Organism name | Pterocarpus santalinus |
---|---|
Genus | Pterocarpus |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Pterocarpus santalinus |
---|---|
Linked NCBI taxonomy ID | 1071199 |
Linked level | species |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
Species | Activity |
---|---|
Pterocarpus santalinus L. f. | Alexeteric |
Pterocarpus santalinus L. f. | Analgesic |
Pterocarpus santalinus L. f. | Anticonvulsant |
Pterocarpus santalinus L. f. | Antidiabetic |
Pterocarpus santalinus L. f. | Antiexudative |
Pterocarpus santalinus L. f. | Antipyretic |
Pterocarpus santalinus L. f. | Antispasmodic |
Pterocarpus santalinus L. f. | Aphrodisiac |
Pterocarpus santalinus L. f. | Astringent |
Pterocarpus santalinus L. f. | CNS Depressant |
Pterocarpus santalinus L. f. | Depurative |
Pterocarpus santalinus L. f. | Diaphoretic |
Pterocarpus santalinus L. f. | Expectorant |
Pterocarpus santalinus L. f. | Fungicide |
Pterocarpus santalinus L. f. | Hypoglycemic |
Pterocarpus santalinus L. f. | Insecticide |
Pterocarpus santalinus L. f. | Nematicide |
Pterocarpus santalinus L. f. | Tonic |
Pterocarpus santalinus L. f. | Tranquilizer |
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 |
---|---|---|---|---|---|---|---|---|
C00019424
![]() |
5,3',4'-Trihydroxy-7-methoxyisoflavone 3'-O-glucoside
|
No. 2 | No. 15 |
![]() |
||||
C00009459
![]() |
Santal
/ 5,3',4'-Trihydroxy-7-methoxyisoflavone |
No. 3 | No. 15 |
![]() |
||||
C00036622
![]() |
6-Hydroxy-7,2',4',5'-tetramethoxyisoflavone
|
No. 8 | No. 15 |
![]() |
||||
C00019047
![]() |
6-Hydroxy-7,2',4',5'-tetramethoxyisoflavone
|
No. 8 | No. 15 |
![]() |
||||
C00019065
![]() |
Erythrodiol
/ 3beta-Erythrodiol |
CHEMBL298604
CHEMBL60687 CHEMBL400074 |
C077953
|
4 / 0 / 1 | No. 13 | No. 51 |
![]() |
|
C00049120
![]() |
beta-Amyrone
|
CHEMBL461060
|
No. 13 | No. 51 |
![]() |
|||
C00003738
![]() |
beta-Amyrin
/ beta-Amirin / beta-Amyrine / beta-Amyrenol |
C036380
|
0 / 4 | No. 23 | No. 51 |
![]() |
||
C00029492
![]() |
epi-Lupeol
/ 3-Epilupeol / (+)-epi-Lupeol |
CHEMBL289191
CHEMBL459702 |
3 / 0 / 0 | No. 23 | No. 51 |
![]() |
||
C00003740
![]() |
Betulin
|
CHEMBL23236
CHEMBL140040 CHEMBL1610940 CHEMBL2000891 CHEMBL2069124 |
C002503
|
18 / 16 / 17 | 0 / 2 | No. 23 | No. 51 |
![]() |
C00003749
![]() |
Lupeol
/ Lupenol / (+)-Lupenol |
CHEMBL289191
CHEMBL459702 |
C010480
|
3 / 0 / 0 | 2 / 6 | No. 23 | No. 51 |
![]() |
C00019220
![]() |
Lupenone
|
CHEMBL486393
CHEMBL575188 |
3 / 4 / 2 | No. 23 | No. 51 |
![]() |
||
C00049211
![]() |
Lup-20(29)-ene-2alpha,3beta-diol
|
CHEMBL1773216
|
No. 23 | No. 51 |
![]() |
|||
C00019435
![]() |
4',5-Dihydroxy-7-methoxyisoflavone 3'-O-(3''-E-cinnamoylglucoside)
|
No. 30 | No. 15 |
![]() |
||||
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 |
![]() |
C00003672
![]() |
Sitosterol
/ beta-sitosterl / (-)-beta-Sitosterol / Stigmast-5-en-3beta-ol |
CHEMBL221542
CHEMBL1398443 CHEMBL1875388 |
17 / 19 / 12 | No. 53 | No. 11 |
![]() |
||
C00006925
![]() |
Isoliquiritigenin
|
CHEMBL129795
CHEMBL1395334 |
C040920
|
59 / 83 / 90 | 12 / 3 | No. 92 | No. 13 |
![]() |
C00011147
![]() |
6,4'-Dihydroxyaurone 4-O-rutinoside
|
No. 169 | No. 13 |
![]() |
||||
C00014665
![]() |
6,4'-Dihydroxyaurone-4-O-neohesperidoside
|
No. 169 | No. 13 |
![]() |
||||
C00002902
![]() |
Pterostilbene
/ 3,5-Dimethoxy-4'-hydroxystilbene |
CHEMBL87712
CHEMBL83527 |
C107773
|
19 / 19 / 20 | 54 / 15 | No. 344 | No. 13 |
![]() |
C00012772
![]() |
Pterocarpdiolone
/ [4R-(4alpha,4aalpha,6beta,8abeta)]-Octahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-2(1H)-naphthalenone |
No. 351 |
![]() |
|||||
C00012771
![]() |
Pterocarptriol
/ [1R-(1alpha,3alpha,4abeta,7beta,8aalpha)]-Decahydro-7-(1-hydroxy-1-methylethyl)-1,4a-dimethyl-1,3-naphthalenediol |
No. 351 |
![]() |
|||||
C00000856
![]() |
4-Hydroxybenzoic acid
/ p-Hydroxybenzoic acid |
CHEMBL441343
|
C038193
|
21 / 7 / 16 | 2 / 1 | No. 817 | No. 81 |
![]() |
C00002648
![]() |
Gentisic acid
/ 2,5-Dihydroxybenzoic acid |
CHEMBL1461
|
C010925
|
15 / 6 / 8 | 2 / 1 | No. 817 | No. 81 |
![]() |
C00002624
![]() |
Savinin
/ (-)-Savinin / (-)-Hibalactone |
CHEMBL395263
CHEMBL459851 |
7 / 10 / 5 | No. 1029 | No. 21 |
![]() |
||
C00002682
![]() |
Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid |
CHEMBL120568
|
D014641
|
5 / 3 / 3 | 5 / 0 | No. 1073 |
![]() |
