Species

KNApSAcK Entry

Organism name Virgilia oroboides
Genus Virgilia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Virgilia oroboides
Linked NCBI taxonomy ID 58847
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 (15)

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
C00006793 External link 512 Cyanidin 3-(6''-acetylglucoside)
No. 2 No. 15
C00006859 External link 512 Peonidin 3-(6''-acetylglucoside)
No. 2 No. 15
C00002525 External link 512 Formononetin
/ 7-Hydroxy-4'-methoxyisoflavone
CHEMBL242341
C007768
24 / 36 / 58 13 / 0 No. 3 No. 15
C00008126 External link 512 7-Hydroxyflavanone
CHEMBL97542
CHEMBL402744
C059353
9 / 18 / 45 1 / 0 No. 25 No. 14
C00010028 External link 512 3-Hydroxy-8,9-methylenedioxypterocarp-6a-ene
No. 27 No. 15
C00000963 External link 512 (2R,3R)-fustin
CHEMBL470267
CHEMBL508731
2 / 3 / 5 No. 42 No. 14
C00008546 External link 512 3,7-dihydroxyflavanone
CHEMBL252667
No. 42 No. 14
C00004579 External link 512 Fisetin
/ 3,3',4',7-Tetrahydroxyflavone
/ 2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-4H-1-benzopyran-4-one
CHEMBL31574
C017875
53 / 51 / 73 37 / 2 No. 71 No. 15
C00002209 External link 512 Aphylline
CHEMBL509343
No. 85 No. 3
C00007744 External link 512 Virgiline
No. 85 No. 3
C00009534 External link 512 Dihydroformononetin
/ 7-Hydroxy-4'-methoxyisoflavanone
CHEMBL1087010
No. 106 No. 14
C00007948 External link 512 2',4',alpha-Trihydroxy-4-methoxydihydrochalcone
No. 548 No. 13
C00002208 External link 512 Angustifoline
CHEMBL459206
C101930
No. 1023 No. 3
C00002214 External link 512 Calpurnine
/ Oroboidine
C013362
0 / 3 No. 1636 No. 3
C00002014 External link 512 (+)-Ammodendrine
/ (+)-Spherocarpine
CHEMBL464776
CHEMBL464777
C068578
No. 2560 No. 1

Human Protein / Gene in interactions

72 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00002525 C00004579 C00008126 7 / 37
P04150 Glucocorticoid receptor NR3C1 C00000963 C00004579 C00008126 0 / 1
P10275 Androgen receptor NR3C4 C00000963 C00004579 C00008126 3 / 4
P10636 Microtubule-associated protein tau Unclassified protein C00002525 C00004579 4 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002525 C00004579 0 / 1
O00255 Menin Unclassified protein C00002525 C00004579 2 / 5
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002525 C00004579 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002525 C00004579 0 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002525 C00004579 2 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002525 C00004579 3 / 3
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002525 C00004579 1 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002525 C00008126 4 / 2
P00352 Retinal dehydrogenase 1 Enzyme C00002525 C00004579 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002525 1 / 0
Q00534 Cyclin-dependent kinase 6 CMGC serine/threonine protein kinase family C00004579 1 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00004579 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00002525 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00004579 0 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00008126 1 / 1
Q00535 Cyclin-dependent kinase 5 Cdk5 C00004579 0 / 0
Q15078 Cyclin-dependent kinase 5 activator 1 REG serine/threonine protein kinase family C00004579 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00004579 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00004579 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00004579 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00004579 1 / 1
P68871 Hemoglobin subunit beta Secreted protein C00004579 4 / 4
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00004579 0 / 0
P02545 Prelamin-A/C Unclassified protein C00004579 11 / 10
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00004579 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00008126 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002525 0 / 0
Q92793 CREB-binding protein Enzyme C00004579 1 / 1
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00008126 2 / 2
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002525 5 / 3
P06276 Cholinesterase Hydrolase C00004579 0 / 0
P04745 Alpha-amylase 1 Enzyme C00004579 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00004579 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00004579 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002525 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004579 2 / 0
P29466 Caspase-1 C14 C00004579 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00004579 0 / 0
P22303 Acetylcholinesterase Hydrolase C00004579 1 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00004579 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00004579 0 / 0
P55210 Caspase-7 C14 C00004579 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002525 1 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00004579 0 / 0
Q15046 Lysine--tRNA ligase Enzyme C00004579 2 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00004579 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00004579 5 / 1
Q16637 Survival motor neuron protein Unclassified protein C00002525 4 / 1
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00004579 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002525 0 / 0
P31639 Sodium/glucose cotransporter 2 Glucose C00002525 1 / 1
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002525 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00004579 0 / 1
Q04760 Lactoylglutathione lyase Enzyme C00004579 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00004579 0 / 0
P13866 Sodium/glucose cotransporter 1 Glucose C00002525 1 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00004579 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00004579 3 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00002525 0 / 0
O95067 G2/mitotic-specific cyclin-B2 Other cytosolic protein C00004579 0 / 0
P14635 G2/mitotic-specific cyclin-B1 Other cytosolic protein C00004579 0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 C00004579 0 / 0
Q8WWL7 G2/mitotic-specific cyclin-B3 Other cytosolic protein C00004579 0 / 0
P49840 Glycogen synthase kinase-3 alpha Gsk C00004579 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00004579 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00008126 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00008126 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002525 0 / 0

