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
Displaying entries 55501 - 55525 of 62743 in total
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