| Organism name | Carex brevicollis DC. | 
|---|---|
| Genus | Carex | 
| Family | Cyperaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Carex brevicollis | 
|---|---|
| Linked NCBI taxonomy ID | 140793 | 
| Linked level | species | 
| Family in NCBI taxonomy | Cyperaceae | 
|---|---|
| ID | 4609 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | Liliopsida | 
|---|---|
| ID | 4447 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| 
                        C00001736
                        
                           | 
                      
                        Harman
                         / Harmane / Indoter / Locuturin / Zygofabagine  | 
                      
                        CHEMBL12014
                         | 
                      
                        C005010
                         | 
                      109 / 46 / 33 | 2 / 2 | No. 1889 | No. 4 | 
                         
                       | 
                    
| 
                        C00001737
                        
                           | 
                      
                        Harmine
                         | 
                      
                        CHEMBL269538
                         | 
                      
                        D006247
                         | 
                      150 / 45 / 26 | 3 / 5 | No. 1889 | No. 4 | 
                         
                       | 
                    
| 
                        C00042574
                        
                           | 
                      
                        Harmol
                         | 
                      
                        CHEMBL14285
                         | 
                      
                        C001326
                         | 
                      30 / 38 / 70 | 3 / 0 | No. 1889 | No. 4 | 
                         
                       | 
                    
| accession | description | class description | KNApSAcK metabolite in interactions | 
                          # of diseases
                           (OMIM / KEGG)  | 
                      
