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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 9801 - 9825 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0050741 alcohol dependence HGNC:8156 Homo sapiens (human) 4988 OPRM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16679777
  • PMID:18250251
  • PMID:20077761
DOID:13544 low tension glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:15226658
  • PMID:15557444
  • PMID:16148883
DOID:1067 open-angle glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:11834836
  • PMID:14627677
DOID:5408 Paget's disease of bone HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:20436471
DOID:1070 primary open angle glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:15226658
  • PMID:15557444
  • RGD:7240710
DOID:332 amyotrophic lateral sclerosis HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:20428114
  • PMID:21613650
DOID:1686 glaucoma HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • PMID:16148883
DOID:0060203 amyotrophic lateral sclerosis type 12 HGNC:17142 Homo sapiens (human) 10133 OPTN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080686 tubular aggregate myopathy 2 HGNC:25896 Homo sapiens (human) 84876 ORAI1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111976 immunodeficiency 9 HGNC:25896 Homo sapiens (human) 84876 ORAI1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080512 Meier-Gorlin syndrome 1 HGNC:8487 Homo sapiens (human) 4998 ORC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma FB:FBgn0037110 Drosophila melanogaster (fruit fly) 40404 ORMDL combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25979522
DOID:0080245 Galloway-Mowat syndrome 3 HGNC:18028 Homo sapiens (human) 55644 OSGEP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080930 primary localized cutaneous amyloidosis 1 HGNC:8507 Homo sapiens (human) 9180 OSMR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110939 autosomal recessive osteopetrosis 5 HGNC:21652 Homo sapiens (human) 28962 OSTM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110480 autosomal recessive nonsyndromic deafness 22 HGNC:16378 Homo sapiens (human) 146183 OTOA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110474 autosomal recessive nonsyndromic deafness 18B HGNC:8516 Homo sapiens (human) 340990 OTOG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:25118 Homo sapiens (human) 90268 OTULIN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080163 otulipenia HGNC:25118 Homo sapiens (human) 90268 OTULIN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9410 combined pituitary hormone deficiency HGNC:8522 Homo sapiens (human) 5015 OTX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111806 syndromic microphthalmia 5 HGNC:8522 Homo sapiens (human) 5015 OTX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080652 calcium oxalate nephrolithiasis HGNC:4531 Homo sapiens (human) 27199 OXGR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070339 cerebellar hyplasia/atrophy, epilepsy, and global developmental delay HGNC:15822 Homo sapiens (human) 55074 OXR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q FB:FBgn0039827 Drosophila melanogaster (fruit fly) 43689 Oadh combinatorial experimental and author inference evidence used in manual assertion
  • PMID:38416643
DOID:0050632 oculocutaneous albinism MGI:97454 Mus musculus (house mouse) 18431 Oca2 author statement supported by traceable reference
  • MGI:5607140
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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: April 7, 2025