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 |
---|---|---|---|---|---|
C2047886 | (Idiopathic) normal pressure hydrocephalus | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C2047886 | (Idiopathic) normal pressure hydrocephalus | NCAN | 1463 | neurocan | O14594 |
C4329210 | 11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency | HSD11B1 | 3290 | hydroxysteroid 11-beta dehydrogenase 1 | P28845 |
C3697269 | 15q24 Microdeletion | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
C3277849 | 17,20-Lyase Deficiency, Isolated | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C3665382 | 2,8-Dihydroxyadenine Urolithiasis | GALNS | 2588 | galactosamine (N-acetyl)-6-sulfatase | P34059 |
C3665382 | 2,8-Dihydroxyadenine Urolithiasis | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
C3665382 | 2,8-Dihydroxyadenine Urolithiasis | UMOD | 7369 | uromodulin | P07911 |
C3266731 | 2-methyl-3-hydroxybutyric aciduria | DHCR7 | 1717 | 7-dehydrocholesterol reductase | Q9UBM7 |
C3266731 | 2-methyl-3-hydroxybutyric aciduria | ACADSB | 36 | acyl-CoA dehydrogenase short/branched chain | P45954 |
C1853490 | 22q13.3 Deletion Syndrome | ARSA | 410 | arylsulfatase A | P15289 |
C1853490 | 22q13.3 Deletion Syndrome | PNPLA3 | 80339 | patatin like phospholipase domain containing 3 | Q9NST1 |
C0342471 | 3 beta-Hydroxysteroid dehydrogenase deficiency | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
C0342471 | 3 beta-Hydroxysteroid dehydrogenase deficiency | HSD3B2 | 3284 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | P26439 |
C0342471 | 3 beta-Hydroxysteroid dehydrogenase deficiency | HSD17B3 | 3293 | hydroxysteroid 17-beta dehydrogenase 3 | P37058 |
C1291230 | 3-Hydroxyacyl-CoA Dehydrogenase Deficiency | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
C3696376 | 3-Methylglutaconic Aciduria | DHCR7 | 1717 | 7-dehydrocholesterol reductase | Q9UBM7 |
C3696376 | 3-Methylglutaconic Aciduria | AGK | 55750 | acylglycerol kinase | Q53H12 |
C3696376 | 3-Methylglutaconic Aciduria | ECHS1 | 1892 | enoyl-CoA hydratase, short chain 1 | P30084 |
C3696376 | 3-Methylglutaconic Aciduria | ACADSB | 36 | acyl-CoA dehydrogenase short/branched chain | P45954 |
C1855126 | 3-Methylglutaconic Aciduria Type IV | SUCLA2 | 8803 | succinate-CoA ligase ADP-forming subunit beta | Q9P2R7 |
C0574083 | 3-Methylglutaconic aciduria type 2 | PNPLA2 | 57104 | patatin like phospholipase domain containing 2 | Q96AD5 |
C0574083 | 3-Methylglutaconic aciduria type 2 | ATRN | 8455 | attractin | O75882 |
C0574083 | 3-Methylglutaconic aciduria type 2 | HADHA | 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | P40939 |
C0574084 | 3-Methylglutaconic aciduria type 3 | ATRN | 8455 | attractin | O75882 |
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Last updated: August 19, 2024