Species

KNApSAcK Entry

Organism name Rheum spp.
Genus Rheum
Family Polygonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Rheum
Linked NCBI taxonomy ID 3620
Linked level genus

Family

Family in NCBI taxonomy Polygonaceae
ID 3615

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (14)

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
C00002378 External link 512 Cyanin
/ Cyanidin 3,5-diglucoside
No. 1 No. 15
C00002376 External link 512 Cyanidin 3-rutinoside
CHEMBL505251
C020386
3 / 0 / 1 No. 1 No. 15
C00015566 External link 512 4'-Methoxy-3,3',5-trihydroxystilbene 3'-O-beta-D-glucopyranoside
No. 36 No. 13
C00002870 External link 512 Astringin
/ (E)-Astringin
/ 3,4,3',5'-Tetrahydroxystilbene 3'-glucoside
CHEMBL358769
CHEMBL469920
No. 36 No. 13
C00002789 External link 512 Aloe emodin
/ Rhabarberone
CHEMBL40275
20 / 21 / 24 No. 41 No. 62
C00000568 External link 512 Chrysophanol
CHEMBL41092
C027113
20 / 17 / 20 1 / 0 No. 41 No. 62
C00000555 External link 512 Emodin
CHEMBL289277
D004642
109 / 88 / 91 68 / 9 No. 41 No. 62
C00002895 External link 512 Piceatannol
/ 3,3',4,5'-Tetrahydroxystilbene
CHEMBL69863
CHEMBL1603409
CHEMBL1972346
117 / 104 / 100 No. 295 No. 13
C00015335 External link 512 3,5-Dihydroxy-4'-methoxystilbene
CHEMBL291501
CHEMBL313687
6 / 13 / 13 No. 295 No. 13
C00015280 External link 512 3,3',4,5'-Tetrahydroxystilbene 3'-O-beta-D-(6''-O-galloylglucopyranoside)
No. 353
C00015565 External link 512 4'-Methoxy-3,3',5-trihydroxystilbene 3'-O-beta-D-(6''-O-galloyl)-glucopyranoside
No. 353
C00015564 External link 512 4'-Methoxy-3,3',5-trihydroxystilbene 3'-O-beta-D-(2''-O-p-coumaryl)-glucopyranoside
No. 353
C00015563 External link 512 4'-Methoxy-3,3',5-trihydroxystilbene 3'-O-beta-D-(2''-O-galloyl)-glucopyranoside
No. 353
C00002861 External link 512 Rhein
CHEMBL418068
C020491
60 / 65 / 46 8 / 1 No. 1811 No. 62

