| Organism name | Leucophyllum ambiguum | 
|---|---|
| Genus | Leucophyllum | 
| Family | Scrophulariaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Leucophyllum | 
|---|---|
| Linked NCBI taxonomy ID | 69911 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Scrophulariaceae | 
|---|---|
| ID | 4149 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | asterids | 
|---|---|
| ID | 71274 | 
| KNApSAcK ID | name | ChEMBL link | CTD link | 
                        # of proteins in
                         ChEMBL interaction / related OMIM / related KEGG DISEASE  | 
                      
                        # of genes in
                         CTD interaction / related diseases  | 
                      
                        KCF-S
                         cluster  | 
                      
                        phytochemical
                         cluster  | 
                      figure | 
|---|---|---|---|---|---|---|---|---|
| 
                        C00001017
                        
                           | 
                      
                        Cosmosiin
                         / Apigenin 7-glucoside / (-)-Apigenin 7-glucoside / Apigenin 7-O-beta-D-glucopyranoside  | 
                      
                        CHEMBL487995
                         CHEMBL487017 CHEMBL1591566 CHEMBL2165585  | 
                      
                        C057792
                         | 
                      5 / 6 / 1 | No. 2 | No. 15 | 
                         
                       | 
                    |
| 
                        C00000643
                        
                           | 
                      
                        Kobusin
                         / (+)-Kobusin / (+)-Spinescin / Methylpiperitol  | 
                      
                        CHEMBL462822
                         | 
                      No. 38 | No. 21 | 
                         
                       | 
                    |||
| 
                        C00003817
                        
                           | 
                      
                        Apigenin
                         / 5,7,4'-Trihydroxyflavone  | 
                      
                        CHEMBL28
                         | 
                      
                        D047310
                         | 
                      164 / 119 / 105 | 68 / 8 | No. 71 | No. 15 | 
                         
                       | 
                    
| 
                        C00000170
                        
                           | 
                      
                        trans-Cinnamate
                         / trans-Cinnamic acid  | 
                      
                        CHEMBL27246
                         | 
                      5 / 2 / 2 | No. 904 | No. 6 | 
                         
                       | 
                    
| accession | description | class description | KNApSAcK metabolite in interactions | 
                          # of diseases
                           (OMIM / KEGG)  | 
                      
