id | C00002895 |
---|---|
Name | Piceatannol / 3,3',4,5'-Tetrahydroxystilbene |
CAS RN | 10083-24-6 |
Standard InChI | InChI=1S/C14H12O4/c15-11-5-10(6-12(16)8-11)2-1-9-3-4-13(17)14(18)7-9/h1-8,15-18H/b2-1+ |
Standard InChI (Main Layer) | InChI=1S/C14H12O4/c15-11-5-10(6-12(16)8-11)2-1-9-3-4-13(17)14(18)7-9/h1-8,15-18H |
Phytochemical cluster | No. 13 |
---|---|
KCF-S cluster | No. 295 |
By standard InChI | CHEMBL69863 |
---|---|
By standard InChI Main Layer | CHEMBL69863 CHEMBL1603409 CHEMBL1972346 |
By LinkDB | C05901 |
---|
By CAS RN |
---|
class name | count |
---|---|
rosids | 16 |
Spermatophyta | 11 |
eudicotyledons | 3 |
Liliopsida | 3 |
family name | count |
---|---|
Fabaceae | 14 |
Pinaceae | 11 |
Polygonaceae | 3 |
Cyperaceae | 2 |
Vitaceae | 1 |
Moraceae | 1 |
Poaceae | 1 |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | CHEMBL1603409 |
CHEMBL1741321
(1)
|
1 / 0 |
P42345 | Serine/threonine-protein kinase mTOR | Enzyme | CHEMBL69863 |
CHEMBL1613805
(1)
CHEMBL1614293
(1)
|
0 / 0 |
Q02750 | Dual specificity mitogen-activated protein kinase kinase 1 | Ste7 | CHEMBL1972346 |
CHEMBL1963692
(1)
|
1 / 1 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | CHEMBL69863 CHEMBL1603409 |
CHEMBL1613992
(1)
CHEMBL1613995
(1)
CHEMBL1738132 (1) |
7 / 44 |
P08922 | Proto-oncogene tyrosine-protein kinase ROS | TK tyrosine-protein kinase SEV | CHEMBL1972346 |
CHEMBL1963751
(1)
|
0 / 1 |
P49336 | Cyclin-dependent kinase 8 | Cdk8 | CHEMBL1972346 |
CHEMBL1963824
(1)
|
0 / 0 |
Q04771 | Activin receptor type-1 | TKL serine/threonine protein kinase STKR1 subfamily | CHEMBL1972346 |
CHEMBL1963721
(1)
|
1 / 2 |
Q16637 | Survival motor neuron protein | Unclassified protein | CHEMBL69863 |
CHEMBL1613842
(3)
|
4 / 2 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | CHEMBL69863 |
CHEMBL1738312
(1)
|
0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | CHEMBL69863 |
CHEMBL1794367
(1)
CHEMBL2114784
(2)
|
1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | CHEMBL69863 |
CHEMBL1794499
(3)
|
2 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | CHEMBL1603409 |
CHEMBL1614177
(1)
CHEMBL1614265
(1)
|
0 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | CHEMBL69863 |
CHEMBL1738091
(1)
|
0 / 0 |
P06746 | DNA polymerase beta | Enzyme | CHEMBL69863 |
CHEMBL1614079
(1)
|
0 / 0 |
P04062 | Glucosylceramidase | Enzyme | CHEMBL69863 |
CHEMBL1613818
(1)
|
6 / 4 |
P29466 | Caspase-1 | C14 | CHEMBL1603409 |
CHEMBL1614158
(1)
|
0 / 0 |
Q04759 | Protein kinase C theta type | Delta | CHEMBL1972346 |
CHEMBL1963687
(1)
|
0 / 1 |
P28907 | ADP-ribosyl cyclase 1 | Enzyme | CHEMBL69863 |
CHEMBL1799589
(1)
|
0 / 1 |
P27448 | MAP/microtubule affinity-regulating kinase 3 | CAMK serine/threonine protein kinase MARK subfamily | CHEMBL1972346 |
CHEMBL1963756
(1)
|
0 / 0 |
Q9UHD2 | Serine/threonine-protein kinase TBK1 | Ikk | CHEMBL1972346 |
CHEMBL1963698
(1)
|
1 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | CHEMBL69863 |
CHEMBL1614310
(1)
CHEMBL1614544
(1)
|
11 / 10 |
P55789 | FAD-linked sulfhydryl oxidase ALR | Enzyme | CHEMBL69863 |
CHEMBL1738573
(1)
|
1 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | CHEMBL69863 |
CHEMBL1614554
(1)
CHEMBL1613776
(1)
|
3 / 1 |
P11309 | Serine/threonine-protein kinase pim-1 | Pim | CHEMBL1972346 |
CHEMBL1963726
(1)
|
0 / 0 |
P48729 | Casein kinase I isoform alpha | Ck1 | CHEMBL1972346 |
CHEMBL1963741
(1)
|
0 / 0 |
P16234 | Platelet-derived growth factor receptor alpha | Pdgfr | CHEMBL1972346 |