Human Protein / Gene in interactions

200 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000555 C00000568 C00002789 C00002861 C00002895 1 / 2
O00255 Menin Unclassified protein C00000555 C00000568 C00002789 C00002861 C00002895 2 / 5
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000555 C00000568 C00002789 C00002861 C00002895 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000555 C00000568 C00002861 C00002895 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000555 C00000568 C00002861 C00002895 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000555 C00000568 C00002861 C00002895 4 / 3
P39748 Flap endonuclease 1 Enzyme C00000555 C00002789 C00002861 C00002895 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000555 C00002789 C00002861 C00002895 0 / 0
P16234 Platelet-derived growth factor receptor alpha Pdgfr C00000555 C00002789 C00002861 C00002895 2 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00000555 C00000568 C00002861 C00002895 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000555 C00002861 C00002895 C00015335 11 / 10
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000555 C00000568 C00002861 C00002895 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000568 C00002861 C00002895 C00015335 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000555 C00000568 C00002861 C00002895 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00000555 C00000568 C00002861 C00002895 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002861 C00002895 C00015335 2 / 0
P11473 Vitamin D3 receptor NR1I1 C00000555 C00000568 C00002861 2 / 3
P08246 Neutrophil elastase S1A C00000555 C00002789 C00002861 2 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00000555 C00002861 C00002895 2 / 0
P04150 Glucocorticoid receptor NR3C1 C00000555 C00000568 C00002861 0 / 1
P06746 DNA polymerase beta Enzyme C00000555 C00002861 C00002895 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00000555 C00002861 C00002895 1 / 0
P54132 Bloom syndrome protein Enzyme C00000555 C00002861 C00002895 1 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000555 C00002861 C00002895 3 / 3
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000555 C00000568 C00002861 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000555 C00002861 C00002895 0 / 0
P03372 Estrogen receptor NR3A1 C00000555 C00002789 C00002861 1 / 1
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00000555 C00002789 C00002861 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00000555 C00002861 C00002895 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000555 C00002789 C00002861 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000555 C00002861 C00002895 1 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00000555 C00000568 C00002861 3 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000555 C00002861 C00002895 0 / 0
P08311 Cathepsin G S1A C00000555 C00002789 C00002861 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00000555 C00002861 C00002895 0 / 0
P09619 Platelet-derived growth factor receptor beta Pdgfr C00000555 C00002789 C00002861 5 / 1
Q92731 Estrogen receptor beta NR3A2 C00000555 C00002789 C00002861 0 / 1
O75496 Geminin Unclassified protein C00000555 C00002861 C00002895 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00000555 C00002861 C00002895 3 / 1
Q99549 M-phase phosphoprotein 8 Unclassified protein C00000555 C00002895 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000555 C00002895 1 / 1
O43451 Maltase-glucoamylase, intestinal Hydrolase C00000555 C00015335 0 / 0
O75116 Rho-associated protein kinase 2 Rock C00000555 C00002895 0 / 0
P10275 Androgen receptor NR3C4 C00000555 C00002789 3 / 4
P48729 Casein kinase I isoform alpha Ck1 C00000555 C00002895 0 / 0
P29466 Caspase-1 C14 C00002861 C00002895 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000555 C00002895 0 / 1
P06239 Tyrosine-protein kinase Lck Src C00000555 C00002895 0 / 1
O15118 Niemann-Pick C1 protein Unclassified protein C00000555 C00002895 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002861 C00002895 2 / 2
P43405 Tyrosine-protein kinase SYK Syk C00000555 C00002895 0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka C00000555 C00002895 0 / 0
Q13627 Dual specificity tyrosine-phosphorylation-regulated kinase 1A CMGC dual-specificity kinase DYRK1 C00000555 C00002895 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000555 C00000568 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00000555 C00002861 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000568 C00002861 0 / 0
P40225 Thrombopoietin Unclassified protein C00000555 C00002895 1 / 1
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00000555 C00002895 0 / 0
Q9H244 P2Y purinoceptor 12 Purine receptor C00000555 C00002789 1 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00000555 C00002861 5 / 3
