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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 |
|---|---|---|---|---|---|
| C0006142 | Malignant neoplasm of breast | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
| C0004364 | Autoimmune Diseases | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
| C0345904 | Malignant neoplasm of liver | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
| C0006826 | Malignant Neoplasms | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
| C0027651 | Neoplasms | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
| C1306459 | Primary malignant neoplasm | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
| C0684249 | Carcinoma of lung | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
| C0025202 | melanoma | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0376358 | Malignant neoplasm of prostate | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0600139 | Prostate carcinoma | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0004096 | Asthma | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0027651 | Neoplasms | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0013274 | Patent ductus arteriosus | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0026764 | Multiple Myeloma | CRYBG1 | 202 | crystallin beta-gamma domain containing 1 | Q9Y4K1 |
| C0027819 | Neuroblastoma | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C4721532 | Lymphoma, Non-Hodgkin, Familial | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0175707 | Asplenia Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3536741 | Discordant ventriculoarterial connection | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1415817 | HETEROTAXY, VISCERAL, 2, AUTOSOMAL | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0700095 | Central neuroblastoma | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3178805 | Heterotaxy Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3178806 | Right Atrial Isomerism | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0040761 | Transposition of Great Vessels | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0010068 | Coronary heart disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1970109 | AROMATASE EXCESS SYNDROME | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
