Species

KNApSAcK Entry

Organism name Virola surinamensis
Genus Virola
Family Myristicaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Virola surinamensis
Linked NCBI taxonomy ID 224910
Linked level species

Family

Family in NCBI taxonomy Myristicaceae
ID 22274

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (30)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00002525 External link 512 Formononetin
/ 7-Hydroxy-4'-methoxyisoflavone
CHEMBL242341
C007768
24 / 36 / 58 13 / 0 No. 3 No. 15
C00002510 External link 512 Olmelin
/ Pratensol
/ Biochanin A
/ Genistein 4'-methyl ether
/ 5,7-Dihydroxy-4'-methoxyisoflavone
CHEMBL131921
C004541
51 / 65 / 83 64 / 2 No. 3 No. 15
C00008126 External link 512 7-Hydroxyflavanone
CHEMBL97542
CHEMBL402744
C059353
9 / 18 / 45 1 / 0 No. 25 No. 14
C00019452 External link 512 2'-Hydroxy-7,4'-dimethoxyisoflavone
No. 35 No. 15
C00031801 External link 512 Galbelgin
CHEMBL56800
CHEMBL57542
CHEMBL418309
CHEMBL291515
CHEMBL56856
CHEMBL56917
CHEMBL112481
CHEMBL469500
1 / 0 / 0 No. 38 No. 21
C00002607 External link 512 Grandisin
/ (-)-Grandisin
CHEMBL459404
CHEMBL459405
CHEMBL1377609
CHEMBL2204392
C074346
4 / 3 / 7 No. 38 No. 21
C00002633 External link 512 (+)-Veraguensin
CHEMBL56800
CHEMBL57542
CHEMBL418309
CHEMBL291515
CHEMBL56856
CHEMBL56917
CHEMBL112481
CHEMBL469500
1 / 0 / 0 No. 38 No. 21
C00007212 External link 512 Galgravin
CHEMBL56800
CHEMBL57542
CHEMBL418309
CHEMBL291515
CHEMBL56856
CHEMBL56917
CHEMBL112481
CHEMBL469500
C084077
1 / 0 / 0 No. 38 No. 21
C00023770 External link 512 Sitosterol
/ Stigmasta-5,22-dien-3beta-ol
/ (24R)24-Ethylcholesta-5,22-dien-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00023774 External link 512 Fucostanol
/ Stigmasterol
/ Dihydro-beta-sitosterol
/ (24S)24-Ethylcholestain-3beta-ol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00040640 External link 512 Virolanol C
No. 96 No. 26
C00040639 External link 512 Virolane
No. 96 No. 26
C00037221 External link 512 Guaiacin
/ (+)-Guaiacin
CHEMBL482239
CHEMBL1080351
No. 406
C00002605 External link 512 (+)-Galbacin
CHEMBL1980140
CHEMBL2151191
2 / 0 / 0 No. 621 No. 21
C00007213 External link 512 (-)-Galbacin
CHEMBL1980140
CHEMBL2151191
2 / 0 / 0 No. 621 No. 21
C00000601 External link 512 (+)-Sesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
C054125
20 / 24 / 15 0 / 5 No. 621 No. 21
C00002608 External link 512 Hinokinin
/ Hinoquinin
/ (-)-Hinokinin
/ (-)-Hinoquinin
CHEMBL180970
CHEMBL182073
CHEMBL242011
C475934
2 / 1 / 1 No. 629 No. 21
C00002599 External link 512 (-)-Dihydrocubebin
CHEMBL486597
CHEMBL1477391
C011228
4 / 8 / 4 No. 629 No. 21
C00031898 External link 512 Isoelemicin
/ (E)-Isoelemicin
CHEMBL121548
No. 723 No. 6
C00038679 External link 512 Cagayanin
CHEMBL407726
No. 1142 No. 21
C00038410 External link 512 alpha,2'-Dihydroxy-4,4'-dimethoxydihydrochalcone
/ (-)-alpha,2'-Dihydroxy-4,4'-dimethoxydihydrochalcone
No. 1331 No. 13
C00002630 External link 512 Surinamensin
CHEMBL464726
CHEMBL464934
CHEMBL2313009
C420461
No. 1500 No. 23
C00032491 External link 512 Virolin
/ Machilin D 4-methyl ether
CHEMBL463080
CHEMBL464725
CHEMBL2313010
No. 1504
C00031949 External link 512 Juruenolide F
/ (+)-Juruenolide F
No. 2162
C00031948 External link 512 Juruenolide E
/ (+)-Juruenolide E
No. 2162
C00031947 External link 512 Juruenolide D
No. 2162
C00031767 External link 512 epi-Juruenolide C
/ (-)-epi-Juruenolide C
No. 2162
C00031946 External link 512 Juruenolide C
/ (+)-Juruenolide C
No. 2162
C00039245 External link 512 Galbulin
CHEMBL1395109
C412027
No. 3582
C00031888 External link 512 Iryelliptin B
No. 6024