|
C00002776
![]() |
Sinapic acid
|
CHEMBL109341
|
C073734
|
5 / 5 / 5 | 0 / 5 | No. 1366 | No. 6 |
![]() |
C00011146
![]() |
6-Hydroxy-5-methyl-3',4',5'-trimethoxyaurone-4-O-alpha-L-rhamnopyranoside
|
No. 3026 |
![]() |
|||||
C00014668
![]() |
6-Hydroxy-7-methyl-3',4',5'-trimethoxyaurone 4-O-rhamnoside
|
No. 3026 |
![]() |
|||||
C00012855
![]() |
Isopterocarpolone
/ [4aR-(4aalpha,6beta,8abeta)]-4a,5,6,7,8,8a-Hexahydro-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-2(1H)-naphthalenone |
No. 3519 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00002648 C00003672 C00003740 C00006925 C00019065 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002624 C00002648 C00002682 C00006925 | 0 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00002776 C00002902 C00003740 C00006925 | 0 / 3 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00003740 C00003749 C00023774 C00029492 | 0 / 0 |
P08047 | Transcription factor Sp1 | Unclassified protein | C00003672 C00003749 C00029492 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00002682 C00006925 C00019065 | 0 / 0 |
P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00002776 C00002902 C00006925 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003672 C00003740 C00006925 | 1 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003672 C00003740 C00006925 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003672 C00003740 C00006925 | 1 / 1 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002624 C00002902 C00006925 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003672 C00003740 C00006925 | 0 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003672 C00003740 C00006925 | 0 / 0 |
P11387 | DNA topoisomerase 1 | Isomerase | C00003740 C00003749 C00029492 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00003672 C00023774 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00000856 C00002648 | 0 / 1 |
P03372 | Estrogen receptor | NR3A1 | C00002682 C00003672 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00002902 C00006925 | 0 / 0 |
Q96RI1 | Bile acid receptor | NR1H4 | C00003740 C00019220 | 0 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00003672 C00019220 | 4 / 2 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00000856 C00006925 | 1 / 8 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00003740 C00006925 | 0 / 0 |
P14780 | Matrix metalloproteinase-9 | M10A | C00002648 C00006925 | 2 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002648 C00006925 | 0 / 0 |
Q8TDU6 | G-protein coupled bile acid receptor 1 | Steroid-like ligand receptor | C00003740 C00019220 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002902 C00006925 | 1 / 2 |
P02545 | Prelamin-A/C | Unclassified protein | C00003740 C00006925 | 11 / 10 |
P51580 | Thiopurine S-methyltransferase | Enzyme | C00000856 C00002682 | 1 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002902 C00006925 | 4 / 3 |
P00915 | Carbonic anhydrase 1 | Lyase | C00000856 C00002648 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00002624 C00006925 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00002902 C00006925 | 0 / 0 |
O43570 | Carbonic anhydrase 12 | Lyase | C00000856 C00002648 | 1 / 2 |
P00918 | Carbonic anhydrase 2 | Lyase | C00000856 C00002648 | 1 / 2 |
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00000856 C00002648 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002624 C00006925 | 0 / 0 |
P08183 | Multidrug resistance protein 1 | drug | C00002902 C00003672 | 1 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002624 C00006925 | 1 / 0 |
O00255 | Menin | Unclassified protein | C00002902 C00006925 | 2 / 5 |
P43166 | Carbonic anhydrase 7 | Lyase | C00000856 C00002648 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002624 C00002902 | 1 / 1 |
Q9HAW7 | UDP-glucuronosyltransferase 1-7 | Enzyme | C00000856 | 0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | C00006925 | 1 / 2 |
Q9UQ49 | Sialidase-3 | Enzyme | C00000856 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00006925 | 2 / 3 |
Q02156 | Protein kinase C epsilon type | Eta | C00003740 | 0 / 0 |
P23280 | Carbonic anhydrase 6 | Lyase | C00000856 | 0 / 0 |
P34969 | 5-hydroxytryptamine receptor 7 | Serotonin receptor | C00023774 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002776 | 2 / 2 |