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001736 C00001737 C00042574 | 1 / 0 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001736 C00001737 C00042574 | 3 / 3 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00001736 C00001737 C00042574 | 2 / 2 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00001736 C00001737 C00042574 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001736 C00001737 C00042574 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001736 C00001737 C00042574 | 0 / 1 | 
| Q00535 | Cyclin-dependent kinase 5 | Cdk5 | C00001736 C00001737 C00042574 | 0 / 0 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001736 C00001737 C00042574 | 0 / 1 | 
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00001736 C00001737 C00042574 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001736 C00001737 C00042574 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001736 C00001737 C00042574 | 0 / 0 | 
| O43781 | Dual specificity tyrosine-phosphorylation-regulated kinase 3 | CMGC dual-specificity kinase DYRK2 | C00001736 C00001737 | 0 / 0 | 
| Q15759 | Mitogen-activated protein kinase 11 | p38 | C00001736 C00001737 | 0 / 0 | 
| Q16539 | Mitogen-activated protein kinase 14 | p38 | C00001736 C00001737 | 0 / 0 | 
| Q8TD08 | Mitogen-activated protein kinase 15 | Mapk | C00001736 C00001737 | 0 / 0 | 
| O15530 | 3-phosphoinositide-dependent protein kinase 1 | Pdk1 | C00001736 C00001737 | 0 / 0 | 
| O00418 | Eukaryotic elongation factor 2 kinase | Atypical serine/threonine protein kinase alpha subfamily | C00001736 C00001737 | 0 / 0 | 
| P41240 | Tyrosine-protein kinase CSK | Csk | C00001736 C00001737 | 0 / 0 | 
| P45984 | Mitogen-activated protein kinase 9 | Jnk | C00001736 C00001737 | 0 / 0 | 
| P17252 | Protein kinase C alpha type | Alpha | C00001736 C00001737 | 0 / 0 | 
| P27361 | Mitogen-activated protein kinase 3 | Erk | C00001736 C00001737 | 0 / 0 | 
| O14757 | Serine/threonine-protein kinase Chk1 | Chk1 | C00001736 C00001737 | 0 / 0 | 
| Q8IWQ3 | Serine/threonine-protein kinase BRSK2 | CAMK serine/threonine protein kinase BRSK subfamily | C00001736 C00001737 | 0 / 0 | 
| P27448 | MAP/microtubule affinity-regulating kinase 3 | CAMK serine/threonine protein kinase MARK subfamily | C00001736 C00001737 | 0 / 0 | 
| P53778 | Mitogen-activated protein kinase 12 | p38 | C00001736 C00001737 | 0 / 0 | 
| Q13627 | Dual specificity tyrosine-phosphorylation-regulated kinase 1A | CMGC dual-specificity kinase DYRK1 | C00001736 C00001737 | 1 / 0 | 
| P17612 | cAMP-dependent protein kinase catalytic subunit alpha | Pka | C00001736 C00001737 | 0 / 0 | 
| Q14012 | Calcium/calmodulin-dependent protein kinase type 1 | Camk1 | C00001736 C00001737 | 0 / 0 | 
| O96017 | Serine/threonine-protein kinase Chk2 | Rad53 | C00001736 C00001737 | 4 / 1 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00001737 C00042574 | 0 / 0 | 
| P20248 | Cyclin-A2 | Other cytosolic protein | C00001736 C00001737 | 0 / 0 | 
| Q05513 | Protein kinase C zeta type | Iota | C00001736 C00001737 | 0 / 0 | 
| Q9H2X6 | Homeodomain-interacting protein kinase 2 | CMGC dual-specificity kinase HIPK | C00001736 C00001737 | 0 / 0 | 
| P11309 | Serine/threonine-protein kinase pim-1 | Pim | C00001736 C00001737 | 0 / 0 | 
| P78396 | Cyclin-A1 | Other cytosolic protein | C00001736 C00001737 | 0 / 0 | 
| Q9HC98 | Serine/threonine-protein kinase Nek6 | Nek | C00001736 C00001737 | 0 / 0 | 
| P68400 | Casein kinase II subunit alpha | Ck2 | C00001736 C00001737 | 0 / 0 | 
| P23443 | Ribosomal protein S6 kinase beta-1 | p70 | C00001736 C00001737 | 0 / 0 | 
| Q8TDX7 | Serine/threonine-protein kinase Nek7 | Nek | C00001736 C00001737 | 0 / 0 | 
| Q9UQB9 | Aurora kinase C | Aur | C00001736 C00001737 | 1 / 1 | 
| Q9P1W9 | Serine/threonine-protein kinase pim-2 | Pim | C00001736 C00001737 | 0 / 0 | 
| Q9HBH9 | MAP kinase-interacting serine/threonine-protein kinase 2 | CAMK serine/threonine protein kinase MNK subfamily | C00001736 C00001737 | 0 / 0 | 
| Q9NQU5 | Serine/threonine-protein kinase PAK 6 | STE serine/threonine protein kinase PAKB subfamily | C00001736 C00001737 | 0 / 0 | 
| Q16644 | MAP kinase-activated protein kinase 3 | CAMK serine/threonine protein kinase MAPKAPK | C00001736 C00001737 | 0 / 0 | 
