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 6751 - 6775 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0036572 Seizures ICAM1 3383 intercellular adhesion molecule 1 P05362
C0036572 Seizures AGRN 375790 agrin O00468
C0036572 Seizures ACAT1 38 acetyl-CoA acetyltransferase 1 P24752
C0036572 Seizures IMPA1 3612 inositol monophosphatase 1 P29218
C0036572 Seizures LGALS3 3958 galectin 3 P17931
C0036572 Seizures STS 412 steroid sulfatase P08842
C0036572 Seizures MBL2 4153 mannose binding lectin 2 P11226
C0036572 Seizures ACHE 43 acetylcholinesterase (Cartwright blood group) P22303
C0036572 Seizures MMUT 4594 methylmalonyl-CoA mutase P22033
C0036572 Seizures MRC1 4360 mannose receptor C-type 1 P22897
C0036572 Seizures NT5E 4907 5'-nucleotidase ecto P21589
C0036572 Seizures PCCB 5096 propionyl-CoA carboxylase subunit beta P05166
C0036572 Seizures PCCA 5095 propionyl-CoA carboxylase subunit alpha P05165
C0036572 Seizures ISYNA1 51477 inositol-3-phosphate synthase 1 Q9NPH2
C0036572 Seizures PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C0036572 Seizures PLA2G2A 5320 phospholipase A2 group IIA P14555
C0036572 Seizures TMED9 54732 transmembrane p24 trafficking protein 9 Q9BVK6
C0036572 Seizures NGLY1 55768 N-glycanase 1 Q96IV0
C0036572 Seizures PLD2 5338 phospholipase D2 O14939
C0036572 Seizures PLCG1 5335 phospholipase C gamma 1 P19174
C0036572 Seizures PRNP 5621 prion protein P04156
C0036572 Seizures RGMA 56963 repulsive guidance molecule BMP co-receptor a Q96B86
C0036572 Seizures ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0036572 Seizures PTGS1 5742 prostaglandin-endoperoxide synthase 1 P23219
C0036572 Seizures PSMD10 5716 proteasome 26S subunit, non-ATPase 10 O75832

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Last updated: August 19, 2024