P51649 | Succinate-semialdehyde dehydrogenase, mitochondrial | Oxidoreductase | C00000856 | 1 / 1 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00003740 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00006925 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00002682 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00006925 | 2 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00003740 | 3 / 1 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00002902 | 0 / 0 |
O60656 | UDP-glucuronosyltransferase 1-9 | Enzyme | C00000856 | 0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00002902 | 4 / 2 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00003672 | 3 / 2 |
P37840 | Alpha-synuclein | Unclassified protein | C00006925 | 4 / 2 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00003672 | 0 / 0 |
P55789 | FAD-linked sulfhydryl oxidase ALR | Enzyme | C00002902 | 1 / 0 |
P03956 | Interstitial collagenase | M10A | C00002648 | 0 / 1 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002624 | 7 / 3 |
Q04206 | Transcription factor p65 | Transcription Factor | C00006925 | 0 / 0 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00003740 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00006925 | 0 / 0 |
P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00006925 | 0 / 0 |
P22894 | Neutrophil collagenase | M10A | C00002648 | 0 / 0 |
P00734 | Prothrombin | S1A | C00003672 | 4 / 2 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00002902 | 2 / 2 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00000856 | 0 / 0 |
P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00006925 | 5 / 3 |
P80404 | 4-aminobutyrate aminotransferase, mitochondrial | Transferase | C00000856 | 1 / 1 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00006925 | 0 / 0 |
P35968 | Vascular endothelial growth factor receptor 2 | Vegfr | C00006925 | 1 / 0 |
Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00000856 | 0 / 0 |
P08581 | Hepatocyte growth factor receptor | TK tyrosine-protein kinase MET subfamily | C00006925 | 2 / 3 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002902 | 1 / 1 |
P04062 | Glucosylceramidase | Enzyme | C00006925 | 6 / 4 |
P21802 | Fibroblast growth factor receptor 2 | TK tyrosine-protein kinase TLK subfamily | C00006925 | 9 / 3 |
P08253 | 72 kDa type IV collagenase | M10A | C00002648 | 1 / 3 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00006925 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00006925 | 2 / 2 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00002902 | 1 / 1 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00006925 | 5 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00006925 | 0 / 0 |
Q9HAW9 | UDP-glucuronosyltransferase 1-8 | Enzyme | C00000856 | 0 / 0 |
Q13093 | Platelet-activating factor acetylhydrolase | Enzyme | C00002776 | 3 / 0 |
P09884 | DNA polymerase alpha catalytic subunit | Transferase | C00023774 | 0 / 0 |
P11362 | Fibroblast growth factor receptor 1 | Fgfr | C00006925 | 4 / 5 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00006925 | 0 / 0 |
P05771 | Protein kinase C beta type | Alpha | C00003740 | 0 / 0 |
Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00006925 | 2 / 2 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00006925 | 0 / 0 |
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00002648 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00006925 | 0 / 0 |
O60218 | Aldo-keto reductase family 1 member B10 | Enzyme | C00019065 | 0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00006925 | 1 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006925 | 0 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003672 | 2 / 0 |
Q99549 | M-phase phosphoprotein 8 | Unclassified protein | C00006925 | 0 / 0 |
P19224 | UDP-glucuronosyltransferase 1-6 | Enzyme | C00000856 | 0 / 0 |
Q9HAW8 | UDP-glucuronosyltransferase 1-10 | Enzyme | C00000856 | 0 / 0 |
P10721 | Mast/stem cell growth factor receptor Kit | Pdgfr | C00006925 | 4 / 3 |
P05412 | Transcription factor AP-1 | Transcription Factor | C00006925 | 0 / 0 |
P07451 | Carbonic anhydrase 3 | Lyase | C00000856 | 0 / 0 |
P17706 | Tyrosine-protein phosphatase non-receptor type 2 | Tyr | C00019065 | 0 / 1 |
P08254 | Stromelysin-1 | M10A | C00002648 | 1 / 0 |
P22748 | Carbonic anhydrase 4 | Lyase | C00000856 | 1 / 1 |
