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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 13951 - 13975 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:10763 hypertension HGNC:59 Homo sapiens (human) 6833 ABCC8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11030411
DOID:0112141 retinitis pigmentosa 84 HGNC:17211 Homo sapiens (human) 9785 DHX38 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8689 anorexia nervosa MGI:109246 Mus musculus (house mouse) 15562 Htr4 author statement supported by traceable reference
  • PMID:17913892
DOID:5419 schizophrenia HGNC:13830 Homo sapiens (human) 26047 CNTNAP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23123147
DOID:12714 Ellis-Van Creveld syndrome MGI:1915775 Mus musculus (house mouse) 68525 Evc2 author statement supported by traceable reference
  • PMID:26219237
DOID:14735 hereditary angioedema HGNC:3656 Homo sapiens (human) 26509 MYOF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4989 pancreatitis HGNC:9475 Homo sapiens (human) 5644 PRSS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8841182
DOID:13141 uveitis HGNC:4932 Homo sapiens (human) 3106 HLA-B direct assay evidence used in manual assertion
  • PMID:9232451
DOID:8893 psoriasis HGNC:5981 Homo sapiens (human) 3605 IL17A mutant phenotype evidence used in manual assertion
  • PMID:20926833
DOID:0080188 chronic myelomonocytic leukemia HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20693430
DOID:674 cleft palate HGNC:10659 Homo sapiens (human) 6383 SDC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18716610
DOID:0080176 meningococcal meningitis HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23691182
DOID:9253 gastrointestinal stromal tumor HGNC:18420 Homo sapiens (human) 29072 SETD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26338826
DOID:219 colon cancer HGNC:9376 Homo sapiens (human) 5562 PRKAA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20622004
DOID:0110376 retinitis pigmentosa 41 HGNC:9454 Homo sapiens (human) 8842 PROM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:10771 Homo sapiens (human) 10262 SF3B4 mutant phenotype evidence used in manual assertion
  • PMID:30391496
DOID:1470 major depressive disorder HGNC:1951 Homo sapiens (human) 1129 CHRM2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12116189
DOID:0060060 non-Hodgkin lymphoma MGI:99569 Mus musculus (house mouse) 14739 S1pr2 author statement supported by traceable reference
  • PMID:19903857
DOID:8577 ulcerative colitis HGNC:602 Homo sapiens (human) 337 APOA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:17206692
DOID:0111261 fumarase deficiency HGNC:3700 Homo sapiens (human) 2271 FH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:15478 Homo sapiens (human) 80332 ADAM33 inference by association of genotype from phenotype used in manual assertion
  • PMID:19284602
  • PMID:20003279
DOID:423 myopathy FB:FBgn0263782 Drosophila melanogaster (fruit fly) 42803 Hmgcr combinatorial experimental and author inference evidence used in manual assertion
  • PMID:36428957
DOID:10579 leukodystrophy HGNC:20 Homo sapiens (human) 16 AARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110486 autosomal recessive nonsyndromic deafness 28 HGNC:17009 Homo sapiens (human) 11078 TRIOBP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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