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 |
C0036341 | Schizophrenia | PLA2G4B | 100137049 | phospholipase A2 group IVB | P0C869 |
C1168401 | Squamous cell carcinoma of the head and neck | PLA2G4B | 100137049 | phospholipase A2 group IVB | P0C869 |
C1168401 | Squamous cell carcinoma of the head and neck | JMJD7-PLA2G4B | 8681 | JMJD7-PLA2G4B readthrough | P0C869 |
C0006142 | Malignant neoplasm of breast | ASAH2B | 653308 | N-acylsphingosine amidohydrolase 2B | P0C7U1 |
C0678222 | Breast Carcinoma | ASAH2B | 653308 | N-acylsphingosine amidohydrolase 2B | P0C7U1 |
C0036341 | Schizophrenia | ALDOC | 230 | aldolase, fructose-bisphosphate C | P09972 |
C2239176 | Liver carcinoma | ALDOC | 230 | aldolase, fructose-bisphosphate C | P09972 |
C0345904 | Malignant neoplasm of liver | ALDOC | 230 | aldolase, fructose-bisphosphate C | P09972 |
C0027819 | Neuroblastoma | ALDOC | 230 | aldolase, fructose-bisphosphate C | P09972 |
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Last updated: August 19, 2024