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DisGeNET
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 |
|---|---|---|---|---|---|
| C0278878 | Adult Glioblastoma | MSLN | 10232 | mesothelin | Q13421 |
| C0740277 | Bile duct carcinoma | MSLN | 10232 | mesothelin | Q13421 |
| C0020538 | Hypertensive disease | MSLN | 10232 | mesothelin | Q13421 |
| C0239946 | Fibrosis, Liver | MSLN | 10232 | mesothelin | Q13421 |
| C0345905 | Intrahepatic Cholangiocarcinoma | MSLN | 10232 | mesothelin | Q13421 |
| C0017636 | Glioblastoma | MSLN | 10232 | mesothelin | Q13421 |
| C0205644 | Carcinoma, Granular Cell | MSLN | 10232 | mesothelin | Q13421 |
| C0025286 | Meningioma | MSLN | 10232 | mesothelin | Q13421 |
| C0011991 | Diarrhea | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0266551 | Congenital coloboma of iris | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0279626 | Squamous cell carcinoma of esophagus | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1832736 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0235946 | Cerebral atrophy | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0006826 | Malignant Neoplasms | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0282577 | Congenital Disorders of Glycosylation | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0006142 | Malignant neoplasm of breast | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0023467 | Leukemia, Myelocytic, Acute | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0038379 | Strabismus | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0678222 | Breast Carcinoma | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0554101 | Villous atrophy | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C4317295 | Congenital disorder of glycosylation type 1s | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1306459 | Primary malignant neoplasm | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1168401 | Squamous cell carcinoma of the head and neck | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0027651 | Neoplasms | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C3279947 | NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
