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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 |
|---|---|---|---|---|---|
| C1306459 | Primary malignant neoplasm | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1853444 | Heterotaxy, Visceral, 3, Autosomal | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C2936858 | Congenital adrenal hyperplasia due to 21 hydroxylase deficiency | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0024305 | Lymphoma, Non-Hodgkin | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0025517 | Metabolic Diseases | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0000768 | Congenital Abnormality | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3151867 | CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3463824 | MYELODYSPLASTIC SYNDROME | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1956412 | Double Outlet Right Ventricle, Subpulmonary VSD | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1275081 | Cardio-facio-cutaneous syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0685938 | Malignant neoplasm of gastrointestinal tract | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0278701 | Gastric Adenocarcinoma | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0041296 | Tuberculosis | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0036341 | Schizophrenia | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0018799 | Heart Diseases | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3553676 | HETEROTAXY, VISCERAL, 6, AUTOSOMAL | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C2931005 | Congenital disorder of glycosylation type 1K | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0018213 | Graves Disease | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0262655 | Recurrent urinary tract infection | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0009375 | Colonic Neoplasms | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0006142 | Malignant neoplasm of breast | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0235991 | Small for gestational age (disorder) | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0282577 | Congenital Disorders of Glycosylation | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0024141 | Lupus Erythematosus, Systemic | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
