KCF-S cluster No. 2068 (5 metabolites)

Corresponding Phytochemical cluster No. 81



Metabolite list (5)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00002678 External link 512 Nasutin B
/ 3,3',4'-tri-O-methylellagic acid
CHEMBL451476
C00011153 External link 512 Gallogen
/ Ellagic acid
/ Elagostasine
/ Alizarin yellow
CHEMBL6246
D004610
104 / 97 / 100 77 / 9
C00011154 External link 512 3-O-Methylellagic acid
CHEMBL564351
C00029474 External link 512 3,3'-Dimethoxyellagic acid
/ 3,3'-di-O-Methylellagic acid
CHEMBL487203
C050401
10 / 11 / 15
C00044433 External link 512 3,3',4-Tri-O-methylflavellagic acid
CHEMBL509184

Human Protein / Gene in interactions

105 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P54132 Bloom syndrome protein Enzyme C00011153 C00029474 1 / 2
O00255 Menin Unclassified protein C00011153 C00029474 2 / 5
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00011153 C00029474 1 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00011153 C00029474 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00011153 C00029474 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00011153 C00029474 4 / 3
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00011153 C00029474 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00011153 C00029474 2 / 2
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00011153 C00029474 1 / 2
Q9UNA4 DNA polymerase iota Enzyme C00011153 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00011153 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00011153 0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00011153 0 / 0
O14965 Aurora kinase A Aur C00011153 0 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00011153 1 / 4
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00011153 0 / 0
P02545 Prelamin-A/C Unclassified protein C00011153 11 / 10
P10828 Thyroid hormone receptor beta NR1A2 C00011153 3 / 1
P68400 Casein kinase II subunit alpha Ck2 C00011153 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00011153 1 / 2
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00011153 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00011153 0 / 1
O00444 Serine/threonine-protein kinase PLK4 PLK serine/threonine protein kinase subfamily C00011153 0 / 0
P11802 Cyclin-dependent kinase 4 CMGC serine/threonine protein kinase family C00011153 1 / 3
P24385 G1/S-specific cyclin-D1 Other cytosolic protein C00011153 1 / 8
P04637 Cellular tumor antigen p53 Transcription Factor C00011153 7 / 37
Q9HC97 G-protein coupled receptor 35 Kynurenic acid receptor C00011153 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00011153 1 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00011153 1 / 8
P11473 Vitamin D3 receptor NR1I1 C00011153 2 / 3
P23280 Carbonic anhydrase 6 Lyase C00011153 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00011153 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00011153 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00029474 0 / 0
P68871 Hemoglobin subunit beta Secreted protein C00011153 4 / 4
O43570 Carbonic anhydrase 12 Lyase C00011153 1 / 2
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00011153 1 / 1
P54760 Ephrin type-B receptor 4 Eph C00011153 0 / 0
P39748 Flap endonuclease 1 Enzyme C00011153 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00011153 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00011153 2 / 0
O75496 Geminin Unclassified protein C00011153 0 / 0
P15121 Aldose reductase Enzyme C00011153 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00011153 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00011153 0 / 0
Q05397 Focal adhesion kinase 1 Fak C00011153 0 / 0
P09211 Glutathione S-transferase P Enzyme C00011153 0 / 1
Q02763 Angiopoietin-1 receptor Tie C00011153 1 / 1
P15056 Serine/threonine-protein kinase B-raf Raf C00011153 6 / 3
P08107 Heat shock 70 kDa protein 1A/1B Unclassified protein C00011153 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00011153 1 / 1
O60285 NUAK family SNF1-like kinase 1 CAMK serine/threonine protein kinase NUAK subfamily C00011153 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00011153 0 / 0
Q4U2R8 Solute carrier family 22 member 6 Antiporter C00011153 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00011153 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00011153 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00011153 0 / 0