P80365 | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Enzyme | C00003672 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00006925 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002902 | 0 / 0 |
P40225 | Thrombopoietin | Unclassified protein | C00006925 | 1 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00006925 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00003672 | 1 / 1 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | C00006925 | 7 / 37 |
P42345 | Serine/threonine-protein kinase mTOR | Enzyme | C00006925 | 0 / 0 |
P00519 | Tyrosine-protein kinase ABL1 | Abl | C00002902 | 1 / 2 |
P11274 | Breakpoint cluster region protein | Bcr | C00002902 | 1 / 2 |
Q02880 | DNA topoisomerase 2-beta | Isomerase | C00023774 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002776 | 0 / 0 |
P51531 | Probable global transcription activator SNF2L2 | Unclassified protein | C00006925 | 1 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00006925 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
6817 | SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 | sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) |
C00000856
C00002648
|
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) |
C00002682
C00006925
|
54577 | UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G | UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) |
C00002682
C00006925
|
54575 | UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J | UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) |
C00002682
C00006925
|
5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A |
C00002902
C00006925
|
598 | BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS | BCL2-like 1 |
C00002902
C00006925
|
4792 | NFKBIA, IKBA, MAD-3, NFKBI | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha |
C00002902
C00006925
|
836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00002902
C00006925
|
4609 | MYC, MRTL, MYCC, bHLHe39, c-Myc | v-myc avian myelocytomatosis viral oncogene homolog |
C00002902
|
329 | BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 | baculoviral IAP repeat containing 2 |
C00006925
|
3952 | LEP, LEPD, OB, OBS | leptin |
C00000856
|
6513 | SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED | solute carrier family 2 (facilitated glucose transporter), member 1 |
C00006925
|
54658 | UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A | UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) |
C00006925
|
1499 | CTNNB1, CTNNB, MRD19, armadillo | catenin (cadherin-associated protein), beta 1, 88kDa |
C00003749
|
2539 | G6PD, G6PD1 | glucose-6-phosphate dehydrogenase (EC:1.1.1.49) |
C00002648
|
5728 | PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 | phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) |
C00003749
|
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) |
C00006925
|
207 | AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA | v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) |
C00002902
|
23600 | AMACR, AMACRD, CBAS4, RACE, RM | alpha-methylacyl-CoA racemase (EC:5.1.99.4) |
C00002902
|
1386 | ATF2, CRE-BP1, CREB2, HB16, TREB7 | activating transcription factor 2 (EC:2.3.1.48) |
C00002902
|
578 | BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 | BCL2-antagonist/killer 1 |
C00002902
|
581 | BAX, BCL2L4 | BCL2-associated X protein |
C00002902
|
596 | BCL2, Bcl-2, PPP1R50 | B-cell CLL/lymphoma 2 |
C00002902
|
842 | CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 | caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) |
C00002902
|
595 | CCND1, BCL1, D11S287E, PRAD1, U21B31 | cyclin D1 |
C00002902
|
1026 | CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | cyclin-dependent kinase inhibitor 1A (p21, Cip1) |
C00002902
|
1027 | CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 | cyclin-dependent kinase inhibitor 1B (p27, Kip1) |
C00002902
|
2921 | CXCL3, CINC-2b, GRO3, GROg, MIP-2b, MIP2B, SCYB3 | chemokine (C-X-C motif) ligand 3 |
C00002902
|
54205 | CYCS, CYC, HCS, THC4 | cytochrome c, somatic |
C00002902
|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00002902
|
1649 | DDIT3, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 | DNA-damage-inducible transcript 3 |
C00002902
|
56616 | DIABLO, DFNA64, SMAC | diablo, IAP-binding mitochondrial protein |
