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 |
---|---|---|---|---|---|
C0028754 | Obesity | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0023903 | Liver neoplasms | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0007137 | Squamous cell carcinoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0684249 | Carcinoma of lung | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0700095 | Central neuroblastoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0153594 | Malignant neoplasm of testis | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0024121 | Lung Neoplasms | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0699791 | Stomach Carcinoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0027819 | Neuroblastoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C1458155 | Mammary Neoplasms | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0017636 | Glioblastoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0020479 | Hyperlipoproteinemia Type III | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SULF2 | 55959 | sulfatase 2 | Q8IWU5 |
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 |
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Last updated: August 19, 2024