Species

KNApSAcK Entry

Organism name Pterocarpus marsupium
Genus Pterocarpus
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pterocarpus marsupium
Linked NCBI taxonomy ID 1071187
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 (30)

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
C00010146 External link 512 5,7-Dihydroxy-6-methoxyisoflavone 7-O-rhamnoside
No. 2 No. 15
C00010145 External link 512 Retusin 7-O-glucoside
No. 2 No. 15
C00010147 External link 512 Irisolidone 7-O-rhamnoside
No. 2 No. 15
C00010170 External link 512 Retusin 8-O-arabinoside
No. 2 No. 15
C00013827 External link 512 6-Hydroxykaempferol 3,5,7,4'-tetramethyl ether 6-rhamnoside
/ 6-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-3,5,7-trimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
No. 2 No. 15
C00008396 External link 512 7,8,4'-Trihydroxy-3',5'-dimethoxyflavanone 4'-O-glucoside
No. 12 No. 14
C00001039 External link 512 8-C-Glucosylfisetin
/ Fisetin 8-C-glucoside
No. 22 No. 15
C00006109 External link 512 8-C-Glucosyl-5-deoxykaempferol
/ 8-beta-D-Glucopyranosyl-3,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
No. 22 No. 15
C00000977 External link 512 Liquiritigenin
CHEMBL252642
CHEMBL271939
C083152
5 / 4 / 4 1 / 1 No. 25 No. 14
C00000982 External link 512 Naringenin
/ (-)-Naringenin
CHEMBL9352
CHEMBL32571
C005273
57 / 46 / 40 35 / 10 No. 25 No. 14
C00008126 External link 512 7-Hydroxyflavanone
CHEMBL97542
CHEMBL402744
C059353
9 / 18 / 45 1 / 0 No. 25 No. 14
C00008064 External link 512 6,4'-Dihydroxy-7-methylaurone 6-rhamnoside
No. 36 No. 13
C00008065 External link 512 4,6,4'-Trihydroxy-7-methylaurone 4-rhamnoside
No. 36 No. 13
C00008042 External link 512 4,6,4'-Trihydroxyaurone 6-rhamnoside
No. 36 No. 13
C00008047 External link 512 Aureusidin 6-rhamnoside
No. 36 No. 13
C00000964 External link 512 Garbanzol
CHEMBL254051
No. 42 No. 14
C00000956 External link 512 (-)-Epicatechin
CHEMBL80941
CHEMBL311498
CHEMBL129482
CHEMBL200715
CHEMBL206452
CHEMBL583912
85 / 58 / 54 No. 52 No. 14
C00020153 External link 512 5,6,7-TrihydroxyIsoflavone
No. 71 No. 15
C00004540 External link 512 Resokaempferol
CHEMBL242383
19 / 22 / 55 No. 76 No. 15
C00003800 External link 512 7,4'-Dihydroxyflavone
CHEMBL294878
C085172
17 / 19 / 16 No. 76 No. 15
C00006925 External link 512 Isoliquiritigenin
CHEMBL129795
CHEMBL1395334
C040920
59 / 83 / 90 12 / 3 No. 92 No. 13
C00019722 External link 512 Formononetin 7-O-(2'',6''-di-O-(E-p-coumaroyl)glucoside)
/ 7-Hydroxy-4'-methoxyisoflavone 7-O-(2'',6'-di-O-E-p-coumaroyl)-glucoside
No. 231
C00006115 External link 512 Coatline A
No. 261 No. 14
C00006117 External link 512 Pterosupin
C083153
No. 261 No. 14
C00002902 External link 512 Pterostilbene
/ 3,5-Dimethoxy-4'-hydroxystilbene
CHEMBL87712
CHEMBL83527
C107773
19 / 19 / 20 54 / 15 No. 344 No. 13
C00012781 External link 512 [2R-(2alpha,4aalpha,5alpha,8abeta)]-Decahydro-5-hydroxy-a,a,4a-trimethyl-8-methylene-2-naphthalenemethanol
CHEMBL1079685
No. 524 No. 38
C00008067 External link 512 Carpusin
CHEMBL512396
No. 1085
C00010152 External link 512 7-Hydroxy-5,4'-dimethoxy-8-methylisoflavone 7-O-rhamnoside
No. 2064
C00002657 External link 512 p-Formylphenol
/ 4-Hydroxybenzaldehyde
/ p-Hydroxybenzaldehyde
CHEMBL14193
C011483
3 / 2 / 2 No. 2076
C00008397 External link 512 7-Hydroxy-6,8-di-C-methylflavanone 7-O-arabinoside
No. 7294

Human Protein / Gene in interactions

169 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P28482 Mitogen-activated protein kinase 1 Erk C00000956 C00002902 C00003800 C00004540 C00006925 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000977 C00000982 C00002902 C00003800 C00008126 2 / 2
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000956 C00000982 C00002902 C00004540 C00006925 1 / 2
O00255 Menin Unclassified protein C00000956 C00000982 C00002902 C00004540 C00006925 2 / 5
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000956 C00000982 C00003800 C00004540 C00006925 3 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000956 C00000982 C00003800 C00004540 C00006925 0 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000956 C00000982 C00004540 C00006925 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00000956 C00002902 C00004540 C00006925 4 / 3
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000956 C00000977 C00000982 C00006925 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000956 C00003800 C00004540 C00006925 2 / 2
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000956 C00002902 C00003800 C00004540 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000956 C00000982 C00002902 C00006925 0 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000956 C00000982 C00004540 C00006925 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000956 C00000982 C00004540 C00006925 1 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000956 C00000982 C00006925 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00000982 C00003800 C00006925 5 / 3
P04637 Cellular tumor antigen p53 Transcription Factor C00004540 C00006925 C00008126 7 / 37
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000956 C00000982 C00006925 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000956 C00004540 C00006925 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002902 C00006925 C00008126 0 / 0