| Q9H422 | Homeodomain-interacting protein kinase 3 | CMGC dual-specificity kinase HIPK | C00001736 C00001737 | 0 / 0 | 
| Q14680 | Maternal embryonic leucine zipper kinase | Melk | C00001736 C00001737 | 0 / 0 | 
| P19784 | Casein kinase II subunit alpha' | Ck2 | C00001736 C00001737 | 0 / 0 | 
| P51812 | Ribosomal protein S6 kinase alpha-3 | Rskb | C00001736 C00001737 | 2 / 2 | 
| Q15746 | Myosin light chain kinase, smooth muscle | Mlck | C00001736 C00001737 | 1 / 1 | 
| Q13188 | Serine/threonine-protein kinase 3 | STE serine/threonine protein kinase MST subfamily | C00001736 C00001737 | 0 / 0 | 
| P31751 | RAC-beta serine/threonine-protein kinase | Akt | C00001736 C00001737 | 2 / 2 | 
| O75582 | Ribosomal protein S6 kinase alpha-5 | CAMK serine/threonine protein kinase MSKB subfamily | C00001736 C00001737 | 0 / 0 | 
| O14920 | Inhibitor of nuclear factor kappa-B kinase subunit beta | Other serine/threonine protein kinase | C00001736 C00001737 | 0 / 0 | 
| Q16513 | Serine/threonine-protein kinase N2 | Pkn | C00001736 C00001737 | 0 / 0 | 
| Q15139 | Serine/threonine-protein kinase D1 | Pkd | C00001736 C00001737 | 0 / 0 | 
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00001736 C00001737 | 0 / 0 | 
| P67870 | Casein kinase II subunit beta | REG serine/threonine protein kinase family | C00001736 C00001737 | 0 / 0 | 
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00001737 C00042574 | 2 / 2 | 
| Q8N5S9 | Calcium/calmodulin-dependent protein kinase kinase 1 | META serine/threonine protein kinase subfamily | C00001736 C00001737 | 0 / 0 | 
| Q9P286 | Serine/threonine-protein kinase PAK 7 | STE serine/threonine protein kinase PAKB subfamily | C00001736 C00001737 | 0 / 0 | 
| O00141 | Serine/threonine-protein kinase Sgk1 | AGC serine/threonine protein kinase SGK subfamily | C00001736 C00001737 | 0 / 0 | 
| P31749 | RAC-alpha serine/threonine-protein kinase | Akt | C00001736 C00001737 | 4 / 1 | 
| Q96SB4 | SRSF protein kinase 1 | Srpk | C00001736 C00001737 | 0 / 0 | 
| Q92630 | Dual specificity tyrosine-phosphorylation-regulated kinase 2 | CMGC dual-specificity kinase DYRK2 | C00001736 C00001737 | 0 / 0 | 
| Q86V86 | Serine/threonine-protein kinase pim-3 | Pim | C00001736 C00001737 | 0 / 0 | 
| O96013 | Serine/threonine-protein kinase PAK 4 | STE serine/threonine protein kinase PAKB subfamily | C00001736 C00001737 | 0 / 0 | 
| O75116 | Rho-associated protein kinase 2 | Rock | C00001736 C00001737 | 0 / 0 | 
| Q8IW41 | MAP kinase-activated protein kinase 5 | CAMK serine/threonine protein kinase MAPKAPK | C00001736 C00001737 | 0 / 0 | 
| P53350 | Serine/threonine-protein kinase PLK1 | PLK serine/threonine protein kinase subfamily | C00001736 C00001737 | 0 / 0 | 
| P22303 | Acetylcholinesterase | Hydrolase | C00001736 C00001737 | 1 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001736 C00042574 | 0 / 0 | 
| Q92698 | DNA repair and recombination protein RAD54-like | Enzyme | C00001736 C00042574 | 0 / 0 | 
| Q02750 | Dual specificity mitogen-activated protein kinase kinase 1 | Ste7 | C00001736 C00001737 | 1 / 1 | 
| P49841 | Glycogen synthase kinase-3 beta | Gsk | C00001736 C00001737 | 0 / 0 | 
| Q15418 | Ribosomal protein S6 kinase alpha-1 | Rskb | C00001736 C00001737 | 0 / 0 | 
| O15264 | Mitogen-activated protein kinase 13 | p38 | C00001736 C00001737 | 0 / 0 | 
| P53779 | Mitogen-activated protein kinase 10 | Jnk | C00001736 C00001737 | 0 / 1 | 
| P51955 | Serine/threonine-protein kinase Nek2 | Nek | C00001736 C00001737 | 0 / 0 | 
| Q96RR4 | Calcium/calmodulin-dependent protein kinase kinase 2 | META serine/threonine protein kinase subfamily | C00001736 C00001737 | 0 / 0 | 
| Q9BUB5 | MAP kinase-interacting serine/threonine-protein kinase 1 | CAMK serine/threonine protein kinase MNK subfamily | C00001736 C00001737 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001736 C00001737 | 0 / 0 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001736 C00042574 | 1 / 2 | 
| P45983 | Mitogen-activated protein kinase 8 | Jnk | C00001736 C00001737 | 0 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00001736 C00001737 | 0 / 0 | 
| P48730 | Casein kinase I isoform delta | Ck1 | C00001736 C00001737 | 1 / 0 | 
| P49137 | MAP kinase-activated protein kinase 2 | CAMK serine/threonine protein kinase MAPKAPK | C00001736 C00001737 | 0 / 0 | 