|---|---|---|---|---|
| Q16637 | Survival motor neuron protein | Unclassified protein | C00001017 C00003817 | 4 / 1 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00001017 C00003817 | 0 / 0 | 
| P03372 | Estrogen receptor | NR3A1 | C00000170 C00003817 | 1 / 1 | 
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00001017 C00003817 | 2 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00001017 C00003817 | 0 / 0 | 
| P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00000170 C00003817 | 1 / 1 | 
| Q9Y4K4 | Mitogen-activated protein kinase kinase kinase kinase 5 | STE serine/threonine protein kinase KHS subfamily | C00003817 | 0 / 0 | 
| Q9NPH5 | NADPH oxidase 4 | Enzyme | C00003817 | 0 / 0 | 
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003817 | 1 / 0 | 
| Q9HAW8 | UDP-glucuronosyltransferase 1-10 | Enzyme | C00003817 | 0 / 0 | 
| Q99700 | Ataxin-2 | Unclassified protein | C00003817 | 1 / 1 | 
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003817 | 2 / 0 | 
| P14618 | Pyruvate kinase PKM | Enzyme | C00003817 | 0 / 0 | 
| P27338 | Amine oxidase [flavin-containing] B | Oxidoreductase | C00003817 | 0 / 0 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00003817 | 0 / 3 | 
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00003817 | 0 / 0 | 
| Q15759 | Mitogen-activated protein kinase 11 | p38 | C00003817 | 0 / 0 | 
| Q16539 | Mitogen-activated protein kinase 14 | p38 | C00003817 | 0 / 0 | 
| O15530 | 3-phosphoinositide-dependent protein kinase 1 | Pdk1 | C00003817 | 0 / 0 | 
| P04062 | Glucosylceramidase | Enzyme | C00003817 | 6 / 4 | 
| P41240 | Tyrosine-protein kinase CSK | Csk | C00003817 | 0 / 0 | 
| P17252 | Protein kinase C alpha type | Alpha | C00003817 | 0 / 0 | 
| Q03181 | Peroxisome proliferator-activated receptor delta | NR1C2 | C00003817 | 0 / 0 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00003817 | 0 / 0 | 
| O14757 | Serine/threonine-protein kinase Chk1 | Chk1 | C00003817 | 0 / 0 | 
| O95271 | Tankyrase-1 | Enzyme | C00003817 | 0 / 0 | 
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00003817 | 0 / 0 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00003817 | 11 / 10 | 
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00003817 | 3 / 2 | 
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00000170 | 0 / 0 | 
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00003817 | 3 / 1 | 
| P19793 | Retinoic acid receptor RXR-alpha | NR2B1 | C00003817 | 0 / 0 | 
| P68400 | Casein kinase II subunit alpha | Ck2 | C00003817 | 0 / 0 | 
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00003817 | 1 / 1 | 
| Q00534 | Cyclin-dependent kinase 6 | CMGC serine/threonine protein kinase family | C00003817 | 1 / 0 | 
| P11309 | Serine/threonine-protein kinase pim-1 | Pim | C00003817 | 0 / 0 | 
| P04798 | Cytochrome P450 1A1 | Cytochrome P450 1A1 | C00003817 | 0 / 0 | 
| P08183 | Multidrug resistance protein 1 | drug | C00003817 | 1 / 0 | 
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00003817 | 0 / 0 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003817 | 0 / 1 | 
| P23443 | Ribosomal protein S6 kinase beta-1 | p70 | C00003817 | 0 / 0 | 
| Q00535 | Cyclin-dependent kinase 5 | Cdk5 | C00003817 | 0 / 0 | 
| Q15078 | Cyclin-dependent kinase 5 activator 1 | REG serine/threonine protein kinase family | C00003817 | 0 / 0 | 
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00003817 | 1 / 8 | 
| P11388 | DNA topoisomerase 2-alpha | Isomerase | C00003817 | 0 / 0 | 
| P11473 | Vitamin D3 receptor | NR1I1 | C00003817 | 2 / 3 | 
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00003817 | 0 / 0 | 
| P41145 | Kappa-type opioid receptor | Opioid receptor | C00003817 | 0 / 0 | 
| O75582 | Ribosomal protein S6 kinase alpha-5 | CAMK serine/threonine protein kinase MSKB subfamily | C00003817 | 0 / 0 | 
| Q9Y3R4 | Sialidase-2 | Enzyme | C00003817 | 0 / 0 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00003817 | 0 / 0 | 
| P68871 | Hemoglobin subunit beta | Secreted protein | C00003817 | 4 / 4 | 
| P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | C00003817 | 1 / 1 | 
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00003817 | 0 / 0 | 
| Q8TDS4 | Hydroxycarboxylic acid receptor 2 | Hydroxycarboxylic acid receptor | C00000170 | 0 / 0 | 
| P09769 | Tyrosine-protein kinase Fgr | Src | C00003817 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00003817 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003817 | 2 / 0 | 
| O75496 | Geminin | Unclassified protein | C00003817 | 0 / 0 | 
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00003817 | 4 / 2 | 
| P54855 | UDP-glucuronosyltransferase 2B15 | Enzyme | C00003817 | 0 / 0 | 
| P41143 | Delta-type opioid receptor | Opioid receptor | C00003817 | 0 / 0 | 
| Q92731 | Estrogen receptor beta | NR3A2 | C00003817 | 0 / 1 | 
| P15121 | Aldose reductase | Enzyme | C00000170 | 0 / 0 | 
| P10145 | Interleukin-8 | Secreted protein | C00003817 | 0 / 0 | 
| P49841 | Glycogen synthase kinase-3 beta | Gsk | C00003817 | 0 / 0 | 
| Q15418 | Ribosomal protein S6 kinase alpha-1 | Rskb | C00003817 | 0 / 0 | 
| O15264 | Mitogen-activated protein kinase 13 | p38 | C00003817 | 0 / 0 | 
| P09874 | Poly [ADP-ribose] polymerase 1 | Enzyme | C00003817 | 0 / 0 | 
| Q12791 | Calcium-activated potassium channel subunit alpha-1 | KCNM, KCa1.x | C00003817 | 1 / 1 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00003817 | 1 / 1 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001017 | 0 / 0 | 
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00003817 | 0 / 0 | 
| P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | C00003817 | 3 / 0 | 
| P04150 | Glucocorticoid receptor | NR3C1 | C00003817 | 0 / 1 | 
| P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00003817 | 2 / 2 | 
| P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00003817 | 5 / 3 | 
| Q16678 | Cytochrome P450 1B1 | Cytochrome P450 1B1 | C00003817 | 4 / 4 | 
| P06276 | Cholinesterase | Hydrolase | C00003817 | 0 / 0 | 
| P49137 | MAP kinase-activated protein kinase 2 | CAMK serine/threonine protein kinase MAPKAPK | C00003817 | 0 / 0 | 
| Q96RI1 | Bile acid receptor | NR1H4 | C00003817 | 0 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00003817 | 0 / 0 | 
| P56817 | Beta-secretase 1 | A1A | C00003817 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003817 | 0 / 0 | 
| P04637 | Cellular tumor antigen p53 | Transcription Factor | C00003817 | 7 / 37 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00003817 | 3 / 3 | 
| P33527 | Multidrug resistance-associated protein 1 | drugs | C00003817 | 0 / 0 | 
| Q92887 | Canalicular multispecific organic anion transporter 1 | Unclassified protein | C00003817 | 1 / 1 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00003817 | 2 / 2 | 