46 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002525 C00004579
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) C00002525 C00004579
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) C00002525 C00004579
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002525 C00004579
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002525 C00004579
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00004579
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00002525
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00002525
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002525
2056 EPO, EP, MVCD2 erythropoietin C00002525
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00002525
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002525
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00002525
367 AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM androgen receptor C00004579
578 BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 BCL2-antagonist/killer 1 C00004579
637 BID, FP497 BH3 interacting domain death agonist C00004579
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00004579
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00004579
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00004579
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00004579
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00004579
891 CCNB1, CCNB cyclin B1 C00004579
958 CD40, Bp50, CDW40, TNFRSF5, p50 CD40 molecule, TNF receptor superfamily member 5 C00004579
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00002525
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00004579
1734 DIO2, 5DII, D2, DIOII, SelY, TXDI2 deiodinase, iodothyronine, type II (EC:1.97.1.10) C00004579
1786 DNMT1, ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT DNA (cytosine-5-)-methyltransferase 1 (EC:2.1.1.37) C00004579
356 FASLG, ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L, FASL, TNFSF6 Fas ligand (TNF superfamily, member 6) C00004579
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00004579
3596 IL13, IL-13, P600 interleukin 13 C00004579
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00004579
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00004579
3567 IL5, EDF, IL-5, TRF interleukin 5 (colony-stimulating factor, eosinophil) C00004579
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00004579
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00004579
354 KLK3, APS, KLK2A1, PSA, hK3 kallikrein-related peptidase 3 (EC:3.4.21.77) C00004579
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00004579
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) C00004579
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00004579
4773 NFATC2, NFAT1, NFATP nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 C00004579
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00004579
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00004579
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00004579
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00004579
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00004579
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00008126

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (72)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#610251 Alcohol sensitivity, acute P05091
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#613985 Beta-thalassemia P68871
#603902 Beta-thalassemia, dominant inclusion body type P68871
#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
#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
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#613916 Deafness, autosomal recessive 89; dfnb89 Q15046
#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
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 P37231
#606824 Glucose/galactose malabsorption; ggm P13866
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#140700 Heinz body anemias P68871
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#211980 Lung cancer 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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#601665 Obesity P37231
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#233100 Renal glucosuria; glys1 P31639
#275210 Restrictive dermopathy, lethal P02545
#180849 Rubinstein-taybi syndrome 1; rsts1 Q92793
#603903 Sickle cell anemia P68871
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
%612223 Stature quantitative trait locus 11; stqtl11 Q00534
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (81)

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)
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)
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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
P68871 (marker)
H00022 Bladder cancer P04637 (related)
P68871 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00028 Choriocarcinoma P04637 (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)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H01071 Acute alcohol sensitivity P05091 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (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)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00192 Xanthinuria P47989 (related)
H00228 Thalassemia P68871 (related)
H00229 Sickle cell anemia (SCA) P68871 (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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00504 Rubinstein-Taybi syndrome Q92793 (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)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D001145 Arrhythmias, Cardiac C00002214
D064420 Drug-Related Side Effects and Adverse Reactions C00002214
D014693 Ventricular Fibrillation C00002214
D009374 Neoplasms, Experimental C00004579
D011471 Prostatic Neoplasms C00004579