| Q96GD4 | Aurora kinase B | Aur | C00001736 C00001737 | 0 / 0 | 
| Q05655 | Protein kinase C delta type | Delta | C00001737 | 0 / 0 | 
| P50406 | 5-hydroxytryptamine receptor 6 | Serotonin receptor | C00001737 | 0 / 0 | 
| P31645 | Sodium-dependent serotonin transporter | Serotonin | C00001737 | 2 / 0 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001737 | 0 / 0 | 
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00042574 | 1 / 2 | 
| P35348 | Alpha-1A adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 0 | 
| P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 0 | 
| O75496 | Geminin | Unclassified protein | C00042574 | 0 / 0 | 
| Q8TF76 | Serine/threonine-protein kinase haspin | Haspin | C00001737 | 0 / 0 | 
| P08588 | Beta-1 adrenergic receptor | Adrenergic receptor | C00001737 | 1 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001737 | 2 / 0 | 
| P28335 | 5-hydroxytryptamine receptor 2C | Serotonin receptor | C00001737 | 0 / 0 | 
| Q9Y463 | Dual specificity tyrosine-phosphorylation-regulated kinase 1B | CMGC dual-specificity kinase DYRK1 | C00001737 | 0 / 0 | 
| P49840 | Glycogen synthase kinase-3 alpha | Gsk | C00001737 | 0 / 0 | 
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00001737 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00001737 | 0 / 0 | 
| P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00001736 | 0 / 0 | 
| P07948 | Tyrosine-protein kinase Lyn | Src | C00001737 | 0 / 0 | 
| P14902 | Indoleamine 2,3-dioxygenase 1 | Enzyme | C00042574 | 0 / 0 | 
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00001737 | 0 / 0 | 
| P54132 | Bloom syndrome protein | Enzyme | C00001736 | 1 / 2 | 
| Q15078 | Cyclin-dependent kinase 5 activator 1 | REG serine/threonine protein kinase family | C00001737 | 0 / 0 | 
| P49761 | Dual specificity protein kinase CLK3 | Clk | C00001737 | 0 / 0 | 
| Q9HAZ1 | Dual specificity protein kinase CLK4 | Clk | C00001737 | 0 / 0 | 
| P06241 | Tyrosine-protein kinase Fyn | Src | C00001737 | 0 / 0 | 
| P47898 | 5-hydroxytryptamine receptor 5A | Serotonin receptor | C00001737 | 0 / 0 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001736 | 0 / 0 | 
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00001736 | 1 / 0 | 
| P34969 | 5-hydroxytryptamine receptor 7 | Serotonin receptor | C00001737 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00001736 | 4 / 3 | 
| P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 0 | 
| P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00001737 | 1 / 0 | 
| P23975 | Sodium-dependent noradrenaline transporter | Norepinephrine | C00001737 | 1 / 1 | 
| P28221 | 5-hydroxytryptamine receptor 1D | Serotonin receptor | C00001737 | 0 / 0 | 
| P35368 | Alpha-1B adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 0 | 
| P18089 | Alpha-2B adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 0 | 
| P06239 | Tyrosine-protein kinase Lck | Src | C00001737 | 0 / 1 | 
| P28222 | 5-hydroxytryptamine receptor 1B | Serotonin receptor | C00001737 | 0 / 0 | 
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00001737 | 1 / 1 | 
| P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00001737 | 0 / 1 | 
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00001736 | 3 / 2 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00042574 | 11 / 10 | 
| P04062 | Glucosylceramidase | Enzyme | C00042574 | 6 / 4 | 
| P49760 | Dual specificity protein kinase CLK2 | Clk | C00001737 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00042574 | 0 / 0 | 
| P27338 | Amine oxidase [flavin-containing] B | Oxidoreductase | C00001737 | 0 / 0 | 
| Q9NR20 | Dual specificity tyrosine-phosphorylation-regulated kinase 4 | Enzyme | C00001737 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00042574 | 0 / 0 | 
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00042574 | 1 / 0 | 
| O00255 | Menin | Unclassified protein | C00001736 | 2 / 5 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00042574 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00042574 | 1 / 4 | 
| Q04759 | Protein kinase C theta type | Delta | C00001737 | 0 / 1 | 
| Q02156 | Protein kinase C epsilon type | Eta | C00001737 | 0 / 0 | 
| O94806 | Serine/threonine-protein kinase D3 | Pkd | C00001737 | 0 / 0 | 
