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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 2726 - 2750 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0080959 arrhythmogenic right ventricular dysplasia 14 HGNC:1759 Homo sapiens (human) 1000 CDH2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110074 arrhythmogenic right ventricular dysplasia 5 HGNC:28472 Homo sapiens (human) 79188 TMEM43 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110076 arrhythmogenic right ventricular dysplasia 8 HGNC:3052 Homo sapiens (human) 1832 DSP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110077 arrhythmogenic right ventricular dysplasia 9 HGNC:9024 Homo sapiens (human) 5318 PKP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050644 arterial calcification of infancy HGNC:57 Homo sapiens (human) 368 ABCC6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050644 arterial calcification of infancy MGI:97370 Mus musculus (house mouse) 18605 Enpp1 author statement supported by traceable reference
  • PMID:23798568
  • PMID:25479107
DOID:0050644 arterial calcification of infancy HGNC:3356 Homo sapiens (human) 5167 ENPP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12881724
  • PMID:15940697
  • PMID:20016754
  • RGD:7240710
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050645 arterial tortuosity syndrome HGNC:3219 Homo sapiens (human) 30008 EFEMP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22943132
DOID:2349 arteriosclerosis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16890863
DOID:2349 arteriosclerosis HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11941274
DOID:2349 arteriosclerosis HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11978651
DOID:2349 arteriosclerosis HGNC:603 Homo sapiens (human) 338 APOB mutant phenotype evidence used in manual assertion
  • PMID:19260948
DOID:2349 arteriosclerosis HGNC:7166 Homo sapiens (human) 4313 MMP2 direct assay evidence used in manual assertion
  • PMID:12526080
DOID:2349 arteriosclerosis HGNC:9204 Homo sapiens (human) 5444 PON1 mutant phenotype evidence used in manual assertion
  • PMID:16627808
DOID:2349 arteriosclerosis HGNC:405 Homo sapiens (human) 218 ALDH3A1 direct assay evidence used in manual assertion
  • PMID:3949078
DOID:2349 arteriosclerosis RGD:1309438 Rattus norvegicus (Norway rat) 313121 Map3k7 mutant phenotype evidence used in manual assertion
  • PMID:35078016
DOID:2349 arteriosclerosis HGNC:7155 Homo sapiens (human) 4312 MMP1 direct assay evidence used in manual assertion
  • PMID:15621056
DOID:2349 arteriosclerosis RGD:3371 Rattus norvegicus (Norway rat) 25664 Pparg direct assay evidence used in manual assertion
  • PMID:15967870
DOID:2349 arteriosclerosis HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15823277
DOID:2349 arteriosclerosis HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • PMID:17664290
DOID:2349 arteriosclerosis HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11099417
DOID:2349 arteriosclerosis HGNC:7159 Homo sapiens (human) 4322 MMP13 inference by association of genotype from phenotype used in manual assertion
  • PMID:12392760
DOID:2349 arteriosclerosis HGNC:6547 Homo sapiens (human) 3949 LDLR direct assay evidence used in manual assertion
  • PMID:12969990
DOID:2349 arteriosclerosis HGNC:5261 Homo sapiens (human) 3329 HSPD1 direct assay evidence used in manual assertion
  • PMID:17070529
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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: December 8, 2025