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 |
---|---|---|---|---|---|
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 |
C0003873 | Rheumatoid Arthritis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0949116 | Congenital hypoplastic anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C3714772 | Recurrent fevers | LPIN2 | 9663 | lipin 2 | Q92539 |
C0020758 | Congenital ichthyosis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0004096 | Asthma | LPIN2 | 9663 | lipin 2 | Q92539 |
C0033687 | Proteinuria | LPIN2 | 9663 | lipin 2 | Q92539 |
C0013604 | Edema | LPIN2 | 9663 | lipin 2 | Q92539 |
C0029443 | Osteomyelitis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0029464 | Osteosclerosis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0600139 | Prostate carcinoma | LPIN2 | 9663 | lipin 2 | Q92539 |
C0268731 | Renal glomerular disease | LPIN2 | 9663 | lipin 2 | Q92539 |
C3875321 | Inflammatory dermatosis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0410422 | Chronic multifocal osteomyelitis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0021831 | Intestinal Diseases | LPIN2 | 9663 | lipin 2 | Q92539 |
C0027947 | Neutropenia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0702166 | Acne | LPIN2 | 9663 | lipin 2 | Q92539 |
C0263859 | Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
C0268238 | Triglyceride storage disease with ichthyosis | LPIN2 | 9663 | lipin 2 | Q92539 |
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Last updated: August 19, 2024