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 |
---|---|---|---|---|---|
C0403447 | Chronic Kidney Insufficiency | GFPT2 | 9945 | glutamine-fructose-6-phosphate transaminase 2 | O94808 |
C0403416 | Idiopathic crescentic glomerulonephritis | DCN | 1634 | decorin | P07585 |
C0403416 | Idiopathic crescentic glomerulonephritis | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0403416 | Idiopathic crescentic glomerulonephritis | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0403416 | Idiopathic crescentic glomerulonephritis | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C0403416 | Idiopathic crescentic glomerulonephritis | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
C0403414 | Acute post-streptococcal glomerulonephritis | GAPDH | 2597 | glyceraldehyde-3-phosphate dehydrogenase | P04406 |
C0403414 | Acute post-streptococcal glomerulonephritis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C0403399 | Finnish congenital nephrotic syndrome | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
C0403399 | Finnish congenital nephrotic syndrome | TREH | 11181 | trehalase | O43280 |
C0403396 | Steroid-sensitive nephrotic syndrome | EXT1 | 2131 | exostosin glycosyltransferase 1 | Q16394 |
C0403396 | Steroid-sensitive nephrotic syndrome | HPSE | 10855 | heparanase | Q9Y251 |
C0403396 | Steroid-sensitive nephrotic syndrome | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0403396 | Steroid-sensitive nephrotic syndrome | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0403396 | Steroid-sensitive nephrotic syndrome | GLO1 | 2739 | glyoxalase I | Q04760 |
C0403396 | Steroid-sensitive nephrotic syndrome | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
C0401067 | Unilateral inguinal hernia NOS | ARSA | 410 | arylsulfatase A | P15289 |
C0400966 | Non-alcoholic Fatty Liver Disease | B3GAT1 | 27087 | beta-1,3-glucuronyltransferase 1 | Q9P2W7 |
C0400966 | Non-alcoholic Fatty Liver Disease | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
C0400966 | Non-alcoholic Fatty Liver Disease | ST3GAL4 | 6484 | ST3 beta-galactoside alpha-2,3-sialyltransferase 4 | Q11206 |
C0400966 | Non-alcoholic Fatty Liver Disease | DDOST | 1650 | dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | P39656 |
C0400966 | Non-alcoholic Fatty Liver Disease | GLB1 | 2720 | galactosidase beta 1 | P16278 |
C0400966 | Non-alcoholic Fatty Liver Disease | LIPA | 3988 | lipase A, lysosomal acid type | P38571 |
C0400966 | Non-alcoholic Fatty Liver Disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0400966 | Non-alcoholic Fatty Liver Disease | NEU1 | 4758 | neuraminidase 1 | Q99519 |
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Last updated: August 19, 2024