CHEMBL1963805
(1)
|
2 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | CHEMBL1603409 |
CHEMBL1614027
(1)
CHEMBL1741325
(1)
|
0 / 1 |
Q06187 | Tyrosine-protein kinase BTK | Tec | CHEMBL1972346 |
CHEMBL1963733
(1)
|
2 / 2 |
Q14680 | Maternal embryonic leucine zipper kinase | Melk | CHEMBL1972346 |
CHEMBL1963804
(1)
|
0 / 0 |
P29376 | Leukocyte tyrosine kinase receptor | Alk | CHEMBL1972346 |
CHEMBL1964115
(1)
|
0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | CHEMBL69863 |
CHEMBL1614522
(1)
CHEMBL1614067
(1)
|
1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | CHEMBL69863 |
CHEMBL1614166
(1)
|
1 / 0 |
Q15746 | Myosin light chain kinase, smooth muscle | Mlck | CHEMBL69863 |
CHEMBL939381
(1)
CHEMBL971891
(1)
|
1 / 1 |
Q13188 | Serine/threonine-protein kinase 3 | STE serine/threonine protein kinase MST subfamily | CHEMBL1972346 |
CHEMBL1964119
(1)
|
0 / 0 |
Q13464 | Rho-associated protein kinase 1 | Rock | CHEMBL1972346 |
CHEMBL1963814
(1)
|
0 / 0 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | CHEMBL69863 CHEMBL1603409 |
CHEMBL1613800
(2)
|
0 / 0 |
P17948 | Vascular endothelial growth factor receptor 1 | Vegfr | CHEMBL1972346 |
CHEMBL1963826
(1)
|
0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL69863 |
CHEMBL1614458
(4)
|
0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | CHEMBL69863 |
CHEMBL1794495
(1)
|
2 / 2 |
Q02779 | Mitogen-activated protein kinase kinase kinase 10 | TKL dual-specificity kinase MLK | CHEMBL1972346 |
CHEMBL1964110
(1)
|
0 / 0 |
Q9UQM7 | Calcium/calmodulin-dependent protein kinase type II subunit alpha | Camk2 | CHEMBL1972346 |
CHEMBL1964111
(1)
|
0 / 0 |
P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | CHEMBL1972346 |
CHEMBL1963779
(1)
|
1 / 1 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | CHEMBL1603409 |
CHEMBL1614456
(1)
CHEMBL1613803
(1)
|
0 / 0 |
Q8IXJ6 | NAD-dependent protein deacetylase sirtuin-2 | Enzyme | CHEMBL69863 |
CHEMBL913334
(1)
|
0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | CHEMBL69863 |
CHEMBL1613922
(1)
CHEMBL1794486
(1)
|
0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | CHEMBL69863 |
CHEMBL1738606
(2)
|
0 / 0 |
Q9Y463 | Dual specificity tyrosine-phosphorylation-regulated kinase 1B | CMGC dual-specificity kinase DYRK1 | CHEMBL1972346 |
CHEMBL1963799
(1)
|
0 / 0 |
O95819 | Mitogen-activated protein kinase kinase kinase kinase 4 | STE serine/threonine protein kinase MSN subfamily | CHEMBL1972346 |
CHEMBL1964101
(1)
|
0 / 0 |
Q9HBY8 | Serine/threonine-protein kinase Sgk2 | AGC serine/threonine protein kinase SGK subfamily | CHEMBL1972346 |
CHEMBL1963793
(1)
|
0 / 0 |
O75496 | Geminin | Unclassified protein | CHEMBL69863 |
CHEMBL1613941
(1)
CHEMBL2114843
(1)
|
0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | CHEMBL69863 |
CHEMBL1613838
(1)
|
0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | CHEMBL69863 |
CHEMBL2114807
(1)
|
4 / 2 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | CHEMBL1972346 |
CHEMBL1963830
(1)
|
0 / 0 |
Q05397 | Focal adhesion kinase 1 | Fak | CHEMBL1972346 |
CHEMBL1963801
(1)
|
0 / 0 |
P53779 | Mitogen-activated protein kinase 10 | Jnk | CHEMBL1972346 |
CHEMBL1964109
(1)
|
0 / 1 |
Q14164 | Inhibitor of nuclear factor kappa-B kinase subunit epsilon | Other serine/threonine protein kinase | CHEMBL1972346 |
CHEMBL1964108
(1)
|
0 / 0 |
Q96RR4 | Calcium/calmodulin-dependent protein kinase kinase 2 | META serine/threonine protein kinase subfamily | CHEMBL1972346 |