P06213 Insulin receptor TK tyrosine-protein kinase INSR subfamily C00011153 5 / 4
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00011153 5 / 9
P09619 Platelet-derived growth factor receptor beta Pdgfr C00011153 5 / 1
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00011153 0 / 0
Q96GD4 Aurora kinase B Aur C00011153 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00011153 1 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00011153 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00011153 0 / 0
P35916 Vascular endothelial growth factor receptor 3 Vegfr C00011153 2 / 1
P00390 Glutathione reductase, mitochondrial Oxidoreductase C00011153 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00011153 0 / 1
P41279 Mitogen-activated protein kinase kinase kinase 8 Ste11 C00011153 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00011153 3 / 3
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00011153 0 / 0
P12821 Angiotensin-converting enzyme M2 C00011153 4 / 2
P53350 Serine/threonine-protein kinase PLK1 PLK serine/threonine protein kinase subfamily C00011153 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00011153 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00011153 0 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt C00011153 4 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00011153 1 / 1
P07949 Proto-oncogene tyrosine-protein kinase receptor Ret Ret C00011153 9 / 4
P43166 Carbonic anhydrase 7 Lyase C00011153 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00011153 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00011153 1 / 1
P06746 DNA polymerase beta Enzyme C00011153 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00011153 0 / 0
Q13627 Dual specificity tyrosine-phosphorylation-regulated kinase 1A CMGC dual-specificity kinase DYRK1 C00011153 1 / 0
P22748 Carbonic anhydrase 4 Lyase C00011153 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00011153 0 / 0
P11142 Heat shock cognate 71 kDa protein Unclassified protein C00011153 0 / 0
P08069 Insulin-like growth factor 1 receptor TK tyrosine-protein kinase INSR subfamily C00011153 1 / 3
P49798 Regulator of G-protein signaling 4 Unclassified protein C00011153 2 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00011153 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00011153 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00011153 1 / 0
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00011153 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00011153 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00011153 1 / 4
Q9NSA0 Solute carrier family 22 member 11 Transporter C00011153 0 / 0
P20248 Cyclin-A2 Other cytosolic protein C00011153 0 / 0
P78396 Cyclin-A1 Other cytosolic protein C00011153 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00011153 0 / 0
P22694 cAMP-dependent protein kinase catalytic subunit beta Pka C00011153 0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka C00011153 0 / 0
P22612 cAMP-dependent protein kinase catalytic subunit gamma Pka C00011153 0 / 0
Q9UM73 ALK tyrosine kinase receptor TKL serine/threonine protein kinase STKR type 1 subfamily C00011153 1 / 1
P06748 Nucleophosmin Other nuclear protein C00011153 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00011153 0 / 0

77 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
55 ACPP, 5'-NT, ACP-3, ACP3, PAP acid phosphatase, prostate (EC:3.1.3.2 3.1.3.5) C00011153
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00011153
317 APAF1, APAF-1, CED4 apoptotic peptidase activating factor 1 C00011153
429 ASCL1, ASH1, HASH1, MASH1, bHLHa46 achaete-scute family bHLH transcription factor 1 C00011153
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00011153
467 ATF3 activating transcription factor 3 C00011153
9474 ATG5, APG5, APG5-LIKE, APG5L, ASP, hAPG5 autophagy related 5 C00011153
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00011153
654 BMP6, VGR, VGR1 bone morphogenetic protein 6 C00011153
2972 BRF1, BRF, BRF-1, GTF3B, TAF3B2, TAF3C, TAFIII90, TF3B90, TFIIIB90, hBRF BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit C00011153
811 CALR, CRT, RO, SSA, cC1qR calreticulin C00011153
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00011153
