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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 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:12849 autistic disorder HGNC:4323 Homo sapiens (human) 2739 GLO1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17346350
DOID:2352 hemochromatosis HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:11389006
  • PMID:16793930
DOID:4947 cholangiocarcinoma HGNC:4392 Homo sapiens (human) 2778 GNAS inference by association of genotype from phenotype used in manual assertion
  • PMID:17356712
DOID:3910 lung adenocarcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1 direct assay evidence used in manual assertion
  • PMID:24736069
DOID:0070296 primary autosomal recessive microcephaly HGNC:8766 Homo sapiens (human) 10015 PDCD6IP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:6724 Homo sapiens (human) 4060 LUM direct assay evidence used in manual assertion
  • PMID:11890723
DOID:0080563 congenital disorder of glycosylation Ik SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1 genetic interaction evidence used in manual assertion
  • PMID:26931382
DOID:0110229 cataract 6 multiple types HGNC:3386 Homo sapiens (human) 1969 EPHA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4492 avian influenza HGNC:13557 Homo sapiens (human) 59272 ACE2 direct assay evidence used in manual assertion
  • PMID:24800825
DOID:9743 diabetic neuropathy RGD:620401 Rattus norvegicus (Norway rat) 81509 Bdkrb1 mutant phenotype evidence used in manual assertion
  • PMID:20587056
DOID:3910 lung adenocarcinoma HGNC:3432 Homo sapiens (human) 2066 ERBB4 inference by association of genotype from phenotype used in manual assertion
  • PMID:26824984
DOID:1612 breast cancer HGNC:18039 Homo sapiens (human) 10765 KDM5B mutant phenotype evidence used in manual assertion
  • PMID:21369698
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:628837 Rattus norvegicus (Norway rat) 81822 Actb direct assay evidence used in manual assertion
  • PMID:25282656
DOID:0110147 Bartter disease type 5 HGNC:16353 Homo sapiens (human) 10916 MAGED2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3525 middle cerebral artery infarction RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1 direct assay evidence used in manual assertion
  • PMID:35218623
DOID:0060300 complement component 7 deficiency HGNC:1346 Homo sapiens (human) 730 C7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9452 steatotic liver disease RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck direct assay evidence used in manual assertion
  • PMID:22925001
DOID:1612 breast cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12631398
DOID:9952 acute lymphoblastic leukemia HGNC:6407 Homo sapiens (human) 3845 KRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:17910045
  • PMID:25917266
DOID:0050861 colorectal adenocarcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21926398
DOID:13481 thanatophoric dysplasia MGI:96257 Mus musculus (house mouse) 15530 Hspg2 author statement supported by traceable reference
  • PMID:10545953
DOID:684 hepatocellular carcinoma HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:24997628
DOID:10763 hypertension RGD:3369 Rattus norvegicus (Norway rat) 25747 Ppara mutant phenotype evidence used in manual assertion
  • PMID:15967866
DOID:0081109 keratosis palmoplantaris striata 2 HGNC:3052 Homo sapiens (human) 1832 DSP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:7646 Homo sapiens (human) 10 NAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20297661
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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: April 7, 2025