CHEMBL1963755
(1)
|
0 / 0 |
Q9UM73 | ALK tyrosine kinase receptor | TKL serine/threonine protein kinase STKR type 1 subfamily | CHEMBL1972346 |
CHEMBL1963704
(1)
|
1 / 1 |
Q9Y253 | DNA polymerase eta | Enzyme | CHEMBL69863 |
CHEMBL1794569
(1)
|
1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | CHEMBL69863 |
CHEMBL1614280
(1)
|
0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | CHEMBL69863 |
CHEMBL1738610
(1)
CHEMBL1794401
(1)
|
0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | CHEMBL69863 |
CHEMBL1963863
(1)
|
0 / 0 |
P11021 | 78 kDa glucose-regulated protein | Unclassified protein | CHEMBL69863 |
CHEMBL1794423
(1)
CHEMBL1963893
(1)
|
0 / 0 |
P34947 | G protein-coupled receptor kinase 5 | AGC serine/threonine protein kinase GRK subfamily | CHEMBL1972346 |
CHEMBL1963789
(1)
|
0 / 0 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | CHEMBL69863 |
CHEMBL823856
(1)
|
0 / 0 |
O60674 | Tyrosine-protein kinase JAK2 | Jakb | CHEMBL1972346 |
CHEMBL1963693
(1)
|
5 / 2 |
P35968 | Vascular endothelial growth factor receptor 2 | Vegfr | CHEMBL1972346 |
CHEMBL1963788
(1)
|
1 / 0 |
P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | CHEMBL69863 CHEMBL1603409 |
CHEMBL1614252
(2)
|
2 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | CHEMBL1603409 |
CHEMBL1741322
(1)
|
0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL1603409 |
CHEMBL1613910
(1)
CHEMBL1614227
(1)
|
3 / 3 |
Q06418 | Tyrosine-protein kinase receptor TYRO3 | TK tyrosine-protein kinase AXL | CHEMBL1972346 |
CHEMBL1963714
(1)
|
0 / 0 |
Q7L7X3 | Serine/threonine-protein kinase TAO1 | STE serine/threonine protein kinase TAO subfamily | CHEMBL1972346 |
CHEMBL1963750
(1)
|
0 / 0 |
Q9H0K1 | Serine/threonine-protein kinase SIK2 | CAMK serine/threonine protein kinase QIK subfamily | CHEMBL1972346 |
CHEMBL1963784
(1)
|
0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL69863 |
CHEMBL1614038
(2)
|
2 / 2 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | CHEMBL69863 |
CHEMBL1614342
(1)
|
1 / 1 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | CHEMBL69863 |
CHEMBL1614171
(1)
|
5 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | CHEMBL69863 |
CHEMBL1738588
(1)
CHEMBL1738675
(1)
CHEMBL1737868 (1) CHEMBL1738317 (1) |
0 / 0 |
P11362 | Fibroblast growth factor receptor 1 | Fgfr | CHEMBL1972346 |
CHEMBL1963740
(1)
|
4 / 5 |
P49840 | Glycogen synthase kinase-3 alpha | Gsk | CHEMBL1972346 |
CHEMBL1963771
(1)
|
0 / 0 |
O75116 | Rho-associated protein kinase 2 | Rock | CHEMBL1972346 |
CHEMBL1963722
(1)
|
0 / 0 |
P08631 | Tyrosine-protein kinase HCK | Src | CHEMBL1972346 |
CHEMBL1963709
(1)
|
0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | CHEMBL1603409 |
CHEMBL1614240
(1)
|
0 / 0 |
P51812 | Ribosomal protein S6 kinase alpha-3 | Rskb | CHEMBL1972346 |
CHEMBL1963690
(1)
|
2 / 2 |
P07333 | Macrophage colony-stimulating factor 1 receptor | Pdgfr | CHEMBL1972346 |
CHEMBL1964104
(1)
|
1 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | CHEMBL1603409 |
CHEMBL1741323
(1)
|
1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | CHEMBL1603409 |
CHEMBL1614108
(1)
CHEMBL1613886
(1)
CHEMBL1741324 (1) |
0 / 1 |
Q8IU85 | Calcium/calmodulin-dependent protein kinase type 1D | Camk1 | CHEMBL1972346 |
CHEMBL1963811
(1)
|
0 / 0 |
P07949 | Proto-oncogene tyrosine-protein kinase receptor Ret | Ret | CHEMBL1972346 |
CHEMBL1963706
(1)
|
9 / 5 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL69863 |
CHEMBL1794483
(2)
|