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003817 | 1 / 1 | 
| Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00003817 | 5 / 2 | 
| P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00003817 | 0 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003817 | 0 / 0 | 
| Q9HAW9 | UDP-glucuronosyltransferase 1-8 | Enzyme | C00003817 | 0 / 0 | 
| Q9H2K2 | Tankyrase-2 | Enzyme | C00003817 | 0 / 0 | 
| O76074 | cGMP-specific 3',5'-cyclic phosphodiesterase | PDE_5A | C00003817 | 0 / 0 | 
| P14061 | Estradiol 17-beta-dehydrogenase 1 | Enzyme | C00003817 | 0 / 0 | 
| P22303 | Acetylcholinesterase | Hydrolase | C00003817 | 1 / 0 | 
| P35372 | Mu-type opioid receptor | Opioid receptor | C00003817 | 0 / 0 | 
| Q8IW41 | MAP kinase-activated protein kinase 5 | CAMK serine/threonine protein kinase MAPKAPK | C00003817 | 0 / 0 | 
| O75116 | Rho-associated protein kinase 2 | Rock | C00003817 | 0 / 0 | 
| P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00003817 | 0 / 0 | 
| P07948 | Tyrosine-protein kinase Lyn | Src | C00003817 | 0 / 0 | 
| Q02880 | DNA topoisomerase 2-beta | Isomerase | C00003817 | 0 / 0 | 
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00003817 | 0 / 0 | 
| P31749 | RAC-alpha serine/threonine-protein kinase | Akt | C00003817 | 4 / 1 | 
| O00141 | Serine/threonine-protein kinase Sgk1 | AGC serine/threonine protein kinase SGK subfamily | C00003817 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003817 | 1 / 1 | 
| P37059 | Estradiol 17-beta-dehydrogenase 2 | Enzyme | C00003817 | 0 / 0 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003817 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00003817 | 0 / 0 | 
| Q15046 | Lysine--tRNA ligase | Enzyme | C00003817 | 2 / 1 | 
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00003817 | 1 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00003817 | 0 / 0 | 
| P22309 | UDP-glucuronosyltransferase 1-1 | Enzyme | C00003817 | 5 / 1 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00003817 | 4 / 3 | 
| Q99549 | M-phase phosphoprotein 8 | Unclassified protein | C00003817 | 0 / 0 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003817 | 0 / 0 | 
| P10275 | Androgen receptor | NR3C4 | C00003817 | 3 / 4 | 
| Q07869 | Peroxisome proliferator-activated receptor alpha | NR1C1 | C00003817 | 0 / 0 | 
| P06239 | Tyrosine-protein kinase Lck | Src | C00003817 | 0 / 1 | 
| P54646 | 5'-AMP-activated protein kinase catalytic subunit alpha-2 | Ampk | C00003817 | 0 / 0 | 
| P35869 | Aryl hydrocarbon receptor | Transcription Factor | C00003817 | 0 / 0 | 
| P43405 | Tyrosine-protein kinase SYK | Syk | C00003817 | 0 / 0 | 
| Q13627 | Dual specificity tyrosine-phosphorylation-regulated kinase 1A | CMGC dual-specificity kinase DYRK1 | C00003817 | 1 / 0 | 
| P53778 | Mitogen-activated protein kinase 12 | p38 | C00003817 | 0 / 0 | 
| Q02750 | Dual specificity mitogen-activated protein kinase kinase 1 | Ste7 | C00003817 | 1 / 1 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00003817 | 0 / 0 | 
| P40225 | Thrombopoietin | Unclassified protein | C00003817 | 1 / 1 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00003817 | 1 / 1 | 
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003817 | 1 / 0 | 
| O00255 | Menin | Unclassified protein | C00003817 | 2 / 5 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00003817 | 1 / 2 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00003817 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00003817 | 1 / 4 | 
| Q9UN88 | Gamma-aminobutyric acid receptor subunit theta | GABA-A theta | C00003817 | 0 / 0 | 
| P28472 | Gamma-aminobutyric acid receptor subunit beta-3 | GABA-A beta | C00003817 | 1 / 0 | 
| P14867 | Gamma-aminobutyric acid receptor subunit alpha-1 | GABA-A alpha | C00003817 | 1 / 1 | 
| P48169 | Gamma-aminobutyric acid receptor subunit alpha-4 | GABA-A alpha | C00003817 | 0 / 0 | 
| O14764 | Gamma-aminobutyric acid receptor subunit delta | GABA-A delta | C00003817 | 1 / 1 | 
| P31644 | Gamma-aminobutyric acid receptor subunit alpha-5 | GABA-A alpha | C00003817 | 0 / 0 | 
| Q99928 | Gamma-aminobutyric acid receptor subunit gamma-3 | GABA-A gamma | C00003817 | 0 / 0 | 
| P78334 | Gamma-aminobutyric acid receptor subunit epsilon | GABA-A epsilon | C00003817 | 0 / 0 | 
| Q8N1C3 | Gamma-aminobutyric acid receptor subunit gamma-1 | GABA-A gamma | C00003817 | 0 / 0 | 
| P34903 | Gamma-aminobutyric acid receptor subunit alpha-3 | GABA-A alpha | C00003817 | 0 / 0 | 
| O00591 | Gamma-aminobutyric acid receptor subunit pi | GABA-A pi | C00003817 | 0 / 0 | 
| P47870 | Gamma-aminobutyric acid receptor subunit beta-2 | GABA-A beta | C00003817 | 0 / 0 | 
| P18507 | Gamma-aminobutyric acid receptor subunit gamma-2 | GABA-A gamma | C00003817 | 4 / 2 | 
| P18505 | Gamma-aminobutyric acid receptor subunit beta-1 | GABA-A beta | C00003817 | 0 / 0 | 
| Q16445 | Gamma-aminobutyric acid receptor subunit alpha-6 | GABA-A alpha | C00003817 | 0 / 0 | 
| P47869 | Gamma-aminobutyric acid receptor subunit alpha-2 | GABA-A alpha | C00003817 | 1 / 0 | 
| P45983 | Mitogen-activated protein kinase 8 | Jnk | C00003817 | 0 / 0 | 
| P53779 | Mitogen-activated protein kinase 10 | Jnk | C00003817 | 0 / 1 | 
| P45984 | Mitogen-activated protein kinase 9 | Jnk | C00003817 | 0 / 0 | 
| O95067 | G2/mitotic-specific cyclin-B2 | Other cytosolic protein | C00003817 | 0 / 0 | 
| P14635 | G2/mitotic-specific cyclin-B1 | Other cytosolic protein | C00003817 | 0 / 0 | 
| P06493 | Cyclin-dependent kinase 1 | Cdc2 | C00003817 | 0 / 0 | 
| Q8WWL7 | G2/mitotic-specific cyclin-B3 | Other cytosolic protein | C00003817 | 0 / 0 | 
| P22694 | cAMP-dependent protein kinase catalytic subunit beta | Pka | C00003817 | 0 / 0 | 
| P17612 | cAMP-dependent protein kinase catalytic subunit alpha | Pka | C00003817 | 0 / 0 | 
| P22612 | cAMP-dependent protein kinase catalytic subunit gamma | Pka | C00003817 | 0 / 0 | 
| P49840 | Glycogen synthase kinase-3 alpha | Gsk | C00003817 | 0 / 0 | 
| Q9HCP0 | Casein kinase I isoform gamma-1 | Ck1 | C00003817 | 0 / 0 | 
| P48730 | Casein kinase I isoform delta | Ck1 | C00003817 | 1 / 0 | 
| P49674 | Casein kinase I isoform epsilon | Ck1 | C00003817 | 0 / 0 | 
| P78368 | Casein kinase I isoform gamma-2 | Ck1 | C00003817 | 0 / 0 | 
| P48729 | Casein kinase I isoform alpha | Ck1 | C00003817 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00003817 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 4363 | ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 | ATP-binding cassette, sub-family C (CFTR/MRP), member 1 | 
                          C00003817
                           | 
                      
