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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 January 28, 2025
Displaying entries 12126 - 12150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▼
DOID:0111799 syndromic microphthalmia 1 HGNC:20893 Homo sapiens (human) 54880 BCOR inference by association of genotype from phenotype used in manual assertion
  • PMID:15004558
DOID:83 cataract HGNC:20893 Homo sapiens (human) 54880 BCOR inference by association of genotype from phenotype used in manual assertion
  • PMID:15004558
DOID:0111809 syndromic microphthalmia 2 HGNC:20893 Homo sapiens (human) 54880 BCOR inference by association of genotype from phenotype used in manual assertion
  • PMID:15004558
  • RGD:7240710
DOID:0080162 lupus nephritis HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:15004265
DOID:11716 prediabetes syndrome HGNC:9677 Homo sapiens (human) 5799 PTPRN2 direct assay evidence used in manual assertion
  • PMID:15004204
DOID:437 myasthenia gravis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15003812
  • PMID:21924912
DOID:0060178 familial hemiplegic migraine MGI:109482 Mus musculus (house mouse) 12286 Cacna1a author statement supported by traceable reference
  • PMID:15003170
  • PMID:19104150
  • PMID:22144569
DOID:0110320 hypertrophic cardiomyopathy 14 MGI:97255 Mus musculus (house mouse) 17888 Myh6 author statement supported by traceable reference
  • PMID:15001446
  • PMID:16332958
  • PMID:20811150
  • PMID:24829265
  • PMID:8614836
DOID:104 bacterial infectious disease RGD:3650 Rattus norvegicus (Norway rat) 24771 Sdc4 mutant phenotype evidence used in manual assertion
  • PMID:15001228
DOID:10286 prostate carcinoma HGNC:3273 Homo sapiens (human) 8667 EIF3H inference by association of genotype from phenotype used in manual assertion
  • PMID:14997205
DOID:9477 pulmonary embolism HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:14996674
DOID:14330 Parkinson's disease HGNC:2689 Homo sapiens (human) 1621 DBH inference by association of genotype from phenotype used in manual assertion
  • PMID:14991826
DOID:0060564 spinal disease HGNC:3755 Homo sapiens (human) 2317 FLNB inference by association of genotype from phenotype used in manual assertion
  • PMID:14991055
DOID:2256 osteochondrodysplasia HGNC:3755 Homo sapiens (human) 2317 FLNB inference by association of genotype from phenotype used in manual assertion
  • PMID:14991055
  • PMID:16752402
DOID:0080006 bone development disease HGNC:3755 Homo sapiens (human) 2317 FLNB inference by association of genotype from phenotype used in manual assertion
  • PMID:14991055
  • PMID:15994868
DOID:4483 rhinitis HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14990915
DOID:4483 rhinitis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14990915
DOID:0050152 aspiration pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE mutant phenotype evidence used in manual assertion
  • PMID:14990394
DOID:219 colon cancer HGNC:11773 Homo sapiens (human) 7048 TGFBR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:14988818
DOID:219 colon cancer HGNC:173 Homo sapiens (human) 92 ACVR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:14988818
DOID:8778 Crohn's disease HGNC:3619 Homo sapiens (human) 2214 FCGR3A inference by association of genotype from phenotype used in manual assertion
  • PMID:14987319
DOID:7188 autoimmune thyroiditis HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:14986169
  • PMID:16352685
  • PMID:9398726
DOID:3083 chronic obstructive pulmonary disease HGNC:2015 Homo sapiens (human) 1179 CLCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14985398
DOID:9240 erythromelalgia HGNC:10597 Homo sapiens (human) 6335 SCN9A inference by association of genotype from phenotype used in manual assertion
  • PMID:14985375
  • PMID:16216943
  • RGD:7240710
DOID:0050458 juvenile myelomonocytic leukemia MGI:97306 Mus musculus (house mouse) 18015 Nf1 author statement supported by traceable reference
  • PMID:14982883

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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 8, 2025