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 |
---|---|---|---|---|---|
C0027765 | nervous system disorder | PLA2G2A | 5320 | phospholipase A2 group IIA | P14555 |
C0027765 | nervous system disorder | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0027765 | nervous system disorder | SMPD3 | 55512 | sphingomyelin phosphodiesterase 3 | Q9NY59 |
C0027765 | nervous system disorder | PRNP | 5621 | prion protein | P04156 |
C0027765 | nervous system disorder | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0027765 | nervous system disorder | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0027765 | nervous system disorder | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0027765 | nervous system disorder | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
C0027765 | nervous system disorder | PLA2G10 | 8399 | phospholipase A2 group X | O15496 |
C0027765 | nervous system disorder | SUCLA2 | 8803 | succinate-CoA ligase ADP-forming subunit beta | Q9P2R7 |
C0027765 | nervous system disorder | DEGS1 | 8560 | delta 4-desaturase, sphingolipid 1 | O15121 |
C0027765 | nervous system disorder | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0027765 | nervous system disorder | CD1D | 912 | CD1d molecule | P15813 |
C0027765 | nervous system disorder | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
C0027765 | nervous system disorder | IDH3A | 3419 | isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | P50213 |
C0027765 | nervous system disorder | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0027765 | nervous system disorder | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0027765 | nervous system disorder | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
C0027765 | nervous system disorder | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
C0027765 | nervous system disorder | CDH13 | 1012 | cadherin 13 | P55290 |
C0027765 | nervous system disorder | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
C0027765 | nervous system disorder | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0027765 | nervous system disorder | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0027765 | nervous system disorder | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0027765 | nervous system disorder | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
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Last updated: August 19, 2024