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 ▲ |
---|---|---|---|---|---|
C0008489 | Chorea | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0234533 | Generalized seizures | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0030567 | Parkinson Disease | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0520947 | Clumsiness - motor delay | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C3714756 | Intellectual Disability | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0036572 | Seizures | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0038273 | Stereotypic Movement Disorder | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0684276 | Hypsarrhythmia | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0011581 | Depressive disorder | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0025958 | Microcephaly | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C0036857 | Severe intellectual disability | PIGC | 5279 | phosphatidylinositol glycan anchor biosynthesis class C | Q92535 |
C1857276 | Trichohepatoenteric Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
C0002876 | Congenital dyserythropoietic anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011849 | Diabetes Mellitus | LPIN2 | 9663 | lipin 2 | Q92539 |
C1834531 | MYOPIA 2 (disorder) | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011847 | Diabetes | LPIN2 | 9663 | lipin 2 | Q92539 |
C0002871 | Anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0010346 | Crohn Disease | LPIN2 | 9663 | lipin 2 | Q92539 |
C0035021 | Relapsing Fever | LPIN2 | 9663 | lipin 2 | Q92539 |
C0039103 | Synovitis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0028754 | Obesity | LPIN2 | 9663 | lipin 2 | Q92539 |
C0027092 | Myopia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0023530 | Leukopenia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0025517 | Metabolic Diseases | LPIN2 | 9663 | lipin 2 | Q92539 |
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Last updated: August 19, 2024