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00011153
929 CD14 CD14 molecule C00011153
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00011153
1616 DAXX, BING2, DAP6, EAP1 death-domain associated protein C00011153
1676 DFFA, DFF-45, DFF1, ICAD DNA fragmentation factor, 45kDa, alpha polypeptide C00011153
1877 E4F1, E4F E4F transcription factor 1 C00011153
1960 EGR3, EGR-3, PILOT early growth response 3 C00011153
2033 EP300, KAT3B, RSTS2, p300 E1A binding protein p300 (EC:2.3.1.48) C00011153
2060 EPS15, AF-1P, AF1P, MLLT5 epidermal growth factor receptor pathway substrate 15 C00011153
2145 EZH1, KMT6B enhancer of zeste homolog 1 (Drosophila) (EC:2.1.1.43) C00011153
2161 F12, HAE3, HAEX, HAF coagulation factor XII (Hageman factor) (EC:3.4.21.38) C00011153
2260 FGFR1, BFGFR, CD331, CEK, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 fibroblast growth factor receptor 1 (EC:2.7.10.1) C00011153
2316 FLNA, ABP-280, ABPX, CSBS, CVD1, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD filamin A, alpha C00011153
2822 GPLD1, GPIPLD, GPIPLDM, PIGPLD, PIGPLD1 glycosylphosphatidylinositol specific phospholipase D1 (EC:3.1.4.50) C00011153
2941 GSTA4, GSTA4-4, GTA4 glutathione S-transferase alpha 4 (EC:2.5.1.18) C00011153
2961 GTF2E2, FE, TF2E2, TFIIE-B general transcription factor IIE, polypeptide 2, beta 34kDa C00011153
2968 GTF2H4, P52, TFB2, TFIIH general transcription factor IIH, polypeptide 4, 52kDa C00011153
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00011153
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00011153
9592 IER2, ETR101 immediate early response 2 C00011153
3485 IGFBP2, IBP2, IGF-BP53 insulin-like growth factor binding protein 2, 36kDa C00011153
3487 IGFBP4, BP-4, HT29-IGFBP, IBP4, IGFBP-4 insulin-like growth factor binding protein 4 C00011153
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00011153
3554 IL1R1, CD121A, D2S1473, IL-1R-alpha, IL1R, IL1RA, P80 interleukin 1 receptor, type I C00011153
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00011153
3635 INPP5D, SHIP, SHIP-1, SHIP1, SIP-145, hp51CN inositol polyphosphate-5-phosphatase, 145kDa (EC:3.1.3.86) C00011153
10788 IQGAP2 IQ motif containing GTPase activating protein 2 C00011153
10379 IRF9, IRF-9, ISGF3, ISGF3G, p48 interferon regulatory factor 9 C00011153
354 KLK3, APS, KLK2A1, PSA, hK3 kallikrein-related peptidase 3 (EC:3.4.21.77) C00011153
9516 LITAF, PIG7, SIMPLE, TP53I7 lipopolysaccharide-induced TNF factor C00011153
4130 MAP1A, MAP1L, MTAP1A microtubule-associated protein 1A C00011153
23531 MMD, MMA, MMD1, PAQR11 monocyte to macrophage differentiation-associated C00011153
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) C00011153
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00011153
4791 NFKB2, H2TF1, LYT-10, LYT10, NF-kB2, p105, p52 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100) C00011153
4826 NNAT, Peg5 neuronatin C00011153
10528 NOP56, NOL5A, SCA36 NOP56 ribonucleoprotein C00011153
4862 NPAS2, MOP4, PASD4, bHLHe9 neuronal PAS domain protein 2 C00011153
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00011153
8505 PARG, PARG99 poly (ADP-ribose) glycohydrolase (EC:3.2.1.143) C00011153
5320 PLA2G2A, MOM1, PLA2, PLA2B, PLA2L, PLA2S, PLAS1, sPLA2 phospholipase A2, group IIA (platelets, synovial fluid) (EC:3.1.1.4) C00011153
5355 PLP2, A4, A4LSB proteolipid protein 2 (colonic epithelium-enriched) C00011153
5371 PML, MYL, PP8675, RNF71, TRIM19 promyelocytic leukemia C00011153
5467 PPARD, FAAR, NR1C2, NUC1, NUCI, NUCII, PPARB peroxisome proliferator-activated receptor delta C00011153
5592 PRKG1, 1, AAT8, PKG, PRKG1B, PRKGR1B, cGK, cGK_1, cGK1, cGKI, cGKI-BETA, cGKI-alpha protein kinase, cGMP-dependent, type I (EC:2.7.11.12) C00011153
5764 PTN, HARP, HBGF8, HBNF, NEGF1 pleiotrophin C00011153
5799 PTPRN2, IA-2beta, IAR, ICAAR, PTPRP, R-PTP-N2 protein tyrosine phosphatase, receptor type, N polypeptide 2 (EC:3.1.3.48) C00011153
5901 RAN, ARA24, Gsp1, TC4 RAN, member RAS oncogene family C00011153
8434 RECK, ST15 reversion-inducing-cysteine-rich protein with kazal motifs C00011153
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00011153
8490 RGS5, MST092, MST106, MST129, MSTP032, MSTP092, MSTP106, MSTP129 regulator of G-protein signaling 5 C00011153
6319 SCD, FADS5, MSTP008, SCD1, SCDOS stearoyl-CoA desaturase (delta-9-desaturase) (EC:1.14.19.1) C00011153
