Species

KNApSAcK Entry

Organism name Lespedeza bicolor
Genus Lespedeza
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lespedeza bicolor
Linked NCBI taxonomy ID 556514
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 (12)

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
C00018971 External link 512 7,4'-Dihydroxy-2'-methoxy-6-geranylisoflavanone
No. 19 No. 14
C00001055 External link 512 Isoorientin
/ Homoorientin
/ Lespecapitioside
/ Luteolin 6-C-beta-D-glucopyranoside
/ 2-(3,4-Dihydroxyphenyl)-6-beta-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one
CHEMBL239559
CHEMBL1302308
C057912
23 / 14 / 17 0 / 1 No. 22 No. 15
C00003740 External link 512 Betulin
CHEMBL23236
CHEMBL140040
CHEMBL1610940
CHEMBL2000891
CHEMBL2069124
C002503
18 / 16 / 17 0 / 2 No. 23 No. 51
C00003741 External link 512 Betulinic acid
CHEMBL269277
CHEMBL71690
CHEMBL519059
CHEMBL1318530
CHEMBL2005635
C002070
34 / 17 / 14 10 / 2 No. 23 No. 51
C00018972 External link 512 2',4'-Dihydroxy-6''-(4-methyl-3-pentenyl)-6''-methylpyrano[2'',3'':7,6]isoflavanone
No. 39
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00009380 External link 512 Daidzein
/ 7,4'-Dihydroxyisoflavone
CHEMBL8145
C004742
60 / 68 / 76 113 / 12 No. 71 No. 15
C00006925 External link 512 Isoliquiritigenin
CHEMBL129795
CHEMBL1395334
C040920
59 / 83 / 90 12 / 3 No. 92 No. 13
C00002668 External link 512 Protocatechuic acid
/ 3,4-Dihydroxybenzoic acid
CHEMBL37537
C009091
33 / 19 / 19 2 / 0 No. 817 No. 81
C00002759 External link 512 Methyl caffeate
CHEMBL17001
C042405
No. 876
C00000615 External link 512 Caffeic acid
CHEMBL145
CHEMBL1320034
68 / 64 / 63 No. 904 No. 6
C00001402 External link 512 Bufotenine
CHEMBL416526
D002027
6 / 3 / 0 No. 1385 No. 4

Human Protein / Gene in interactions

169 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000615 C00003672 C00003740 C00003741 C00006925 C00009380 1 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000615 C00003672 C00003740 C00003741 C00006925 C00009380 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000615 C00003672 C00003740 C00003741 C00006925 C00009380 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000615 C00003672 C00003740 C00003741 C00006925 C00009380 0 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000615 C00003672 C00003740 C00003741 C00006925 C00009380 0 / 1
P02545 Prelamin-A/C Unclassified protein C00000615 C00003740 C00003741 C00006925 C00009380 11 / 10
P06746 DNA polymerase beta Enzyme C00000615 C00001055 C00002668 C00003672 C00003741 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000615 C00001055 C00002668 C00006925 C00009380 4 / 3
P15121 Aldose reductase Enzyme C00000615 C00002668 C00003741 C00006925 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000615 C00001055 C00001402 C00002668 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000615 C00001055 C00006925 C00009380 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000615 C00003672 C00003740 C00006925 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000615 C00003741 C00006925 C00009380 0 / 0
P03372 Estrogen receptor NR3A1 C00000615 C00002668 C00003672 C00009380 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00000615 C00001055 C00003741 C00006925 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000615 C00001055 C00002668 C00009380 0 / 0
O75496 Geminin Unclassified protein C00002668 C00003741 C00006925 C00009380 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000615 C00001055 C00003672 C00009380 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00000615 C00006925 C00009380 5 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001055 C00006925 C00009380 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000615 C00003740 C00006925 0 / 3
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000615 C00006925 C00009380 1 / 8
P11387 DNA topoisomerase 1 Isomerase C00003740 C00003741 C00009380 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003740 C00003741 C00009380 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00000615 C00001055 C00002668 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 C00003741 C00009380 2 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000615 C00006925 C00009380 2 / 2
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000615 C00006925 C00009380 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000615 C00006925 C00009380 3 / 3
O00255 Menin Unclassified protein C00000615 C00001055 C00006925 2 / 5
P10828 Thyroid hormone receptor beta NR1A2 C00000615 C00003740 C00009380 3 / 1
P14780 Matrix metalloproteinase-9 M10A C00000615 C00002668 C00006925 2 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000615 C00003740 C00003741 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001055 C00002668 C00006925 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000615 C00001055 C00006925 1 / 2
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003740 C00003741 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003740 C00003741 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001055 C00006925 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000615 C00003672 3 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000615 C00009380 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00000615 C00001055 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00000615 C00002668 1 / 2
P43166 Carbonic anhydrase 7 Lyase C00000615 C00002668 0 / 0
P05771 Protein kinase C beta type Alpha C00003740 C00003741 0 / 0
