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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 9976 - 10000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:10652 Alzheimer's disease HGNC:1318 Homo sapiens (human) 718 C3 inference by association of genotype from phenotype used in manual assertion
  • PMID:22300950
DOID:5327 retinal detachment RGD:2559 Rattus norvegicus (Norway rat) 24335 Epo direct assay evidence used in manual assertion
  • PMID:22020175
DOID:12361 Graves' disease HGNC:12373 Homo sapiens (human) 7253 TSHR direct assay evidence used in manual assertion
  • PMID:24518168
  • PMID:7828357
DOID:1441 autosomal dominant cerebellar ataxia HGNC:1349 Homo sapiens (human) 219285 SAMD9L inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2986 IgA glomerulonephritis HGNC:8784 Homo sapiens (human) 8654 PDE5A inference by association of genotype from phenotype used in manual assertion
  • PMID:20563733
DOID:3393 coronary artery disease HGNC:3662 Homo sapiens (human) 2244 FGB inference by association of genotype from phenotype used in manual assertion
  • PMID:8565160
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A inference by association of genotype from phenotype used in manual assertion
  • PMID:23269818
DOID:10763 hypertension RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2 mutant phenotype evidence used in manual assertion
  • PMID:19680135
  • PMID:21040717
DOID:11716 prediabetes syndrome HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18096169
DOID:8283 peritonitis HGNC:3823 Homo sapiens (human) 27086 FOXP1 mutant phenotype evidence used in manual assertion
  • PMID:18799727
DOID:10629 microphthalmia HGNC:6697 Homo sapiens (human) 4041 LRP5 inference by association of genotype from phenotype used in manual assertion
  • PMID:28111184
DOID:3393 coronary artery disease HGNC:10718 Homo sapiens (human) 6401 SELE inference by association of genotype from phenotype used in manual assertion
  • PMID:17578587
DOID:9074 systemic lupus erythematosus HGNC:1318 Homo sapiens (human) 718 C3 direct assay evidence used in manual assertion
  • PMID:7510492
DOID:5082 liver cirrhosis HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:19456900
DOID:0112313 brain small vessel disease HGNC:3661 Homo sapiens (human) 2243 FGA inference by association of genotype from phenotype used in manual assertion
  • PMID:17951283
DOID:8619 recurrent hypersomnia HGNC:1938 Homo sapiens (human) 1120 CHKB inference by association of genotype from phenotype used in manual assertion
  • PMID:19404393
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12200370
DOID:9849 Meniere's disease HGNC:5232 Homo sapiens (human) 3303 HSPA1A inference by association of genotype from phenotype used in manual assertion
  • PMID:19241595
DOID:0111473 combined oxidative phosphorylation deficiency 5 HGNC:14508 Homo sapiens (human) 56945 MRPS22 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6000 congestive heart failure MGI:1100846 Mus musculus (house mouse) 19014 Med1 author statement supported by traceable reference
  • PMID:27548259
DOID:10808 gastric ulcer RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad direct assay evidence used in manual assertion
  • PMID:24378970
DOID:0070070 autosomal dominant intellectual developmental disorder 40 HGNC:20311 Homo sapiens (human) 283489 CHAMP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1307 dementia HGNC:6700 Homo sapiens (human) 7804 LRP8 inference by association of genotype from phenotype used in manual assertion
  • PMID:17614163
DOID:0081453 Dent disease 1 HGNC:2023 Homo sapiens (human) 1184 CLCN5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060692 platelet-type bleeding disorder 8 MGI:1918089 Mus musculus (house mouse) 70839 P2ry12 author statement supported by traceable reference
  • PMID:11413167
  • PMID:12897207

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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