Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
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DOID:0111366 | familial hepatic adenoma | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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DOID:2043 | hepatitis B | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
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DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
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DOID:7693 | abdominal aortic aneurysm | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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DOID:0070354 | cataract 48 | HGNC:30373 | Homo sapiens (human) | 23268 | DNMBP |
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DOID:686 | liver carcinoma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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DOID:3907 | lung squamous cell carcinoma | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
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DOID:9261 | nasopharynx carcinoma | HGNC:7381 | Homo sapiens (human) | 4486 | MST1R |
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DOID:10283 | prostate cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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DOID:13166 | allergic bronchopulmonary aspergillosis | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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DOID:865 | vasculitis | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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DOID:10966 | lipoid nephrosis | HGNC:11368 | Homo sapiens (human) | 6778 | STAT6 |
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DOID:8778 | Crohn's disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:0111153 | congenital mirror movement disorder | HGNC:2701 | Homo sapiens (human) | 1630 | DCC |
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DOID:0110482 | autosomal recessive nonsyndromic deafness 24 | HGNC:9944 | Homo sapiens (human) | 5962 | RDX |
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DOID:612 | primary immunodeficiency disease | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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DOID:2513 | basal cell carcinoma | HGNC:9871 | Homo sapiens (human) | 5921 | RASA1 |
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DOID:5517 | stomach carcinoma | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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DOID:13241 | Behcet's disease | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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DOID:0070467 | carpal tunnel syndrome 2 | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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DOID:0111212 | autosomal dominant distal hereditary motor neuronopathy 9 | HGNC:12729 | Homo sapiens (human) | 7453 | WARS1 |
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DOID:0081182 | autosomal recessive intellectual developmental disorder 6 | HGNC:4580 | Homo sapiens (human) | 2898 | GRIK2 |
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DOID:0050211 | swine influenza | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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DOID:2256 | osteochondrodysplasia | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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DOID:332 | amyotrophic lateral sclerosis | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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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 v4.1.0
Last updated: December 9, 2024