Q02156 Protein kinase C epsilon type Eta C00003740 C00003741 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00006925 C00009380 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00000615 C00002668 1 / 1
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00000615 C00002668 3 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000615 C00006925 2 / 2
Q9GZT9 Egl nine homolog 1 Enzyme C00000615 C00002668 1 / 1
P54132 Bloom syndrome protein Enzyme C00006925 C00009380 1 / 2
P40225 Thrombopoietin Unclassified protein C00006925 C00009380 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00000615 C00002668 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00006925 C00009380 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00000615 C00003741 0 / 0
Q99700 Ataxin-2 Unclassified protein C00006925 C00009380 1 / 1
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000615 C00006925 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000615 C00001055 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00000615 C00002668 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00000615 C00002668 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000615 C00009380 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003741 C00006925 1 / 0
O43570 Carbonic anhydrase 12 Lyase C00000615 C00002668 1 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00006925 C00009380 7 / 37
Q16790 Carbonic anhydrase 9 Lyase C00000615 C00002668 0 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00001055 C00002668 0 / 1
P39748 Flap endonuclease 1 Enzyme C00001055 C00006925 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000615 C00006925 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00003740 C00003741 0 / 0
Q01196 Runt-related transcription factor 1 Unclassified protein C00001055 C00002668 1 / 4
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00006925 C00009380 5 / 3
P14679 Tyrosinase Oxidoreductase C00000615 C00003672 4 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003740 C00006925 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00001055 C00009380 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00000615 C00002668 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 C00003741 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00006925 C00009380 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00003741 C00006925 0 / 0
P03956 Interstitial collagenase M10A C00000615 C00002668 0 / 1
Q04206 Transcription factor p65 Transcription Factor C00003741 C00006925 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00001055 C00003741 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001055 C00002668 0 / 0
P08253 72 kDa type IV collagenase M10A C00000615 C00002668 1 / 3
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00009380 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00003741 0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00009380 1 / 0
P07711 Cathepsin L1 C1A C00002668 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00009380 0 / 1
P00734 Prothrombin S1A C00003672 4 / 2
P04150 Glucocorticoid receptor NR3C1 C00009380 0 / 1
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00009380 2 / 2
P41143 Delta-type opioid receptor Opioid receptor C00009380 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001402 2 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00009380 0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00006925 0 / 0
P06280 Alpha-galactosidase A Enzyme C00000615 1 / 1
P04745 Alpha-amylase 1 Enzyme C00009380 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00006925 1 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00006925 2 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003741 0 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00006925 2 / 3
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00000615 0 / 0
P08151 Zinc finger protein GLI1 Unclassified protein C00003741 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00000615 0 / 0
P42330 Aldo-keto reductase family 1 member C3 Enzyme C00000615 0 / 0
P16581 E-selectin Adhesion C00002668 0 / 0
P55055 Oxysterols receptor LXR-beta NR1H3 C00003741 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00009380 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00009380 2 / 0
Q04828 Aldo-keto reductase family 1 member C1 Enzyme C00000615 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00006925 2 / 3
O15118 Niemann-Pick C1 protein Unclassified protein C00009380 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001055 1 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00009380 0 / 0
P15559 NAD(P)H dehydrogenase [quinone] 1 Enzyme C00003741 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001402 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001402 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00009380 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00006925 4 / 5
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00000615 0 / 0
P02768 Serum albumin Secreted protein C00002668 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00006925 0 / 0
P14151 L-selectin Adhesion C00002668 0 / 0
P16109 P-selectin Adhesion C00002668 1 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00009380 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00006925 0 / 0
P37840 Alpha-synuclein Unclassified protein C00006925 4 / 2
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00006925 1 / 0