| 196 | AHR, bHLHe76 | aryl hydrocarbon receptor | 
                          C00003817
                           | 
                      
| 207 | AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA | v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) | 
                          C00003817
                           | 
                      
| 405 | ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 | aryl hydrocarbon receptor nuclear translocator | 
                          C00003817
                           | 
                      
| 596 | BCL2, Bcl-2, PPP1R50 | B-cell CLL/lymphoma 2 | 
                          C00003817
                           | 
                      
| 330 | BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 | baculoviral IAP repeat containing 3 | 
                          C00003817
                           | 
                      
| 836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) | 
                          C00003817
                           | 
                      
| 840 | CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 | caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) | 
                          C00003817
                           | 
                      
| 841 | CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 | caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) | 
                          C00003817
                           | 
                      
| 842 | CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 | caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) | 
                          C00003817
                           | 
                      
| 847 | CAT | catalase (EC:1.11.1.6) | 
                          C00003817
                           | 
                      
| 891 | CCNB1, CCNB | cyclin B1 | 
                          C00003817
                           | 
                      
| 958 | CD40, Bp50, CDW40, TNFRSF5, p50 | CD40 molecule, TNF receptor superfamily member 5 | 
                          C00003817
                           | 
                      
| 983 | CDK1, CDC2, CDC28A, P34CDC2 | cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) | 
                          C00003817
                           | 
                      
| 1026 | CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | cyclin-dependent kinase inhibitor 1A (p21, Cip1) | 
                          C00003817
                           | 
                      
| 1031 | CDKN2C, INK4C, p18, p18-INK4C | cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) | 
                          C00003817
                           | 
                      
| 1080 | CFTR, ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1 | cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (EC:3.6.3.49) | 
                          C00003817
                           | 
                      
| 6387 | CXCL12, IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1, SDF1A, SDF1B | chemokine (C-X-C motif) ligand 12 | 
                          C00003817
                           | 
                      
| 54205 | CYCS, CYC, HCS, THC4 | cytochrome c, somatic | 
                          C00003817
                           | 
                      
| 1584 | CYP11B1, CPN1, CYP11B, FHI, P450C11 | cytochrome P450, family 11, subfamily B, polypeptide 1 (EC:1.14.15.4) | 
                          C00003817
                           | 
                      
| 1586 | CYP17A1, CPT7, CYP17, P450C17, S17AH | cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) | 
                          C00003817
                           | 
                      
| 1588 | CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM | cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) | 
                          C00003817
                           | 
                      
| 1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) | 
                          C00003817
                           | 
                      
| 1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) | 
                          C00003817
                           | 
                      
| 1545 | CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 | cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) | 
                          C00003817
                           | 
                      
| 1589 | CYP21A2, CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B | cytochrome P450, family 21, subfamily A, polypeptide 2 (EC:1.14.99.10) | 
                          C00003817
                           | 
                      
| 1559 | CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 | cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) | 
                          C00003817
                           | 
                      
| 1576 | CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 | cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) | 
                          C00003817
                           | 
                      
| 2064 | ERBB2, CD340, HER-2, HER-2/neu, HER2, MLN_19, NEU, NGL, TKR1 | v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (EC:2.7.10.1) | 
                          C00003817
                           | 
                      
| 2099 | ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 | estrogen receptor 1 | 
                          C00003817
                           | 
                      
| 2100 | ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 | estrogen receptor 2 (ER beta) | 
                          C00003817
                           | 
                      
| 2203 | FBP1, FBP | fructose-1,6-bisphosphatase 1 (EC:3.1.3.11) | 
                          C00003817
                           | 
                      
| 2353 | FOS, AP-1, C-FOS, p55 | FBJ murine osteosarcoma viral oncogene homolog | 
                          C00003817
                           | 
                      
| 2729 | GCLC, GCL, GCS, GLCL, GLCLC | glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) | 
                          C00003817
                           | 
                      
| 3091 | HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 | hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) | 
                          C00003817
                           | 
                      
| 3284 | HSD3B2, HSD3B, HSDB, SDR11E2 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 (EC:1.1.1.145 5.3.3.1) | 
                          C00003817
                           | 
                      
| 3383 | ICAM1, BB2, CD54, P3.58 | intercellular adhesion molecule 1 | 
                          C00003817
                           | 
                      
| 3565 | IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 | interleukin 4 | 
                          C00003817
                           | 
                      
| 3725 | JUN, AP-1, AP1, c-Jun | jun proto-oncogene | 
                          C00003817
                           | 
                      
| 5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) | 
                          C00003817
                           | 
                      
| 5595 | MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK | mitogen-activated protein kinase 3 (EC:2.7.11.24) | 
                          C00003817
                           | 
                      
| 4312 | MMP1, CLG, CLGN | matrix metallopeptidase 1 (interstitial collagenase) (EC:3.4.24.7) | 
                          C00003817
                           | 
                      
| 4318 | MMP9, CLG4B, GELB, MANDP2, MMP-9 | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) | 
                          C00003817
                           | 
                      
| 4792 | NFKBIA, IKBA, MAD-3, NFKBI | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha | 
                          C00003817
                           | 
                      
| 4793 | NFKBIB, IKBB, TRIP9 | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, beta | 
                          C00003817
                           | 
                      
| 5241 | PGR, NR3C3, PR | progesterone receptor | 
                          C00003817
                           | 
                      
| 5562 | PRKAA1, AMPK, AMPKa1 | protein kinase, AMP-activated, alpha 1 catalytic subunit (EC:2.7.11.1 2.7.11.26 2.7.11.27 2.7.11.31) | 
                          C00003817
                           | 
                      
| 8000 | PSCA, PRO232 | prostate stem cell antigen | 
                          C00003817
                           | 
                      
| 5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A | 
                          C00003817
                           | 
                      
| 6198 | RPS6KB1, PS6K, S6K, S6K-beta-1, S6K1, STK14A, p70_S6KA, p70(S6K)-alpha, p70-S6K, p70-alpha | ribosomal protein S6 kinase, 70kDa, polypeptide 1 (EC:2.7.11.1) | 
                          C00003817
                           | 
                      
| 6401 | SELE, CD62E, ELAM, ELAM1, ESEL, LECAM2 | selectin E | 
                          C00003817
                           | 
                      
| 6817 | SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 | sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) | 
                          C00003817
                           | 
                      
