Species

KNApSAcK Entry

Organism name Caragana frutex
Genus Caragana
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Caragana frutex
Linked NCBI taxonomy ID 47643
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (7)

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
C00004635 External link 512 Isorhamnetin
/ 3'-O-Methylquercetin
/ 3,4',5,7-Tetrahydroxy-3'-methoxyflavone
/ 3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL379064
C047368
12 / 10 / 13 10 / 0 No. 3 No. 15
C00001071 External link 512 Myricetin
CHEMBL164
C040015
78 / 70 / 56 39 / 2 No. 3 No. 15
C00002547 External link 512 (-)-Medicarpin
/ 3-Hydroxy-9-methoxypterocarpan
CHEMBL238845
CHEMBL413297
C047353
3 / 1 / 1 No. 66 No. 15
C00002546 External link 512 Inermin
/ Maackiain
/ (-)-Maackiain
/ Demethylpterocarpin
/ 3-Hydroxy-8,9-methylenedioxypterocarpan
CHEMBL334918
CHEMBL239047
CHEMBL445279
3 / 2 / 3 No. 66 No. 15
C00002499 External link 512 Scopoletin
CHEMBL71851
D012603
48 / 37 / 34 9 / 0 No. 864 No. 25
C00000576 External link 512 Xanthotoxin
CHEMBL416
D008730
104 / 55 / 45 22 / 18 No. 1282 No. 25
C00000575 External link 512 Bergaptan
CHEMBL24171
C022909
22 / 22 / 17 0 / 3 No. 1282 No. 25

