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 | PSAP | 5660 | prosaposin | P07602 |
C0016057 | Fibrosarcoma | PSAP | 5660 | prosaposin | P07602 |
C1306459 | Primary malignant neoplasm | PSAP | 5660 | prosaposin | P07602 |
C1136084 | Plasma cell dyscrasia | PSAP | 5660 | prosaposin | P07602 |
C0233844 | Clumsiness | PSAP | 5660 | prosaposin | P07602 |
C0006840 | Candidiasis | PSAP | 5660 | prosaposin | P07602 |
C0268255 | Farber Lipogranulomatosis | PSAP | 5660 | prosaposin | P07602 |
C0036572 | Seizures | PSAP | 5660 | prosaposin | P07602 |
C0153252 | Systemic candidiasis | PSAP | 5660 | prosaposin | P07602 |
C0030486 | Paraplegia | PSAP | 5660 | prosaposin | P07602 |
C3714731 | Early childhood caries | PSAP | 5660 | prosaposin | P07602 |
C0006846 | Cutaneous Candidiasis | PSAP | 5660 | prosaposin | P07602 |
C0019693 | HIV Infections | PSAP | 5660 | prosaposin | P07602 |
C0278595 | Adult Fibrosarcoma | PSAP | 5660 | prosaposin | P07602 |
C0699791 | Stomach Carcinoma | PSAP | 5660 | prosaposin | P07602 |
C0029124 | Optic Atrophy | PSAP | 5660 | prosaposin | P07602 |
C0233794 | Memory impairment | PSAP | 5660 | prosaposin | P07602 |
C0036341 | Schizophrenia | PSAP | 5660 | prosaposin | P07602 |
C0021390 | Inflammatory Bowel Diseases | PSAP | 5660 | prosaposin | P07602 |
C0026764 | Multiple Myeloma | PSAP | 5660 | prosaposin | P07602 |
C0023520 | Leukodystrophy | PSAP | 5660 | prosaposin | P07602 |
C0017636 | Glioblastoma | PSAP | 5660 | prosaposin | P07602 |
C0033860 | Psoriasis | PSAP | 5660 | prosaposin | P07602 |
C0023903 | Liver neoplasms | PSAP | 5660 | prosaposin | P07602 |
C0003507 | Aortic Valve Stenosis | PSAP | 5660 | prosaposin | P07602 |
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Last updated: August 19, 2024