P52895 Aldo-keto reductase family 1 member C2 Enzyme C00000615 1 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00009380 0 / 0
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00000615 4 / 2
P22894 Neutrophil collagenase M10A C00002668 0 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00006925 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00000615 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00001402 1 / 0
P10275 Androgen receptor NR3C4 C00009380 3 / 4
P28221 5-hydroxytryptamine receptor 1D Serotonin receptor C00001402 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00009380 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00006925 4 / 3
P05412 Transcription factor AP-1 Transcription Factor C00006925 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00000615 0 / 0
P35869 Aryl hydrocarbon receptor Transcription Factor C00009380 0 / 0
P08254 Stromelysin-1 M10A C00002668 1 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00000615 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q12794 Hyaluronidase-1 Enzyme C00000615 1 / 2
P04062 Glucosylceramidase Enzyme C00006925 6 / 4
P24298 Alanine aminotransferase 1 Enzyme C00000615 0 / 0
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00006925 9 / 3
P21728 D(1A) dopamine receptor Dopamine receptor C00006925 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00009380 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00009380 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00009380 4 / 1
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00003741 0 / 0
P17516 Aldo-keto reductase family 1 member C4 Enzyme C00000615 1 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00009380 3 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00009380 0 / 0
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00000615 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00000615 0 / 0
Q9UBT2 SUMO-activating enzyme subunit 2 Enzyme C00003741 0 / 0
Q9UBE0 SUMO-activating enzyme subunit 1 Unclassified protein C00003741 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00009380 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00009380 1 / 1
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00009380 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00006925 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00001055 2 / 1
P51531 Probable global transcription activator SNF2L2 Unclassified protein C00006925 1 / 0

124 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) C00003741 C00006925 C00009380
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00003741 C00009380
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) C00006925 C00009380
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00006925 C00009380
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00006925 C00009380
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00003741 C00009380
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) C00006925 C00009380
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) C00003741 C00009380
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00006925 C00009380
6513 SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED solute carrier family 2 (facilitated glucose transporter), member 1 C00006925 C00009380
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00002668 C00009380
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00006925 C00009380
5747 PTK2, FADK, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK protein tyrosine kinase 2 (EC:2.7.10.2) C00009380
10057 ABCC5, ABC33, EST277145, MOAT-C, MOATC, MRP5, SMRP, pABC11 ATP-binding cassette, sub-family C (CFTR/MRP), member 5 C00009380
119 ADD2, ADDB adducin 2 (beta) C00009380
196 AHR, bHLHe76 aryl hydrocarbon receptor C00009380
249 ALPL, AP-TNAP, APTNAP, HOPS, TNAP, TNSALP alkaline phosphatase, liver/bone/kidney (EC:3.1.3.1) C00009380
251 ALPPL2, ALPG, ALPPL, GCAP alkaline phosphatase, placental-like 2 (EC:3.1.3.1) C00009380
367 AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM androgen receptor C00009380
396 ARHGDIA, GDIA1, NPHS8, RHOGDI, RHOGDI-1 Rho GDP dissociation inhibitor (GDI) alpha C00009380
23545 ATP6V0A2, A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS ATPase, H+ transporting, lysosomal V0 subunit a2 (EC:3.6.3.6) C00009380
11177 BAZ1A, ACF1, WALp1, WCRF180, hACF1 bromodomain adjacent to zinc finger domain, 1A C00009380
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00009380
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00009380
632 BGLAP, BGP, OC, OCN bone gamma-carboxyglutamate (gla) protein C00009380
672 BRCA1, BRCAI, BRCC1, BROVCA1, IRIS, PNCA4, PPP1R53, PSCP, RNF53 breast cancer 1, early onset C00009380
103993 C00009380
890 CCNA2, CCN1, CCNA cyclin A2 C00009380
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00009380
1017 CDK2, p33(CDK2) cyclin-dependent kinase 2 (EC:2.7.11.22) C00009380
1019 CDK4, CMM3, PSK-J3 cyclin-dependent kinase 4 (EC:2.7.11.22) C00009380
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00009380
1103 CHAT, CHOACTASE, CMS1A, CMS1A2 choline O-acetyltransferase (EC:2.3.1.6) C00009380
1152 CKB, B-CK, CKBB creatine kinase, brain (EC:2.7.3.2) C00009380
19 ABCA1, ABC-1, ABC1, CERP, HDLDT1, TGD ATP-binding cassette, sub-family A (ABC1), member 1 C00009380
9167 COX7A2L, COX7AR, COX7RP, EB1, SIG81 cytochrome c oxidase subunit VIIa polypeptide 2 like C00009380
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00009380