Human Protein / Gene in interactions

206 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000575 C00000576 C00001071 C00002499 C00002546 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000575 C00000576 C00001071 C00002499 1 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000575 C00000576 C00001071 C00002499 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000575 C00000576 C00001071 C00002499 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000576 C00001071 C00002499 C00004635 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001071 C00002499 C00004635 1 / 2
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000575 C00001071 C00002499 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000575 C00000576 C00002499 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00000575 C00000576 C00001071 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000575 C00001071 C00002499 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000576 C00001071 C00002499 0 / 3
O00255 Menin Unclassified protein C00001071 C00002499 C00004635 2 / 5
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00001071 C00002499 C00004635 1 / 1
P22303 Acetylcholinesterase Hydrolase C00000576 C00001071 C00002499 1 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000575 C00001071 C00002499 3 / 3
P56817 Beta-secretase 1 A1A C00000575 C00000576 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001071 C00002499 2 / 2
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002499 C00004635 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00000576 C00001071 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001071 C00004635 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000575 C00002547 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001071 C00002499 1 / 1
P04745 Alpha-amylase 1 Enzyme C00001071 C00004635 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00001071 C00004635 4 / 4
P10275 Androgen receptor NR3C4 C00000575 C00000576 3 / 4
Q9UBT6 DNA polymerase kappa Enzyme C00001071 C00004635 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001071 C00002499 0 / 0
P04062 Glucosylceramidase Enzyme C00001071 C00002499 6 / 4
P15121 Aldose reductase Enzyme C00001071 C00002499 0 / 0
O75496 Geminin Unclassified protein C00002499 C00002547 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001071 C00004635 0 / 0
P29466 Caspase-1 C14 C00000576 C00002499 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001071 C00002499 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000575 C00000576 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001071 C00002499 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000576 C00001071 2 / 3
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001071 C00002499 0 / 0
Q09470 Potassium voltage-gated channel subfamily A member 1 KCNA, Kv1.x (Shaker) C00000575 C00000576 1 / 1
P20813 Cytochrome P450 2B6 Cytochrome P450 2B6 C00000575 C00000576 1 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00001071 C00004635 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00000576 C00002499 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000576 C00002547 1 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00000575 C00000576 3 / 2
Q01453 Peripheral myelin protein 22 Unclassified protein C00001071 5 / 2
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00001071 0 / 0
P17658 Potassium voltage-gated channel subfamily A member 6 K C00000575 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00000576 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00000576 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00000576 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00000576 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00000576 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00000576 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00000576 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00000576 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00001071 0 / 0
P28907 ADP-ribosyl cyclase 1 Enzyme C00001071 0 / 1
P08183 Multidrug resistance protein 1 drug C00000575 1 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00000576 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00000576 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00000576 0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00002499 0 / 0
P23443 Ribosomal protein S6 kinase beta-1 p70 C00000576 0 / 0
P04792 Heat shock protein beta-1 Unclassified protein C00004635 2 / 1
P54132 Bloom syndrome protein Enzyme C00001071 1 / 2
Q9HC97 G-protein coupled receptor 35 Kynurenic acid receptor C00001071 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001071 1 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000576 1 / 8
P11387 DNA topoisomerase 1 Isomerase C00001071 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00001071 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000576 2 / 2
P14416 D(2) dopamine receptor Dopamine receptor C00000576 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000576 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00000576 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00000576 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00000576 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00000576 0 / 0
Q15746 Myosin light chain kinase, smooth muscle Mlck C00001071 1 / 1
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00000576 0 / 0
P16389 Potassium voltage-gated channel subfamily A member 2 KCNA, Kv1.x (Shaker) C00000575 0 / 0
Q9Y3R4 Sialidase-2 Enzyme C00001071 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00000576 1 / 1
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001071 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00000576 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00000576 1 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002499 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002499 1 / 2
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00001071 1 / 1
P27361 Mitogen-activated protein kinase 3 Erk C00000576 0 / 0
P17252 Protein kinase C alpha type Alpha C00000576 0 / 0
P42336 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform Enzyme C00001071 9 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00002499 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00002499 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002499 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002499 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00000576 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00000576 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00000576 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00000576 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00000576 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000576 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00000576 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00000576 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002499 1 / 1
P25101 Endothelin-1 receptor Endothelin receptor C00000576 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00000576 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00000576 1 / 0
P00915 Carbonic anhydrase 1 Lyase C00002499 0 / 0
Q14790 Caspase-8 C14 C00001071 2 / 1
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00000576 0 / 0
P08311 Cathepsin G S1A C00000576 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00000576 1 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000576 0 / 0
P03956 Interstitial collagenase M10A C00000576 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00000576 0 / 0
P22001 Potassium voltage-gated channel subfamily A member 3 KCNA, Kv1.x (Shaker) C00000575 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00002499 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00001071 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00001071 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00001071 3 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001071 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00000576 0 / 0
P06746 DNA polymerase beta Enzyme C00001071 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00001071 0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00000576 1 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001071 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000576 0 / 1
P06213 Insulin receptor TK tyrosine-protein kinase INSR subfamily C00001071 5 / 4
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00000576 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00000576 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001071 2 / 2
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00000576 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00000576 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00000576 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00000576 1 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00000576 0 / 0
P21452 Substance-K receptor Neurokinin receptor C00000576 0 / 0
P06276 Cholinesterase Hydrolase C00001071 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00000576 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00000576 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00000576 0 / 0
P06280 Alpha-galactosidase A Enzyme C00002499 1 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00000576 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00001071 2 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00000576 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000576 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00001071 0 / 1
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00000576 2 / 1
P08246 Neutrophil elastase S1A C00000576 2 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000576 2 / 2
Q16790 Carbonic anhydrase 9 Lyase C00002499 0 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001071 2 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00001071 1 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002499 0 / 0
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002499 1 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000576 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00002499 0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002499 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000576 0 / 0
P03372 Estrogen receptor NR3A1 C00000576 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00000576 1 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000576 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00000576 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00000576 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00000576 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00000576 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00000576 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00000576 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00000576 0 / 0
Q00796 Sorbitol dehydrogenase Enzyme C00002499 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00001071 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00001071 0 / 0
P55210 Caspase-7 C14 C00002499 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001071 0 / 0
P31941 DNA dC->dU-editing enzyme APOBEC-3A Enzyme C00001071 0 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00000576 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001071 0 / 0
Q15046 Lysine--tRNA ligase Enzyme C00001071 2 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00001071 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00000576 1 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002499 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00001071 4 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein C00001071 0 / 0
P48547 Potassium voltage-gated channel subfamily C member 1 K C00000575 0 / 0
O75795 UDP-glucuronosyltransferase 2B17 Enzyme C00002499 1 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00000576 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00000576 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00000576 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00000576 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00000576 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00000576 0 / 1
P22460 Potassium voltage-gated channel subfamily A member 5 KCNA, Kv1.x (Shaker) C00000575 1 / 1
Q04760 Lactoylglutathione lyase Enzyme C00001071 0 / 0
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00000576 0 / 0
P31639 Sodium/glucose cotransporter 2 Glucose C00002546 1 / 1
P13866 Sodium/glucose cotransporter 1 Glucose C00002546 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002499 0 / 0
P40225 Thrombopoietin Unclassified protein C00001071 1 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002499 3 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001071 1 / 1
P33527 Multidrug resistance-associated protein 1 drugs C00001071 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00001071 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001071 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001071 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00001071 2 / 1
P42345 Serine/threonine-protein kinase mTOR Enzyme C00001071 0 / 0
Q9HCT0 Fibroblast growth factor 22 Unclassified protein C00001071 0 / 0

