Organism name | Bauhinia candicans |
---|---|
Genus | Bauhinia |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Bauhinia forficata subsp. pruinosa |
---|---|
Linked NCBI taxonomy ID | 72379 |
Linked level | subspecies |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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
![]() |
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
![]() |
Kaempferol 3-rutinoside-7-rhamnoside
|
No. 5 | No. 15 |
![]() |
||||
C00003647
![]() |
Campesterol
/ 24alpha-Methylcholesterol / (24R)24-Methylcholest-5-en-3beta-ol |
CHEMBL520535
CHEMBL485421 CHEMBL1836653 |
C021273
|
No. 53 | No. 11 |
![]() |
||
C00003672
![]() |
Sitosterol
/ beta-sitosterl / (-)-beta-Sitosterol / Stigmast-5-en-3beta-ol |
CHEMBL221542
CHEMBL1398443 CHEMBL1875388 |
17 / 19 / 12 | No. 53 | No. 11 |
![]() |
||
C00003648
![]() |
Cholesterol
/ Cholesterin / Cholest-5-en-3beta-ol |
CHEMBL112570
CHEMBL1597825 CHEMBL1867358 |
D002784
|
20 / 28 / 24 | 45 / 23 | No. 53 | No. 11 |
![]() |
C00023774
![]() |
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
![]() |
Trigonelline
|
CHEMBL350675
|
C009560
|
3 / 1 / 0 | No. 3681 | No. 1 |
![]() |
|
C00007298
![]() |
Choline
|
CHEMBL920
|
D002794
|
11 / 5 / 5 | 51 / 20 | No. 5945 |
![]() |
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 |
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
|
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 | 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)
|
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
|