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 |
---|---|---|---|---|---|
C3179455 | Niemann-Pick Disease, Type C1 | GPC1 | 2817 | glypican 1 | P35052 |
C0268247 | Niemann-Pick Disease, Type D | LIPA | 3988 | lipase A, lysosomal acid type | P38571 |
C0268248 | Niemann-Pick Disease, Type E | SMPD1 | 6609 | sphingomyelin phosphodiesterase 1 | P17405 |
C0028064 | Niemann-Pick Diseases | GALC | 2581 | galactosylceramidase | P54803 |
C0028064 | Niemann-Pick Diseases | GBA | 2629 | glucosylceramidase beta | P04062 |
C0028064 | Niemann-Pick Diseases | GLA | 2717 | galactosidase alpha | P06280 |
C0028064 | Niemann-Pick Diseases | IDUA | 3425 | alpha-L-iduronidase | P35475 |
C0028064 | Niemann-Pick Diseases | SMPD1 | 6609 | sphingomyelin phosphodiesterase 1 | P17405 |
C0028064 | Niemann-Pick Diseases | OGA | 10724 | O-GlcNAcase | O60502 |
C0028064 | Niemann-Pick Diseases | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0028064 | Niemann-Pick Diseases | SMPDL3A | 10924 | sphingomyelin phosphodiesterase acid like 3A | Q92484 |
C0028064 | Niemann-Pick Diseases | SMPD2 | 6610 | sphingomyelin phosphodiesterase 2 | O60906 |
C3495587 | Night Blindness, Congenital Stationary, Type 1A | NYX | 60506 | nyctalopin | Q9GZU5 |
C0339535 | Night blindness, congenital stationary | NYX | 60506 | nyctalopin | Q9GZU5 |
C0398791 | Nijmegen Breakage Syndrome | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
C0398791 | Nijmegen Breakage Syndrome | IDH1 | 3417 | isocitrate dehydrogenase (NADP(+)) 1 | O75874 |
C0398791 | Nijmegen Breakage Syndrome | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0398791 | Nijmegen Breakage Syndrome | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0398791 | Nijmegen Breakage Syndrome | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0398791 | Nijmegen Breakage Syndrome | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0398791 | Nijmegen Breakage Syndrome | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0398791 | Nijmegen Breakage Syndrome | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0264893 | Nodal rhythm disorder | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0264893 | Nodal rhythm disorder | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
C0018023 | Nodular Goiter | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
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Last updated: August 19, 2024