Species

KNApSAcK Entry

Organism name Bauhinia guianensis
Genus Bauhinia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Bauhinia guianensis
Linked NCBI taxonomy ID 508984
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 (9)

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
C00001029 External link 512 Chrysoeriol
/ Luteolin 3'-methyl ether
CHEMBL214321
C007054
20 / 24 / 20 8 / 0 No. 3 No. 15
C00000960 External link 512 Eriodictyol
CHEMBL8996
CHEMBL307893
CHEMBL1975989
C007619
32 / 29 / 55 5 / 0 No. 25 No. 14
C00000982 External link 512 Naringenin
/ (-)-Naringenin
CHEMBL9352
CHEMBL32571
C005273
57 / 46 / 40 35 / 10 No. 25 No. 14
C00000977 External link 512 Liquiritigenin
CHEMBL252642
CHEMBL271939
C083152
5 / 4 / 4 1 / 1 No. 25 No. 14
C00003998 External link 512 Bausplendin
/ 7-Methoxy-5,6:3',4'-bis(methylenedioxy)flavone
No. 27 No. 15
C00020217 External link 512 Pratol
/ 7-Hydroxy-4'-methoxyflavone
CHEMBL16751
16 / 25 / 52 No. 76 No. 15
C00003801 External link 512 Isopratol
/ 4'-Hydroxy-7-methoxyflavone
CHEMBL1600520
14 / 27 / 57 No. 76 No. 15
C00006927 External link 512 Isoliquiritigenin 2'-methy ether
/ 4,4'-Dihydroxy-2'-methoxychalcone
CHEMBL253777
7 / 20 / 19 No. 92 No. 13
C00020663 External link 512 Obtustyrene
CHEMBL243670
No. 379

Human Protein / Gene in interactions

101 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O00255 Menin Unclassified protein C00000982 C00001029 C00003801 C00020217 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000982 C00001029 C00003801 C00020217 1 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000960 C00000982 C00003801 C00020217 0 / 1
O75496 Geminin Unclassified protein C00000960 C00000982 C00001029 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000960 C00000982 C00001029 4 / 4
P04637 Cellular tumor antigen p53 Transcription Factor C00000960 C00003801 C00020217 7 / 37
P00352 Retinal dehydrogenase 1 Enzyme C00000960 C00001029 C00003801 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000960 C00000982 C00001029 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000960 C00001029 C00003801 4 / 3
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000960 C00000982 C00001029 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000960 C00000982 C00003801 3 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000982 C00003801 C00020217 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000982 C00003801 C00020217 0 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001029 C00020217 0 / 0
P06746 DNA polymerase beta Enzyme C00000960 C00001029 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00000982 C00001029 0 / 0
P22303 Acetylcholinesterase Hydrolase C00000960 C00000982 1 / 0
P04062 Glucosylceramidase Enzyme C00000982 C00003801 6 / 4
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000960 C00003801 2 / 2
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00000982 C00001029 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00000960 C00000982 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000960 C00003801 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00000982 C00001029 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000960 C00020217 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000977 C00000982 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00000982 C00001029 5 / 3
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000977 C00000982 2 / 2
P11021 78 kDa glucose-regulated protein Unclassified protein C00000960 C00020217 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000960 C00003801 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00001029 C00020217 4 / 2
P33527 Multidrug resistance-associated protein 1 drugs C00000982 C00001029 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000982 C00003801 1 / 0
P39748 Flap endonuclease 1 Enzyme C00000960 C00001029 0 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00000960 C00000982 1 / 1
P03372 Estrogen receptor NR3A1 C00000982 1 / 1
P17405 Sphingomyelin phosphodiesterase Enzyme C00020217 2 / 2
P16152 Carbonyl reductase [NADPH] 1 Enzyme C00000982 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001029 2 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000960 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00000982 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00000982 0 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000982 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00000982 0 / 1
P15121 Aldose reductase Enzyme C00000982 0 / 0
P09874 Poly [ADP-ribose] polymerase 1 Enzyme C00020217 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00020217 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00000977 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000960 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00000960 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00000960 3 / 1
P11308 Transcriptional regulator ERG Unclassified protein C00020217 1 / 2
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00006927 1 / 8
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00000982 1 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001029 1 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000982 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000982 0 / 1
O75828 Carbonyl reductase [NADPH] 3 Enzyme C00000982 0 / 0
P24864 G1/S-specific cyclin-E1 Other cytosolic protein C00000982 0 / 2
P24941 Cyclin-dependent kinase 2 Cdc2 C00000982 0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00006927 0 / 0
P04745 Alpha-amylase 1 Enzyme C00000982 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00006927 1 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00000982 2 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00006927 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00000960 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00000960 0 / 1
P08183 Multidrug resistance protein 1 drug C00000982 1 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000982 1 / 1
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00000982 2 / 0
O95271 Tankyrase-1 Enzyme C00020217 0 / 0
P62158 Calmodulin Unclassified protein C00000982 1 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001029 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000982 0 / 0
Q9H2K2 Tankyrase-2 Enzyme C00020217 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000982 0 / 0
P04278 Sex hormone-binding globulin Secreted protein C00000982 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000977 2 / 2
P35372 Mu-type opioid receptor Opioid receptor C00000982 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00006927 4 / 5
P16050 Arachidonate 15-lipoxygenase Enzyme C00000960 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00000960 1 / 1
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00000982 0 / 0
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00006927 9 / 3
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000982 0 / 3
O75164 Lysine-specific demethylase 4A Enzyme C00000960 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00000960 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00000982 5 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000982 0 / 0
P10275 Androgen receptor NR3C4 C00000982 3 / 4
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000982 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00006927 4 / 3
P05412 Transcription factor AP-1 Transcription Factor C00000977 0 / 0
Q04760 Lactoylglutathione lyase Enzyme C00000982 0 / 0
P49888 Estrogen sulfotransferase Enzyme C00000982 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00000982 1 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00000982 3 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000960 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000982 1 / 1
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00000982 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000960 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00000960 2 / 1

