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 ▲ |
---|---|---|---|---|---|
C0043459 | Zellweger Syndrome | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C1263846 | Attention deficit hyperactivity disorder | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0008445 | Chondrodysplasia Punctata | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0036341 | Schizophrenia | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0025958 | Microcephaly | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0004352 | Autistic Disorder | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0041671 | Attention Deficit Disorder | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0006826 | Malignant Neoplasms | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0036439 | Scoliosis, unspecified | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0345904 | Malignant neoplasm of liver | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C1306459 | Primary malignant neoplasm | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0086543 | Cataract | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0002395 | Alzheimer's Disease | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C2239176 | Liver carcinoma | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0239946 | Fibrosis, Liver | GNPAT | 8443 | glyceronephosphate O-acyltransferase | O15228 |
C0600139 | Prostate carcinoma | ACOX3 | 8310 | acyl-CoA oxidase 3, pristanoyl | O15254 |
C0033578 | Prostatic Neoplasms | ACOX3 | 8310 | acyl-CoA oxidase 3, pristanoyl | O15254 |
C0376358 | Malignant neoplasm of prostate | ACOX3 | 8310 | acyl-CoA oxidase 3, pristanoyl | O15254 |
C0004936 | Mental disorders | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0020071 | Hereditary Sensory Autonomic Neuropathy, Type 1 | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0033975 | Psychotic Disorders | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0086405 | Hereditary Sensory Radicular Neuropathy | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0006118 | Brain Neoplasms | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0007959 | Charcot-Marie-Tooth Disease | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
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Last updated: August 19, 2024