O75496 Geminin Unclassified protein C00000982 C00002902 C00006925 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000956 C00002902 C00006925 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000956 C00000982 C00006925 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000956 C00003800 C00004540 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00000956 C00002902 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00000956 C00006925 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000956 C00006925 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00000982 C00003800 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000977 C00006925 2 / 2
P35372 Mu-type opioid receptor Opioid receptor C00000956 C00000982 0 / 0
Q01453 Peripheral myelin protein 22 Unclassified protein C00000956 C00006925 5 / 2
P04062 Glucosylceramidase Enzyme C00000982 C00006925 6 / 4
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00000956 C00006925 1 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00000956 C00000982 5 / 1
P10275 Androgen receptor NR3C4 C00000982 C00008126 3 / 4
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00000956 C00006925 2 / 3
P04745 Alpha-amylase 1 Enzyme C00000956 C00000982 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000956 C00000982 1 / 1
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00000982 C00003800 0 / 0
P05412 Transcription factor AP-1 Transcription Factor C00000977 C00006925 0 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00003800 C00008126 1 / 1
P04150 Glucocorticoid receptor NR3C1 C00000982 C00008126 0 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00000956 C00006925 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000956 C00006925 0 / 0
P08183 Multidrug resistance protein 1 drug C00000982 C00002902 1 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000956 C00000982 1 / 1
Q16637 Survival motor neuron protein Unclassified protein C00000956 C00003800 4 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00000956 C00000982 3 / 0
P15121 Aldose reductase Enzyme C00000982 C00006925 0 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000956 C00000982 0 / 0
P54132 Bloom syndrome protein Enzyme C00000956 C00006925 1 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002902 C00008126 4 / 2
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00003800 C00008126 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000956 C00006925 2 / 3
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00003800 C00008126 1 / 1
P41145 Kappa-type opioid receptor Opioid receptor C00000956 C00000982 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000956 C00006925 2 / 0
Q9Y3R4 Sialidase-2 Enzyme C00000956 C00003800 0 / 0
P39748 Flap endonuclease 1 Enzyme C00000956 C00006925 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00000977 C00006925 0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00000982 1 / 0
P04278 Sex hormone-binding globulin Secreted protein C00000982 0 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00000982 1 / 1
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00002657 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00000956 0 / 0
P07998 Ribonuclease pancreatic Enzyme C00000956 0 / 0
P16152 Carbonyl reductase [NADPH] 1 Enzyme C00000982 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00000956 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00000956 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002902 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00006925 1 / 8
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00000982 0 / 0
O75828 Carbonyl reductase [NADPH] 3 Enzyme C00000982 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00000982 0 / 1
P24864 G1/S-specific cyclin-E1 Other cytosolic protein C00000982 0 / 2
P00915 Carbonic anhydrase 1 Lyase C00000956 0 / 0
P07711 Cathepsin L1 C1A C00000956 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00000982 0 / 0
P49327 Fatty acid synthase Transferase C00000956 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000956 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00000956 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00000956 3 / 1
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000982 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00006925 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00000956 1 / 2
P11021 78 kDa glucose-regulated protein Unclassified protein C00006925 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00004540 0 / 0
P00734 Prothrombin S1A C00000956 4 / 2
P02768 Serum albumin Secreted protein C00000956 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00000956 1 / 2
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002657 1 / 1
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002657 1 / 1
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000982 4 / 4
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00006925 0 / 0
P06280 Alpha-galactosidase A Enzyme C00003800 1 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00000956 3 / 2
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00006925 1 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00000982 2 / 0
P37840 Alpha-synuclein Unclassified protein C00006925 4 / 2
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002902 1 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00000956 0 / 1
P56817 Beta-secretase 1 A1A C00000956 0 / 0
P02545 Prelamin-A/C Unclassified protein C00006925 11 / 10
Q16790 Carbonic anhydrase 9 Lyase C00000956 0 / 1
P62158 Calmodulin Unclassified protein C00000982 1 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00000982 2 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00000982 1 / 1
P28907 ADP-ribosyl cyclase 1 Enzyme C00000956 0 / 1