| P06280 | Alpha-galactosidase A | Enzyme | C00042574 | 1 / 1 | 
| P05129 | Protein kinase C gamma type | Alpha | C00001737 | 1 / 1 | 
| P05771 | Protein kinase C beta type | Alpha | C00001737 | 0 / 0 | 
| P24723 | Protein kinase C eta type | Eta | C00001737 | 1 / 0 | 
| P41743 | Protein kinase C iota type | Iota | C00001737 | 0 / 0 | 
| Q9UN88 | Gamma-aminobutyric acid receptor subunit theta | GABA-A theta | C00001736 | 0 / 0 | 
| P28472 | Gamma-aminobutyric acid receptor subunit beta-3 | GABA-A beta | C00001736 | 1 / 0 | 
| P14867 | Gamma-aminobutyric acid receptor subunit alpha-1 | GABA-A alpha | C00001736 | 1 / 1 | 
| P48169 | Gamma-aminobutyric acid receptor subunit alpha-4 | GABA-A alpha | C00001736 | 0 / 0 | 
| O14764 | Gamma-aminobutyric acid receptor subunit delta | GABA-A delta | C00001736 | 1 / 1 | 
| P31644 | Gamma-aminobutyric acid receptor subunit alpha-5 | GABA-A alpha | C00001736 | 0 / 0 | 
| Q99928 | Gamma-aminobutyric acid receptor subunit gamma-3 | GABA-A gamma | C00001736 | 0 / 0 | 
| P78334 | Gamma-aminobutyric acid receptor subunit epsilon | GABA-A epsilon | C00001736 | 0 / 0 | 
| Q8N1C3 | Gamma-aminobutyric acid receptor subunit gamma-1 | GABA-A gamma | C00001736 | 0 / 0 | 
| P34903 | Gamma-aminobutyric acid receptor subunit alpha-3 | GABA-A alpha | C00001736 | 0 / 0 | 
| O00591 | Gamma-aminobutyric acid receptor subunit pi | GABA-A pi | C00001736 | 0 / 0 | 
| P47870 | Gamma-aminobutyric acid receptor subunit beta-2 | GABA-A beta | C00001736 | 0 / 0 | 
| P18507 | Gamma-aminobutyric acid receptor subunit gamma-2 | GABA-A gamma | C00001736 | 4 / 2 | 
| P18505 | Gamma-aminobutyric acid receptor subunit beta-1 | GABA-A beta | C00001736 | 0 / 0 | 
| Q16445 | Gamma-aminobutyric acid receptor subunit alpha-6 | GABA-A alpha | C00001736 | 0 / 0 | 
| P47869 | Gamma-aminobutyric acid receptor subunit alpha-2 | GABA-A alpha | C00001736 | 1 / 0 | 
| P08172 | Muscarinic acetylcholine receptor M2 | Acetylcholine receptor | C00001737 | 2 / 0 | 
| P20309 | Muscarinic acetylcholine receptor M3 | Acetylcholine receptor | C00001737 | 1 / 0 | 
| P08912 | Muscarinic acetylcholine receptor M5 | Acetylcholine receptor | C00001737 | 0 / 0 | 
| P11229 | Muscarinic acetylcholine receptor M1 | Acetylcholine receptor | C00001737 | 0 / 0 | 
| P08173 | Muscarinic acetylcholine receptor M4 | Acetylcholine receptor | C00001737 | 0 / 0 | 
| P51946 | Cyclin-H | Other cytosolic protein | C00001737 | 0 / 0 | 
| P50613 | Cyclin-dependent kinase 7 | Cdk7 | C00001737 | 0 / 0 | 
| O95067 | G2/mitotic-specific cyclin-B2 | Other cytosolic protein | C00001737 | 0 / 0 | 
| P14635 | G2/mitotic-specific cyclin-B1 | Other cytosolic protein | C00001737 | 0 / 0 | 
| P06493 | Cyclin-dependent kinase 1 | Cdc2 | C00001737 | 0 / 0 | 
| Q8WWL7 | G2/mitotic-specific cyclin-B3 | Other cytosolic protein | C00001737 | 0 / 0 | 
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00001736 | 2 / 0 | 
| Q99700 | Ataxin-2 | Unclassified protein | C00001737 | 1 / 1 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00001737 | 4 / 1 | 
| P49759 | Dual specificity protein kinase CLK1 | Clk | C00001737 | 0 / 0 | 
| P04637 | Cellular tumor antigen p53 | Transcription Factor | C00042574 | 7 / 37 | 
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00001737 | 0 / 0 | 
| P21917 | D(4) dopamine receptor | Dopamine receptor | C00001737 | 0 / 0 | 
| P21918 | D(1B) dopamine receptor | Dopamine receptor | C00001737 | 1 / 0 | 
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00001737 | 2 / 0 | 
| P35462 | D(3) dopamine receptor | Dopamine receptor | C00001737 | 1 / 0 | 
| P46098 | 5-hydroxytryptamine receptor 3A | NS | C00001737 | 0 / 0 | 
| O95264 | 5-hydroxytryptamine receptor 3B | NS | C00001737 | 0 / 0 | 
| O60563 | Cyclin-T1 | Other cytosolic protein | C00001737 | 0 / 0 | 
| P50750 | Cyclin-dependent kinase 9 | Cdk9 | C00001737 | 0 / 0 | 
| Q9Y2I1 | Nischarin | Other cytosolic protein | C00001737 | 0 / 0 | 
| P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00042574 | 0 / 3 | 
| Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00042574 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) | 
                          C00001736
                          C00001737
                          C00042574
                           | 
                      
