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 ▲ |
---|---|---|---|---|---|
C0023467 | Leukemia, Myelocytic, Acute | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
C0025202 | melanoma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0017636 | Glioblastoma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C1621958 | Glioblastoma Multiforme | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0017638 | Glioma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0278878 | Adult Glioblastoma | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
C0400966 | Non-alcoholic Fatty Liver Disease | ELOVL2 | 54898 | ELOVL fatty acid elongase 2 | Q9NXB9 |
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 |
C0025958 | Microcephaly | SMPD4 | 55627 | sphingomyelin phosphodiesterase 4 | Q9NXE4 |
C0027051 | Myocardial Infarction | SMPD4 | 55627 | sphingomyelin phosphodiesterase 4 | Q9NXE4 |
C0011311 | Dengue Fever | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0008373 | Cholesteatoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0029463 | Osteosarcoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0019100 | Severe Dengue | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0278878 | Adult Glioblastoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0017636 | Glioblastoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0585442 | Osteosarcoma of bone | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0017638 | Glioma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0032302 | Mycoplasma pneumonia | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0003850 | Arteriosclerosis | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
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