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 |
---|---|---|---|---|---|
C1956097 | Wolf-Hirschhorn Syndrome | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
C0043194 | Wiskott-Aldrich Syndrome | FUT1 | 2523 | fucosyltransferase 1 (H blood group) | P19526 |
C0043194 | Wiskott-Aldrich Syndrome | FCER2 | 2208 | Fc fragment of IgE receptor II | P06734 |
C0043194 | Wiskott-Aldrich Syndrome | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
C0043194 | Wiskott-Aldrich Syndrome | PGK1 | 5230 | phosphoglycerate kinase 1 | P00558 |
C0043194 | Wiskott-Aldrich Syndrome | G6PC3 | 92579 | glucose-6-phosphatase catalytic subunit 3 | Q9BUM1 |
C0043194 | Wiskott-Aldrich Syndrome | PKD2 | 5311 | polycystin 2, transient receptor potential cation channel | Q13563 |
C0175702 | Williams Syndrome | ARSD | 414 | arylsulfatase D | P51689 |
C0175702 | Williams Syndrome | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
C0949570 | Wheat Hypersensitivity | ENPP3 | 5169 | ectonucleotide pyrophosphatase/phosphodiesterase 3 | O14638 |
C0949570 | Wheat Hypersensitivity | HACD1 | 9200 | 3-hydroxyacyl-CoA dehydratase 1 | B0YJ81 |
C3888896 | Wet age-related macular degeneration | PNPLA2 | 57104 | patatin like phospholipase domain containing 2 | Q96AD5 |
C0037769 | West Syndrome | PIGW | 284098 | phosphatidylinositol glycan anchor biosynthesis class W | Q7Z7B1 |
C0037769 | West Syndrome | PIGA | 5277 | phosphatidylinositol glycan anchor biosynthesis class A | P37287 |
C0037769 | West Syndrome | ST3GAL3 | 6487 | ST3 beta-galactoside alpha-2,3-sialyltransferase 3 | Q11203 |
C0037769 | West Syndrome | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
C0037769 | West Syndrome | PIGQ | 9091 | phosphatidylinositol glycan anchor biosynthesis class Q | Q9BRB3 |
C0037769 | West Syndrome | PMM2 | 5373 | phosphomannomutase 2 | O15305 |
C0037769 | West Syndrome | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
C0037769 | West Syndrome | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
C0037769 | West Syndrome | PLCB1 | 23236 | phospholipase C beta 1 | Q9NQ66 |
C0037769 | West Syndrome | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
C0037769 | West Syndrome | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
C0037769 | West Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0037769 | West Syndrome | PIGP | 51227 | phosphatidylinositol glycan anchor biosynthesis class P | P57054 |
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Last updated: August 19, 2024