| 196 | AHR, bHLHe76 | aryl hydrocarbon receptor | 
                          C00001736
                           | 
                      
| 6818 | SULT1A3, HAST, HAST3, M-PST, ST1A3/ST1A4, ST1A5, STM, TL-PST | sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 (EC:2.8.2.1) | 
                          C00042574
                           | 
                      
| 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) | 
                          C00042574
                           | 
                      
| 1859 | DYRK1A, DYRK, DYRK1, HP86, MNB, MNBH, MRD7 | dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A (EC:2.7.12.1) | 
                          C00001737
                           | 
                      
| 4137 | MAPT, DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, TAU | microtubule-associated protein tau | 
                          C00001737
                           | 
                      
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | 
                            Q99714
                             | 
                        
| #100100 | Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism | 
                            P20309
                             | 
                        
| #202300 | Adrenocortical carcinoma, hereditary; adcc | 
                            P04637
                             | 
                        
| #615224 | Advanced sleep phase syndrome, familial, 2; fasps2 | 
                            P48730
                             | 
                        
| #103780 | Alcohol dependence | 
                            P08172
                             P14416 P31645 P47869  | 
                        
| #613780 | Aortic aneurysm, familial thoracic 7; aat7 | 
                            Q15746
                             | 
                        
| #608584 | Asthma-related traits, susceptibility to, 2 | 
                            Q6W5P4
                             | 
                        
| #614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 | 
                            P04637
                             | 
                        
| #606798 | Blepharospasm, benign essential | 
                            P21918
                             | 
                        
| #210900 | Bloom syndrome; blm | 
                            P54132
                             | 
                        
| #114480 | Breast cancer | 
                            O96017
                             P31749  | 
                        
| #300615 | Brunner syndrome | 
                            P21397
                             | 
                        
| #615279 | Cardiofaciocutaneous syndrome 3; cfc3 | 
                            Q02750
                             | 
                        
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | 
                            P02545
                             | 
                        
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | 
                            P02545
                             | 
                        
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | 
                            P02545
                             | 
                        
| #303600 | Coffin-lowry syndrome; cls | 
                            P51812
                             | 
                        
| #114500 | Colorectal cancer; crc | 
                            P31749
                             P84022  | 
                        
| #615109 | Cowden syndrome 6; cws6 | 
                            P31749
                             | 
                        
| #125853 | Diabetes mellitus, noninsulin-dependent; niddm | 
                            P31751
                             | 
                        
| #119900 | Digital clubbing, isolated congenital | 
                            P15428
                             | 
                        
| #607208 | Dravet syndrome | 
                            P18507
                             | 
                        
| #609535 | Drug metabolism, poor, cyp2c19-related | 
                            P33261
                             | 
                        
| #608902 | Drug metabolism, poor, cyp2d6-related | 
                            P10635
                             | 
                        
| #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
                             | 
                        
| #612219 | Ewing sarcoma; es | 
                            P11308
                             | 
                        
| #301500 | Fabry disease | 
                            P06280
                             | 
                        
| #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
                             | 
                        
| #604233 | Generalized epilepsy with febrile seizures plus, type 1; gefsp1 | 
                            P18507
                             | 
                        
| #611277 | Generalized epilepsy with febrile seizures plus, type 3; gefsp3 | 
                            P18507
                             | 
                        
| #137800 | Glioma susceptibility 1; glm1 | 
                            O75874
                             | 
                        
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | 
                            Q03164
                             | 
                        
| #610140 | Heart-hand syndrome, slovenian type | 
                            P02545
                             | 
                        
| #176670 | Hutchinson-gilford progeria syndrome; hgps | 
                            P02545
                             | 
                        
| #145000 | Hyperparathyroidism 1; hrpt1 | 
                            O00255
                             | 
                        
| #603373 | Hyperthyroidism, familial gestational | 
                            P16473
                             | 
                        
| #609152 | Hyperthyroidism, nonautoimmune | 
                            P16473
                             | 
                        
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 | 
                            P15428
                             | 
                        
| #240900 | Hypoinsulinemic hypoglycemia with hemihypertrophy; hihghh | 
                            P31751
                             | 
                        