0 / 0 |
Q15046 | Lysine--tRNA ligase | Enzyme | CHEMBL69863 |
CHEMBL2173407
(1)
CHEMBL2173422
(1)
|
2 / 1 |
O75164 | Lysine-specific demethylase 4A | Enzyme | CHEMBL69863 |
CHEMBL1737991
(1)
|
0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL69863 |
CHEMBL1614211
(4)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL69863 |
CHEMBL1614421
(4)
CHEMBL1614502
(4)
|
4 / 3 |
Q99549 | M-phase phosphoprotein 8 | Unclassified protein | CHEMBL69863 |
CHEMBL1738402
(2)
|
0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | CHEMBL69863 |
CHEMBL1737980
(1)
CHEMBL1738184
(1)
|
0 / 0 |
Q5S007 | Leucine-rich repeat serine/threonine-protein kinase 2 | TKL serine/threonine protein kinase LRRK subfamily | CHEMBL1972346 |
CHEMBL1963806
(1)
|
2 / 2 |
P06239 | Tyrosine-protein kinase Lck | Src | CHEMBL69863 CHEMBL1972346 |
CHEMBL765997
(1)
CHEMBL818321
(1)
CHEMBL842076 (1) CHEMBL841383 (1) CHEMBL985774 (1) CHEMBL941407 (1) CHEMBL971894 (1) CHEMBL976939 (1) CHEMBL1963718 (1) |
0 / 1 |
P52333 | Tyrosine-protein kinase JAK3 | Jakb | CHEMBL1972346 |
CHEMBL1963742
(1)
|
1 / 1 |
P43405 | Tyrosine-protein kinase SYK | Syk | CHEMBL69863 |
CHEMBL808354
(1)
CHEMBL937049
(1)
CHEMBL1022010 (1) |
0 / 0 |
P17612 | cAMP-dependent protein kinase catalytic subunit alpha | Pka | CHEMBL1972346 |
CHEMBL1963835
(1)
|
0 / 0 |
Q13627 | Dual specificity tyrosine-phosphorylation-regulated kinase 1A | CMGC dual-specificity kinase DYRK1 | CHEMBL1972346 |
CHEMBL1964107
(1)
|
1 / 0 |
P49760 | Dual specificity protein kinase CLK2 | Clk | CHEMBL1972346 |
CHEMBL1963691
(1)
|
0 / 0 |
Q07912 | Activated CDC42 kinase 1 | TK tyrosine-protein kinase ACK subfamily | CHEMBL1972346 |
CHEMBL1963777
(1)
|
0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | CHEMBL69863 |
CHEMBL1794536
(5)
|
0 / 0 |
Q96L34 | MAP/microtubule affinity-regulating kinase 4 | CAMK serine/threonine protein kinase MARK subfamily | CHEMBL1972346 |
CHEMBL1963713
(1)
|
0 / 0 |
P51817 | cAMP-dependent protein kinase catalytic subunit PRKX | Pka | CHEMBL1972346 |
CHEMBL1963800
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL69863 |
CHEMBL1613914
(1)
|
0 / 0 |
P40225 | Thrombopoietin | Unclassified protein | CHEMBL1603409 |
CHEMBL1614086
(1)
CHEMBL1614034
(1)
|
1 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL69863 |
CHEMBL1738442
(6)
|
0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL69863 |
CHEMBL1614364
(1)
|
1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | CHEMBL69863 |
CHEMBL2354311
(1)
|
1 / 0 |
O00255 | Menin | Unclassified protein | CHEMBL69863 |
CHEMBL1614257
(2)
|
2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | CHEMBL69863 |
CHEMBL1614257
(2)
|
1 / 3 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | CHEMBL69863 |
CHEMBL1613933
(1)
|
0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | CHEMBL69863 |
CHEMBL1613933
(1)
|
1 / 6 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL69863 |
CHEMBL2114738
(1)
|
0 / 0 |
Q9HCT0 | Fibroblast growth factor 22 | Unclassified protein | CHEMBL1972346 |
CHEMBL2354256
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#300755 | Agammaglobulinemia, x-linked; xla |
Q06187
|
#613780 | Aortic aneurysm, familial thoracic 7; aat7 |
Q15746
|
#614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
#210900 | Bloom syndrome; blm |
P54132
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#600880 | Budd-chiari syndrome; bdchs |
O60674
|
#615279 | Cardiofaciocutaneous syndrome 3; cfc3 |
Q02750