O15118 Niemann-Pick C1 protein Unclassified protein C00002902 1 / 1
Q8N1Q1 Carbonic anhydrase 13 Lyase C00000956 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00006925 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000982 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000982 0 / 0
P00374 Dihydrofolate reductase Oxidoreductase C00000956 1 / 1
P03372 Estrogen receptor NR3A1 C00000982 1 / 1
P22303 Acetylcholinesterase Hydrolase C00000982 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00006925 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00006925 4 / 5
P52209 6-phosphogluconate dehydrogenase, decarboxylating Enzyme C00000956 0 / 0
P29466 Caspase-1 C14 C00004540 0 / 0
P55210 Caspase-7 C14 C00004540 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00000956 0 / 0
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00000982 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00000956 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00000956 0 / 0
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00006925 9 / 3
P06746 DNA polymerase beta Enzyme C00000956 0 / 0
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00000956 3 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00006925 2 / 2
Q99549 M-phase phosphoprotein 8 Unclassified protein C00006925 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00006925 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00006925 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00006925 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00006925 4 / 3
Q99700 Ataxin-2 Unclassified protein C00006925 1 / 1
P07451 Carbonic anhydrase 3 Lyase C00000956 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00003800 0 / 1
Q04760 Lactoylglutathione lyase Enzyme C00000982 0 / 0
P49888 Estrogen sulfotransferase Enzyme C00000982 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00000956 1 / 1
P10415 Apoptosis regulator Bcl-2 Other cytosolic protein C00000956 0 / 7
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000982 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000982 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000956 0 / 0
P40225 Thrombopoietin Unclassified protein C00006925 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000956 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00000982 1 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00006925 1 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00000982 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00004540 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00004540 1 / 4
Q05513 Protein kinase C zeta type Iota C00000956 0 / 0
Q04759 Protein kinase C theta type Delta C00000956 0 / 1
Q02156 Protein kinase C epsilon type Eta C00000956 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00000956 0 / 0
P17252 Protein kinase C alpha type Alpha C00000956 0 / 0
Q05655 Protein kinase C delta type Delta C00000956 0 / 0
P05129 Protein kinase C gamma type Alpha C00000956 1 / 1
P05771 Protein kinase C beta type Alpha C00000956 0 / 0
P24723 Protein kinase C eta type Eta C00000956 1 / 0
P41743 Protein kinase C iota type Iota C00000956 0 / 0
Q15139 Serine/threonine-protein kinase D1 Pkd C00000956 0 / 0
P00519 Tyrosine-protein kinase ABL1 Abl C00002902 1 / 2
P11274 Breakpoint cluster region protein Bcr C00002902 1 / 2
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00000982 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00006925 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00000956 0 / 0
P51531 Probable global transcription activator SNF2L2 Unclassified protein C00006925 1 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002902 1 / 1

85 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000982 C00002902 C00006925
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00000982 C00006925
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002902 C00006925
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002902 C00006925
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) C00000982 C00006925
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) C00000982 C00006925
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00000982 C00006925
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00000982 C00006925
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002902 C00006925
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00000982 C00002902
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00000982 C00002902
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00000982 C00002902
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00000982 C00008126
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00000982 C00002902
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00000982 C00002902
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000982 C00002902
6513 SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED solute carrier family 2 (facilitated glucose transporter), member 1 C00000982 C00006925
3717 JAK2, JTK10, THCYT3 Janus kinase 2 (EC:2.7.10.2) C00002902
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00000982
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00000982
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00000982
3757 KCNH2, ERG1, HERG, HERG1, Kv11.1, LQT2, SQT1 potassium voltage-gated channel, subfamily H (eag-related), member 2 C00000982
5444 PON1, ESA, MVCD5, PON paraoxonase 1 (EC:3.1.1.2 3.1.8.1 3.1.1.81) C00000982
