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 |
---|---|---|---|---|---|
C0019163 | Hepatitis B | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0006845 | Candidiasis, Chronic Mucocutaneous | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1859353 | Candidiasis, Familial, 2 | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1306459 | Primary malignant neoplasm | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0085253 | Adult-Onset Still Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0038034 | Sporotrichosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0024141 | Lupus Erythematosus, Systemic | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1868684 | EAR, PATELLA, SHORT STATURE SYNDROME | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0006826 | Malignant Neoplasms | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0002395 | Alzheimer's Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0042384 | Vasculitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0028754 | Obesity | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0004943 | Behcet Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0026691 | Mucocutaneous Lymph Node Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0008582 | Chromoblastomycosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0027651 | Neoplasms | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0376358 | Malignant neoplasm of prostate | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C1306459 | Primary malignant neoplasm | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C1956346 | Coronary Artery Disease | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0010054 | Coronary Arteriosclerosis | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0010068 | Coronary heart disease | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0009402 | Colorectal Carcinoma | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0006826 | Malignant Neoplasms | NDST4 | 64579 | N-deacetylase and N-sulfotransferase 4 | Q9H3R1 |
C0086647 | Mucopolysaccharidosis Type IIIA | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
C0026706 | Mucopolysaccharidosis III | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
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