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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 9951 - 9975 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0060757 sclerosteosis 2 HGNC:6696 Homo sapiens (human) 4038 LRP4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:8031 Homo sapiens (human) 4914 NTRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18780967
DOID:8778 Crohn's disease HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:20848524
DOID:9744 type 1 diabetes mellitus HGNC:5209 Homo sapiens (human) 3291 HSD11B2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11916625
DOID:0081319 multiple synostoses syndrome 3 HGNC:3687 Homo sapiens (human) 2254 FGF9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:7215 Homo sapiens (human) 10198 MPHOSPH9 inference by association of genotype from phenotype used in manual assertion
  • PMID:19879194
DOID:707 B-cell lymphoma HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21918980
DOID:0111731 familial episodic pain syndrome 3 HGNC:10583 Homo sapiens (human) 11280 SCN11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:4439 Homo sapiens (human) 2811 GP1BA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:10632 Homo sapiens (human) 6352 CCL5 inference by association of genotype from phenotype used in manual assertion
  • PMID:19335954
DOID:10584 retinitis pigmentosa HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18024811
  • PMID:9466990
DOID:0080000 muscular disease HGNC:6143 Homo sapiens (human) 3679 ITGA7 inference by association of genotype from phenotype used in manual assertion
  • PMID:9590299
DOID:0070257 congenital disorder of glycosylation type IIe HGNC:18622 Homo sapiens (human) 91949 COG7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1387 hypolipoproteinemia HGNC:600 Homo sapiens (human) 335 APOA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9931341
DOID:10283 prostate cancer HGNC:4910 Homo sapiens (human) 3091 HIF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:19106642
DOID:1793 pancreatic cancer HGNC:6140 Homo sapiens (human) 3676 ITGA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18772397
DOID:1205 allergic disease HGNC:5973 Homo sapiens (human) 3596 IL13 inference by association of genotype from phenotype used in manual assertion
  • PMID:11588017
DOID:0111385 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 HGNC:12666 Homo sapiens (human) 7415 VCP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12849 autistic disorder HGNC:9957 Homo sapiens (human) 5649 RELN inference by association of genotype from phenotype used in manual assertion
  • PMID:11317216
  • PMID:20436377
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:20663564
DOID:9352 type 2 diabetes mellitus HGNC:18590 Homo sapiens (human) 80339 PNPLA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:31377187
DOID:8432 polycythemia HGNC:4827 Homo sapiens (human) 3043 HBB inference by association of genotype from phenotype used in manual assertion
  • PMID:4719677
DOID:0112300 spondylometaphyseal dysplasia with cone-rod dystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060227 Adams-Oliver syndrome HGNC:29216 Homo sapiens (human) 57514 ARHGAP31 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8869 neuromyelitis optica HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21748712
  • PMID:27049564
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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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