1401 CRP, PTX1 C-reactive protein, pentraxin-related C00009380
6387 CXCL12, IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1, SDF1A, SDF1B chemokine (C-X-C motif) ligand 12 C00009380
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00009380
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00009380
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00009380
1589 CYP21A2, CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B cytochrome P450, family 21, subfamily A, polypeptide 2 (EC:1.14.99.10) C00009380
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) C00009380
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) C00009380
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) C00009380
1795 DOCK3, MOCA, PBP dedicator of cytokinesis 3 C00009380
1846 DUSP4, HVH2, MKP-2, MKP2, TYP dual specificity phosphatase 4 (EC:3.1.3.16 3.1.3.48) C00009380
9166 EBAG9, EB9, PDAF estrogen receptor binding site associated, antigen, 9 C00009380
2027 ENO3, GSD13, MSE enolase 3 (beta, muscle) (EC:4.2.1.11) C00009380
2041 EPHA1, EPH, EPHT, EPHT1 EPH receptor A1 (EC:2.7.10.1) C00009380
83715 ESPN, DFNB36 espin C00009380
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00009380
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00009380
2101 ESRRA, ERR1, ERRa, ERRalpha, ESRL1, NR3B1 estrogen-related receptor alpha C00009380
2103 ESRRB, DFNB35, ERR2, ERRb, ESRL2, NR3B2 estrogen-related receptor beta C00009380
2104 ESRRG, ERR3, ERRgamma, NR3B3 estrogen-related receptor gamma C00009380
56776 FMN2 formin 2 C00009380
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00009380
9687 GREB1 growth regulation by estrogen in breast cancer 1 C00009380
3284 HSD3B2, HSD3B, HSDB, SDR11E2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 (EC:1.1.1.145 5.3.3.1) C00009380
7866 IFRD2, IFNRP, SKMc15, SM15 interferon-related developmental regulator 2 C00009380
3480 IGF1R, CD221, IGFIR, IGFR, JTK13 insulin-like growth factor 1 receptor (EC:2.7.10.1) C00009380
3487 IGFBP4, BP-4, HT29-IGFBP, IBP4, IGFBP-4 insulin-like growth factor binding protein 4 C00009380
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00009380
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00009380
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00009380
26145 IRF2BP1 interferon regulatory factor 2 binding protein 1 C00009380
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00009380
26251 KCNG2, KCNF2, KV6.2 potassium voltage-gated channel, subfamily G, member 2 C00009380
354 KLK3, APS, KLK2A1, PSA, hK3 kallikrein-related peptidase 3 (EC:3.4.21.77) C00009380
27074 LAMP3, CD208, DC_LAMP, DC-LAMP, DCLAMP, LAMP, LAMP-3, TSC403 lysosomal-associated membrane protein 3 C00009380
4199 ME1, HUMNDME, MES malic enzyme 1, NADP(+)-dependent, cytosolic (EC:1.1.1.40) C00009380
4502 MT2A, MT2 metallothionein 2A C00009380
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00009380
10499 NCOA2, GRIP1, KAT13C, NCoA-2, SRC2, TIF2, bHLHe75 nuclear receptor coactivator 2 C00009380
4824 NKX3-1, BAPX2, NKX3, NKX3.1, NKX3A NK3 homeobox 1 C00009380
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00009380
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00009380
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00009380
8204 NRIP1, RIP140 nuclear receptor interacting protein 1 C00009380
56944 OLFML3, HNOEL-iso, OLF44 olfactomedin-like 3 C00009380
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00009380
5111 PCNA proliferating cell nuclear antigen C00009380
64236 PDLIM2, MYSTIQUE, SLIM PDZ and LIM domain 2 (mystique) C00009380
5174 PDZK1, CAP70, CLAMP, NHERF-3, NHERF3, PDZD1 PDZ domain containing 1 C00009380
5241 PGR, NR3C3, PR progesterone receptor C00009380
5411 PNN, DRS, DRSP, SDK3, memA pinin, desmosome associated protein C00009380
10957 PNRC1, B4-2, PNAS-145, PROL2, PRR2 proline-rich nuclear receptor coactivator 1 C00009380
5458 POU4F2, BRN3.2, BRN3B, Brn-3b POU class 4 homeobox 2 C00009380
5580 PRKCD, MAY1, PKCD, nPKC-delta protein kinase C, delta (EC:2.7.10.2 2.7.11.13) C00009380
11098 PRSS23, SIG13, SPUVE, ZSIG13 protease, serine, 23 C00009380
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) C00009380
10257 ABCC4, EST170205, MOAT-B, MOATB, MRP4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4 C00009380
5932 RBBP8, COM1, CTIP, JWDS, RIM, SAE2, SCKL2 retinoblastoma binding protein 8 C00009380
6197 RPS6KA3, CLS, HU-3, ISPK-1, MAPKAPK1B, MRX19, RSK, RSK2, S6K-alpha3, p90-RSK2, pp90RSK2 ribosomal protein S6 kinase, 90kDa, polypeptide 3 (EC:2.7.11.1) C00009380
81537 SGPP1, SPPase1 sphingosine-1-phosphate phosphatase 1 C00009380
6558 SLC12A2, BSC, BSC2, NKCC1 solute carrier family 12 (sodium/potassium/chloride transporter), member 2 C00009380
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00003741
8140 SLC7A5, 4F2LC, CD98, D16S469E, E16, LAT1, MPE16, hLAT1 solute carrier family 7 (amino acid transporter light chain, L system), member 5 C00009380
6781 STC1, STC stanniocalcin 1 C00009380
27347 STK39, DCHT, PASK, SPAK serine threonine kinase 39 (EC:2.7.11.1) C00009380
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) C00009380
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) C00009380
6870 TACR3, HH11, NK-3R, NK3R, NKR, TAC3RL tachykinin receptor 3 C00009380
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00009380
7041 TGFB1I1, ARA55, HIC-5, HIC5, TSC-5 transforming growth factor beta 1 induced transcript 1 C00009380
7130 TNFAIP6, TSG-6, TSG6 tumor necrosis factor, alpha-induced protein 6 C00009380
