Species

KNApSAcK Entry

Organism name Sophora prostrata
Genus Sophora
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Sophora prostrata
Linked NCBI taxonomy ID 76398
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 (18)

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
C00020212 External link 512 7,3',4'-Trihydroxyflavone 6,8-diglucoside
No. 1 No. 15
C00019534 External link 512 Prostratol A
/ 7,2',4'-Trihydroxy-5'-((2E)-3,7-dimethyl-2,6-octadienyl)isoflavanone
No. 19 No. 14
C00019535 External link 512 Prostratol B
/ 7,2',4'-Trihydroxy-6,5'-diprenylisoflavanone
No. 19 No. 14
C00014185 External link 512 Prostratol F
/ (2S)-7,4'-Dihydroxy-8-geranylflavanone
No. 19 No. 14
C00008611 External link 512 3-Hydroxyglabrol
CHEMBL463947
No. 19 No. 14
C00008459 External link 512 Glabrol
CHEMBL462721
7 / 12 / 6 No. 19 No. 14
C00019536 External link 512 Prostratol C
/ 7,2'-Dihydroxy-4'-methoxy-5'-prenylisoflavanone
CHEMBL1811967
1 / 0 / 0 No. 28 No. 14
C00003825 External link 512 3',4',7-Trihydroxyflavone
/ 7,3',4'-Trihydroxyflavone
CHEMBL301624
4 / 5 / 5 No. 71 No. 15
C00000674 External link 512 Luteolin
CHEMBL151
D047311
99 / 91 / 95 76 / 6 No. 71 No. 15
C00003800 External link 512 7,4'-Dihydroxyflavone
CHEMBL294878
C085172
17 / 19 / 16 No. 76 No. 15
C00002381 External link 512 Corylifolinin
/ Isobavachalcone
/ 2',4,4'-Trihydroxy-3'-(3-methyl-2-butenyl)chalcone
CHEMBL253467
C468754
8 / 22 / 21 No. 133 No. 13
C00007070 External link 512 Bavachalcone
No. 133 No. 13
C00010002 External link 512 Isoneorautenol
/ 3-Hydroxy-6'',6''-dimethylpyrano[2'',3'':9,8]pterocarpan
CHEMBL1098729
No. 135 No. 15
C00019533 External link 512 Prostratol G
CHEMBL34333
CHEMBL561966
No. 170 No. 14
C00019531 External link 512 Prostratol D
/ (6aR,11aR)-3-Hydroxy-9-methoxy-8-prenylpterocarpan
No. 188 No. 15
C00009668 External link 512 Ficifolinol
/ 3,9-Dihydroxy-2,8-diprenylpterocarpan
No. 460
C00019532 External link 512 Prostratol E
/ (6aR,11aR)-3-Hydroxy-9-methoxy-8-((2E)-3,7-dimethyl-2,6-octadienhyl)pterocarpan
No. 460
C00009669 External link 512 Erythrabyssin II
/ 3,9-Dihydroxy-2,10-diprenylpterocarpan
CHEMBL455372
1 / 0 / 0 No. 460