C00002902
|
1950 | EGF, HOMG4, URG | epidermal growth factor |
C00002902
|
1956 | EGFR, ERBB, ERBB1, HER1, PIG61, mENA | epidermal growth factor receptor (EC:2.7.10.1) |
C00002902
|
2002 | ELK1 | ELK1, member of ETS oncogene family |
C00002902
|
2523 | FUT1, H, HH, HSC | fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group) (EC:2.4.1.69) |
C00002902
|
9518 | GDF15, GDF-15, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB | growth differentiation factor 15 |
C00002902
|
3162 | HMOX1, HMOX1D, HO-1, HSP32, bK286B10 | heme oxygenase (decycling) 1 (EC:1.14.99.3) |
C00002902
|
4670 | HNRNPM, CEAR, HNRNPM4, HNRPM, HNRPM4, HTGR1, NAGR1, hnRNP_M | heterogeneous nuclear ribonucleoprotein M |
C00002902
|
3313 | HSPA9, CSA, GRP-75, GRP75, HSPA9B, MOT, MOT2, MTHSP75, PBP74 | heat shock 70kDa protein 9 (mortalin) |
C00002902
|
3458 | IFNG, IFG, IFI | interferon, gamma |
C00002902
|
3553 | IL1B, IL-1, IL1-BETA, IL1F2 | interleukin 1, beta |
C00002902
|
3696 | ITGB8 | integrin, beta 8 |
C00002902
|
3717 | JAK2, JTK10, THCYT3 | Janus kinase 2 (EC:2.7.10.2) |
C00002902
|
3949 | LDLR, FH, FHC, LDLCQ2 | low density lipoprotein receptor |
C00002902
|
5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) |
C00002902
|
1432 | MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA | mitogen-activated protein kinase 14 (EC:2.7.11.24) |
C00002902
|
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) |
C00002902
|
5599 | MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c | mitogen-activated protein kinase 8 (EC:2.7.11.24) |
C00002902
|
5601 | MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK | mitogen-activated protein kinase 9 (EC:2.7.11.24) |
C00002902
|
4170 | MCL1, BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1, TM, bcl2-L-3, mcl1/EAT | myeloid cell leukemia sequence 1 (BCL2-related) |
C00002902
|
4318 | MMP9, CLG4B, GELB, MANDP2, MMP-9 | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) |
C00002902
|
330 | BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 | baculoviral IAP repeat containing 3 |
C00006925
|
4790 | NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 | nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 |
C00002902
|
4843 | NOS2, HEP-NOS, INOS, NOS, NOS2A | nitric oxide synthase 2, inducible (EC:1.14.13.39) |
C00002902
|
8856 | NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR | nuclear receptor subfamily 1, group I, member 2 |
C00002902
|
9970 | NR1I3, CAR, CAR1, MB67 | nuclear receptor subfamily 1, group I, member 3 |
C00002902
|
142 | PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 | poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) |
C00002902
|
5743 | PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 | prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) |
C00002902
|
6301 | SARS, SERRS, SERS | seryl-tRNA synthetase (EC:6.1.1.11) |
C00002902
|
6648 | SOD2, IPOB, MNSOD, MVCD6 | superoxide dismutase 2, mitochondrial (EC:1.15.1.1) |
C00002902
|
6667 | SP1 | Sp1 transcription factor |
C00002902
|
6774 | STAT3, APRF, HIES | signal transducer and activator of transcription 3 (acute-phase response factor) |
C00002902
|
7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor |
C00002902
|
7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 |
C00002902
|
9189 | ZBED1, ALTE, DREF, TRAMP, hDREF | zinc finger, BED-type containing 1 |
C00002902
|
118738 | ZNF488 | zinc finger protein 488 |
C00002902
|
10599 | SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 | solute carrier organic anion transporter family, member 1B1 |
C00023774
|
4846 | NOS3, ECNOS, eNOS | nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) |
C00002682
|
54659 | UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C | UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) |
C00002682
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#207410 | Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 |
P21802
|
#101200 | Apert syndrome |
P21802
|
#218030 | Apparent mineralocorticoid excess; ame |
P80365
|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#600807 | Asthma, susceptibility to |
Q13093
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
#123790 | Beare-stevenson cutis gyrata syndrome; bstvs |
P21802
|
#614592 | Bent bone dysplasia syndrome; bbds |
P21802
|
#210900 | Bloom syndrome; blm |
