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 |
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DisGeNET | July 29, 2024 |
Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0524851 | Neurodegenerative Disorders | HK2 | 3099 | hexokinase 2 | P52789 |
C0524851 | Neurodegenerative Disorders | IDH2 | 3418 | isocitrate dehydrogenase (NADP(+)) 2 | P48735 |
C0524851 | Neurodegenerative Disorders | MUTYH | 4595 | mutY DNA glycosylase | Q9UIF7 |
C0524851 | Neurodegenerative Disorders | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
C0524851 | Neurodegenerative Disorders | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0524851 | Neurodegenerative Disorders | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0524851 | Neurodegenerative Disorders | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
C0524851 | Neurodegenerative Disorders | RENBP | 5973 | renin binding protein | P51606 |
C0524851 | Neurodegenerative Disorders | UNG | 7374 | uracil DNA glycosylase | P13051 |
C0524851 | Neurodegenerative Disorders | PARP10 | 84875 | poly(ADP-ribose) polymerase family member 10 | Q53GL7 |
C0524851 | Neurodegenerative Disorders | GPNMB | 10457 | glycoprotein nmb | Q14956 |
C0524851 | Neurodegenerative Disorders | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0524851 | Neurodegenerative Disorders | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0524851 | Neurodegenerative Disorders | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0524851 | Neurodegenerative Disorders | DLST | 1743 | dihydrolipoamide S-succinyltransferase | P36957 |
C0524851 | Neurodegenerative Disorders | DHCR24 | 1718 | 24-dehydrocholesterol reductase | Q15392 |
C0524851 | Neurodegenerative Disorders | FCN2 | 2220 | ficolin 2 | Q15485 |
C0524851 | Neurodegenerative Disorders | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0524851 | Neurodegenerative Disorders | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
C0524851 | Neurodegenerative Disorders | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
C0524851 | Neurodegenerative Disorders | PDIA3 | 2923 | protein disulfide isomerase family A member 3 | P30101 |
C0524851 | Neurodegenerative Disorders | MTM1 | 4534 | myotubularin 1 | Q13496 |
C0524851 | Neurodegenerative Disorders | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0524851 | Neurodegenerative Disorders | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0524851 | Neurodegenerative Disorders | PLA2G1B | 5319 | phospholipase A2 group IB | P04054 |
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Last updated: August 19, 2024