| 6783 | SULT1E1, EST, EST-1, ST1E1, STE | sulfotransferase family 1E, estrogen-preferring, member 1 (EC:2.8.2.4) | 
                          C00003817
                           | 
                      
| 7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor | 
                          C00003817
                           | 
                      
| 7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 | 
                          C00003817
                           | 
                      
| 9540 | TP53I3, PIG3 | tumor protein p53 inducible protein 3 | 
                          C00003817
                           | 
                      
| 8626 | TP63, AIS, B(p51A), B(p51B), EEC3, KET, LMS, NBP, OFC8, RHS, SHFM4, TP53CP, TP53L, TP73L, p40, p51, p53CP, p63, p73H, p73L | tumor protein p63 | 
                          C00003817
                           | 
                      
| 7161 | TP73, P73 | tumor protein p73 | 
                          C00003817
                           | 
                      
| 54658 | UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A | UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 54575 | UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J | UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 54577 | UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G | UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 54576 | UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H | UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 54600 | UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I | UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 7366 | UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 | UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) | 
                          C00003817
                           | 
                      
| 7402 | UTRN, DMDL, DRP, DRP1 | utrophin | 
                          C00003817
                           | 
                      
| 7412 | VCAM1, CD106, INCAM-100 | vascular cell adhesion molecule 1 | 
                          C00003817
                           | 
                      
| 7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A | 
                          C00003817
                           | 
                      
| 8839 | WISP2, CCN5, CT58, CTGF-L | WNT1 inducible signaling pathway protein 2 | 
                          C00003817
                           | 
                      
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | 
                            Q99714
                             | 
                        
| #202300 | Adrenocortical carcinoma, hereditary; adcc | 
                            P04637
                             | 
                        
| #615224 | Advanced sleep phase syndrome, familial, 2; fasps2 | 
                            P48730
                             | 
                        
| #103780 | Alcohol dependence | 
                            P47869
                             | 
                        
| #300068 | Androgen insensitivity syndrome; ais | 
                            P10275
                             | 
                        
| #312300 | Androgen insensitivity, partial; pais | 
                            P10275
                             | 
                        
| #613546 | Aromatase deficiency | 
                            P11511
                             | 
                        
| #139300 | Aromatase excess syndrome; aexs | 
                            P11511
                             | 
                        
| #608584 | Asthma-related traits, susceptibility to, 2 | 
                            Q6W5P4
                             | 
                        
| #614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 | 
                            P04637
                             | 
                        
| #613985 | Beta-thalassemia | 
                            P68871
                             | 
                        
| #603902 | Beta-thalassemia, dominant inclusion body type | 
                            P68871
                             | 
                        
| #601816 | Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 | 
                            P22309
                             | 
                        
| #614490 | Blood group, junior system; jr | 
                            Q9UNQ0
                             | 
                        
| %606641 | Body mass index; bmi | 
                            P37231
                             | 
                        
| #114480 | Breast cancer | 
                            P31749
                             P38398  | 
                        
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 | 
                            P38398
                             | 
                        
| #300615 | Brunner syndrome | 
                            P21397
                             | 
                        
| #615279 | Cardiofaciocutaneous syndrome 3; cfc3 | 
                            Q02750
                             | 
                        
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | 
                            P02545
                             | 
                        
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | 
                            P02545
                             | 
                        
| #609338 | Carotid intimal medial thickness 1 | 
                            P37231
                             | 
                        
| #118300 | Charcot-marie-tooth disease and deafness | 
                            Q01453
                             | 
                        
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | 
                            P02545
                             | 
                        
| #118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a | 
                            Q01453
                             | 
                        
| #613641 | Charcot-marie-tooth disease, recessive intermediate b; cmtrib | 
                            Q15046
                             | 
                        
| #114500 | Colorectal cancer; crc | 
                            P31749
                             P84022  | 
                        
| #615109 | Cowden syndrome 6; cws6 | 
                            P31749
                             | 
                        
| #218800 | Crigler-najjar syndrome, type i | 
                            P22309
                             P22310  | 
                        
| #606785 | Crigler-najjar syndrome, type ii | 
                            P22309
                             P22310  | 
                        
| #613916 | Deafness, autosomal recessive 89; dfnb89 | 
                            Q15046
                             | 
                        
| #119900 | Digital clubbing, isolated congenital | 
                            P15428
                             | 
                        
| #607208 | Dravet syndrome | 
                            P18507
                             | 
                        
| #609535 | Drug metabolism, poor, cyp2c19-related | 
                            P33261
                             | 
                        
| #608902 | Drug metabolism, poor, cyp2d6-related | 
                            P10635
                             | 
                        
| #237500 | Dubin-johnson syndrome; djs | 
                            Q92887
                             | 
                        
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | 
                            P02545
                             | 
                        
| #607681 | Epilepsy, childhood absence, susceptibility to, 2; eca2 | 
                            P18507
                             | 
                        
| #612269 | Epilepsy, childhood absence, susceptibility to, 5; eca5 | 
                            P28472
                             | 
                        
| #613060 | Epilepsy, idiopathic generalized, susceptibility to, 10; eig10 | 
                            O14764
                             | 
                        
| #611136 | Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 | 
                            P14867
                             | 
                        
| #133239 | Esophageal cancer | 
                            P04637
                             | 
                        
| #615363 | Estrogen resistance; estrr | 
                            P03372
                             | 
                        
| #600274 | Frontotemporal dementia; ftd | 
                            P10636
                             | 
                        
| #608013 | Gaucher disease, perinatal lethal | 
                            P04062
                             | 
                        
| #230800 | Gaucher disease, type i | 
                            P04062
                             | 
                        
| #230900 | Gaucher disease, type ii | 
                            P04062
                             | 
                        
| #231000 | Gaucher disease, type iii | 
                            P04062
                             | 
                        
| #231005 | Gaucher disease, type iiic | 
                            P04062
                             | 
                        
| #609446 | Generalized epilepsy and paroxysmal dyskinesia; gepd | 
                            Q12791
                             | 
                        
| #604233 | Generalized epilepsy with febrile seizures plus, type 1; gefsp1 | 
                            P18507
                             | 
                        
| #611277 | Generalized epilepsy with febrile seizures plus, type 3; gefsp3 | 
                            P18507
                             | 
                        
| #143500 | Gilbert syndrome | 
                            P22309
                             P22310  | 
                        
| #137750 | Glaucoma 1, open angle, a; glc1a | 
                            Q16678
                             | 
                        
| #231300 | Glaucoma 3, primary congenital, a; glc3a | 
                            Q16678
                             | 
                        
| #137760 | Glaucoma, primary open angle; poag | 
                            Q16678
                             | 
                        
| #137800 | Glioma susceptibility 1; glm1 | 
                            O75874
                             P37231  | 
                        
| #139393 | Guillain-barre syndrome, familial; gbs | 
                            Q01453
                             | 
                        