6566 SLC16A1, HHF7, MCT, MCT1 solute carrier family 16 (monocarboxylate transporter), member 1 C00000982
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) C00000982
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) C00000982
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) C00000982
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00000982
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00000982
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00000982
249 ALPL, AP-TNAP, APTNAP, HOPS, TNAP, TNSALP alkaline phosphatase, liver/bone/kidney (EC:3.1.3.1) C00000982
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00000982
8644 AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) C00000982
1645 AKR1C1, 2-ALPHA-HSD, 20-ALPHA-HSD, C9, DD1, DD1/DD2, DDH, DDH1, H-37, HAKRC, HBAB, MBAB aldo-keto reductase family 1, member C1 (EC:1.3.1.20 1.1.1.149 1.1.1.112) C00000982
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00000982
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000982
329 BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 baculoviral IAP repeat containing 2 C00006925
330 BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 baculoviral IAP repeat containing 3 C00006925
10057 ABCC5, ABC33, EST277145, MOAT-C, MOATC, MRP5, SMRP, pABC11 ATP-binding cassette, sub-family C (CFTR/MRP), member 5 C00000982
10257 ABCC4, EST170205, MOAT-B, MOATB, MRP4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4 C00000982
1831 TSC22D3, DIP, DSIPI, GILZ, TSC-22R, hDIP TSC22 domain family, member 3 C00000977
23600 AMACR, AMACRD, CBAS4, RACE, RM alpha-methylacyl-CoA racemase (EC:5.1.99.4) C00002902
1386 ATF2, CRE-BP1, CREB2, HB16, TREB7 activating transcription factor 2 (EC:2.3.1.48) C00002902
578 BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 BCL2-antagonist/killer 1 C00002902
581 BAX, BCL2L4 BCL2-associated X protein C00002902
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00002902
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00002902
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00002902
2921 CXCL3, CINC-2b, GRO3, GROg, MIP-2b, MIP2B, SCYB3 chemokine (C-X-C motif) ligand 3 C00002902
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00002902
1649 DDIT3, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 DNA-damage-inducible transcript 3 C00002902
56616 DIABLO, DFNA64, SMAC diablo, IAP-binding mitochondrial protein C00002902
1950 EGF, HOMG4, URG epidermal growth factor C00002902
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00002902
2002 ELK1 ELK1, member of ETS oncogene family C00002902
2523 FUT1, H, HH, HSC fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group) (EC:2.4.1.69) C00002902
9518 GDF15, GDF-15, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB growth differentiation factor 15 C00002902
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00002902
4670 HNRNPM, CEAR, HNRNPM4, HNRPM, HNRPM4, HTGR1, NAGR1, hnRNP_M heterogeneous nuclear ribonucleoprotein M C00002902
3313 HSPA9, CSA, GRP-75, GRP75, HSPA9B, MOT, MOT2, MTHSP75, PBP74 heat shock 70kDa protein 9 (mortalin) C00002902
3458 IFNG, IFG, IFI interferon, gamma C00002902
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00002902
3696 ITGB8 integrin, beta 8 C00002902
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) C00000982
3949 LDLR, FH, FHC, LDLCQ2 low density lipoprotein receptor C00002902
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00002902
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00002902
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00002902
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00002902
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00002902
4170 MCL1, BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1, TM, bcl2-L-3, mcl1/EAT myeloid cell leukemia sequence 1 (BCL2-related) C00002902
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002902
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00002902
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 C00002902
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00002902
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00002902
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00002902
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00002902
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) C00002902
6301 SARS, SERRS, SERS seryl-tRNA synthetase (EC:6.1.1.11) C00002902
6648 SOD2, IPOB, MNSOD, MVCD6 superoxide dismutase 2, mitochondrial (EC:1.15.1.1) C00002902
6667 SP1 Sp1 transcription factor C00002902
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00002902
9189 ZBED1, ALTE, DREF, TRAMP, hDREF zinc finger, BED-type containing 1 C00002902
118738 ZNF488 zinc finger protein 488 C00002902

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (145)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#610251 Alcohol sensitivity, acute P05091
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#207410 Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 P21802
#101200 Apert syndrome P21802
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#600807 Asthma, susceptibility to Q13093
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#123790 Beare-stevenson cutis gyrata syndrome; bstvs P21802
#614592 Bent bone dysplasia syndrome; bbds P21802
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#614490 Blood group, junior system; jr Q9UNQ0
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#114500 Colorectal cancer; crc P18054
P84022
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#123500 Crouzon syndrome P21802