43 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 C00000960 C00000982 C00001029
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00000982 C00001029
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00000982 C00001029
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000982 C00001029
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 C00001029
3757 KCNH2, ERG1, HERG, HERG1, Kv11.1, LQT2, SQT1 potassium voltage-gated channel, subfamily H (eag-related), member 2 C00000982
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
249 ALPL, AP-TNAP, APTNAP, HOPS, TNAP, TNSALP alkaline phosphatase, liver/bone/kidney (EC:3.1.3.1) C00000982
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00000982
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00000982
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000982
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00000982
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) 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
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
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
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
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
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
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
6513 SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED solute carrier family 2 (facilitated glucose transporter), member 1 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
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000982
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00000982
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00000982
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00000982
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
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
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
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00000982
4543 MTNR1A, MEL-1A-R, MT1 melatonin receptor 1A C00001029
4544 MTNR1B, FGQTL2, MEL-1B-R, MT2 melatonin receptor 1B C00001029
4835 NQO2, DHQV, DIA6, NMOR2, QR2 NAD(P)H dehydrogenase, quinone 2 (EC:1.10.99.2) C00001029
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00000960
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00000960
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00000960
29110 TBK1, NAK, T2K TANK-binding kinase 1 (EC:2.7.11.1) C00000960
1831 TSC22D3, DIP, DSIPI, GILZ, TSC-22R, hDIP TSC22 domain family, member 3 C00000977

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (100)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#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
#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
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P18054
P84022
Q14191
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#123500 Crouzon syndrome P21802
#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
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#612219 Ewing sarcoma; es P11308
#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 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 P37231
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P08581
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#145000 Hyperparathyroidism 1; hrpt1 O00255
#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
#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
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P00533
P04637
#174800 Mccune-albright syndrome; mas P63092
#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
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#166250 Osteoglophonic dysplasia; ogd P11362
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#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
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#190440 Trigonocephaly 1; trigno1 P11362
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#614916 Ventricular tachycardia, catecholaminergic polymorphic, 4; cpvt4 P62158
#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 (93)

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)
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)
P24864 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P04637 (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)
P24864 (related)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (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)
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)
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)
H00213 Hypophosphatasia P05186 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
P11308 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
P10721 (marker)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
P36888 (related)
H00170 Piebaldism P10721 (related)
H00035 Ewing's sarcoma P11308 (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)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00192 Xanthinuria P47989 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00296 Defects in RecQ helicases Q14191 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00000982
D001932 Brain Neoplasms C00000982
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
D009120 Muscle Cramp C00000977