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 51626 - 51650 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0751781 Dentatorubral-Pallidoluysian Atrophy PRNP 5621 prion protein P04156
C0751781 Dentatorubral-Pallidoluysian Atrophy CERS1 10715 ceramide synthase 1 P27544
C0751781 Dentatorubral-Pallidoluysian Atrophy PRNP 5621 prion protein F7VJQ1
C0751782 May-White Syndrome NEU1 4758 neuraminidase 1 Q99519
C0751782 May-White Syndrome EPM2A 7957 EPM2A glucan phosphatase, laforin O95278
C0751782 May-White Syndrome PRNP 5621 prion protein P04156
C0751782 May-White Syndrome CERS1 10715 ceramide synthase 1 P27544
C0751782 May-White Syndrome PRNP 5621 prion protein F7VJQ1
C0751783 Lafora Disease GBA 2629 glucosylceramidase beta P04062
C0751783 Lafora Disease CHI3L1 1116 chitinase 3 like 1 P36222
C0751783 Lafora Disease CLN5 1203 CLN5 intracellular trafficking protein O75503
C0751783 Lafora Disease GYG1 2992 glycogenin 1 P46976
C0751783 Lafora Disease PFKL 5211 phosphofructokinase, liver type P17858
C0751783 Lafora Disease EPM2A 7957 EPM2A glucan phosphatase, laforin O95278
C0751783 Lafora Disease PPP1R3B 79660 protein phosphatase 1 regulatory subunit 3B Q86XI6
C0751783 Lafora Disease GLUL 2752 glutamate-ammonia ligase P15104
C0751783 Lafora Disease ACHE 43 acetylcholinesterase (Cartwright blood group) P22303
C0751783 Lafora Disease PTEN 5728 phosphatase and tensin homolog P60484
C0751785 Unverricht-Lundborg Syndrome ARSA 410 arylsulfatase A P15289
C0751785 Unverricht-Lundborg Syndrome ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0751785 Unverricht-Lundborg Syndrome NEU1 4758 neuraminidase 1 Q99519
C0751785 Unverricht-Lundborg Syndrome PFKL 5211 phosphofructokinase, liver type P17858
C0751785 Unverricht-Lundborg Syndrome EPM2A 7957 EPM2A glucan phosphatase, laforin O95278
C0751785 Unverricht-Lundborg Syndrome TMED9 54732 transmembrane p24 trafficking protein 9 Q9BVK6
C0751785 Unverricht-Lundborg Syndrome PRNP 5621 prion protein P04156

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Last updated: August 19, 2024