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 |
---|---|---|---|---|---|
C0015695 | Fatty Liver | LPIN1 | 23175 | lipin 1 | Q14693 |
C0271650 | Impaired glucose tolerance | LPIN1 | 23175 | lipin 1 | Q14693 |
C0206708 | Cervical Intraepithelial Neoplasia | LPIN1 | 23175 | lipin 1 | Q14693 |
C0442874 | Neuropathy | LPIN1 | 23175 | lipin 1 | Q14693 |
C0023434 | Chronic Lymphocytic Leukemia | LPIN1 | 23175 | lipin 1 | Q14693 |
C0400966 | Non-alcoholic Fatty Liver Disease | LPIN1 | 23175 | lipin 1 | Q14693 |
C1848296 | DOSAGE-SENSITIVE SEX REVERSAL | LPIN1 | 23175 | lipin 1 | Q14693 |
C0011849 | Diabetes Mellitus | LPIN1 | 23175 | lipin 1 | Q14693 |
C0009375 | Colonic Neoplasms | LPIN1 | 23175 | lipin 1 | Q14693 |
C0376358 | Malignant neoplasm of prostate | LPIN1 | 23175 | lipin 1 | Q14693 |
C0343641 | Human papilloma virus infection | LPIN1 | 23175 | lipin 1 | Q14693 |
C0007222 | Cardiovascular Diseases | LPIN1 | 23175 | lipin 1 | Q14693 |
C0524620 | Metabolic Syndrome X | LPIN1 | 23175 | lipin 1 | Q14693 |
C0022661 | Kidney Failure, Chronic | LPIN1 | 23175 | lipin 1 | Q14693 |
C0026848 | Myopathy | LPIN1 | 23175 | lipin 1 | Q14693 |
C0007097 | Carcinoma | LPIN1 | 23175 | lipin 1 | Q14693 |
C0152013 | Adenocarcinoma of lung (disorder) | LPIN1 | 23175 | lipin 1 | Q14693 |
C0020538 | Hypertensive disease | LPIN1 | 23175 | lipin 1 | Q14693 |
C0006826 | Malignant Neoplasms | LPIN1 | 23175 | lipin 1 | Q14693 |
C0231528 | Myalgia | LPIN1 | 23175 | lipin 1 | Q14693 |
C1867300 | RETINITIS PIGMENTOSA 9 | LPIN1 | 23175 | lipin 1 | Q14693 |
C2239176 | Liver carcinoma | LPIN1 | 23175 | lipin 1 | Q14693 |
C0009402 | Colorectal Carcinoma | LPIN1 | 23175 | lipin 1 | Q14693 |
C0241005 | Creatine phosphokinase serum increased | LPIN1 | 23175 | lipin 1 | Q14693 |
C3887523 | Very long chain acyl-CoA dehydrogenase deficiency | LPIN1 | 23175 | lipin 1 | Q14693 |
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Last updated: August 19, 2024