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 ▲ |
---|---|---|---|---|---|
C0019196 | Hepatitis C | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C0019163 | Hepatitis B | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C3150651 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C2750440 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C0376358 | Malignant neoplasm of prostate | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C0000768 | Congenital Abnormality | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0235974 | Pancreatic carcinoma | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C4551974 | DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1 | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0027651 | Neoplasms | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C1306459 | Primary malignant neoplasm | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0014550 | Myoclonic Epilepsy | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0005695 | Bladder Neoplasm | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0004096 | Asthma | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0006826 | Malignant Neoplasms | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0005684 | Malignant neoplasm of urinary bladder | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0007131 | Non-Small Cell Lung Carcinoma | INPP4A | 3631 | inositol polyphosphate-4-phosphatase type I A | Q96PE3 |
C0220981 | Metabolic acidosis | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0268583 | Methylmalonic acidemia | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0268468 | Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0025517 | Metabolic Diseases | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0017168 | Gastroesophageal reflux disease | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0032285 | Pneumonia | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
C0600139 | Prostate carcinoma | SIGLEC12 | 89858 | sialic acid binding Ig like lectin 12 (gene/pseudogene) | Q96PQ1 |
C0028754 | Obesity | SIGLEC12 | 89858 | sialic acid binding Ig like lectin 12 (gene/pseudogene) | Q96PQ1 |
C0024141 | Lupus Erythematosus, Systemic | SIGLEC12 | 89858 | sialic acid binding Ig like lectin 12 (gene/pseudogene) | Q96PQ1 |
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Last updated: August 19, 2024