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | 
                            Q03164
                             | 
                        
| #610140 | Heart-hand syndrome, slovenian type | 
                            P02545
                             | 
                        
| #140700 | Heinz body anemias | 
                            P68871
                             | 
                        
| #176670 | Hutchinson-gilford progeria syndrome; hgps | 
                            P02545
                             | 
                        
| #237900 | Hyperbilirubinemia, transient familial neonatal; hblrtfn | 
                            P22309
                             | 
                        
| #145000 | Hyperparathyroidism 1; hrpt1 | 
                            O00255
                             | 
                        
| #603373 | Hyperthyroidism, familial gestational | 
                            P16473
                             | 
                        
| #609152 | Hyperthyroidism, nonautoimmune | 
                            P16473
                             | 
                        
| #145900 | Hypertrophic neuropathy of dejerine-sottas | 
                            Q01453
                             | 
                        
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 | 
                            P15428
                             | 
                        
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 | 
                            P16473
                             | 
                        
| #612244 | Inflammatory bowel disease 13; ibd13 | 
                            P08183
                             | 
                        
| #601626 | Leukemia, acute myeloid; aml | 
                            P36888
                             | 
                        
| #151623 | Li-fraumeni syndrome 1; lfs1 | 
                            P04637
                             | 
                        
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | 
                            P02545
                             | 
                        
| #604367 | Lipodystrophy, familial partial, type 3; fpld3 | 
                            P37231
                             | 
                        
| #613795 | Loeys-dietz syndrome, type 3; lds3 | 
                            P84022
                             | 
                        
| #211980 | Lung cancer | 
                            P00533
                             P04637  | 
                        
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada | 
                            P02545
                             | 
                        
| #614104 | Mental retardation, autosomal dominant 7; mrd7 | 
                            Q13627
                             | 
                        
| #300705 | Mental retardation, x-linked 17; mrx17 | 
                            Q99714
                             | 
                        
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 | 
                            Q99714
                             | 
                        
| #131100 | Multiple endocrine neoplasia, type i; men1 | 
                            O00255
                             | 
                        
| #613205 | Muscular dystrophy, congenital, lmna-related | 
                            P02545
                             | 
                        
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | 
                            P02545
                             | 
                        
| #607948 | Mycobacterium tuberculosis, susceptibility to | 
                            P11473
                             | 
                        
| #162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp | 
                            Q01453
                             | 
                        
| #257220 | Niemann-pick disease, type c1; npc1 | 
                            O15118
                             | 
                        
| #601665 | Obesity | 
                            P37231
                             | 
                        
| #167000 | Ovarian cancer | 
                            P38398
                             | 
                        
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 | 
                            P38398
                             | 
                        
| #260500 | Papilloma of choroid plexus; cpp | 
                            P04637
                             | 
                        
| #168600 | Parkinson disease, late-onset; pd | 
                            P04062
                             | 
                        
| #260540 | Parkinson-dementia syndrome | 
                            P10636
                             | 
                        
| #604229 | Peters anomaly | 
                            Q16678
                             | 
                        
| #172700 | Pick disease of brain | 
                            P10636
                             | 
                        
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | 
                            Q01196
                             | 
                        
| #176920 | Proteus syndrome | 
                            P31749
                             | 
                        
| #275210 | Restrictive dermopathy, lethal | 
                            P02545
                             | 
                        
| #604906 | Schizophrenia 9; sczd9 | 
                            P49798
                             | 
                        
| #181500 | Schizophrenia; sczd | 
                            P49798
                             | 
                        
| #603903 | Sickle cell anemia | 
                            P68871
                             | 
                        
| #313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 | 
                            P10275
                             | 
                        
| #253300 | Spinal muscular atrophy, type i; sma1 | 
                            Q16637
                             | 
                        
| #253550 | Spinal muscular atrophy, type ii; sma2 | 
                            Q16637
                             | 
                        
| #253400 | Spinal muscular atrophy, type iii; sma3 | 
                            Q16637
                             | 
                        
| #271150 | Spinal muscular atrophy, type iv; sma4 | 
                            Q16637
                             | 
                        
| #183090 | Spinocerebellar ataxia 2; sca2 | 
                            Q99700
                             | 
                        
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 | 
                            Q9NUW8
                             | 
                        
| #275355 | Squamous cell carcinoma, head and neck; hnscc | 
                            P04637
                             | 
                        
| %612223 | Stature quantitative trait locus 11; stqtl11 | 
                            Q00534
                             | 
                        
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | 
                            P10636
                             | 
                        
| #187950 | Thrombocythemia 1; thcyt1 | 
                            P40225
                             | 
                        
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth | 
                            P10828
                             | 
                        
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth | 
                            P10828
                             | 
                        
| #145650 | Thyroid hormone resistance, selective pituitary; prth | 
                            P10828
                             | 
                        
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 | 
                            Q9UNQ0
                             | 
                        
