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Alliance of Genome Resources

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
Alliance of Genome Resources July 29, 2024
Displaying entries 10801 - 10825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10003 sensorineural hearing loss HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22574884
DOID:10300 Raynaud disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17401513
DOID:9182 pemphigus HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22738420
DOID:8947 diabetic retinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:3770 pulmonary fibrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:21190578
DOID:5679 retinal disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:3717 gastric adenocarcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:31396300
DOID:12361 Graves' disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12919155
DOID:13208 background diabetic retinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:24092995
DOID:13207 proliferative diabetic retinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:24092995
DOID:2876 laryngeal squamous cell carcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:8138195
DOID:9201 lichen planus HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20372767
DOID:10808 gastric ulcer HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:2527 nephrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20685819
DOID:10159 osteonecrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:18353692
DOID:5844 myocardial infarction HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:1596 depressive disorder HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:31396300
DOID:6543 acne HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:11349462
  • PMID:16489259
  • PMID:23174057
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:10450379
DOID:8893 psoriasis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12165738
  • PMID:12602965
DOID:874 bacterial pneumonia HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:9970 obesity HGNC:1473 Homo sapiens (human) 821 CANX
  • PMID:18567819
DOID:14330 Parkinson's disease HGNC:20407 Homo sapiens (human) 125972 CALR3
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:1455 Homo sapiens (human) 811 CALR
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024