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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 |
|---|---|---|---|---|---|
| C0042373 | Vascular Diseases | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0002895 | Anemia, Sickle Cell | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C2239176 | Liver carcinoma | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0004096 | Asthma | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0279639 | Mucinous adenocarcinoma of colon | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0027651 | Neoplasms | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0009319 | Colitis | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0029408 | Degenerative polyarthritis | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0699790 | Colon Carcinoma | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0007102 | Malignant tumor of colon | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| 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 |