4735 SEPT2, DIFF6, NEDD-5, NEDD5, Pnutl3, hNedd5 septin 2 C00011153
6649 SOD3, EC-SOD superoxide dismutase 3, extracellular (EC:1.15.1.1) C00011153
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00011153
9013 TAF1C, MGC:39976, SL1, TAFI110, TAFI95 TATA box binding protein (TBP)-associated factor, RNA polymerase I, C, 110kDa C00011153
6938 TCF12, CRS3, HEB, HTF4, HsT17266, bHLHb20 transcription factor 12 C00011153
7015 TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT telomerase reverse transcriptase (EC:2.7.7.49) C00011153
7019 TFAM, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2, TCF6L3 transcription factor A, mitochondrial C00011153
7040 TGFB1, CED, DPD1, LAP, TGFB, TGFbeta transforming growth factor, beta 1 C00011153
7360 UGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379 UDP-glucose pyrophosphorylase 2 (EC:2.7.7.9) C00011153
7375 USP4, UNP, Unph ubiquitin specific peptidase 4 (proto-oncogene) (EC:3.4.19.12) C00011153
7453 WARS, GAMMA-2, IFI53, IFP53 tryptophanyl-tRNA synthetase (EC:6.1.1.2) C00011153
7704 ZBTB16, PLZF, ZNF145 zinc finger and BTB domain containing 16 C00011153
7750 ZMYM2, FIM, MYM, RAMP, SCLL, ZNF198 zinc finger, MYM-type 2 C00011153

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (97)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#615007 Basal ganglia calcification, idiopathic, 4; ibgc4 P09619
#613985 Beta-thalassemia P68871
#603902 Beta-thalassemia, dominant inclusion body type P68871
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer P31749
#115150 Cardiofaciocutaneous syndrome 1; cfc1 P15056
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#209880 Central hypoventilation syndrome, congenital; cchs P07949
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P07949
P15056
P31749
P84022
#615109 Cowden syndrome 6; cws6 P31749
#610549 Diabetes mellitus, insulin-resistant, with acanthosis nigricans P06213
#125853 Diabetes mellitus, noninsulin-dependent; niddm P06213
#119900 Digital clubbing, isolated congenital P15428
#246200 Donohue syndrome P06213
#609535 Drug metabolism, poor, cyp2c19-related P33261
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#137800 Glioma susceptibility 1; glm1 O75874
P04626
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#140700 Heinz body anemias P68871
#602089 Hemangioma, capillary infantile P35916
P35968
#614519 Hemorrhage, intracerebral, susceptibility to; ich P12821
#114550 Hepatocellular carcinoma P08581
#142623 Hirschsprung disease, susceptibility to, 1; hscr1 P07949
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#143860 Hyperchlorhidrosis, isolated O43570
#609968 Hyperinsulinemic hypoglycemia, familial, 5; hhf5 P06213
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#270450 Insulin-like growth factor i, resistance to P08069
#607785 Juvenile myelomonocytic leukemia; jmml P09619
#613707 Leopard syndrome 3 P15056
#601626 Leukemia, acute myeloid; aml P09619
P36888
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P00533
P04626
P04637
P15056
#153100 Lymphedema, hereditary, ia P35916
#605027 Lymphoma, non-hodgkin, familial P15056
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#609048 Melanoma, cutaneous malignant, susceptibility to, 3; cmm3 P11802
#614104 Mental retardation, autosomal dominant 7; mrd7 Q13627
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#612624 Microvascular complications of diabetes, susceptibility to, 3; mvcd3 P12821
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#171400 Multiple endocrine neoplasia, type iia; men2a P07949
#162300 Multiple endocrine neoplasia, type iib; men2b P07949
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#254500 Myeloma, multiple P24385
#131440 Myeloproliferative disorder, chronic, with eosinophilia P09619
#228550 Myofibromatosis, infantile, 1; imf1 P09619
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#613014 Neuroblastoma, susceptibility to, 3; nblst3 Q9UM73
#613706 Noonan syndrome 7; ns7 P15056
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#171300 Pheochromocytoma P07949
#172700 Pick disease of brain P10636
#262190 Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities P06213
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#176920 Proteus syndrome P31749
#191830 Renal adysplasia P07949
