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 |
---|---|---|---|---|---|
C1956346 | Coronary Artery Disease | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0027051 | Myocardial Infarction | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0742343 | Acute Chest Syndrome | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C1510586 | Autism Spectrum Disorders | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C2239176 | Liver carcinoma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0238463 | Papillary thyroid carcinoma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0013595 | Eczema | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0011847 | Diabetes | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0233794 | Memory impairment | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0376358 | Malignant neoplasm of prostate | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0020757 | Ichthyoses | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0600139 | Prostate carcinoma | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0011615 | Dermatitis, Atopic | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0011849 | Diabetes Mellitus | ELOVL3 | 83401 | ELOVL fatty acid elongase 3 | Q9HB03 |
C0009398 | Color vision defect | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0020757 | Ichthyoses | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0242383 | Age related macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0036572 | Seizures | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0456909 | Blindness | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0020620 | Hypohidrosis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0265961 | Erythrokeratodermia variabilis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C2239176 | Liver carcinoma | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C1838644 | Stargardt disease 3 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C0015397 | Disorder of eye | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
C4282180 | Juvenile macular degeneration | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
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