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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 6001 - 6025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:5082 liver cirrhosis HGNC:3691 Homo sapiens (human) 2264 FGFR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:25860955
DOID:6000 congestive heart failure HGNC:4396 Homo sapiens (human) 2782 GNB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:33779075
DOID:0112382 muscular dystrophy-dystroglycanopathy type C8 HGNC:25902 Homo sapiens (human) 84892 POMGNT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:13919 Homo sapiens (human) 7917 BAG6 inference by association of genotype from phenotype used in manual assertion
  • PMID:25231575
DOID:1883 hepatitis C HGNC:5432 Homo sapiens (human) 3454 IFNAR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21756311
DOID:0080978 arthrogryposis multiplex congenita-1 HGNC:18712 Homo sapiens (human) 163175 LGI4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9296 cleft lip HGNC:9202 Homo sapiens (human) 10585 POMT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18640039
DOID:0050211 swine influenza HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • PMID:29867955
DOID:0110961 atypical Gaucher's disease due to saposin c deficiency HGNC:9498 Homo sapiens (human) 5660 PSAP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2842 Jervell-Lange Nielsen syndrome HGNC:6240 Homo sapiens (human) 3753 KCNE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16987820
  • PMID:9445165
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:11891 Homo sapiens (human) 7123 CLEC3B inference by association of genotype from phenotype used in manual assertion
  • PMID:15334463
DOID:0111758 Y-linked deafness 2 HGNC:18502 Homo sapiens (human) 90665 TBL1Y inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11719 oculopharyngeal muscular dystrophy HGNC:8565 Homo sapiens (human) 8106 PABPN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:26890368
DOID:3083 chronic obstructive pulmonary disease HGNC:4583 Homo sapiens (human) 2901 GRIK5 inference by association of genotype from phenotype used in manual assertion
  • PMID:28900078
DOID:11105 fundus albipunctatus HGNC:9942 Homo sapiens (human) 5961 PRPH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8485575
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:7029 Homo sapiens (human) 4233 MET inference by association of genotype from phenotype used in manual assertion
  • PMID:9140397
DOID:0070508 metabolic dysfunction and alcohol associated liver disease HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:9214463
DOID:0111907 thrombophilia due to thrombin defect HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:8513325
DOID:1682 congenital heart disease HGNC:4214 Homo sapiens (human) 2657 GDF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23076529
  • PMID:26656983
DOID:13378 Kawasaki disease HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17672867
DOID:9074 systemic lupus erythematosus HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12651073
  • PMID:18552411
  • PMID:21658414
DOID:37 skin disease HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:21357384
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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