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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 13451 - 13475 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:0111380 solitary median maxillary central incisor HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:12671028
DOID:9351 diabetes mellitus HGNC:5006 Homo sapiens (human) 3156 HMGCR mutant phenotype evidence used in manual assertion
  • PMID:15476492
DOID:1787 pericarditis HGNC:9364 Homo sapiens (human) 10216 PRG4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16429407
DOID:0112330 pontocerebellar hypoplasia type 1E HGNC:25198 Homo sapiens (human) 91137 SLC25A46 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9051 Homo sapiens (human) 5327 PLAT inference by association of genotype from phenotype used in manual assertion
  • PMID:11848437
DOID:628 combined T cell and B cell immunodeficiency HGNC:6010 Homo sapiens (human) 3561 IL2RG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10609 rickets HGNC:2606 Homo sapiens (human) 1594 CYP27B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9486994
DOID:0110163 Charcot-Marie-Tooth disease axonal type 2F HGNC:5246 Homo sapiens (human) 3315 HSPB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer SGD:S000006387 Saccharomyces cerevisiae S288C 856313 DPM1 sequence similarity evidence used in manual assertion
  • PMID:30637701
DOID:3883 Lynch syndrome HGNC:7329 Homo sapiens (human) 2956 MSH6 inference by association of genotype from phenotype used in manual assertion
  • PMID:15571801
  • PMID:28218421
  • PMID:7604266
DOID:2841 asthma HGNC:5970 Homo sapiens (human) 3593 IL12B inference by association of genotype from phenotype used in manual assertion
  • PMID:12241719
  • PMID:15322986
  • PMID:16210052
DOID:649 prion disease HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:18559949
DOID:684 hepatocellular carcinoma HGNC:9346 Homo sapiens (human) 639 PRDM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31376415
DOID:0110480 autosomal recessive nonsyndromic deafness 22 MGI:2149209 Mus musculus (house mouse) 246190 Otoa author statement supported by traceable reference
  • PMID:23129639
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26591766
DOID:1612 breast cancer MGI:97250 Mus musculus (house mouse) 17869 Myc author statement supported by traceable reference
  • PMID:22525269
DOID:10983 Alport syndrome HGNC:2204 Homo sapiens (human) 1285 COL4A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:7987301
DOID:2841 asthma HGNC:11849 Homo sapiens (human) 7098 TLR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:17434873
DOID:0070235 Loeys-Dietz syndrome 1 HGNC:11772 Homo sapiens (human) 7046 TGFBR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112230 lissencephaly 5 HGNC:6486 Homo sapiens (human) 3912 LAMB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:12426569
  • PMID:23398946
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:12825 Homo sapiens (human) 7514 XPO1 mutant phenotype evidence used in manual assertion
  • PMID:26603256
  • PMID:33745946
DOID:1588 thrombocytopenia HGNC:11283 Homo sapiens (human) 6714 SRC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060001 withdrawal disorder HGNC:7978 Homo sapiens (human) 2908 NR3C1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27397864
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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