Human Protein / Gene in interactions

84 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000601 C00002510 C00002525 C00002599 C00002608 C00023770 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000601 C00002510 C00002525 C00002599 C00002608 C00023770 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000601 C00002510 C00002525 C00023770 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000601 C00002510 C00002525 C00023770 0 / 1
Q16637 Survival motor neuron protein Unclassified protein C00000601 C00002510 C00002525 4 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00002510 C00002525 C00008126 7 / 37
O00255 Menin Unclassified protein C00002510 C00002525 C00002607 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002510 C00002525 C00002607 1 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000601 C00002510 C00002599 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000601 C00002510 C00002525 2 / 2
P25105 Platelet-activating factor receptor PAF receptor C00002633 C00007212 C00031801 0 / 0
O75496 Geminin Unclassified protein C00000601 C00002510 C00002607 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002510 C00002525 C00008126 4 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000601 C00002510 C00008126 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000601 C00002510 C00002525 4 / 3
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002510 C00008126 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00000601 C00002607 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000601 C00002525 0 / 0
P45984 Mitogen-activated protein kinase 9 Jnk C00002605 C00007213 0 / 0
P10275 Androgen receptor NR3C4 C00002510 C00008126 3 / 4
P06746 DNA polymerase beta Enzyme C00023770 C00023774 0 / 0
P08183 Multidrug resistance protein 1 drug C00002510 C00023770 1 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00002605 C00007213 0 / 0
P03372 Estrogen receptor NR3A1 C00002510 C00023770 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002510 C00002525 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002510 C00008126 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002510 C00002525 3 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00002510 C00002525 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000601 C00002510 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002510 C00008126 2 / 2
P04150 Glucocorticoid receptor NR3C1 C00002510 C00008126 0 / 1
P33527 Multidrug resistance-associated protein 1 drugs C00002510 C00002525 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002510 C00002525 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002510 C00008126 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000601 C00002599 7 / 3
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000601 C00002510 1 / 1
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00002510 1 / 2
P49841 Glycogen synthase kinase-3 beta Gsk C00023770 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002510 0 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00000601 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002510 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000601 0 / 0
P00734 Prothrombin S1A C00023770 4 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000601 2 / 0
P16152 Carbonyl reductase [NADPH] 1 Enzyme C00002510 0 / 0
P14679 Tyrosinase Oxidoreductase C00023770 4 / 2
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002525 5 / 3
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002510 2 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002510 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00023770 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000601 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00002510 2 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00002510 1 / 1
P11473 Vitamin D3 receptor NR1I1 C00000601 2 / 3
O15118 Niemann-Pick C1 protein Unclassified protein C00002510 1 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002510 1 / 8
O75828 Carbonyl reductase [NADPH] 3 Enzyme C00002510 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00002525 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00002510 0 / 0
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00002510 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00023770 3 / 2
P08047 Transcription factor Sp1 Unclassified protein C00023770 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002510 11 / 10
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002525 0 / 0
P04062 Glucosylceramidase Enzyme C00002510 6 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002525 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00023770 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00023770 2 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002510 0 / 0
P42224 Signal transducer and activator of transcription 1-alpha/beta Unclassified protein C00002510 3 / 3
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00023770 1 / 1
P31639 Sodium/glucose cotransporter 2 Glucose C00002525 1 / 1
P13866 Sodium/glucose cotransporter 1 Glucose C00002525 1 / 1
P11388 DNA topoisomerase 2-alpha Isomerase C00023774 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00023774 0 / 0
Q00653 Nuclear factor NF-kappa-B p100 subunit Transcription Factor C00002510 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00002510 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00002510 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00023770 0 / 0
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00002510 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002525 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002510 0 / 0