Human Protein / Gene in interactions

116 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75164 Lysine-specific demethylase 4A Enzyme C00000674 C00008459 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00009669 C00019536 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000674 C00003800 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00000674 C00003800 0 / 1
Q16637 Survival motor neuron protein Unclassified protein C00000674 C00003800 4 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000674 C00003800 0 / 1
Q99700 Ataxin-2 Unclassified protein C00000674 C00008459 1 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00000674 C00003800 0 / 0
Q9H2K2 Tankyrase-2 Enzyme C00000674 C00003825 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000674 C00003800 2 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000674 C00003800 3 / 3
P06280 Alpha-galactosidase A Enzyme C00000674 C00003800 1 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00003800 C00008459 5 / 3
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002381 C00003800 2 / 2
P09874 Poly [ADP-ribose] polymerase 1 Enzyme C00000674 C00003825 0 / 0
O75496 Geminin Unclassified protein C00000674 C00008459 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000674 C00008459 2 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000674 C00003800 0 / 0
O95271 Tankyrase-1 Enzyme C00000674 C00003825 0 / 0
Q9Y3R4 Sialidase-2 Enzyme C00000674 C00003800 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00000674 C00003800 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000674 1 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000674 1 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00000674 3 / 1
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00003800 1 / 1
P37840 Alpha-synuclein Unclassified protein C00008459 4 / 2
Q00534 Cyclin-dependent kinase 6 CMGC serine/threonine protein kinase family C00000674 1 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00000674 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000674 0 / 0
P08183 Multidrug resistance protein 1 drug C00000674 1 / 0
P49327 Fatty acid synthase Transferase C00000674 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00000674 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000674 0 / 1
Q00535 Cyclin-dependent kinase 5 Cdk5 C00000674 0 / 0
Q15078 Cyclin-dependent kinase 5 activator 1 REG serine/threonine protein kinase family C00000674 0 / 0
P54132 Bloom syndrome protein Enzyme C00000674 1 / 2
P51570 Galactokinase Enzyme C00000674 1 / 1
Q9HC97 G-protein coupled receptor 35 Kynurenic acid receptor C00000674 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00000674 1 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002381 1 / 8
P11387 DNA topoisomerase 1 Isomerase C00000674 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00000674 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000674 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000674 11 / 10
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000674 0 / 0
P28907 ADP-ribosyl cyclase 1 Enzyme C00000674 0 / 1
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00000674 1 / 1
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000674 0 / 0
P39748 Flap endonuclease 1 Enzyme C00000674 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000674 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000674 2 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00000674 4 / 2
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00003800 0 / 0
P03956 Interstitial collagenase M10A C00000674 0 / 1
Q9Y253 DNA polymerase eta Enzyme C00000674 1 / 1
P11021 78 kDa glucose-regulated protein Unclassified protein C00000674 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000674 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000674 0 / 1
P39900 Macrophage metalloelastase M10A C00000674 0 / 0
P14679 Tyrosinase Oxidoreductase C00000674 4 / 2
P10253 Lysosomal alpha-glucosidase Hydrolase C00000674 1 / 1
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000674 4 / 4
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00002381 0 / 0
P06276 Cholinesterase Hydrolase C00000674 0 / 0
P04062 Glucosylceramidase Enzyme C00000674 6 / 4
P04745 Alpha-amylase 1 Enzyme C00000674 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00002381 1 / 0
P45452 Collagenase 3 M10A C00000674 1 / 1
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00000674 2 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00002381 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00003800 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000674 0 / 0
P08253 72 kDa type IV collagenase M10A C00000674 1 / 3
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00002381 9 / 3
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00000674 2 / 0
P06746 DNA polymerase beta Enzyme C00000674 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000674 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000674 0 / 3
O14763 Tumor necrosis factor receptor superfamily member 10B Unclassified protein C00000674 1 / 0
P03372 Estrogen receptor NR3A1 C00000674 1 / 1
P22303 Acetylcholinesterase Hydrolase C00000674 1 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00002381 4 / 5
P16050 Arachidonate 15-lipoxygenase Enzyme C00000674 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000674 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000674 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000674 0 / 0
Q15046 Lysine--tRNA ligase Enzyme C00000674 2 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00000674 3 / 2
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000674 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000674 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000674 0 / 0
P10275 Androgen receptor NR3C4 C00000674 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00003800 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00002381 4 / 3
Q9NPH5 NADPH oxidase 4 Enzyme C00000674 0 / 0
Q04760 Lactoylglutathione lyase Enzyme C00000674 0 / 0
P08254 Stromelysin-1 M10A C00000674 1 / 0
O14746 Telomerase reverse transcriptase Enzyme C00003825 5 / 5
Q9UBT6 DNA polymerase kappa Enzyme C00000674 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00000674 7 / 37
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000674 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000674 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000674 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00008459 1 / 0
O00255 Menin Unclassified protein C00000674 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000674 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00000674 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000674 1 / 4
O95067 G2/mitotic-specific cyclin-B2 Other cytosolic protein C00000674 0 / 0
P14635 G2/mitotic-specific cyclin-B1 Other cytosolic protein C00000674 0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 C00000674 0 / 0
Q8WWL7 G2/mitotic-specific cyclin-B3 Other cytosolic protein C00000674 0 / 0
P49840 Glycogen synthase kinase-3 alpha Gsk C00000674 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00000674 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000674 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00000674 2 / 1