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 | 
                            P16473
                             | 
                        
| #151623 | Li-fraumeni syndrome 1; lfs1 | 
                            P04637
                             | 
                        
| #609265 | Li-fraumeni syndrome 2; lfs2 | 
                            O96017
                             | 
                        
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | 
                            P02545
                             | 
                        
| #613795 | Loeys-dietz syndrome, type 3; lds3 | 
                            P84022
                             | 
                        
| #211980 | Lung cancer | 
                            P04637
                             | 
                        
| #608516 | Major depressive disorder; mdd | 
                            P08172
                             | 
                        
| #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
                             | 
                        
| #300844 | Mental retardation, x-linked 19; mrx19 | 
                            P51812
                             | 
                        
| #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
                             | 
                        
| #159900 | Myoclonic dystonia | 
                            P14416
                             | 
                        
| #257200 | Niemann-pick disease, type a | 
                            P17405
                             | 
                        
| #607616 | Niemann-pick disease, type b | 
                            P17405
                             | 
                        
| #164230 | Obsessive-compulsive disorder; ocd | 
                            P31645
                             | 
                        
| #604715 | Orthostatic intolerance | 
                            P23975
                             | 
                        
| #259500 | Osteogenic sarcoma | 
                            O96017
                             | 
                        
| #260500 | Papilloma of choroid plexus; cpp | 
                            P04637
                             | 
                        
| #168600 | Parkinson disease, late-onset; pd | 
                            P04062
                             | 
                        
| #260540 | Parkinson-dementia syndrome | 
                            P10636
                             | 
                        
| #614674 | Periodic fever, menstrual cycle-dependent | 
                            P08908
                             | 
                        
| #172700 | Pick disease of brain | 
                            P10636
                             | 
                        
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | 
                            Q01196
                             | 
                        
| #176807 | Prostate cancer | 
                            O96017
                             | 
                        
| #176920 | Proteus syndrome | 
                            P31749
                             | 
                        
| #607276 | Resting heart rate, variation in | 
                            P08588
                             | 
                        
| #275210 | Restrictive dermopathy, lethal | 
                            P02545
                             | 
                        
| #604906 | Schizophrenia 9; sczd9 | 
                            P49798
                             | 
                        
| #181500 | Schizophrenia; sczd | 
                            P49798
                             | 
                        
| #243060 | Spermatogenic failure 5; spgf5 | 
                            Q9UQB9
                             | 
                        
| #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
                             | 
                        
| #605361 | Spinocerebellar ataxia 14; sca14 | 
                            P05129
                             | 
                        
| #183090 | Spinocerebellar ataxia 2; sca2 | 
                            Q99700
                             | 
                        
| #275355 | Squamous cell carcinoma, head and neck; hnscc | 
                            P04637
                             | 
                        
| #601367 | Stroke, ischemic | 
                            P24723
                             | 
                        
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | 
                            P10636
                             | 
                        
| #190300 | Tremor, hereditary essential, 1; etm1 | 
                            P35462
                             | 
                        
| #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)  | 
                        
| H00881 | Li-Fraumeni syndrome | 
                            O96017
                            (related)
                             P04637 (related)  | 
                        
| H00081 | Hashimoto's thyroiditis | 
                            P01215
                            (marker)
                             | 
                        
| H00082 | Graves' disease | 
                            P01215
                            (marker)
                             | 
                        
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) | 
                            P01215
                            (marker)
                             P16473 (related)  | 
                        
| H00264 | Charcot-Marie-Tooth disease (CMT) | 
                            P02545
                            (related)
                             | 
                        
| H00294 | Dilated cardiomyopathy (DCM) | 
                            P02545
                            (related)
                             | 
                        
| H00420 | Familial partial lipodystrophy (FPL) | 
                            P02545
                            (related)
                             P31751 (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)
                             | 
                        
| 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)
                             | 
                        
| 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)
                             | 
                        
| H00016 | Oral cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00017 | Esophageal cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00018 | Gastric cancer | 
                            P04637
                            (related)
                             | 
                        
| H00019 | Pancreatic cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00020 | Colorectal cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00022 | Bladder cancer | 
                            P04637
                            (related)
                             | 
                        
| H00025 | Penile cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00026 | Endometrial Cancer | 
                            P04637
                            (related)
                             | 
                        
| H00027 | Ovarian cancer | 
                            P04637
                            (related)
                             P31751 (related)  | 
                        
| H00028 | Choriocarcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00029 | Vulvar cancer | 
                            P04637
                            (related)
                             | 
                        
