Species

KNApSAcK Entry

Organism name Bauhinia candicans
Genus Bauhinia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Bauhinia forficata subsp. pruinosa
Linked NCBI taxonomy ID 72379
Linked level subspecies

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 (8)

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
C00005169 External link 512 Nicotiflorin
/ Nicotifloroside
/ Kaempferol 3-O-rutinoside
/ Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside
/ (-)-Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside
CHEMBL431610
CHEMBL79790
CHEMBL255020
CHEMBL501550
CHEMBL498879
CHEMBL1419228
CHEMBL1875691
22 / 10 / 12 No. 1 No. 15
C00005240 External link 512 Kaempferol 3-rutinoside-7-rhamnoside
No. 5 No. 15
C00003647 External link 512 Campesterol
/ 24alpha-Methylcholesterol
/ (24R)24-Methylcholest-5-en-3beta-ol
CHEMBL520535
CHEMBL485421
CHEMBL1836653
C021273
No. 53 No. 11
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00003648 External link 512 Cholesterol
/ Cholesterin
/ Cholest-5-en-3beta-ol
CHEMBL112570
CHEMBL1597825
CHEMBL1867358
D002784
20 / 28 / 24 45 / 23 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
C00001555 External link 512 Trigonelline
CHEMBL350675
C009560
3 / 1 / 0 No. 3681 No. 1
C00007298 External link 512 Choline
CHEMBL920
D002794
11 / 5 / 5 51 / 20 No. 5945

Human Protein / Gene in interactions

64 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00003672 C00005169 C00023774 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00003648 C00023774 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003648 C00023774 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00003648 C00005169 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003672 C00007298 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 C00007298 1 / 1
Q02880 DNA topoisomerase 2-beta Isomerase C00003648 C00023774 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003672 C00007298 1 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 C00007298 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00003648 C00005169 2 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 C00007298 0 / 1
P08183 Multidrug resistance protein 1 drug C00003648 C00003672 1 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00001555 C00003648 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003648 0 / 1
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P37840 Alpha-synuclein Unclassified protein C00003648 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00005169 1 / 1
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
Q16850 Lanosterol 14-alpha demethylase Cytochrome P450 51A1 C00003648 0 / 0
O15245 Solute carrier family 22 member 1 Drug uniporter C00007298 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005169 0 / 0
P07237 Protein disulfide-isomerase Enzyme C00005169 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005169 1 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00003648 0 / 0
P39748 Flap endonuclease 1 Enzyme C00005169 0 / 0
O75496 Geminin Unclassified protein C00005169 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00005169 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00005169 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001555 0 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P02545 Prelamin-A/C Unclassified protein C00003648 11 / 10
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003648 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005169 1 / 1
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00003648 2 / 0
P03372 Estrogen receptor NR3A1 C00003672 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
P22303 Acetylcholinesterase Hydrolase C00007298 1 / 0
Q99700 Ataxin-2 Unclassified protein C00005169 1 / 1
O00204 Sulfotransferase family cytosolic 2B member 1 Enzyme C00003648 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00005169 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00005169 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005169 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003648 0 / 0
P10275 Androgen receptor NR3C4 C00003648 3 / 4
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
O15244 Solute carrier family 22 member 2 Drug uniporter C00007298 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00005169 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00007298 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001555 1 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00005169 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00005169 1 / 4
Q9H015 Solute carrier family 22 member 4 Unclassified protein C00007298 1 / 1
O76082 Solute carrier family 22 member 5 Unclassified protein C00007298 1 / 2
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00005169 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00003648 0 / 0
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00003648 2 / 2
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00003648 3 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005169 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00005169 2 / 1

