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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 13126 - 13150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:2559 opiate dependence HGNC:15998 Homo sapiens (human) 89795 NAV3 inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:9256 colorectal cancer HGNC:1511 Homo sapiens (human) 842 CASP9 inference by association of genotype from phenotype used in manual assertion
  • PMID:21538054
DOID:0111223 centronuclear myopathy 1 SGD:S000001709 Saccharomyces cerevisiae S288C 853870 VPS1 sequence similarity evidence used in manual assertion
  • PMID:28357347
  • PMID:37060997
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A combinatorial experimental and curator inference evidence used in manual assertion
  • PMID:38124489
DOID:0080553 congenital disorder of glycosylation Iaa HGNC:21042 Homo sapiens (human) 116150 NUS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:10473 Homo sapiens (human) 864 RUNX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16230397
DOID:1289 neurodegenerative disease FB:FBgn0041579 Drosophila melanogaster (fruit fly) 36484 AttC combinatorial experimental and author inference evidence used in manual assertion
  • PMID:23613578
DOID:9352 type 2 diabetes mellitus HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:10332679
  • PMID:11689270
DOID:0050873 follicular lymphoma HGNC:11935 Homo sapiens (human) 959 CD40LG mutant phenotype evidence used in manual assertion
  • PMID:25582824
DOID:4184 pseudohypoparathyroidism MGI:95777 Mus musculus (house mouse) 14683 Gnas author statement supported by traceable reference
  • PMID:26671181
DOID:1572 normal pressure hydrocephalus MGI:2444131 Mus musculus (house mouse) 231293 Cwh43 author statement supported by traceable reference
  • PMID:33459505
DOID:4195 hyperglycemia SGD:S000000545 Saccharomyces cerevisiae S288C 850317 GLK1 sequence similarity evidence used in manual assertion
  • PMID:37101203
DOID:0080581 hyperekplexia 4 HGNC:25903 Homo sapiens (human) 84896 ATAD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:23631 Homo sapiens (human) 387129 NPSR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15073379
  • PMID:17702965
  • PMID:18285428
  • RGD:7240710
DOID:9993 hypoglycemia HGNC:4195 Homo sapiens (human) 2645 GCK inference by association of genotype from phenotype used in manual assertion
  • PMID:9435328
DOID:612 primary immunodeficiency disease HGNC:12016 Homo sapiens (human) 7174 TPP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:865 vasculitis HGNC:7218 Homo sapiens (human) 4353 MPO mutant phenotype evidence used in manual assertion
  • PMID:21071471
DOID:8893 psoriasis MGI:108074 Mus musculus (house mouse) 20773 Sptlc2 author statement supported by traceable reference
  • PMID:23633022
DOID:0080326 familial hypertrophic cardiomyopathy HGNC:7551 Homo sapiens (human) 4607 MYBPC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:12110947
  • PMID:16004897
  • PMID:9048664
  • PMID:9562578
DOID:3144 cutis laxa HGNC:3602 Homo sapiens (human) 10516 FBLN5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12189163
DOID:12132 granulomatosis with polyangiitis HGNC:12724 Homo sapiens (human) 7448 VTN direct assay evidence used in manual assertion
  • PMID:12126637
DOID:0112125 alpha-thalassemia myelodysplasia syndrome HGNC:886 Homo sapiens (human) 546 ATRX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110699 hypotrichosis 2 HGNC:1802 Homo sapiens (human) 1041 CDSN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112035 non-syndromic X-linked intellectual disability 96 HGNC:11506 Homo sapiens (human) 6855 SYP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060673 Peters anomaly HGNC:2597 Homo sapiens (human) 1545 CYP1B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15621878
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: December 8, 2025