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00009380
9537 TP53I11, PIG11 tumor protein p53 inducible protein 11 C00009380
7164 TPD52L1, D53, hD53 tumor protein D52-like 1 C00009380
7345 UCHL1, NDGOA, PARK5, PGP_9.5, PGP9.5, PGP95, Uch-L1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) (EC:3.4.19.12) C00009380
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00003741
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003741
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00003741
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00003741
581 BAX, BCL2L4 BCL2-associated X protein C00003741
7367 UGT2B17, BMND12, UDPGT2B17 UDP glucuronosyltransferase 2 family, polypeptide B17 (EC:2.4.1.17) C00009380
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00009380
2023 ENO1, ENO1L1, MPB1, NNE, PPH enolase 1, (alpha) (EC:4.2.1.11) C00002668
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
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00006925
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00006925

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (146)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#614279 46,xy sex reversal 8; srxy8 P17516
P52895
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P31645
#610251 Alcohol sensitivity, acute P05091
#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
#218030 Apparent mineralocorticoid excess; ame P80365
#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
#614490 Blood group, junior system; jr Q9UNQ0
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#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 P84022
Q14191
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#218800 Crigler-najjar syndrome, type i P22310
#606785 Crigler-najjar syndrome, type ii 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
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#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 P22310
#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
#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
#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
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#151100 Leopard syndrome 1 Q06124
#601626 Leukemia, acute myeloid; aml P10721
#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
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#156250 Metachondromatosis; metcds Q06124
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#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
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#601358 Nicolaides-baraitser syndrome; ncbrs P51531
#257220 Niemann-pick disease, type c1; npc1 O15118
#163950 Noonan syndrome 1; ns1 Q06124
#601665 Obesity P37231
#164230 Obsessive-compulsive disorder; ocd P31645
#166250 Osteoglophonic dysplasia; ogd P11362
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#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
#614674 Periodic fever, menstrual cycle-dependent P08908
#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
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#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
#601367 Stroke, ischemic P00734
P16109
#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
#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
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278300 Xanthinuria, type i P47989
#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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
P08581 (related)
Q16790 (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)
P08581 (related)
P21802 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04637 (related)
P08253 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P08253 (related)
P14780 (related)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
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)
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)
H00125 Fabry disease P06280 (related)
H00472 Torg-Winchester syndrome P08253 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00170 Piebaldism P10721 (related)
H00023 Testicular cancer P10721 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (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)
H00168 Oculocutaneous albinism (OCA) P14679 (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)
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)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (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)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00236 Congenital polycythemia Q9GZT9 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

20 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008103 Liver Cirrhosis C00003741
D008545 Melanoma C00003741
D003110 Colonic Neoplasms C00003740
D064420 Drug-Related Side Effects and Adverse Reactions C00003740
D000230 Adenocarcinoma C00009380
D000647 Amnesia C00009380
D002318 Cardiovascular Diseases C00009380
D003924 Diabetes Mellitus, Type 2 C00009380
D004487 Edema C00009380
D016889 Endometrial Neoplasms C00009380
D007172 Erectile Dysfunction C00009380
D006965 Hyperplasia C00009380
D006973 Hypertension C00009380
D017254 Leukemic Infiltration C00009380
D008569 Memory Disorders C00009380
D014693 Ventricular Fibrillation C00009380
D001927 Brain Diseases C00006925
D009120 Muscle Cramp C00006925
D009422 Nervous System Diseases C00006925
D008104 Liver Cirrhosis, Alcoholic C00001055