DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0521694 | Atrophic retina | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
C0521694 | Atrophic retina | ARSG | 22901 | arylsulfatase G | Q96EG1 |
C0152014 | Atrophy of pancreas | CEL | 1056 | carboxyl ester lipase | P19835 |
C0156296 | Atrophy of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0156312 | Atrophy of testis | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
C0156312 | Atrophy of testis | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
C0156312 | Atrophy of testis | HPRT1 | 3251 | hypoxanthine phosphoribosyltransferase 1 | P00492 |
C0156312 | Atrophy of testis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0156312 | Atrophy of testis | HMMR | 3161 | hyaluronan mediated motility receptor | O75330 |
C0041671 | Attention Deficit Disorder | AGA | 175 | aspartylglucosaminidase | P20933 |
C0041671 | Attention Deficit Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0041671 | Attention Deficit Disorder | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0041671 | Attention Deficit Disorder | HPRT1 | 3251 | hypoxanthine phosphoribosyltransferase 1 | P00492 |
C0041671 | Attention Deficit Disorder | CD38 | 952 | CD38 molecule | P28907 |
C0041671 | Attention Deficit Disorder | THEM4 | 117145 | thioesterase superfamily member 4 | Q5T1C6 |
C0041671 | Attention Deficit Disorder | LGALS3 | 3958 | galectin 3 | P17931 |
C0041671 | Attention Deficit Disorder | STS | 412 | steroid sulfatase | P08842 |
C0041671 | Attention Deficit Disorder | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0041671 | Attention Deficit Disorder | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0041671 | Attention Deficit Disorder | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0041671 | Attention Deficit Disorder | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0041671 | Attention Deficit Disorder | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0041671 | Attention Deficit Disorder | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C1263846 | Attention deficit hyperactivity disorder | ST3GAL3 | 6487 | ST3 beta-galactoside alpha-2,3-sialyltransferase 3 | Q11203 |
C1263846 | Attention deficit hyperactivity disorder | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
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Last updated: August 19, 2024