Q9Y3R4 Sialidase-2 Enzyme C00000555 C00002861 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002861 C00002895 1 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002861 C00002895 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000555 C00000568 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002861 C00002895 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00000555 C00002895 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002861 C00002895 4 / 1
P11308 Transcriptional regulator ERG Unclassified protein C00000555 C00002861 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00000555 C00002895 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000555 C00002895 1 / 4
P53779 Mitogen-activated protein kinase 10 Jnk C00000555 C00002895 0 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00000555 C00002895 7 / 37
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 C00000555 C00002895 1 / 1
P49841 Glycogen synthase kinase-3 beta Gsk C00000555 C00002895 0 / 0
P10145 Interleukin-8 Secreted protein C00000555 C00002861 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002861 C00002895 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00000568 C00002895 4 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000555 C00002895 1 / 0
P51817 cAMP-dependent protein kinase catalytic subunit PRKX Pka C00002895 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002895 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000555 0 / 0
Q9HBY8 Serine/threonine-protein kinase Sgk2 AGC serine/threonine protein kinase SGK subfamily C00002895 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00000555 0 / 0
O95819 Mitogen-activated protein kinase kinase kinase kinase 4 STE serine/threonine protein kinase MSN subfamily C00002895 0 / 0
Q9Y463 Dual specificity tyrosine-phosphorylation-regulated kinase 1B CMGC dual-specificity kinase DYRK1 C00002895 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002895 0 / 0
P09769 Tyrosine-protein kinase Fgr Src C00000555 0 / 0
Q15418 Ribosomal protein S6 kinase alpha-1 Rskb C00000555 0 / 0
O15264 Mitogen-activated protein kinase 13 p38 C00000555 0 / 0
Q05397 Focal adhesion kinase 1 Fak C00002895 0 / 0
Q8IXJ6 NAD-dependent protein deacetylase sirtuin-2 Enzyme C00002895 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002789 0 / 0
Q14164 Inhibitor of nuclear factor kappa-B kinase subunit epsilon Other serine/threonine protein kinase C00002895 0 / 0
Q96RR4 Calcium/calmodulin-dependent protein kinase kinase 2 META serine/threonine protein kinase subfamily C00002895 0 / 0
Q9UM73 ALK tyrosine kinase receptor TKL serine/threonine protein kinase STKR type 1 subfamily C00002895 1 / 1
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00002895 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00002789 0 / 0
Q16611 Bcl-2 homologous antagonist/killer Unclassified protein C00002376 0 / 0
O43521 Bcl-2-like protein 11 Unclassified protein C00002376 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00002789 3 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002895 0 / 0
Q9UQM7 Calcium/calmodulin-dependent protein kinase type II subunit alpha Camk2 C00002895 0 / 0
Q02779 Mitogen-activated protein kinase kinase kinase 10 TKL dual-specificity kinase MLK C00002895 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002895 2 / 2
P11021 78 kDa glucose-regulated protein Unclassified protein C00002895 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00002895 0 / 0
P34947 G protein-coupled receptor kinase 5 AGC serine/threonine protein kinase GRK subfamily C00002895 0 / 0
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00002861 0 / 0
Q13464 Rho-associated protein kinase 1 Rock C00002895 0 / 0
O75582 Ribosomal protein S6 kinase alpha-5 CAMK serine/threonine protein kinase MSKB subfamily C00000555 0 / 0
Q13188 Serine/threonine-protein kinase 3 STE serine/threonine protein kinase MST subfamily C00002895 0 / 0
Q15746 Myosin light chain kinase, smooth muscle Mlck C00002895 1 / 1
O60674 Tyrosine-protein kinase JAK2 Jakb C00002895 5 / 1
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00002895 1 / 0
P49137 MAP kinase-activated protein kinase 2 CAMK serine/threonine protein kinase MAPKAPK C00000555 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00015335 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002789 1 / 8
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00002861 0 / 0
P15311 Ezrin Unclassified protein C00000555 0 / 1
P10696 Alkaline phosphatase, placental-like Enzyme C00002789 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002895 0 / 0
Q9Y4K4 Mitogen-activated protein kinase kinase kinase kinase 5 STE serine/threonine protein kinase KHS subfamily C00000555 0 / 0
P29376 Leukocyte tyrosine kinase receptor Alk C00002895 0 / 0
Q06418 Tyrosine-protein kinase receptor TYRO3 TK tyrosine-protein kinase AXL C00002895 0 / 0
Q7L7X3 Serine/threonine-protein kinase TAO1 STE serine/threonine protein kinase TAO subfamily C00002895 0 / 0
Q9H0K1 Serine/threonine-protein kinase SIK2 CAMK serine/threonine protein kinase QIK subfamily C00002895 0 / 0
Q15149 Plectin Unclassified protein C00002861 4 / 3
