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 ▼ |
---|---|---|---|---|---|
C0011603 | Dermatitis | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
C0019693 | HIV Infections | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
C0008445 | Chondrodysplasia Punctata | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
C0041296 | Tuberculosis | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
C0162309 | Adrenoleukodystrophy | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
C0021364 | Male infertility | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
C0003811 | Cardiac Arrhythmia | ALG10 | 84920 | ALG10 alpha-1,2-glucosyltransferase | Q5BKT4 |
C0023976 | Long QT Syndrome | ALG10 | 84920 | ALG10 alpha-1,2-glucosyltransferase | Q5BKT4 |
C3150943 | Long Qt Syndrome 2 | ALG10 | 84920 | ALG10 alpha-1,2-glucosyltransferase | Q5BKT4 |
C0019196 | Hepatitis C | ALG10 | 84920 | ALG10 alpha-1,2-glucosyltransferase | Q5BKT4 |
C0678222 | Breast Carcinoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C2717836 | Steroid Sulfatase Deficiency Disease | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0002395 | Alzheimer's Disease | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0079744 | Diffuse Large B-Cell Lymphoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0220597 | Adult Hodgkin Lymphoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C2931822 | Nasopharyngeal carcinoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0152018 | Esophageal carcinoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0038012 | Spondylitis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C1541923 | Infective endocarditis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C1168401 | Squamous cell carcinoma of the head and neck | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C1306459 | Primary malignant neoplasm | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0162529 | Colitis, Ischemic | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0233794 | Memory impairment | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0006826 | Malignant Neoplasms | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
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Last updated: August 19, 2024