Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 ▲ |
|---|---|---|---|---|---|
| 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 |
| 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 |
| C0023895 | Liver diseases | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1389016 | ATRIOVENTRICULAR CANAL DEFECT | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0520463 | Chronic active hepatitis | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0265357 | Polysplenia Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1876172 | VAH, AUTOSOMAL RECESSIVE | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0018817 | Atrial Septal Defects | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0344692 | Isomerism of atrial appendages | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1956413 | Taussig-Bing Anomaly | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0002395 | Alzheimer's Disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0152021 | Congenital heart disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0005411 | Biliary Atresia | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C4520983 | Congenital atresia of extrahepatic bile duct | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