Q14680 Maternal embryonic leucine zipper kinase Melk C00002895 0 / 0
Q06187 Tyrosine-protein kinase BTK Tec C00002895 2 / 2
Q01453 Peripheral myelin protein 22 Unclassified protein C00002895 5 / 2
P23443 Ribosomal protein S6 kinase beta-1 p70 C00000555 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002895 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000555 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00000555 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00002895 4 / 5
P49840 Glycogen synthase kinase-3 alpha Gsk C00002895 0 / 0
Q8IW41 MAP kinase-activated protein kinase 5 CAMK serine/threonine protein kinase MAPKAPK C00000555 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00002895 0 / 0
P08631 Tyrosine-protein kinase HCK Src C00002895 0 / 0
P07948 Tyrosine-protein kinase Lyn Src C00000555 0 / 0
P68400 Casein kinase II subunit alpha Ck2 C00000555 0 / 0
P55210 Caspase-7 C14 C00002861 0 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt C00000555 4 / 1
O00141 Serine/threonine-protein kinase Sgk1 AGC serine/threonine protein kinase SGK subfamily C00000555 0 / 0
P51812 Ribosomal protein S6 kinase alpha-3 Rskb C00002895 2 / 2
P07333 Macrophage colony-stimulating factor 1 receptor Pdgfr C00002895 1 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00000555 0 / 0
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002895 1 / 0
Q8IU85 Calcium/calmodulin-dependent protein kinase type 1D Camk1 C00002895 0 / 0
O75365 Protein tyrosine phosphatase type IVA 3 Tyr C00000555 0 / 0
P07949 Proto-oncogene tyrosine-protein kinase receptor Ret Ret C00002895 9 / 4
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00000568 0 / 0
Q15046 Lysine--tRNA ligase Enzyme C00002895 2 / 1
Q07812 Apoptosis regulator BAX Unclassified protein C00002376 0 / 1
Q9UHD2 Serine/threonine-protein kinase TBK1 Ikk C00002895 1 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00000555 5 / 1
P27448 MAP/microtubule affinity-regulating kinase 3 CAMK serine/threonine protein kinase MARK subfamily C00002895 0 / 0
P28907 ADP-ribosyl cyclase 1 Enzyme C00002895 0 / 1
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00000555 0 / 0
O14757 Serine/threonine-protein kinase Chk1 Chk1 C00000555 0 / 0
Q5S007 Leucine-rich repeat serine/threonine-protein kinase 2 TKL serine/threonine protein kinase LRRK subfamily C00002895 2 / 2
Q04759 Protein kinase C theta type Delta C00002895 0 / 1
P17252 Protein kinase C alpha type Alpha C00000555 0 / 0
P42336 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform Enzyme C00000555 9 / 1
P54646 5'-AMP-activated protein kinase catalytic subunit alpha-2 Ampk C00000555 0 / 0
P35869 Aryl hydrocarbon receptor Transcription Factor C00000555 0 / 0
P52333 Tyrosine-protein kinase JAK3 Jakb C00002895 1 / 1
P41240 Tyrosine-protein kinase CSK Csk C00000555 0 / 0
P04062 Glucosylceramidase Enzyme C00002895 6 / 4
O15530 3-phosphoinositide-dependent protein kinase 1 Pdk1 C00000555 0 / 0
P53778 Mitogen-activated protein kinase 12 p38 C00000555 0 / 0
P49760 Dual specificity protein kinase CLK2 Clk C00002895 0 / 0
Q07912 Activated CDC42 kinase 1 TK tyrosine-protein kinase ACK subfamily C00002895 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00000555 0 / 0
Q96L34 MAP/microtubule affinity-regulating kinase 4 CAMK serine/threonine protein kinase MARK subfamily C00002895 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002861 2 / 0
Q15759 Mitogen-activated protein kinase 11 p38 C00000555 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000555 2 / 2
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00015335 0 / 3
P21728 D(1A) dopamine receptor Dopamine receptor C00002895 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00002895 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002895 1 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000555 0 / 0
Q04771 Activin receptor type-1 TKL serine/threonine protein kinase STKR1 subfamily C00002895 1 / 1
P49336 Cyclin-dependent kinase 8 Cdk8 C00002895 0 / 0
P08922 Proto-oncogene tyrosine-protein kinase ROS TK tyrosine-protein kinase SEV C00002895 0 / 1
P45983 Mitogen-activated protein kinase 8 Jnk C00000555 0 / 0
P45984 Mitogen-activated protein kinase 9 Jnk C00000555 0 / 0
P22694 cAMP-dependent protein kinase catalytic subunit beta Pka C00000555 0 / 0
P22612 cAMP-dependent protein kinase catalytic subunit gamma Pka C00000555 0 / 0
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00002861 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00002861 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00000555 3 / 0
Q9HCP0 Casein kinase I isoform gamma-1 Ck1 C00000555 0 / 0
P48730 Casein kinase I isoform delta Ck1 C00000555 1 / 0
P49674 Casein kinase I isoform epsilon Ck1 C00000555 0 / 0
P78368 Casein kinase I isoform gamma-2 Ck1 C00000555 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00002895 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00002861 2 / 1
Q9HCT0 Fibroblast growth factor 22 Unclassified protein C00002895 0 / 0

