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 |
---|---|---|---|---|---|
C2239176 | Liver carcinoma | GPC5 | 2262 | glypican 5 | P78333 |
C0796154 | SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 | GPC5 | 2262 | glypican 5 | P78333 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | GPC5 | 2262 | glypican 5 | P78333 |
C0039685 | Tetralogy of Fallot | GPC5 | 2262 | glypican 5 | P78333 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | GPC5 | 2262 | glypican 5 | P78333 |
C1261473 | Sarcoma | GPC5 | 2262 | glypican 5 | P78333 |
C0080178 | Spina Bifida | GPC5 | 2262 | glypican 5 | P78333 |
C0677886 | Epithelial ovarian cancer | GPC5 | 2262 | glypican 5 | P78333 |
C0392514 | Hereditary hemochromatosis | GPC5 | 2262 | glypican 5 | P78333 |
C0035412 | Rhabdomyosarcoma | GPC5 | 2262 | glypican 5 | P78333 |
C0027873 | Neuromyelitis Optica | GPC5 | 2262 | glypican 5 | P78333 |
C0027404 | Narcolepsy | GPC5 | 2262 | glypican 5 | P78333 |
C0001925 | Albuminuria | GPC5 | 2262 | glypican 5 | P78333 |
C0018790 | Cardiac Arrest | GPC5 | 2262 | glypican 5 | P78333 |
C0009691 | Congenital cataract | GPC5 | 2262 | glypican 5 | P78333 |
C0575158 | Kyphoscoliosis deformity of spine | GPC5 | 2262 | glypican 5 | P78333 |
C0600139 | Prostate carcinoma | GPC5 | 2262 | glypican 5 | P78333 |
C0003873 | Rheumatoid Arthritis | GPC5 | 2262 | glypican 5 | P78333 |
C0346647 | Malignant neoplasm of pancreas | GPC5 | 2262 | glypican 5 | P78333 |
C0011303 | Demyelinating Diseases | GPC5 | 2262 | glypican 5 | P78333 |
C4551686 | Malignant neoplasm of soft tissue | GPC5 | 2262 | glypican 5 | P78333 |
C0007131 | Non-Small Cell Lung Carcinoma | GPC5 | 2262 | glypican 5 | P78333 |
C0376358 | Malignant neoplasm of prostate | GPC5 | 2262 | glypican 5 | P78333 |
C0342770 | Fumarase deficiency | FH | 2271 | fumarate hydratase | P07954 |
C1306459 | Primary malignant neoplasm | FH | 2271 | fumarate hydratase | P07954 |
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Last updated: August 19, 2024