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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 2526 - 2550 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0060212 amyotrophic lateral sclerosis type 21 HGNC:6912 Homo sapiens (human) 9782 MATR3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:30651232
DOID:0111589 COACH syndrome HGNC:28396 Homo sapiens (human) 91147 TMEM67 inference by association of genotype from phenotype used in manual assertion
  • PMID:19058225
  • PMID:19574260
DOID:0110265 cataract 31 multiple types HGNC:16171 Homo sapiens (human) 128866 CHMP4B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9252 amino acid metabolic disorder HGNC:8653 Homo sapiens (human) 5095 PCCA inference by association of genotype from phenotype used in manual assertion
  • PMID:9385377
DOID:11054 urinary bladder cancer HGNC:2623 Homo sapiens (human) 1559 CYP2C9 inference by association of genotype from phenotype used in manual assertion
  • PMID:16985032
DOID:0110548 autosomal dominant nonsyndromic deafness 17 HGNC:7579 Homo sapiens (human) 4627 MYH9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:12975417
DOID:1380 endometrial cancer HGNC:583 Homo sapiens (human) 324 APC inference by association of genotype from phenotype used in manual assertion
  • PMID:29876005
DOID:1574 alcohol use disorder FB:FBgn0027932 Drosophila melanogaster (fruit fly) 34170 Akap200 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:29444420
DOID:0060041 autism spectrum disorder MGI:1917780 Mus musculus (house mouse) 70530 Lrfn2 author statement supported by traceable reference
  • PMID:28604739
DOID:11476 osteoporosis MGI:1100089 Mus musculus (house mouse) 21943 Tnfsf11 author statement supported by traceable reference
  • PMID:12434161
DOID:0111464 combined oxidative phosphorylation deficiency 35 HGNC:20286 Homo sapiens (human) 54802 TRIT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060654 lethal congenital contracture syndrome 4 HGNC:7549 Homo sapiens (human) 4604 MYBPC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12800 mucopolysaccharidosis VI RGD:2158 Rattus norvegicus (Norway rat) 25227 Arsb inference by association of genotype from phenotype used in manual assertion
  • PMID:21887218
  • PMID:8575749
DOID:7148 rheumatoid arthritis HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:25311255
DOID:8893 psoriasis HGNC:11364 Homo sapiens (human) 6774 STAT3 mutant phenotype evidence used in manual assertion
  • PMID:20811392
DOID:3526 cerebral infarction HGNC:9603 Homo sapiens (human) 5740 PTGIS inference by association of genotype from phenotype used in manual assertion
  • PMID:11130769
  • PMID:28108096
  • PMID:28478978
DOID:9884 muscular dystrophy WB:WBGene00002248 Caenorhabditis elegans 172952 lam-3 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:12783803
DOID:0050570 congenital disorder of glycosylation type I SGD:S000005593 Saccharomyces cerevisiae S288C 854233 ALG8 sequence similarity evidence used in manual assertion
  • PMID:15235028
DOID:6000 congestive heart failure HGNC:10483 Homo sapiens (human) 6261 RYR1 direct assay evidence used in manual assertion
  • PMID:29593014
DOID:11678 onchocerciasis HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22117902
DOID:684 hepatocellular carcinoma HGNC:3432 Homo sapiens (human) 2066 ERBB4 inference by association of genotype from phenotype used in manual assertion
  • PMID:22294845
DOID:2377 multiple sclerosis HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10082437
  • PMID:19740340
DOID:0080821 exercise-induced bronchoconstriction HGNC:11526 Homo sapiens (human) 6869 TACR1 mutant phenotype evidence used in manual assertion
  • PMID:8630576
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International Collaboration

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: December 8, 2025