75 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000555 C00000568 C00002861
10055 SAE1, AOS1, HSPC140, SUA1, UBLE1A SUMO1 activating enzyme subunit 1 C00000555
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) C00002861
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00002861
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002861
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002861
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002861
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00002861
58 ACTA1, ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3 actin, alpha 1, skeletal muscle C00000555
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00000555
472 ATM, AT1, ATA, ATC, ATD, ATDC, ATE, TEL1, TELO1 ataxia telangiectasia mutated (EC:2.7.11.1) C00000555
9529 BAG5, BAG-5 BCL2-associated athanogene 5 C00000555
51283 BFAR, BAR, RNF47 bifunctional apoptosis regulator C00000555
821 CANX, CNX, IP90, P90 calnexin C00000555
9133 CCNB2, HsT17299 cyclin B2 C00000555
8621 CDK13, CDC2L, CDC2L5, CHED, hCDK13 cyclin-dependent kinase 13 (EC:2.7.11.23 2.7.11.22) C00000555
1019 CDK4, CMM3, PSK-J3 cyclin-dependent kinase 4 (EC:2.7.11.22) C00000555
1951 CELSR3, CDHF11, EGFL1, FMI1, HFMI1, MEGF2, RESDA1 cadherin, EGF LAG seven-pass G-type receptor 3 C00000555
10987 COPS5, CSN5, JAB1, MOV-34, SGN5 COP9 signalosome subunit 5 C00000555
1509 CTSD, CLN10, CPSD cathepsin D (EC:3.4.23.5) C00000555
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00000555
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00000555
1719 DHFR, DHFRP1, DYR dihydrofolate reductase (EC:1.5.1.3) C00000555
3337 DNAJB1, HSPF1, Hdj1, Hsp40, RSPH16B, Sis1 DnaJ (Hsp40) homolog, subfamily B, member 1 C00000555
1875 E2F5, E2F-5 E2F transcription factor 5, p130-binding C00000555
9538 EI24, EPG4, PIG8, TP53I8 etoposide induced 2.4 C00000555
1967 EIF2B1, EIF2B, EIF2BA eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa C00000555
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00000555
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00000555
2308 FOXO1, FKH1, FKHR, FOXO1A forkhead box O1 C00000555
2620 GAS2 growth arrest-specific 2 C00000555
2876 GPX1, GPXD, GSHPX1 glutathione peroxidase 1 (EC:1.11.1.9) C00000555
2947 GSTM3, GST5, GSTB, GSTM3-3, GTM3 glutathione S-transferase mu 3 (brain) (EC:2.5.1.18) C00000555
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00000555
3014 H2AFX, H2A.X, H2A/X, H2AX H2A histone family, member X C00000555
3440 IFNA2, IFN-alphaA, IFNA, IFNA2B, INFA2 interferon, alpha 2 C00000555
3708 ITPR1, INSP3R1, IP3R, IP3R1, SCA15, SCA16, SCA29 inositol 1,4,5-trisphosphate receptor, type 1 C00000555
3727 JUND, AP-1 jun D proto-oncogene C00000555
3880 KRT19, CK19, K19, K1CS keratin 19 C00000555
23499 MACF1, ABP620, ACF7, MACF, OFC4 microtubule-actin crosslinking factor 1 C00000555
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00000555
4137 MAPT, DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, TAU microtubule-associated protein tau C00000555
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00000555
5082 PDCL, PhLP phosducin-like C00000555
5289 PIK3C3, VPS34, hVps34 phosphatidylinositol 3-kinase, catalytic subunit type 3 (EC:2.7.1.137) C00000555
8493 PPM1D, PP2C-DELTA, WIP1 protein phosphatase, Mg2+/Mn2+ dependent, 1D (EC:3.1.3.16) C00000555
9588 PRDX6, 1-Cys, AOP2, NSGPx, PRX, aiPLA2, p29 peroxiredoxin 6 (EC:1.11.1.9 1.11.1.15) C00000555
5580 PRKCD, MAY1, PKCD, nPKC-delta protein kinase C, delta (EC:2.7.10.2 2.7.11.13) C00000555
51495 PTPLAD1, B-IND1, HACD3, HSPC121 protein tyrosine phosphatase-like A domain containing 1 (EC:4.2.1.134) C00000555
5894 RAF1, CRAF, NS5, Raf-1, c-Raf v-raf-1 murine leukemia viral oncogene homolog 1 (EC:2.7.11.1) C00000555
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00000555
5955 RCN2, E6BP, ERC-55, ERC55, TCBP49 reticulocalbin 2, EF-hand calcium binding domain C00000555
387 RHOA, ARH12, ARHA, RHO12, RHOH12 ras homolog family member A C00000555
6093 ROCK1, P160ROCK, ROCK-I Rho-associated, coiled-coil containing protein kinase 1 (EC:2.7.11.1) C00000555
9475 ROCK2, ROCK-II Rho-associated, coiled-coil containing protein kinase 2 (EC:2.7.11.1) C00000555
1950 EGF, HOMG4, URG epidermal growth factor C00002861
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00000555
6489 ST8SIA1, GD3S, SIAT8, SIAT8-A, SIAT8A, ST8SiaI ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 (EC:2.4.99.8) C00000555
10963 STIP1, HOP, IEF-SSP-3521, P60, STI1, STI1L stress-induced-phosphoprotein 1 C00000555
55578 SUPT20H, C13, C13orf19, FAM48A, P38IP, SPT20 suppressor of Ty 20 homolog (S. cerevisiae) C00000555
51347 TAOK3, DPK, JIK, MAP3K18 TAO kinase 3 (EC:2.7.11.1) C00000555
6903 TBCC, CFC tubulin folding cofactor C C00000555
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000555
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00000555
7186 TRAF2, MGC:45012, TRAP, TRAP3 TNF receptor-associated factor 2 C00000555
10381 TUBB3, CDCBM, CDCBM1, CFEOM3A, TUBB4, beta-4 tubulin, beta 3 class III C00000555
54957 TXNL4B, DLP, Dim2 thioredoxin-like 4B C00000555
7296 TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR thioredoxin reductase 1 (EC:1.8.1.9) C00000555
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00000555
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00000555
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00000555
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) C00000555
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) C00000555
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00000555
7416 VDAC1, PORIN, VDAC-1 voltage-dependent anion channel 1 C00000555

