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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 14201 - 14225 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:9884 muscular dystrophy HGNC:2213 Homo sapiens (human) 1293 COL6A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9536084
DOID:1827 generalized epilepsy MGI:95613 Mus musculus (house mouse) 14394 Gabra1 author statement supported by traceable reference
  • PMID:22812724
  • PMID:26054439
DOID:1059 intellectual disability FB:FBgn0015380 Drosophila melanogaster (fruit fly) 44355 drl combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25935478
DOID:750 peptic ulcer disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20405713
DOID:8466 retinal degeneration HGNC:11761 Homo sapiens (human) 7980 TFPI2 direct assay evidence used in manual assertion
  • PMID:15184935
DOID:1485 cystic fibrosis HGNC:16 Homo sapiens (human) 12 SERPINA3 direct assay evidence used in manual assertion
  • PMID:11120905
DOID:0070043 autosomal dominant intellectual developmental disorder 13 HGNC:2961 Homo sapiens (human) 1778 DYNC1H1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15505619
DOID:0060956 dystonia 37, early-onset with striatal lesions HGNC:17359 Homo sapiens (human) 53371 NUP54 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10286 prostate carcinoma HGNC:1733 Homo sapiens (human) 8621 CDK13 mutant phenotype evidence used in manual assertion
  • PMID:33390186
DOID:0080642 Middle East respiratory syndrome HGNC:3009 Homo sapiens (human) 1803 DPP4 mutant phenotype evidence used in manual assertion
  • PMID:30256968
  • PMID:30626685
  • PMID:31838832
DOID:0111077 congenital nonspherocytic hemolytic anemia 2 HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:16704447
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy MGI:97603 Mus musculus (house mouse) 18763 Pkd1 author statement supported by traceable reference
  • MGI:5284969
DOID:576 proteinuria RGD:2070 Rattus norvegicus (Norway rat) 24180 Agtr1a mutant phenotype evidence used in manual assertion
  • PMID:20042458
DOID:0050741 alcohol dependence HGNC:6553 Homo sapiens (human) 3952 LEP direct assay evidence used in manual assertion
  • PMID:19884906
  • PMID:29912265
DOID:1574 alcohol use disorder WB:WBGene00016872 Caenorhabditis elegans 183715 dop-4 mutant phenotype evidence used in manual assertion
  • PMID:24681782
DOID:9352 type 2 diabetes mellitus HGNC:12762 Homo sapiens (human) 7466 WFS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11916957
  • PMID:12107816
  • PMID:18040659
  • PMID:21713316
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:336 Homo sapiens (human) 185 AGTR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12975417
DOID:9970 obesity MGI:101909 Mus musculus (house mouse) 14738 Gpr12 author statement supported by traceable reference
  • PMID:16887097
DOID:0070600 intellectual disability and myopathy syndrome HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease FB:FBgn0030522 Drosophila melanogaster (fruit fly) 32342 amrt combinatorial experimental and author inference evidence used in manual assertion
  • PMID:34905536
DOID:0112231 lissencephaly 7 with cerebellar hypoplasia HGNC:1774 Homo sapiens (human) 1020 CDK5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:11290 Homo sapiens (human) 6721 SREBF2 direct assay evidence used in manual assertion
  • PMID:15026365
DOID:0050563 nonsyndromic deafness HGNC:12601 Homo sapiens (human) 7399 USH2A inference by association of genotype from phenotype used in manual assertion
  • PMID:23767834
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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

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Last updated: December 8, 2025