71 Gene in CTD interactions

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) C00000576 C00001071 C00004635
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00000576 C00001071
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001071 C00004635
581 BAX, BCL2L4 BCL2-associated X protein C00000576 C00001071
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000576 C00001071
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000576 C00001071
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00000576 C00001071
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00001071 C00004635
1553 CYP2A13, CPAD, CYP2A, CYPIIA13 cytochrome P450, family 2, subfamily A, polypeptide 13 (EC:1.14.14.1) C00000576
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00001071
1031 CDKN2C, INK4C, p18, p18-INK4C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) C00001071
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00001071
1499 CTNNB1, CTNNB, MRD19, armadillo catenin (cadherin-associated protein), beta 1, 88kDa C00001071
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00001071
847 CAT catalase (EC:1.11.1.6) C00001071
397 ARHGDIB, D4, GDIA2, GDID4, LYGDI, Ly-GDI, RAP1GN1, RhoGDI2 Rho GDP dissociation inhibitor (GDI) beta C00001071
1786 DNMT1, ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT DNA (cytosine-5-)-methyltransferase 1 (EC:2.1.1.37) C00001071
54583 EGLN1, C1orf12, ECYT3, HIF-PH2, HIFPH2, HPH-2, HPH2, PHD2, SM20, ZMYND6 egl-9 family hypoxia-inducible factor 1 (EC:1.14.11.29) C00001071
2203 FBP1, FBP fructose-1,6-bisphosphatase 1 (EC:3.1.3.11) C00001071
3082 HGF, DFNB39, F-TCF, HGFB, HPTA, SF hepatocyte growth factor (hepapoietin A; scatter factor) C00001071
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00001071
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00001071
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00001071
4233 MET, AUTS9, HGFR, RCCP2, c-Met met proto-oncogene (EC:2.7.10.1) C00001071
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00001071
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00001071
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00001071
8505 PARG, PARG99 poly (ADP-ribose) glycohydrolase (EC:3.2.1.143) C00001071
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00001071
8000 PSCA, PRO232 prostate stem cell antigen C00001071
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) C00001071
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00001071
23411 SIRT1, SIR2L1 sirtuin 1 C00001071
6513 SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED solute carrier family 2 (facilitated glucose transporter), member 1 C00001071
1244 ABCC2, ABC30, CMOAT, DJS, MRP2, cMRP ATP-binding cassette, sub-family C (CFTR/MRP), member 2 C00001071
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00001071
9540 TP53I3, PIG3 tumor protein p53 inducible protein 3 C00001071
8626 TP63, AIS, B(p51A), B(p51B), EEC3, KET, LMS, NBP, OFC8, RHS, SHFM4, TP53CP, TP53L, TP73L, p40, p51, p53CP, p63, p73H, p73L tumor protein p63 C00001071
7161 TP73, P73 tumor protein p73 C00001071
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00004635
196 AHR, bHLHe76 aryl hydrocarbon receptor C00004635
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00004635
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00004635
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00004635
4973 OLR1, CLEC8A, LOX1, LOXIN, SCARE1, SLOX1 oxidized low density lipoprotein (lectin-like) receptor 1 C00004635
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00004635
8553 BHLHE40, BHLHB2, DEC1, HLHB2, SHARP-2, STRA13, Stra14 basic helix-loop-helix family, member e40 C00000576
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00000576
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00000576
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00000576
8824 CES2, CE-2, CES2A1, PCE-2, iCE carboxylesterase 2 (EC:3.1.1.1 3.1.1.84 3.1.1.56) C00000576
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00000576
891 CCNB1, CCNB cyclin B1 C00001071
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00000576
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00000576
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00000576
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00000576
3034 HAL, HIS, HSTD histidine ammonia-lyase (EC:4.3.1.3) C00000576
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00000576
3355109 C00000576
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00000576
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00000576
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002499
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002499
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002499
54578 UGT1A6, GNT1, HLUGP, HLUGP1, UDPGT, UDPGT_1-6, UGT1, UGT1A6S, UGT1F UDP glucuronosyltransferase 1 family, polypeptide A6 (EC:2.4.1.17) C00002499
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002499
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) C00002499
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) C00002499
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00002499
7508 XPC, RAD4, XP3, XPCC xeroderma pigmentosum, complementation group C C00002499