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#267430 Renal tubular dysgenesis; rtd P12821
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#603903 Sickle cell anemia P68871
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601367 Stroke, ischemic P12821
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#155240 Thyroid carcinoma, familial medullary; mtc P07949
#188550 Thyroid carcinoma, papillary P07949
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#600195 Venous malformations, multiple cutaneous and mucosal; vmcm Q02763
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (100)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
P08581 (related)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P24385 (related)
P24385 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
P24385 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
P04637 (related)
P08581 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
P04637 (related)
P68871 (marker)
H00028 Choriocarcinoma P00533 (related)
P04626 (related)
P04637 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
P11802 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P09619 (related)
P11802 (related)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
P24385 (related)
P24385 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (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)
H00019 Pancreatic cancer P04626 (related)
P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04626 (related)
P04637 (related)
H00027 Ovarian cancer P04626 (related)
P04637 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
P04637 (related)
P24385 (related)
H00046 Cholangiocarcinoma P04626 (related)
P04637 (related)
P08581 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (related)
H00006 Hairy-cell leukemia P04637 (related)
P24385 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
P24385 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
Q9UM73 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
P08069 (related)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
P68871 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00029 Vulvar cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P07949 (related)
P07949 (marker)
P15056 (related)
H00036 Osteosarcoma P04637 (related)
H00038 Malignant melanoma P04637 (related)
P11802 (related)
P15056 (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)
H00047 Gallbladder cancer P04637 (related)
P24385 (marker)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00719 Leprechaunism P06213 (related)
H00942 Rabson-Mendenhall syndrome P06213 (related)
H01228 Insulin-resistant diabetes mellitus with acanthosis nigricans (IRAN) P06213 (related)
H01267 Familial hyperinsulinemic hypoglycemia (HHF) P06213 (related)
H00822 Renal agenesis and Renal adysplasia P07949 (related)
H00910 Hirschsprung disease (HD) P07949 (related)
H00916 Congenital central hypoventilation syndrome (CCHS) P07949 (related)
H00050 Synovial sarcoma P08069 (related)
H01274 Growth delay due to insulin-like growth factor I resistance P08069 (related)
H00024 Prostate cancer P09211 (related)
P09211 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00083 Allograft rejection P12821 (related)
H00575 Renal tubular dysgenesis P12821 (related)
H00523 Noonan syndrome and related disorders P15056 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H00559 von Hippel-Lindau syndrome P24385 (related)
H00539 PTEN hamartoma tumor syndrome (PHTS) P31749 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00535 Lymphedemas P35916 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00094 DNA repair defects P54132 (related)
Q13315 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00228 Thalassemia P68871 (related)
H00229 Sickle cell anemia (SCA) P68871 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00531 Venous malformations Q02763 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (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

9 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000014 Abnormalities, Drug-Induced C00011153
D002471 Cell Transformation, Neoplastic C00011153
D006965 Hyperplasia C00011153
D007248 Infertility, Male C00011153
D009203 Myocardial Infarction C00011153
D015427 Reperfusion Injury C00011153
D012878 Skin Neoplasms C00011153
D013471 Sunburn C00011153
D013733 Testicular Diseases C00011153