P54132
|
%606641 | Body mass index; bmi |
P37231
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#609338 | Carotid intimal medial thickness 1 |
P37231
|
#118300 | Charcot-marie-tooth disease and deafness |
Q01453
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a |
Q01453
|
#114500 | Colorectal cancer; crc |
P84022
|
#614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
#123500 | Crouzon syndrome |
P21802
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#133239 | Esophageal cancer |
P04637
|
#615363 | Estrogen resistance; estrr |
P03372
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#613163 | Gaba-transaminase deficiency |
P80404
|
#606764 | Gastrointestinal stromal tumor; gist |
P10721
|
#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 |
#232300 | Glycogen storage disease ii |
P10253
|
#139393 | Guillain-barre syndrome, familial; gbs |
Q01453
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#602089 | Hemangioma, capillary infantile |
P35968
|
#114550 | Hepatocellular carcinoma |
P08581
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#145900 | Hypertrophic neuropathy of dejerine-sottas |
Q01453
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#147950 | Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 |
P11362
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#147050 | Ige responsiveness, atopic; iger |
Q13093
|
#612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#123150 | Jackson-weiss syndrome; jws |
P21802
|
#149730 | Lacrimoauriculodentodigital syndrome; ladd |
P21802
|
#601626 | Leukemia, acute myeloid; aml |
P10721
|
#608232 | Leukemia, chronic myeloid; cml |
P00519
P11274 |
#151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#613688 | Long qt syndrome 2; lqt2 |
Q12809
|
#211980 | Lung cancer |
P00533
P04637 |
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#613076 | Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay |
P55789
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#601358 | Nicolaides-baraitser syndrome; ncbrs |
P51531
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#601665 | Obesity |
P37231
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#166250 | Osteoglophonic dysplasia; ogd |
P11362
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#260500 | Papilloma of choroid plexus; cpp |
P04637
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P04062
P37840 |
#260540 | Parkinson-dementia syndrome |
P10636
|
#101600 | Pfeiffer syndrome |
P11362
P21802 |
#172700 | Pick disease of brain |
P10636
|
#172800 | Piebald trait; pbt |
P10721
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#614278 | Platelet-activating factor acetylhydrolase deficiency; pafad |
Q13093
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#605074 | Renal cell carcinoma, papillary, 1; rccp1 |
P08581
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
#609579 | Scaphocephaly, maxillary retrusion, and mental retardation |
P21802
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#609620 | Short qt syndrome 1; sqt1 |
Q12809
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
#601367 | Stroke, ischemic |
P00734
|
#271980 | Succinic semialdehyde dehydrogenase deficiency; ssadhd |
P51649
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#273300 | Testicular germ cell tumor; tgct |
P10721
|
#610460 | Thiopurine s-methyltransferase deficiency |
P51580
|
#187950 | Thrombocythemia 1; thcyt1 |
P40225
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
#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
|
#190440 | Trigonocephaly 1; trigno1 |
P11362
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
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)
|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
P04637 (marker) P08581 (related) Q16790 (marker) |
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
P00519
(related)
P00519 (marker) P11274 (related) P11274 (marker) Q03164 (related) Q03164 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
P00519
(related)
P00519 (marker) P04637 (related) P11274 (related) P11274 (marker) |
H00016 | Oral cancer |
P00533
(related)
P00533 (marker) P04637 (related) P04637 (marker) |
H00017 | Esophageal cancer |
P00533
(related)
P04637 (related) P04637 (marker) P35354 (related) |
H00018 | Gastric cancer |
P00533