| H00031 | Breast cancer | 
                            P04637
                            (related)
                             | 
                        
| H00032 | Thyroid cancer | 
                            P04637
                            (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)
                             | 
                        
| H00042 | Glioma | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H00044 | Cancer of the anal canal | 
                            P04637
                            (related)
                             | 
                        
| H00046 | Cholangiocarcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00047 | Gallbladder cancer | 
                            P04637
                            (related)
                             | 
                        
| H00048 | Hepatocellular carcinoma | 
                            P04637
                            (related)
                             | 
                        
| H00055 | Laryngeal cancer | 
                            P04637
                            (related)
                             P04637 (marker)  | 
                        
| H01007 | Choroid plexus papilloma | 
                            P04637
                            (related)
                             | 
                        
| H00021 | Renal cell carcinoma | 
                            P04637
                            (marker)
                             | 
                        
| H00063 | Spinocerebellar ataxia (SCA) | 
                            P05129
                            (related)
                             Q99700 (related)  | 
                        
| H00093 | Combined immunodeficiencies (CIDs) | 
                            P06239
                            (related)
                             | 
                        
| H00125 | Fabry disease | 
                            P06280
                            (related)
                             | 
                        
| H00079 | Asthma | 
                            P07550
                            (related)
                             | 
                        
| H00058 | Amyotrophic lateral sclerosis (ALS) | 
                            P10636
                            (related)
                             | 
                        
| H00077 | Progressive supranuclear palsy (PSP) | 
                            P10636
                            (related)
                             | 
                        
| H00078 | Frontotemporal lobar degeneration (FTLD) | 
                            P10636
                            (related)
                             | 
                        
| H00024 | Prostate cancer | 
                            P11308
                            (related)
                             | 
                        
| H00035 | Ewing's sarcoma | 
                            P11308
                            (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)
                             | 
                        
| H01269 | Congenital hyperthyroidism | 
                            P16473
                            (related)
                             | 
                        
| H00137 | Niemann-Pick disease (NPD) typeA and B | 
                            P17405
                            (related)
                             | 
                        
| H00424 | Defects in the degradation of sphingomyelin | 
                            P17405
                            (related)
                             | 
                        
| H00548 | Brunner syndrome | 
                            P21397
                            (related)
                             | 
                        
| H01031 | Orthostatic intolerance (OI) | 
                            P23975
                            (related)
                             | 
                        
| H00539 | PTEN hamartoma tumor syndrome (PHTS) | 
                            P31749
                            (related)
                             | 
                        
| H01171 | Poor drug metabolism (PM) | 
                            P33261
                            (related)
                             | 
                        
| H00480 | Non-syndromic X-linked mental retardation | 
                            P51812
                            (related)
                             Q99714 (related)  | 
                        
| H00574 | Coffin-Lowry syndrome (CLS) | 
                            P51812
                            (related)
                             | 
                        
| H00606 | Early infantile epileptic encephalopathy | 
                            P53779
                            (related)
                             | 
                        
| H00094 | DNA repair defects | 
                            P54132
                            (related)
                             | 
                        
| H00296 | Defects in RecQ helicases | 
                            P54132
                            (related)
                             | 
                        
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | 
                            Q01196
                            (related)
                             Q01196 (marker) Q03164 (related) Q03164 (marker)  | 
                        
| H00003 | Acute myeloid leukemia (AML) | 
                            Q01196
                            (related)
                             Q01196 (marker) Q13951 (marker)  | 
                        
| H00978 | Thrombocytopenia (THC) | 
                            Q01196
                            (related)
                             | 
                        
| H00523 | Noonan syndrome and related disorders | 
                            Q02750
                            (related)
                             | 
                        
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | 
                            Q03164
                            (related)
                             | 
                        
| H00408 | Type I diabetes mellitus | 
                            Q04759
                            (related)
                             | 
                        
| H00801 | Familial thoracic aortic aneurysm and dissection (TAAD) | 
                            Q15746
                            (related)
                             | 
                        
| H00455 | Spinal muscular atrophy (SMA) | 
                            Q16637
                            (related)
                             | 
                        
| H00658 | Syndromic X-linked mental retardation | 
                            Q99714
                            (related)
                             | 
                        
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency | 
                            Q99714
                            (related)
                             | 
                        
| H01282 | Spermatogenic failure | 
                            Q9UQB9
                            (related)
                             |