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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 October 9, 2024
Displaying entries 65876 - 65900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:11400 pyelonephritis HGNC:914 Homo sapiens (human) 567 B2M
  • MGI:6194238
DOID:3407 carotid artery disease HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:21546482
DOID:10763 hypertension HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:15957539
DOID:14330 Parkinson's disease HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:7605592
DOID:417 autoimmune disease HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:17214095
DOID:0050830 peripheral artery disease HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:21314441
DOID:576 proteinuria HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:17634209
DOID:9538 multiple myeloma HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:32856850
DOID:2349 arteriosclerosis HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:16221094
DOID:0111981 immunodeficiency 43 HGNC:914 Homo sapiens (human) 567 B2M
  • RGD:7240710
DOID:8622 measles HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:1402029
DOID:2352 hemochromatosis HGNC:914 Homo sapiens (human) 567 B2M
  • MGI:6194238
DOID:3021 acute kidney failure HGNC:914 Homo sapiens (human) 567 B2M
  • MGI:6194238
DOID:848 arthritis HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:16575857
DOID:9352 type 2 diabetes mellitus HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:15127324
DOID:83 cataract HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:12567748
DOID:9970 obesity HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:15517379
DOID:5199 ureteral obstruction HGNC:914 Homo sapiens (human) 567 B2M
  • MGI:6194238
DOID:640 encephalomyelitis HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:1402029
DOID:0060704 lymphoproliferative syndrome HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:9067691
DOID:0050589 inflammatory bowel disease HGNC:914 Homo sapiens (human) 567 B2M
  • PMID:20015205
DOID:0070311 oligoasthenoteratozoospermia WB:WBGene00015204 Caenorhabditis elegans 174243 B0495.5
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis MGI:103163 Mus musculus (house mouse) 12007 Azgp1
  • MGI:6194238
DOID:10286 prostate carcinoma MGI:103163 Mus musculus (house mouse) 12007 Azgp1
  • MGI:6194238
DOID:5517 stomach carcinoma MGI:103163 Mus musculus (house mouse) 12007 Azgp1
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024