Species

KNApSAcK Entry

Organism name Hedysarum multijugum
Genus Hedysarum
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Hedysarum
Linked NCBI taxonomy ID 47034
Linked level genus

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 (6)

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
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
C00002525 External link 512 Formononetin
/ 7-Hydroxy-4'-methoxyisoflavone
CHEMBL242341
C007768
24 / 36 / 58 13 / 0 No. 3 No. 15
C00019759 External link 512 1,7-Dihydroxy-3,9-dimethoxypterocarpene
No. 3 No. 15
C00009897 External link 512 Gancanin M
/ 5,7-Dihydroxy-4'-methoxy-8-prenylisoflavone
No. 15 No. 15
C00003741 External link 512 Betulinic acid
CHEMBL269277
CHEMBL71690
CHEMBL519059
CHEMBL1318530
CHEMBL2005635
C002070
34 / 17 / 14 10 / 2 No. 23 No. 51
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11

Human Protein / Gene in interactions

90 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002510 C00002525 C00003672 C00003741 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002510 C00002525 C00003672 C00003741 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002510 C00002525 C00003672 C00003741 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002510 C00002525 C00003672 C00003741 0 / 1
P03372 Estrogen receptor NR3A1 C00002510 C00003672 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00002510 C00002525 7 / 37
P10636 Microtubule-associated protein tau Unclassified protein C00002510 C00002525 4 / 3
Q16637 Survival motor neuron protein Unclassified protein C00002510 C00002525 4 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 C00003741 2 / 0
O00255 Menin Unclassified protein C00002510 C00002525 2 / 5
P06746 DNA polymerase beta Enzyme C00003672 C00003741 0 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00002510 C00002525 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00002510 C00003741 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002510 C00002525 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002510 C00002525 2 / 2
P02545 Prelamin-A/C Unclassified protein C00002510 C00003741 11 / 10
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002510 C00002525 3 / 3
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 C00003741 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002510 C00002525 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00002510 C00003741 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002510 C00003741 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 C00003741 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002510 C00002525 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002510 C00002525 1 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002510 C00002525 4 / 2
O75496 Geminin Unclassified protein C00002510 C00003741 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002510 C00003741 0 / 0
P08183 Multidrug resistance protein 1 drug C00002510 C00003672 1 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003741 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00003741 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002510 1 / 8
P08151 Zinc finger protein GLI1 Unclassified protein C00003741 0 / 0
P16152 Carbonyl reductase [NADPH] 1 Enzyme C00002510 0 / 0
O75828 Carbonyl reductase [NADPH] 3 Enzyme C00002510 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002510 0 / 0
P15559 NAD(P)H dehydrogenase [quinone] 1 Enzyme C00003741 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002510 0 / 1
P15121 Aldose reductase Enzyme C00003741 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00002525 0 / 0
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00002510 1 / 2
Q02156 Protein kinase C epsilon type Eta C00003741 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00002510 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00003741 1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00003741 0 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002510 1 / 1
P00734 Prothrombin S1A C00003672 4 / 2
P04150 Glucocorticoid receptor NR3C1 C00002510 0 / 1
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002510 2 / 2
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002525 5 / 3
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002510 2 / 0
Q96RI1 Bile acid receptor NR1H4 C00003741 0 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003741 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002510 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P55055 Oxysterols receptor LXR-beta NR1H3 C00003741 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 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
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003741 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002510 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002510 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003741 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002525 0 / 0
P05771 Protein kinase C beta type Alpha C00003741 0 / 0
P04062 Glucosylceramidase Enzyme C00002510 6 / 4
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00002510 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00003741 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002510 0 / 0
P31639 Sodium/glucose cotransporter 2 Glucose C00002525 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002525 0 / 0
P10275 Androgen receptor NR3C4 C00002510 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002525 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00003741 0 / 0
P13866 Sodium/glucose cotransporter 1 Glucose C00002525 1 / 1
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 C00003672 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003741 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00003741 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00002510 0 / 0
Q00653 Nuclear factor NF-kappa-B p100 subunit Transcription Factor C00002510 0 / 0
Q9UBT2 SUMO-activating enzyme subunit 2 Enzyme C00003741 0 / 0
Q9UBE0 SUMO-activating enzyme subunit 1 Unclassified protein C00003741 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002510 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002510 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002525 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002510 1 / 1

76 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002510 C00003741
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
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00002510 C00002525
55183 RIF1 RAP1 interacting factor homolog (yeast) C00002510
375790 AGRN agrin C00002510
196 AHR, bHLHe76 aryl hydrocarbon receptor 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
84159 ARID5B, DESRT, MRF-2, MRF2 AT rich interactive domain 5B (MRF1-like) C00002510
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002510
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002510
9577 BRE, BRCC4, BRCC45 brain and reproductive organ-expressed (TNFRSF1A modulator) C00002510
1000 CDH2, CD325, CDHN, CDw325, NCAD cadherin 2, type 1, N-cadherin (neuronal) C00002510
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00002510
1152 CKB, B-CK, CKBB creatine kinase, brain (EC:2.7.3.2) C00002510
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002510
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00003741
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002510
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00003741
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
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00003741
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00003741
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
1244 ABCC2, ABC30, CMOAT, DJS, MRP2, cMRP ATP-binding cassette, sub-family C (CFTR/MRP), member 2 C00002510
285367 RPUSD3 RNA pseudouridylate synthase domain containing 3 C00002510
6455 SH3GL1, CNSA1, EEN, SH3D2B, SH3P8 SH3-domain GRB2-like 1 C00002510
5250 SLC25A3, PHC, PTP solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 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
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00003741
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003741
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00003741
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00003741
581 BAX, BCL2L4 BCL2-associated X protein C00003741
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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (88)

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
#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
#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 O75874
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
#211980 Lung cancer P00533
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#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
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#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
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#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
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (94)

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)
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)
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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008103 Liver Cirrhosis C00003741
D008545 Melanoma C00003741
D005909 Glioblastoma C00002510
D011471 Prostatic Neoplasms C00002510