(related)
P04637 (related) P08581 (related) P21802 (related) |
H00022 | Bladder cancer |
P00533
(related)
P04637 (related) |
H00028 | Choriocarcinoma |
P00533
(related)
P03956 (related) P04637 (related) P08253 (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)
|
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)
Q01453 (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) |
H00066 | Lewy body dementia (LBD) |
P04062
(related)
P37840 (related) |
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(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) P08253 (related) P14780 (related) P35354 (related) |
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)
P08581 (related) P35354 (related) |
H00047 | Gallbladder cancer |
P04637
(related)
|
H00048 | Hepatocellular carcinoma |
P04637
(related)
|
H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
H01007 | Choroid plexus papilloma |
P04637
(related)
|
H00472 | Torg-Winchester syndrome |
P08253
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P10721
(related)
P10721 (marker) |
H00170 | Piebaldism |
P10721
(related)
|
H00023 | Testicular cancer |
P10721
(marker)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00255 | Hypogonadotropic hypogonadism |
P11362
(related)
|
H00443 | Osteoglophonic dysplasia (OD) |
P11362
(related)
|
H00458 | Craniosynostosis |
P11362
(related)
P21802 (related) |
H00516 | Isolated orofacial clefts |
P11362
(related)
|
H01207 | Trigonocephaly |
P11362
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
H00794 | Aromatase excess syndrome |
P11511
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00479 | Metaphyseal dysplasias |
P14780
(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)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00408 | Type I diabetes mellitus |
P17706
(related)
|
H00642 | Lacrimo-auriculo-dento-digital syndrome (LADD) |
P21802
(related)
|
H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00409 | Type II diabetes mellitus |
P37231
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00227 | Congenital amegakaryocytic thrombocytopenia (CAMT) |
P40225
(marker)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00964 | Thiopurine S-methyltransferase deficiency (TPMT deficiency) |
P51580
(related)
|
H00835 | Succinic semialdehyde dehydrogenase (SSADH) deficiency |
P51649
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00259 | Apparent mineralocorticoid excess syndrome |
P80365
(related)
|
H01257 | GABA-transaminase deficiency |
P80404
(related)
|
H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) |
Q01453
(related)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00720 | Long QT syndrome |
Q12809
(related)
|
H00725 | Short QT syndrome |
Q12809
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (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)
|
MESH or OMIM | name |
KNApSAcK
metabolite |
---|---|---|
D003110 | Colonic Neoplasms |
C00003740
C00002902 |
D007249 | Inflammation |
C00003738
C00002902 |
D006528 | Carcinoma, Hepatocellular |
C00003749
C00002902 |
D012878 | Skin Neoplasms |
C00003749
C00002902 |
D009422 | Nervous System Diseases |
C00006925
|
D009374 | Neoplasms, Experimental |
C00003749
|
D009202 | Cardiomyopathies |
C00003749
|
D014947 | Wounds and Injuries |
C00003749
|
D006461 | Hemolysis |
C00002648
|
D005157 | Facial Pain |
C00003738
|
D006930 | Hyperalgesia |
C00003738
|
D064420 | Drug-Related Side Effects and Adverse Reactions |
C00003740
|
D010146 | Pain |
C00003738
|
D012220 | Rhinitis |
C00000856
|
D001927 | Brain Diseases |
C00006925
|
D009120 | Muscle Cramp |
C00006925
|
D006937 | Hypercholesterolemia |
C00003749
|
D000647 | Amnesia |
C00002776
|
D000860 | Anoxia |
C00002776
|
D001930 | Brain Injuries |
C00002776
|
D056486 | Drug-Induced Liver Injury |
C00002776
|
D004487 | Edema |
C00002776
|
D058739 | Aberrant Crypt Foci |
C00002902
|
D000236 | Adenoma |
C00002902
|
D001943 | Breast Neoplasms |
C00002902
|
D002471 | Cell Transformation, Neoplastic |
C00002902
|
D015179 | Colorectal Neoplasms |
C00002902
|
D015464 | Leukemia, Myelogenous, Chronic, BCR-ABL Positive |
C00002902
|
D009361 | Neoplasm Invasiveness |
C00002902
|
D009362 | Neoplasm Metastasis |
C00002902
|
D012516 | Osteosarcoma |
C00002902
|
D010190 | Pancreatic Neoplasms |
C00002902
|
D010212 | Papilloma |
C00002902
|