97 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
19 ABCA1, ABC-1, ABC1, CERP, HDLDT1, TGD ATP-binding cassette, sub-family A (ABC1), member 1 C00003648
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00003648
64240 ABCG5, STSL ATP-binding cassette, sub-family G (WHITE), member 5 C00003648
64241 ABCG8, GBD4, STSL ATP-binding cassette, sub-family G (WHITE), member 8 C00003648
177 AGER, RAGE advanced glycosylation end product-specific receptor C00003648
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00003648
335 APOA1 apolipoprotein A-I C00003648
857 CAV1, BSCL3, CGL3, MSTP085, PPH3, VIP21, CAV caveolin 1, caveolae protein, 22kDa C00003648
859 CAV3, LGMD1C, LQT9, VIP-21, VIP21 caveolin 3 C00003648
1050 CEBPA, C/EBP-alpha, CEBP CCAAT/enhancer binding protein (C/EBP), alpha C00003648
1066 CES1, ACAT, CE-1, CEH, CES2, HMSE, HMSE1, PCE-1, REH, SES1, TGH, hCE-1 carboxylesterase 1 (EC:3.1.1.1 3.1.1.56) C00003648
1583 CYP11A1, CYP11A, CYPXIA1, P450SCC cytochrome P450, family 11, subfamily A, polypeptide 1 (EC:1.14.15.6) C00003648
1593 CYP27A1, CP27, CTX, CYP27 cytochrome P450, family 27, subfamily A, polypeptide 1 (EC:1.14.13.15) C00003648
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00003648
10858 CYP46A1, CP46, CYP46 cytochrome P450, family 46, subfamily A, polypeptide 1 (EC:1.14.13.98) C00003648
1581 CYP7A1, CP7A, CYP7, CYPVII cytochrome P450, family 7, subfamily A, polypeptide 1 (EC:1.14.13.17) C00003648
1718 DHCR24, DCE, Nbla03646, SELADIN1, seladin-1 24-dehydrocholesterol reductase (EC:1.3.1.72) C00003648
1717 DHCR7, SLOS 7-dehydrocholesterol reductase (EC:1.3.1.21) C00003648
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00003648
2222 FDFT1, DGPT, ERG9, SQS, SS farnesyl-diphosphate farnesyltransferase 1 (EC:2.5.1.21) C00003648
2252 FGF7, HBGF-7, KGF fibroblast growth factor 7 C00003648
2264 FGFR4, CD334, JTK2, TKF fibroblast growth factor receptor 4 (EC:2.7.10.1) C00003648
2773 GNAI3, 87U6, ARCND1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3 C00003648
2778 GNAS, AHO, C20orf45, GNAS1, GPSA, GSA, GSP, NESP, PHP1A, PHP1B, PHP1C, POH GNAS complex locus C00003648
338442 HCAR2, GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG, Puma-g hydroxycarboxylic acid receptor 2 C00003648
3156 HMGCR, LDLCQ3 3-hydroxy-3-methylglutaryl-CoA reductase (EC:1.1.1.34) C00003648
3667 IRS1, HIRS-1 insulin receptor substrate 1 C00003648
3931 LCAT lecithin-cholesterol acyltransferase (EC:2.3.1.43) C00003648
3949 LDLR, FH, FHC, LDLCQ2 low density lipoprotein receptor C00003648
4481 MSR1, CD204, SCARA1, SR-A, SRA, phSR1, phSR2 macrophage scavenger receptor 1 C00003648
4864 NPC1, NPC Niemann-Pick disease, type C1 C00003648
7376 NR1H2, LXR-b, LXRB, NER, NER-I, RIP15, UNR nuclear receptor subfamily 1, group H, member 2 C00003648
10062 NR1H3, LXR-a, LXRA, RLD-1 nuclear receptor subfamily 1, group H, member 3 C00003648
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00003648
5338 PLD2 phospholipase D2 (EC:3.1.4.4) C00003648
5444 PON1, ESA, MVCD5, PON paraoxonase 1 (EC:3.1.1.2 3.1.8.1 3.1.1.81) C00003648
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00003648
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00003648
5879 RAC1, Rac-1, TC-25, p21-Rac1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1) C00003648
6256 RXRA, NR2B1 retinoid X receptor, alpha C00003648
6319 SCD, FADS5, MSTP008, SCD1, SCDOS stearoyl-CoA desaturase (delta-9-desaturase) (EC:1.14.19.1) C00003648
6721 SREBF2, SREBP-2, SREBP2, bHLHd2 sterol regulatory element binding transcription factor 2 C00003648
6770 STAR, STARD1 steroidogenic acute regulatory protein C00003648
27346 TMEM97, MAC30 transmembrane protein 97 C00003648
7421 VDR, NR1I1 vitamin D (1,25- dihydroxyvitamin D3) receptor C00003648
43 ACHE, ACEE, ARACHE, N-ACHE, YT acetylcholinesterase (EC:3.1.1.7) C00007298
8854 ALDH1A2, RALDH(II), RALDH2, RALDH2-T aldehyde dehydrogenase 1 family, member A2 (EC:1.2.1.36) C00007298
64333 ARHGAP9, 10C, RGL1 Rho GTPase activating protein 9 C00007298
590 BCHE, CHE1, CHE2, E1 butyrylcholinesterase (EC:3.1.1.8) C00007298
701 BUB1B, BUB1beta, BUBR1, Bub1A, MAD3L, MVA1, SSK1, hBUBR1 BUB1 mitotic checkpoint serine/threonine kinase B (EC:2.7.11.1) C00007298
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00007298
9332 CD163, M130, MM130 CD163 molecule C00007298