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a | 
                            P11473
                             | 
                        
| #278300 | Xanthinuria, type i | 
                            P47989
                             | 
                        
| #278750 | Xeroderma pigmentosum, variant type; xpv | 
                            Q9Y253
                             | 
                        
| #112100 | Yt blood group antigen | 
                            P22303
                             | 
                        
| KEGG | name | UniProt | 
|---|---|---|
| H00033 | Adrenal carcinoma | 
                            O00255
                            (related)
                             P04637 (related)  | 
                        
| H00034 | Carcinoid | 
                            O00255
                            (related)
                             | 
                        
| H00045 | Malignant islet cell carcinoma | 
                            O00255
                            (related)
                             | 
                        
| H00246 | Primary hyperparathyroidism | 
                            O00255
                            (related)
                             | 
                        
| H01102 | Pituitary adenomas | 
                            O00255
                            (related)
                             | 
                        
| H00783 | Febrile seizures | 
                            O14764
                            (related)
                             P18507 (related)  | 
                        
| H00136 | Niemann-Pick disease type C (NPC) | 
                            O15118
                            (related)
                             | 
                        
| H00016 | Oral cancer | 
                            P00533
                            (related)
                             P00533 (marker) P04637 (related) P04637 (marker)  | 
                        
| H00017 | Esophageal cancer | 
                            P00533
                            (related)
                             P04637 (related) P04637 (marker) P35354 (related)  | 
                        
| H00018 | Gastric cancer | 
                            P00533
                            (related)
                             P04637 (related)  | 
                        
| H00022 | Bladder cancer | 
                            P00533
                            (related)
                             P04637 (related) P68871 (marker)  | 
                        
| H00028 | Choriocarcinoma | 
                            P00533
                            (related)
                             P04637 (related)  | 
                        
| H00030 | Cervical cancer | 
                            P00533
                            (related)
                             | 
                        
| H00042 | Glioma | 
                            P00533
                            (related)
                             P00533 (marker) P04637 (related) P04637 (marker)  | 
                        
| H00055 | Laryngeal cancer | 
                            P00533
                            (related)
                             P00533 (marker) P04637 (related) P04637 (marker)  | 
                        
| H00264 | Charcot-Marie-Tooth disease (CMT) | 
                            P02545
                            (related)
                             Q01453 (related) Q15046 (related)  | 
                        
| H00294 | Dilated cardiomyopathy (DCM) | 
                            P02545
                            (related)
                             | 
                        
| H00420 | Familial partial lipodystrophy (FPL) | 
                            P02545
                            (related)
                             P37231 (related)  | 
                        
| H00563 | Emery-Dreifuss muscular dystrophy | 
                            P02545
                            (related)
                             | 
                        
| H00590 | Congenital muscular dystrophies (CMD/MDC) | 
                            P02545
                            (related)
                             | 
                        
| H00593 | Limb-girdle muscular dystrophy (LGMD) | 
                            P02545
                            (related)
                             | 
                        
| H00601 | Hutchinson-Gilford progeria syndrome | 
                            P02545
                            (related)
                             | 
                        
| H00663 | Restrictive dermopathy | 
                            P02545
                            (related)
                             | 
                        
| H00665 | Mandibuloacral dysplasia | 
                            P02545
                            (related)
                             | 
                        
| H01216 | Left ventricular noncompaction (LVNC) | 
                            P02545
                            (related)
                             | 
                        
| H00026 | Endometrial Cancer | 
                            P03372
                            (marker)
                             P04637 (related) Q92731 (marker)  | 
                        
| H00066 | Lewy body dementia (LBD) | 
                            P04062
                            (related)
                             | 
                        
| H00126 | Gaucher disease | 
                            P04062
                            (related)
                             | 
                        
| H00426 | Defects in the degradation of ganglioside | 
                            P04062
                            (related)
                             | 
                        
| H00810 | Progressive myoclonic epilepsy (PME) | 
                            P04062
                            (related)
                             | 
                        
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) | 
                            P04150
                            (related)
                             P11511 (related)  | 
                        
| H00004 | Chronic myeloid leukemia (CML) | 
                            P04637
                            (related)
                             Q01196 (related)  | 
                        
| H00005 | Chronic lymphocytic leukemia (CLL) | 
                            P04637
                            (related)
                             | 
                        
| H00006 | Hairy-cell leukemia | 
                            P04637
                            (related)
                             | 
                        
| H00008 | Burkitt lymphoma | 
                            P04637
                            (related)
                             | 
                        
| H00009 | Adult T-cell leukemia | 
                            P04637
                            (related)
                             | 
                        
| H00010 | Multiple myeloma | 
                            P04637
                            (related)
                             | 
                        
| H00013 | Small cell lung cancer | 
                            P04637
                            (related)
                             | 
                        
| H00014 | Non-small cell lung cancer | 
                            P04637
                            (related)
                             | 
                        
| H00015 | Malignant pleural mesothelioma | 
                            P04637
                            (related)
                             | 
                        
| H00019 | Pancreatic cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00020 | Colorectal cancer | 
                            P04637
                            (related)
                             P04637 (marker) P68871 (marker)  | 
                        
| H00025 | Penile cancer | 
                            P04637
                            (related)
                             P04637 (marker) P35354 (related)  | 
                        
| H00027 | Ovarian cancer | 
                            P04637
                            (related)
                             P38398 (related)  | 
                        
| H00029 | Vulvar cancer | 
                            P04637
                            (related)
                             | 
                        
| H00031 | Breast cancer | 
                            P04637
                            (related)
                             P38398 (related)  | 
                        
| H00032 | Thyroid cancer | 
                            P04637
                            (related)
                             P37231 (related)  | 
                        
| H00036 | Osteosarcoma | 
                            P04637
                            (related)
                             P08684 (marker)  | 
                        
| H00038 | Malignant melanoma | 
                            P04637
                            (related)
                             | 
                        
| H00039 | Basal cell carcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00040 | Squamous cell carcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00041 | Kaposi's sarcoma | 
                            P04637
                            (related)
                             | 
                        
| H00044 | Cancer of the anal canal | 
                            P04637
                            (related)
                             | 
                        
| H00046 | Cholangiocarcinoma | 
                            P04637
                            (related)
                             P35354 (related)  | 
                        
| H00047 | Gallbladder cancer | 
                            P04637
                            (related)
                             | 
                        
| H00048 | Hepatocellular carcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00881 | Li-Fraumeni syndrome | 
                            P04637
                            (related)
                             | 
                        