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#209880 | Central hypoventilation syndrome, congenital; cchs |
P07949
|
#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
|
#613641 | Charcot-marie-tooth disease, recessive intermediate b; cmtrib |
Q15046
|
#303600 | Coffin-lowry syndrome; cls |
P51812
|
#114500 | Colorectal cancer; crc |
P07949
P18054 |
#613916 | Deafness, autosomal recessive 89; dfnb89 |
Q15046
|
#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
P18054 |
#135100 | Fibrodysplasia ossificans progressiva; fop |
Q04771
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#606764 | Gastrointestinal stromal tumor; gist |
P16234
|
#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
|
#177700 | Glaucoma 1, open angle, p; glc1p |
Q9UHD2
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#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
|
#142623 | Hirschsprung disease, susceptibility to, 1; hscr1 |
P07949
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#607685 | Hypereosinophilic syndrome, idiopathic; hes |
P16234
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#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
|
#307200 | Isolated growth hormone deficiency, type iii; ighd3 |
Q06187
|
#601626 | Leukemia, acute myeloid; aml |
O60674
P36888 |
#221820 | Leukoencephalopathy, diffuse hereditary, with spheroids; hdls |
P07333
|
#151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#211980 | Lung cancer |
P04637
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#614104 | Mental retardation, autosomal dominant 7; mrd7 |
Q13627
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300844 | Mental retardation, x-linked 19; mrx19 |
P51812
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#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
|
#254450 | Myelofibrosis |
O60674
|
#613076 | Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay |
P55789
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#613014 | Neuroblastoma, susceptibility to, 3; nblst3 |
Q9UM73
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#166250 | Osteoglophonic dysplasia; ogd |
P11362
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#260500 | Papilloma of choroid plexus; cpp |
P04637
|
#607060 | Parkinson disease 8, autosomal dominant; park8 |
Q5S007
|
#168600 | Parkinson disease, late-onset; pd |
P04062
Q5S007 |
#260540 | Parkinson-dementia syndrome |
P10636
|
#101600 | Pfeiffer syndrome |
P11362
|
#171300 | Pheochromocytoma |
P07949
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#263300 | Polycythemia vera; pv |
O60674
|
#191830 | Renal adysplasia |
P07949
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#600802 | Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative |
P52333
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#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
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#187950 | Thrombocythemia 1; thcyt1 |
P40225
|
#614521 | Thrombocythemia 3; thcyt3 |
O60674
|
#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
|
#190440 | Trigonocephaly 1; trigno1 |
P11362
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | disease 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)
|
H00012 | Polycythemia vera |
O60674
(related)
O60674 (marker) |
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
Q01453 (related) Q15046 (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)
|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
