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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 11501 - 11525 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:14701 propionic acidemia HGNC:8654 Homo sapiens (human) 5096 PCCB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2152 ovary epithelial cancer HGNC:2681 Homo sapiens (human) 1616 DAXX direct assay evidence used in manual assertion
  • PMID:23539629
DOID:0081263 neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities HGNC:15717 Homo sapiens (human) 50628 GEMIN4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:83 cataract HGNC:5227 Homo sapiens (human) 3299 HSF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12089525
DOID:9778 irritable bowel syndrome MGI:1927999 Mus musculus (house mouse) 58805 Mlxipl author statement supported by traceable reference
  • PMID:29669261
DOID:0080726 Ehlers-Danlos syndrome classic type 2 HGNC:2210 Homo sapiens (human) 1290 COL5A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050453 lissencephaly HGNC:19139 Homo sapiens (human) 55624 POMGNT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17559086
DOID:0111541 pigmented paravenous chorioretinal atrophy HGNC:2343 Homo sapiens (human) 23418 CRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15623792
  • RGD:7240710
DOID:10534 stomach cancer HGNC:820 Homo sapiens (human) 496 ATP4B direct assay evidence used in manual assertion
  • PMID:23317218
DOID:2340 craniosynostosis HGNC:12428 Homo sapiens (human) 7291 TWIST1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080171 esophageal atresia/tracheoesophageal fistula MGI:104327 Mus musculus (house mouse) 18121 Nog author statement supported by traceable reference
  • PMID:17260385
DOID:0080694 Galloway-Mowat syndrome HGNC:18016 Homo sapiens (human) 55746 NUP133 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110173 Charcot-Marie-Tooth disease axonal type 2U HGNC:6898 Homo sapiens (human) 4141 MARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111944 immunodeficiency 31B HGNC:11362 Homo sapiens (human) 6772 STAT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10487 Hirschsprung's disease MGI:96610 Mus musculus (house mouse) 16412 Itgb1 author statement supported by traceable reference
  • PMID:16571628
DOID:0050671 female breast cancer HGNC:9181 Homo sapiens (human) 5429 POLH inference by association of genotype from phenotype used in manual assertion
  • PMID:30303537
DOID:0110143 Bartter disease type 2 HGNC:6255 Homo sapiens (human) 3758 KCNJ1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:18636032
DOID:1059 intellectual disability MGI:2442071 Mus musculus (house mouse) 245607 Gprasp2 author statement supported by traceable reference
  • PMID:30926797
DOID:1686 glaucoma RGD:619991 Rattus norvegicus (Norway rat) 83785 Vegfa mutant phenotype evidence used in manual assertion
  • PMID:23416159
DOID:0050534 congenital stationary night blindness HGNC:7146 Homo sapiens (human) 4308 TRPM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19878917
  • PMID:19896109
  • PMID:19896113
DOID:0110295 autosomal recessive limb-girdle muscular dystrophy type 2U HGNC:37276 Homo sapiens (human) 729920 CRPPA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050888 syndromic intellectual disability FB:FBgn0259168 Drosophila melanogaster (fruit fly) 32771 mnb combinatorial experimental and author inference evidence used in manual assertion
  • PMID:32555303
DOID:90 degenerative disc disease HGNC:14872 Homo sapiens (human) 54829 ASPN inference by association of genotype from phenotype used in manual assertion
  • PMID:18304494
DOID:783 end stage renal disease RGD:3184 Rattus norvegicus (Norway rat) 24598 Nos1 direct assay evidence used in manual assertion
  • PMID:23185775
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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: April 6, 2026