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (134)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103780 Alcohol dependence P08172
P14416
P31645
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613780 Aortic aneurysm, familial thoracic 7; aat7 Q15746
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#612240 Atrial fibrillation, familial, 7; atfb7 P22460
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#210900 Bloom syndrome; blm P54132
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#612560 Bone mineral density quantitative trait locus 12; bmnd12 O75795
#114480 Breast cancer P42336
#300615 Brunner syndrome P21397
#607271 Caspase 8 deficiency Q14790
#118300 Charcot-marie-tooth disease and deafness Q01453
#606595 Charcot-marie-tooth disease, axonal, type 2f; cmt2f P04792
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#613641 Charcot-marie-tooth disease, recessive intermediate b; cmtrib Q15046
#114500 Colorectal cancer; crc P18054
P42336
Q14191
#612918 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi P42336
#615108 Cowden syndrome 5; cws5 P42336
#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
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#610549 Diabetes mellitus, insulin-resistant, with acanthosis nigricans P06213
#125853 Diabetes mellitus, noninsulin-dependent; niddm P06213
#119900 Digital clubbing, isolated congenital P15428
#246200 Donohue syndrome P06213
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#614546 Efavirenz, poor metabolism of P20813
#160120 Episodic ataxia, type 1; ea1 Q09470
#133239 Esophageal cancer P18054
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#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
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#143500 Gilbert syndrome P22309
P22310
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#137800 Glioma susceptibility 1; glm1 P04626
#606824 Glucose/galactose malabsorption; ggm P13866
#232300 Glycogen storage disease ii P10253
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#114550 Hepatocellular carcinoma P42336
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#609968 Hyperinsulinemic hypoglycemia, familial, 5; hhf5 P06213
#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
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#182000 Keratosis, seborrheic P42336
#601626 Leukemia, acute myeloid; aml P36888
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
Q14790
#608516 Major depressive disorder; mdd P08172
#174800 Mccune-albright syndrome; mas P63092
#602501 Megalencephaly-capillary malformation-polymicrogyria syndrome; mcap P42336
#603387 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome; mpph P42336
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#159900 Myoclonic dystonia P14416
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#608634 Neuronopathy, distal hereditary motor, type iib; hmn2b P04792
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
P42336
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#262190 Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities P06213
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#233100 Renal glucosuria; glys1 P31639
#607276 Resting heart rate, variation in P08588
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#190300 Tremor, hereditary essential, 1; etm1 P35462
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (96)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
P42336 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00856 Distal hereditary motor neuropathies (dHMN) P04792 (related)
H00213 Hypophosphatasia P05186 (related)
H00719 Leprechaunism P06213 (related)
H00942 Rabson-Mendenhall syndrome P06213 (related)
H01228 Insulin-resistant diabetes mellitus with acanthosis nigricans (IRAN) P06213 (related)
H01267 Familial hyperinsulinemic hypoglycemia (HHF) P06213 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H00731 Atrial fibrillation P22460 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H00005 Chronic lymphocytic leukemia (CLL) P28907 (marker)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00264 Charcot-Marie-Tooth disease (CMT) Q01453 (related)
Q15046 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00749 Episodic ataxias Q09470 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00108 Autoimmune lymphoproliferative syndromes (ALPS) Q14790 (related)
H00801 Familial thoracic aortic aneurysm and dissection (TAAD) Q15746 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

22 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D011565 Psoriasis C00000575
C00000576
D008175 Lung Neoplasms C00000576
D006505 Hepatitis C00000575
D005909 Glioblastoma C00001071
D009203 Myocardial Infarction C00001071
D015746 Abdominal Pain C00000576
D056486 Drug-Induced Liver Injury C00000576
D004485 Eczema C00000576
D006261 Headache C00000576
D007674 Kidney Diseases C00000576
D017114 Liver Failure, Acute C00000576
D010787 Photosensitivity Disorders C00000575
D016410 Lymphoma, T-Cell, Cutaneous C00000576
D008881 Migraine Disorders C00000576
D009182 Mycosis Fungoides C00000576
D009325 Nausea C00000576
D000857 Olfaction Disorders C00000576
D011693 Purpura C00000576
D007319 Sleep Initiation and Maintenance Disorders C00000576
D014006 Tinea Capitis C00000576
D015837 Vestibular Diseases C00000576
D014820 Vitiligo C00000576