Q5S007 (related) |
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
Q01196 (related) |
H00005 | Chronic lymphocytic leukemia (CLL) |
P04637
(related)
P28907 (marker) |
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)
P08922 (related) Q9UM73 (related) |
H00015 | Malignant pleural mesothelioma |
P04637
(related)
|
H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
H00018 | Gastric cancer |
P04637
(related)
|
H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
H00022 | Bladder cancer |
P04637
(related)
|
H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
H00026 | Endometrial Cancer |
P04637
(related)
|
H00027 | Ovarian cancer |
P04637
(related)
P38398 (related) |
H00028 | Choriocarcinoma |
P04637
(related)
P07333 (related) |
H00029 | Vulvar cancer |
P04637
(related)
|
H00031 | Breast cancer |
P04637
(related)
P38398 (related) |
H00032 | Thyroid cancer |
P04637
(related)
P07949 (related) P07949 (marker) |
H00036 | Osteosarcoma |
P04637
(related)
P08684 (marker) |
H00038 | Malignant melanoma |
P04637
(related)
|
H00039 | Basal cell carcinoma |
P04637
(related)
|
H00040 | Squamous cell carcinoma |
P04637
(related)
|
H00041 | Kaposi's sarcoma |
P04637
(related)
|
H00042 | Glioma |
P04637
(related)
P04637 (marker) P16234 (related) |
H00044 | Cancer of the anal canal |
P04637
(related)
|
H00046 | Cholangiocarcinoma |
P04637
(related)
|
H00047 | Gallbladder cancer |
P04637
(related)
|
H00048 | Hepatocellular carcinoma |
P04637
(related)
|
H00055 | Laryngeal cancer |
P04637
(related)
P04637 (marker) |
H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
H01007 | Choroid plexus papilloma |
P04637
(related)
|
H00021 | Renal cell carcinoma |
P04637
(marker)
|
H00093 | Combined immunodeficiencies (CIDs) |
P06239
(related)
|
H00822 | Renal agenesis and Renal adysplasia |
P07949
(related)
|
H00910 | Hirschsprung disease (HD) |
P07949
(related)
|
H00916 | Congenital central hypoventilation syndrome (CCHS) |
P07949
(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)
|
H00255 | Hypogonadotropic hypogonadism |
P11362
(related)
|
H00443 | Osteoglophonic dysplasia (OD) |
P11362
(related)
|
H00458 | Craniosynostosis |
P11362
(related)
|
H00516 | Isolated orofacial clefts |
P11362
(related)
|
H01207 | Trigonocephaly |
P11362
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P36888
(related)
Q01196 (related) Q01196 (marker) Q13951 (marker) |
H00227 | Congenital amegakaryocytic thrombocytopenia (CAMT) |
P40225
(marker)
|
H00480 | Non-syndromic X-linked mental retardation |
P51812
(related)
Q99714 (related) |
H00574 | Coffin-Lowry syndrome (CLS) |
P51812
(related)
|
H00091 | T-B+Severe combined immunodeficiencies (SCIDs) |
P52333
(related)
|
H00606 | Early infantile epileptic encephalopathy |
P53779
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) |
Q01453
(related)
|
H00523 | Noonan syndrome and related disorders |
Q02750
(related)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00408 | Type I diabetes mellitus |
Q04759
(related)
|
H00430 | Fibrodysplasia ossificans progressiva (FOP) |
Q04771
(related)
Q04771 (marker) |
H00085 | Agammaglobulinemias |
Q06187
(related)
|
H00254 | Pituitary Dwarfism (PD) |
Q06187
(related)
|
H00801 | Familial thoracic aortic aneurysm and dissection (TAAD) |
Q15746
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
Q16637 (related) |
H00057 | Parkinson's disease (PD) |
Q5S007
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|