68 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 C00002510 C00002525
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) C00002510 C00002525
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) C00002510 C00002525
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002510 C00002525
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002510 C00002525
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002510 C00002525
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00002510 C00002525
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00002510 C00002525
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00002510 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) C00002510 C00002525
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002510 C00008126
5250 SLC25A3, PHC, PTP solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 C00002510
1152 CKB, B-CK, CKBB creatine kinase, brain (EC:2.7.3.2) C00002510
1000 CDH2, CD325, CDHN, CDw325, NCAD cadherin 2, type 1, N-cadherin (neuronal) C00002510
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002510
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002510
9577 BRE, BRCC4, BRCC45 brain and reproductive organ-expressed (TNFRSF1A modulator) C00002510
1594 CYP27B1, CP2B, CYP1, CYP1alpha, CYP27B, P450c1, PDDR, VDD1, VDDR, VDDRI, VDR cytochrome P450, family 27, subfamily B, polypeptide 1 (EC:1.14.13.13) C00002510
51071 DERA, DEOC deoxyribose-phosphate aldolase (putative) (EC:4.1.2.4) C00002510
1983 EIF5, EIF-5, EIF-5A eukaryotic translation initiation factor 5 C00002510
59084 ENPP5 ectonucleotide pyrophosphatase/phosphodiesterase 5 (putative) C00002510
2060 EPS15, AF-1P, AF1P, MLLT5 epidermal growth factor receptor pathway substrate 15 C00002510
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002510
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002510
2101 ESRRA, ERR1, ERRa, ERRalpha, ESRL1, NR3B1 estrogen-related receptor alpha C00002510
2103 ESRRB, DFNB35, ERR2, ERRb, ESRL2, NR3B2 estrogen-related receptor beta C00002510
2104 ESRRG, ERR3, ERRgamma, NR3B3 estrogen-related receptor gamma C00002510
2091 FBL, FIB, FLRN, RNU3IP1 fibrillarin C00002510
2348 FOLR1, FBP, FOLR folate receptor 1 (adult) C00002510
2760 GM2A, GM2-AP, SAP-3 GM2 ganglioside activator C00002510
2773 GNAI3, 87U6, ARCND1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3 C00002510
2876 GPX1, GPXD, GSHPX1 glutathione peroxidase 1 (EC:1.11.1.9) C00002510
9766 KIAA0247 C00002510
753 LDLRAD4, C18orf1 low density lipoprotein receptor class A domain containing 4 C00002510
56925 LXN, ECI, TCI latexin C00002510
4323 MMP14, MMP-14, MMP-X1, MT-MMP, MT-MMP_1, MT1-MMP, MT1MMP, MTMMP1, WNCHRS matrix metallopeptidase 14 (membrane-inserted) (EC:3.4.24.80) C00002510
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00002510
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002510
4502 MT2A, MT2 metallothionein 2A C00002510
4698 NDUFA5, B13, CI-13KD-B, CI-13kB, NUFM, UQOR13 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 (EC:1.6.5.3 1.6.99.3) C00002510
4841 NONO, NMT55, NRB54, P54, P54NRB non-POU domain containing, octamer-binding C00002510
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00002510
5204 PFDN5, MM-1, MM1, PFD5 prefoldin subunit 5 C00002510
5241 PGR, NR3C3, PR progesterone receptor C00002510
5329 PLAUR, CD87, U-PAR, UPAR, URKR plasminogen activator, urokinase receptor C00002510
10957 PNRC1, B4-2, PNAS-145, PROL2, PRR2 proline-rich nuclear receptor coactivator 1 C00002510
55684 RABL6, C9orf86, PARF, RBEL1, pp8875 RAB, member RAS oncogene family-like 6 C00002510
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002510
55183 RIF1 RAP1 interacting factor homolog (yeast) C00002510
285367 RPUSD3 RNA pseudouridylate synthase domain containing 3 C00002510
6455 SH3GL1, CNSA1, EEN, SH3D2B, SH3P8 SH3-domain GRB2-like 1 C00002510
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00002510
6426 SRSF1, ASF, SF2, SF2p33, SFRS1, SRp30a serine/arginine-rich splicing factor 1 C00002510
84222 TMEM191A, TMEM191AP transmembrane protein 191A (pseudogene) C00002510
27242 TNFRSF21, BM-018, CD358, DR6 tumor necrosis factor receptor superfamily, member 21 C00002510
203068 TUBB, M40, OK/SW-cl.56, TUBB1, TUBB5 tubulin, beta class I C00002510
7322 UBE2D2, E2(17)KB2, PUBC1, UBC4, UBC4/5, UBCH5B ubiquitin-conjugating enzyme E2D 2 (EC:6.3.2.19) C00002510
84159 ARID5B, DESRT, MRF-2, MRF2 AT rich interactive domain 5B (MRF1-like) C00002510
501 ALDH7A1, ATQ1, EPD, PDE aldehyde dehydrogenase 7 family, member A1 (EC:1.2.1.3 1.2.1.8 1.2.1.31) C00002510
196 AHR, bHLHe76 aryl hydrocarbon receptor C00002510
375790 AGRN agrin C00002510
1244 ABCC2, ABC30, CMOAT, DJS, MRP2, cMRP ATP-binding cassette, sub-family C (CFTR/MRP), member 2 C00002510
54663 WDR74 WD repeat domain 74 C00002510
80014 WWC2, BOMB WW and C2 domain containing 2 C00002510
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
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
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00023774