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (150)

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
#300755 Agammaglobulinemia, x-linked; xla Q06187
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613780 Aortic aneurysm, familial thoracic 7; aat7 Q15746
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#615007 Basal ganglia calcification, idiopathic, 4; ibgc4 P09619
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#609821 Bleeding disorder, platelet-type, 8; bdplt8 Q9H244
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#114480 Breast cancer P31749
P38398
P42336
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#600880 Budd-chiari syndrome; bdchs O60674
#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
#209880 Central hypoventilation syndrome, congenital; cchs P07949
#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
#303600 Coffin-lowry syndrome; cls P51812
#114500 Colorectal cancer; crc P07949
P18054
P31749
P42336
P84022
Q14191
#612918 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi P42336
#615108 Cowden syndrome 5; cws5 P42336
#615109 Cowden syndrome 6; cws6 P31749
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#162800 Cyclic neutropenia P08246
#613916 Deafness, autosomal recessive 89; dfnb89 Q15046
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#226670 Epidermolysis bullosa simplex with muscular dystrophy Q15149
#612138 Epidermolysis bullosa simplex with pyloric atresia Q15149
#131950 Epidermolysis bullosa simplex, ogna type Q15149
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#612219 Ewing sarcoma; es P11308
#135100 Fibrodysplasia ossificans progressiva; fop Q04771
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P16234
#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
#143500 Gilbert syndrome P22309
P22310
#177700 Glaucoma 1, open angle, p; glc1p Q9UHD2
#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
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P42336
#142623 Hirschsprung disease, susceptibility to, 1; hscr1 P07949
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#607685 Hypereosinophilic syndrome, idiopathic; hes P16234
#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
#147950 Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 P11362
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#307200 Isolated growth hormone deficiency, type iii; ighd3 Q06187
#607785 Juvenile myelomonocytic leukemia; jmml P09619
#182000 Keratosis, seborrheic P42336
#601626 Leukemia, acute myeloid; aml O60674
P09619
P36888
#221820 Leukoencephalopathy, diffuse hereditary, with spheroids; hdls P07333
#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
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#602501 Megalencephaly-capillary malformation-polymicrogyria syndrome; mcap P42336
#603387 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome; mpph P42336
#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
#171400 Multiple endocrine neoplasia, type iia; men2a P07949
#162300 Multiple endocrine neoplasia, type iib; men2b P07949
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#613723 Muscular dystrophy, limb-girdle, type 2q; lgmd2q Q15149
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#254450 Myelofibrosis O60674
#131440 Myeloproliferative disorder, chronic, with eosinophilia P09619
#228550 Myofibromatosis, infantile, 1; imf1 P09619
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#613014 Neuroblastoma, susceptibility to, 3; nblst3 Q9UM73
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166250 Osteoglophonic dysplasia; ogd P11362
#167000 Ovarian cancer P38398
P42336
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#607060 Parkinson disease 8, autosomal dominant; park8 Q5S007
#168600 Parkinson disease, late-onset; pd P04062
Q5S007
#260540 Parkinson-dementia syndrome P10636
#101600 Pfeiffer syndrome P11362
#171300 Pheochromocytoma P07949
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#263300 Polycythemia vera; pv O60674
#176920 Proteus syndrome P31749
#191830 Renal adysplasia P07949
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#600802 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative P52333
#609620 Short qt syndrome 1; sqt1 Q12809
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#614521 Thrombocythemia 3; thcyt3 O60674
#155240 Thyroid carcinoma, familial medullary; mtc P07949
#188550 Thyroid carcinoma, papillary P07949
#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
#190440 Trigonocephaly 1; trigno1 P11362
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (122)

