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 |
---|---|---|---|---|---|
C0022661 | Kidney Failure, Chronic | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0019196 | Hepatitis C | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0025202 | melanoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C1257931 | Mammary Neoplasms, Human | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0018801 | Heart failure | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0011849 | Diabetes Mellitus | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C3203102 | Idiopathic pulmonary arterial hypertension | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0342788 | Renal carnitine transport defect | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0001126 | Renal tubular acidosis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C1449563 | Cardiomyopathy, Familial Idiopathic | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0751674 | Lymphangioleiomyomatosis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0007194 | Hypertrophic Cardiomyopathy | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0011570 | Mental Depression | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0344315 | Depressed mood | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0001306 | Acute alcoholic liver disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0002395 | Alzheimer's Disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0018802 | Congestive heart failure | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0029456 | Osteoporosis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0003872 | Arthritis, Psoriatic | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0376358 | Malignant neoplasm of prostate | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0014070 | Encephalomyelitis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0011847 | Diabetes | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0220710 | Medium-chain acyl-coenzyme A dehydrogenase deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0220756 | Niemann-Pick Disease, Type C | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024