DisGeNET

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
Displaying entries 62451 - 62475 of 62743 in total
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