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)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00012 Polycythemia vera O60674 (related)
O60674 (marker)
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)
H00028 Choriocarcinoma P00533 (related)
P04637 (related)
P07333 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P09619 (related)
P16234 (related)
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)
Q15149 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
Q15149 (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)
Q5S007 (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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
P28907 (marker)
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)
P08922 (related)
Q9UM73 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
Q07812 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
P42336 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
P07949 (related)
P07949 (marker)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
P15311 (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)
H00213 Hypophosphatasia P05186 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00822 Renal agenesis and Renal adysplasia P07949 (related)
H00910 Hirschsprung disease (HD) P07949 (related)
H00916 Congenital central hypoventilation syndrome (CCHS) P07949 (related)
H00100 Neutropenic disorders P08246 (related)
H00024 Prostate cancer P10275 (related)
P11308 (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)
H00023 Testicular cancer P10696 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00035 Ewing's sarcoma P11308 (related)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
H00516 Isolated orofacial clefts P11362 (related)
H01207 Trigonocephaly P11362 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (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)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00208 Hyperbilirubinemia P22309 (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)
H00480 Non-syndromic X-linked mental retardation P51812 (related)
Q99714 (related)
H00574 Coffin-Lowry syndrome (CLS) P51812 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P52333 (related)
H00606 Early infantile epileptic encephalopathy P53779 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (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)
H00408 Type I diabetes mellitus Q04759 (related)
H00430 Fibrodysplasia ossificans progressiva (FOP) Q04771 (related)
Q04771 (marker)
H00085 Agammaglobulinemias Q06187 (related)
H00254 Pituitary Dwarfism (PD) Q06187 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00585 Epidermolysis bullosa, hemidesmosomal Q15149 (related)
H00801 Familial thoracic aortic aneurysm and dissection (TAAD) Q15746 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00057 Parkinson's disease (PD) Q5S007 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H01235 Bleeding disorder platelet-type Q9H244 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

9 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008106 Liver Cirrhosis, Experimental C00002861
C00000555
D005327 Fetal Resorption C00000555
D004802 Eosinophilia C00000555
D005317 Fetal Growth Retardation C00000555
D001249 Asthma C00000555
D020567 Fetal Weight C00000555
D005355 Fibrosis C00000555
D015459 Leukemia-Lymphoma, Adult T-Cell C00000555
D010922 Placenta Diseases C00000555