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#613163 Gaba-transaminase deficiency P80404
#606764 Gastrointestinal stromal tumor; gist P10721
#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
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#232300 Glycogen storage disease ii P10253
#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 P08581
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#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
#147050 Ige responsiveness, atopic; iger Q13093
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#123150 Jackson-weiss syndrome; jws P21802
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#601626 Leukemia, acute myeloid; aml P10721
P36888
#608232 Leukemia, chronic myeloid; cml P00519
P11274
#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
#613839 Megaloblastic anemia due to dihydrofolate reductase deficiency P00374
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#601358 Nicolaides-baraitser syndrome; ncbrs P51531
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166250 Osteoglophonic dysplasia; ogd P11362
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P04062
P37840
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#101600 Pfeiffer syndrome P11362
P21802
#172700 Pick disease of brain P10636
#172800 Piebald trait; pbt P10721
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614278 Platelet-activating factor acetylhydrolase deficiency; pafad Q13093
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#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
#605361 Spinocerebellar ataxia 14; sca14 P05129
#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
#601367 Stroke, ischemic P00734
P24723
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#187950 Thrombocythemia 1; thcyt1 P40225
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#190440 Trigonocephaly 1; trigno1 P11362
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#614916 Ventricular tachycardia, catecholaminergic polymorphic, 4; cpvt4 P62158
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (125)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
P08581 (related)
Q16790 (marker)
H01197 Dihydrofolate reductase (DHFR) deficiency P00374 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) P00519 (related)
P00519 (marker)
P11274 (related)
P11274 (marker)
Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00004 Chronic myeloid leukemia (CML) P00519 (related)
P00519 (marker)
P04637 (related)
P11274 (related)
P11274 (marker)
Q01196 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04637 (related)
P08581 (related)
P10415 (related)
P21802 (related)
P24864 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P04637 (related)
P10415 (related)
H00030 Cervical cancer P00533 (related)
P10415 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P24864 (related)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
P37840 (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)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
P10415 (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)
P10415 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P14780 (related)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
P10415 (related)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P08581 (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)
H01071 Acute alcohol sensitivity P05091 (related)
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
Q99700 (related)
Q9NUW8 (related)
H00213 Hypophosphatasia P05186 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
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)
H00054 Nasopharyngeal cancer P10415 (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)
P10721 (marker)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
P36888 (related)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00170 Piebaldism P10721 (related)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
P21802 (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)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (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)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00192 Xanthinuria P47989 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00408 Type I diabetes mellitus Q04759 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

28 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009120 Muscle Cramp C00006925
C00000977
D000236 Adenoma C00002902
D009202 Cardiomyopathies C00000982
D056486 Drug-Induced Liver Injury C00000982
D064420 Drug-Related Side Effects and Adverse Reactions C00000982
D007674 Kidney Diseases C00000982
D008106 Liver Cirrhosis, Experimental C00000982
D008107 Liver Diseases C00000982
D009369 Neoplasms C00000982
D009374 Neoplasms, Experimental C00000982
D001927 Brain Diseases C00006925
D000647 Amnesia C00000982
D009422 Nervous System Diseases C00006925
D058739 Aberrant Crypt Foci C00002902
D001932 Brain Neoplasms C00000982
D001943 Breast Neoplasms C00002902
D006528 Carcinoma, Hepatocellular C00002902
D002471 Cell Transformation, Neoplastic C00002902
D003110 Colonic Neoplasms C00002902
D015179 Colorectal Neoplasms C00002902
D007249 Inflammation C00002902
D015464 Leukemia, Myelogenous, Chronic, BCR-ABL Positive C00002902
D009361 Neoplasm Invasiveness C00002902
D009362 Neoplasm Metastasis C00002902
D012516 Osteosarcoma C00002902
D010190 Pancreatic Neoplasms C00002902
D010212 Papilloma C00002902
D012878 Skin Neoplasms C00002902