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (97)

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
#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
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#209950 Atypical mycobacteriosis, familial P42224
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#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
#614162 Candidiasis, familial, 7; candf7 P42224
#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
#114500 Colorectal cancer; crc P18054
P84022
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#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
#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
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#147060 Hyper-ige recurrent infection syndrome, autosomal dominant P40763
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#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
#174800 Mccune-albright syndrome; mas P63092
#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
#613796 Mycobacterial and viral infections, susceptibility to, autosomal recessive P42224
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#233100 Renal glucosuria; glys1 P31639
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (99)

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)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P40763 (related)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
H00018 Gastric cancer P00533 (related)
P04637 (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)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (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)
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)
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)
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)
H01071 Acute alcohol sensitivity P05091 (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)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (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)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00107 Other well-defined immunodeficiency syndromes P40763 (related)
H00089 IFN-gamma/IL-12 axis P42224 (related)
H00363 Candidiasis P42224 (related)
H01109 Chronic mucocutaneous candidiasis (CMC) P42224 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (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)
H00208 Hyperbilirubinemia Q92887 (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)

Diseases related to CTD interactions

7 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D005909 Glioblastoma C00002510
D011471 Prostatic Neoplasms C00002510
D001930 Brain Injuries C00000601
D002375 Catalepsy C00000601
D018476 Hypokinesia C00000601
D020244 Infarction, Middle Cerebral Artery C00000601
D020734 Parkinsonian Disorders C00000601