76 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00000674
9429 ABCG2, ABC15, ABCP, BCRP, BCRP1, BMDP, CD338, CDw338, EST157481, GOUT1, MRX, MXR, MXR1, UAQTL1 ATP-binding cassette, sub-family G (WHITE), member 2 C00000674
177 AGER, RAGE advanced glycosylation end product-specific receptor C00000674
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000674
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00000674
581 BAX, BCL2L4 BCL2-associated X protein C00000674
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00000674
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00000674
329 BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 baculoviral IAP repeat containing 2 C00000674
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000674
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00000674
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00000674
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00000674
847 CAT catalase (EC:1.11.1.6) C00000674
890 CCNA2, CCN1, CCNA cyclin A2 C00000674
891 CCNB1, CCNB cyclin B1 C00000674
958 CD40, Bp50, CDW40, TNFRSF5, p50 CD40 molecule, TNF receptor superfamily member 5 C00000674
972 CD74, DHLAG, HLADG, II, Ia-GAMMA CD74 molecule, major histocompatibility complex, class II invariant chain C00000674
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00000674
1017 CDK2, p33(CDK2) cyclin-dependent kinase 2 (EC:2.7.11.22) C00000674
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00000674
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00000674
1031 CDKN2C, INK4C, p18, p18-INK4C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) C00000674
1437 CSF2, GMCSF colony stimulating factor 2 (granulocyte-macrophage) C00000674
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00000674
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00000674
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) C00000674
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00000674
1950 EGF, HOMG4, URG epidermal growth factor C00000674
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00000674
1958 EGR1, AT225, G0S30, KROX-24, NGFI-A, TIS8, ZIF-268, ZNF225 early growth response 1 C00000674
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00000674
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00000674
2203 FBP1, FBP fructose-1,6-bisphosphatase 1 (EC:3.1.3.11) C00000674
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00000674
2354 FOSB, AP-1, G0S3, GOS3, GOSB FBJ murine osteosarcoma viral oncogene homolog B C00000674
4616 GADD45B, GADD45BETA, MYD118 growth arrest and DNA-damage-inducible, beta C00000674
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00000674
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00000674
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00000674
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00000674
3726 JUNB, AP-1 jun B proto-oncogene C00000674
3727 JUND, AP-1 jun D proto-oncogene C00000674
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00000674
5602 MAPK10, JNK3, JNK3A, PRKM10, SAPK1b, p493F12, p54bSAPK mitogen-activated protein kinase 10 (EC:2.7.11.24) C00000674
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) C00000674
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00000674
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00000674
4312 MMP1, CLG, CLGN matrix metallopeptidase 1 (interstitial collagenase) (EC:3.4.24.7) C00000674
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00000674
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 C00000674
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00000674
4793 NFKBIB, IKBB, TRIP9 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, beta C00000674
9572 NR1D1, EAR1, THRA1, THRAL, ear-1, hRev nuclear receptor subfamily 1, group D, member 1 C00000674
5347 PLK1, PLK, STPK13 polo-like kinase 1 (EC:2.7.11.21) C00000674
8000 PSCA, PRO232 prostate stem cell antigen C00000674
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) C00000674
5747 PTK2, FADK, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK protein tyrosine kinase 2 (EC:2.7.10.2) C00000674
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00000674
6401 SELE, CD62E, ELAM, ELAM1, ESEL, LECAM2 selectin E C00000674
2810 SFN, YWHAS stratifin C00000674
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00000674
29110 TBK1, NAK, T2K TANK-binding kinase 1 (EC:2.7.11.1) C00000674
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000674
7128 TNFAIP3, A20, OTUD7C, TNFA1P2 tumor necrosis factor, alpha-induced protein 3 (EC:3.4.19.12) C00000674
8743 TNFSF10, APO2L, Apo-2L, CD253, TL2, TRAIL tumor necrosis factor (ligand) superfamily, member 10 C00000674
9540 TP53I3, PIG3 tumor protein p53 inducible protein 3 C00000674
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 C00000674
7161 TP73, P73 tumor protein p73 C00000674
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00000674
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00000674
10451 VAV3 vav 3 guanine nucleotide exchange factor C00000674
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00000674
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00000674
8839 WISP2, CCN5, CT58, CTGF-L WNT1 inducible signaling pathway protein 2 C00000674
331 XIAP, API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 X-linked inhibitor of apoptosis C00000674

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (125)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#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
#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
#609135 Aplastic anemia O14746
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#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
#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
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#613641 Charcot-marie-tooth disease, recessive intermediate b; cmtrib Q15046
#114500 Colorectal cancer; crc P18054
P84022
Q14191
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#123500 Crouzon syndrome P21802
#613916 Deafness, autosomal recessive 89; dfnb89 Q15046
#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
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#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
#230200 Galactokinase deficiency P51570
#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
#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
#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
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#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
#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
#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
#211980 Lung cancer P00533
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#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
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#601665 Obesity P37231
#166250 Osteoglophonic dysplasia; ogd P11362
#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
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#275210 Restrictive dermopathy, lethal P02545
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#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
#602111 Spondyloepimetaphyseal dysplasia, missouri type P45452
#275355 Squamous cell carcinoma, head and neck; hnscc O14763
P04637
%612223 Stature quantitative trait locus 11; stqtl11 Q00534
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#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
#277700 Werner syndrome; wrn Q14191
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (111)

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)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
P00533 (related)
P04637 (related)
H00024 Prostate cancer O14746 (marker)
P10275 (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)
P21802 (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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q15046 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
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)
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)
P28907 (marker)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
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)
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)
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)
H00021 Renal cell carcinoma P04637 (marker)
P08581 (related)
H01071 Acute alcohol sensitivity P05091 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00069 Glycogen storage diseases (GSD) P10253 (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)
P36888 (related)
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)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00479 Metaphyseal dysplasias P14780 (related)
P45452 (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)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00192 Xanthinuria P47989 (related)
H00070 Galactosemia P51570 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)
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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

6 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009202 Cardiomyopathies C00000674
D002386 Cataract C00000674
D005483 Flushing C00000674
D006529 Hepatomegaly C00000674
D008103 Liver Cirrhosis C00000674
D010051 Ovarian Neoplasms C00000674