| H01007 | Choroid plexus papilloma | 
                            P04637
                            (related)
                             | 
                        
| H00021 | Renal cell carcinoma | 
                            P04637
                            (marker)
                             | 
                        
| H00093 | Combined immunodeficiencies (CIDs) | 
                            P06239
                            (related)
                             | 
                        
| H00024 | Prostate cancer | 
                            P10275
                            (related)
                             | 
                        
| H00062 | Spinal and bulbar muscular atrophy (SBMA) | 
                            P10275
                            (related)
                             | 
                        
| H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) | 
                            P10275
                            (related)
                             | 
                        
| H00609 | 46,XY disorders of sex development (Other) | 
                            P10275
                            (related)
                             | 
                        
| H00058 | Amyotrophic lateral sclerosis (ALS) | 
                            P10636
                            (related)
                             | 
                        
| H00077 | Progressive supranuclear palsy (PSP) | 
                            P10636
                            (related)
                             | 
                        
| H00078 | Frontotemporal lobar degeneration (FTLD) | 
                            P10636
                            (related)
                             | 
                        
| H00249 | Thyroid hormone resistance syndrome | 
                            P10828
                            (related)
                             | 
                        
| H00342 | Tuberculosis | 
                            P11473
                            (related)
                             | 
                        
| H00784 | Localized autosomal recessive hypotrichosis | 
                            P11473
                            (related)
                             | 
                        
| H01143 | Vitamin D-dependent rickets | 
                            P11473
                            (related)
                             | 
                        
| H00794 | Aromatase excess syndrome | 
                            P11511
                            (related)
                             | 
                        
| H01205 | Coumarin resistance | 
                            P11712
                            (related)
                             | 
                        
| H00808 | Idiopathic generalized epilepsies (IGEs) | 
                            P14867
                            (related)
                             P18507 (related)  | 
                        
| H00457 | Primary hypertrophic osteoarthropathy (PHO) | 
                            P15428
                            (related)
                             | 
                        
| H01246 | Isolated congenital nail clubbing (ICNC) | 
                            P15428
                            (related)
                             | 
                        
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) | 
                            P16473
                            (related)
                             | 
                        
| H01269 | Congenital hyperthyroidism | 
                            P16473
                            (related)
                             | 
                        
| H00548 | Brunner syndrome | 
                            P21397
                            (related)
                             | 
                        
| H00208 | Hyperbilirubinemia | 
                            P22309
                            (related)
                             Q92887 (related)  | 
                        
| H00539 | PTEN hamartoma tumor syndrome (PHTS) | 
                            P31749
                            (related)
                             | 
                        
| H01171 | Poor drug metabolism (PM) | 
                            P33261
                            (related)
                             | 
                        
| H00003 | Acute myeloid leukemia (AML) | 
                            P36888
                            (related)
                             Q01196 (related) Q01196 (marker) Q13951 (marker)  | 
                        
| H00409 | Type II diabetes mellitus | 
                            P37231
                            (related)
                             | 
                        
| H00227 | Congenital amegakaryocytic thrombocytopenia (CAMT) | 
                            P40225
                            (marker)
                             | 
                        
| H00192 | Xanthinuria | 
                            P47989
                            (related)
                             | 
                        
| H00606 | Early infantile epileptic encephalopathy | 
                            P53779
                            (related)
                             | 
                        
| H00228 | Thalassemia | 
                            P68871
                            (related)
                             | 
                        
| H00229 | Sickle cell anemia (SCA) | 
                            P68871
                            (related)
                             | 
                        
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | 
                            Q01196
                            (related)
                             Q01196 (marker) Q03164 (related) Q03164 (marker)  | 
                        
| H00978 | Thrombocytopenia (THC) | 
                            Q01196
                            (related)
                             | 
                        
| H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) | 
                            Q01453
                            (related)
                             | 
                        
| H00523 | Noonan syndrome and related disorders | 
                            Q02750
                            (related)
                             | 
                        
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | 
                            Q03164
                            (related)
                             | 
                        
| H01258 | Generalized epilepsy and paroxysmal dyskinesia (GEPD) | 
                            Q12791
                            (related)
                             | 
                        
| H00455 | Spinal muscular atrophy (SMA) | 
                            Q16637
                            (related)
                             | 
                        
| H00612 | Primary open angle glaucoma | 
                            Q16678
                            (related)
                             | 
                        
| H01075 | Peters anomaly | 
                            Q16678
                            (related)
                             | 
                        
| H01159 | Anterior segment dysgenesis (ASD) | 
                            Q16678
                            (related)
                             | 
                        
| H01203 | Primary congenital glaucoma (PCG) | 
                            Q16678
                            (related)
                             | 
                        
| H00063 | Spinocerebellar ataxia (SCA) | 
                            Q99700
                            (related)
                             Q9NUW8 (related)  | 
                        
| H00480 | Non-syndromic X-linked mental retardation | 
                            Q99714
                            (related)
                             | 
                        
| H00658 | Syndromic X-linked mental retardation | 
                            Q99714
                            (related)
                             | 
                        
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency | 
                            Q99714
                            (related)
                             | 
                        
| H00403 | Disorders of nucleotide excision repair | 
                            Q9Y253
                            (related)
                             | 
                        
| MESH or OMIM | name | 
                            KNApSAcK
                             metabolite  | 
                        
|---|---|---|
| D000257 | Adenoviridae Infections | 
                            C00003817
                             | 
                        
| D001943 | Breast Neoplasms | 
                            C00003817
                             | 
                        
| D003110 | Colonic Neoplasms | 
                            C00003817
                             | 
                        
| D056486 | Drug-Induced Liver Injury | 
                            C00003817
                             | 
                        
| D009361 | Neoplasm Invasiveness | 
                            C00003817
                             | 
                        
| D009362 | Neoplasm Metastasis | 
                            C00003817
                             | 
                        
| D011041 | Poisoning | 
                            C00003817
                             | 
                        
| D011471 | Prostatic Neoplasms | 
                            C00003817
                             |