948 CD36, BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3 CD36 molecule (thrombospondin receptor) C00007298
55143 CDCA8, BOR, BOREALIN, DasraB, MESRGP cell division cycle associated 8 C00007298
55349 CHDH choline dehydrogenase (EC:1.1.99.1) C00007298
1111 CHEK1, CHK1 checkpoint kinase 1 (EC:2.7.11.1) C00007298
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00007298
1139 CHRNA7, CHRNA7-2, NACHRA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) C00007298
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00007298
81035 COLEC12, CLP1, NSR2, SCARA4, SRCL collectin sub-family member 12 C00007298
1440 CSF3, C17orf33, CSF3OS, GCSF, G-CSF colony stimulating factor 3 (granulocyte) C00007298
1471 CST3, ARMD11 cystatin C C00007298
1514 CTSL, CATL, CTSL1, MEP cathepsin L (EC:3.4.22.15) C00007298
1524 CX3CR1, CCRL1, CMKBRL1, CMKDR1, GPR13, GPRV28, V28 chemokine (C-X3-C motif) receptor 1 C00007298
1794 DOCK2 dedicator of cytokinesis 2 C00007298
3169 FOXA1, HNF3A, TCF3A forkhead box A1 C00007298
2632 GBE1, APBD, GBE, GSD4 glucan (1,4-alpha-), branching enzyme 1 (EC:2.4.1.18) C00007298
3003 GZMK, TRYP2 granzyme K (granzyme 3; tryptase II) (EC:3.4.21.-) C00007298
3309 HSPA5, BIP, GRP78, MIF2 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) C00007298
396742 C00007298
3560 IL2RB, CD122, IL15RB, P70-75 interleukin 2 receptor, beta C00007298
10112 KIF20A, MKLP2, RAB6KIFL kinesin family member 20A C00007298
9493 KIF23, CHO1, KNSL5, MKLP-1, MKLP1 kinesin family member 23 C00007298
51348 KLRF1, CLEC5C, NKp80 killer cell lectin-like receptor subfamily F, member 1 C00007298
114569 MAL2 mal, T-cell differentiation protein 2 (gene/pseudogene) C00007298
55016 MARCH1, MARCH-I, RNF171 membrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase C00007298
4256 MGP, MGLAP, NTI matrix Gla protein C00007298
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) C00007298
4522 MTHFD1, MTHFC, MTHFD methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase (EC:1.5.1.5 6.3.4.3 3.5.4.9) C00007298
9172 MYOM2, TTNAP myomesin 2 C00007298
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00007298
11333 PDAP1, HASPP28, PAP, PAP1 PDGFA associated protein 1 C00007298
10400 PEMT, PEAMT, PEMPT, PEMT2, PNMT phosphatidylethanolamine N-methyltransferase (EC:2.1.1.17 2.1.1.71) C00007298
5329 PLAUR, CD87, U-PAR, UPAR, URKR plasminogen activator, urokinase receptor C00007298
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00007298
23532 PRAME, CT130, MAPE, OIP-4, OIP4 preferentially expressed antigen in melanoma C00007298
5790 PTPRCAP, CD45-AP, LPAP protein tyrosine phosphatase, receptor type, C-associated protein C00007298
10287 RGS19, GAIP, RGSGAIP regulator of G-protein signaling 19 C00007298
57140 RNPEPL1 arginyl aminopeptidase (aminopeptidase B)-like 1 C00007298
6422 SFRP1, FRP, FRP-1, FRP1, FrzA, SARP2 secreted frizzled-related protein 1 C00007298
6584 SLC22A5, CDSP, OCTN2, OCTN2VT solute carrier family 22 (organic cation/carnitine transporter), member 5 C00007298
9056 SLC7A7, LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 C00007298
6594 SMARCA1, ISWI, NURF140, SNF2L, SNF2L1, SNF2LB, SNF2LT, SWI, SWI2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 C00007298
7015 TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT telomerase reverse transcriptase (EC:2.7.7.49) C00007298
7128 TNFAIP3, A20, OTUD7C, TNFA1P2 tumor necrosis factor, alpha-induced protein 3 (EC:3.4.19.12) C00007298
83549 UCK1, URK1 uridine-cytidine kinase 1 (EC:2.7.1.48) C00007298
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 (58)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#614490 Blood group, junior system; jr Q9UNQ0
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#212140 Carnitine deficiency, systemic primary; cdsp O76082
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc Q14191
#127750 Dementia, lewy body; dlb P37840
#607208 Dravet syndrome P35498
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#615363 Estrogen resistance; estrr P03372
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#275210 Restrictive dermopathy, lethal P02545
#180300 Rheumatoid arthritis; ra Q9H015
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#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
#277700 Werner syndrome; wrn Q14191
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (46)

