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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 13076 - 13100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:3320 Tay-Sachs disease MGI:96073 Mus musculus (house mouse) 15211 Hexa author statement supported by traceable reference
  • PMID:7937929
  • PMID:8747922
  • PMID:8789434
DOID:10763 hypertension RGD:69051 Rattus norvegicus (Norway rat) 59086 Tgfb1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11682445
DOID:0070140 autosomal recessive cutis laxa type IIC HGNC:857 Homo sapiens (human) 529 ATP6V1E1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9743 diabetic neuropathy HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • PMID:19608431
DOID:0111945 immunodeficiency 31A HGNC:11362 Homo sapiens (human) 6772 STAT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:32653938
DOID:9268 glycine encephalopathy HGNC:473 Homo sapiens (human) 275 AMT inference by association of genotype from phenotype used in manual assertion
  • PMID:8005589
  • PMID:9600239
  • PMID:9621520
DOID:1574 alcohol use disorder HGNC:8154 Homo sapiens (human) 4986 OPRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31004399
  • PMID:37177778
DOID:5082 liver cirrhosis HGNC:5423 Homo sapiens (human) 3440 IFNA2 direct assay evidence used in manual assertion
  • PMID:7646558
DOID:14330 Parkinson's disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8872868
DOID:8893 psoriasis HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:12709814
DOID:4906 small intestine adenocarcinoma HGNC:6840 Homo sapiens (human) 5604 MAP2K1 mutant phenotype evidence used in manual assertion
  • PMID:19014680
DOID:12714 Ellis-Van Creveld syndrome HGNC:19747 Homo sapiens (human) 132884 EVC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12571802
  • RGD:7240710
DOID:1909 melanoma HGNC:1516 Homo sapiens (human) 847 CAT direct assay evidence used in manual assertion
  • PMID:9758419
DOID:0050700 cardiomyopathy HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:25699607
DOID:0111981 immunodeficiency 43 HGNC:914 Homo sapiens (human) 567 B2M inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:850 lung disease HGNC:10803 Homo sapiens (human) 6441 SFTPD direct assay evidence used in manual assertion
  • PMID:17974096
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:2666 Homo sapiens (human) 1605 DAG1 direct assay evidence used in manual assertion
  • PMID:15833425
DOID:0070389 developmental and epileptic encephalopathy 103 HGNC:6234 Homo sapiens (human) 3747 KCNC2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12930 dilated cardiomyopathy MGI:106658 Mus musculus (house mouse) 20807 Srf author statement supported by traceable reference
  • PMID:16260633
DOID:0081265 intellectual developmental disorder with abnormal behavior, microcephaly, and short stature HGNC:26033 Homo sapiens (human) 54517 PUS7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12361 Graves' disease HGNC:12373 Homo sapiens (human) 7253 TSHR mutant phenotype evidence used in manual assertion
  • PMID:9528975
DOID:9744 type 1 diabetes mellitus HGNC:1121 Homo sapiens (human) 685 BTC inference by association of genotype from phenotype used in manual assertion
  • PMID:16683131
DOID:12720 cerebral atherosclerosis HGNC:4814 Homo sapiens (human) 8997 KALRN inference by association of genotype from phenotype used in manual assertion
  • PMID:30232674
DOID:9352 type 2 diabetes mellitus HGNC:4498 Homo sapiens (human) 2864 FFAR1 direct assay evidence used in manual assertion
  • PMID:19758793

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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