KEGG name UniProt
H00286 Crohn's disease O76082 (related)
Q9H015 (related)
H00525 Disorders of fatty-acid oxidation O76082 (related)
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)
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)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00192 Xanthinuria P47989 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

39 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006528 Carcinoma, Hepatocellular C00003648
C00007298
D007859 Learning Disorders C00003648
C00007298
D005234 Fatty Liver C00003648
C00007298
D056486 Drug-Induced Liver Injury C00003648
C00007298
D009369 Neoplasms C00003648
D002779 Cholestasis C00003648
D050171 Dyslipidemias C00003648
D001161 Arteriosclerosis C00003648
D006471 Gastrointestinal Hemorrhage C00003648
D006529 Hepatomegaly C00003648
D006937 Hypercholesterolemia C00003648
D006949 Hyperlipidemias C00003648
D006951 Hyperlipoproteinemias C00003648
D006965 Hyperplasia C00003648
D015228 Hypertriglyceridemia C00003648
D007037 Hypothyroidism C00003648
D007680 Kidney Neoplasms C00003648
D050197 Atherosclerosis C00003648
D009336 Necrosis C00003648
D003327 Coronary Disease C00003648
D052556 Niemann-Pick Disease, Type C C00003648
D058226 Plaque, Atherosclerotic C00003648
D014456 Ulcer C00003648
D000647 Amnesia C00007298
D001321 Autistic Disorder C00007298
D003072 Cognition Disorders C00007298
D003866 Depressive Disorder C00007298
D002658 Developmental Disabilities C00007298
D005235 Fatty Liver, Alcoholic C00007298
D006505 Hepatitis C00007298
D007249 Inflammation C00007298
D008103 Liver Cirrhosis C00007298
D008113 Liver Neoplasms C00007298
D008569 Memory Disorders C00007298
C541083 Non-alcoholic Fatty Liver Disease C00007298
D010195 Pancreatitis C00007298
D016137 Spina Bifida Cystica C00007298
D013226 Status Epilepticus C00007298
D052878 Urolithiasis C00007298