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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 July 29, 2024
Displaying entries 2476 - 2500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:162 cancer SGD:S000001085 Saccharomyces cerevisiae S288C 856439 DOG2
  • PMID:31481524
DOID:0080565 congenital disorder of glycosylation Im HGNC:23406 Homo sapiens (human) 22845 DOLK
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:23406 Homo sapiens (human) 22845 DOLK
  • MGI:6194238
DOID:0110676 congenital myasthenic syndrome 13 HGNC:2995 Homo sapiens (human) 1798 DPAGT1
  • RGD:7240710
DOID:0080562 congenital disorder of glycosylation Ij HGNC:2995 Homo sapiens (human) 1798 DPAGT1
  • MGI:6194238
  • RGD:7240710
DOID:687 hepatoblastoma HGNC:3002 Homo sapiens (human) 1800 DPEP1
  • PMID:31541079
DOID:0050570 congenital disorder of glycosylation type I HGNC:3005 Homo sapiens (human) 8813 DPM1
  • MGI:6194238
DOID:0080557 congenital disorder of glycosylation Ie HGNC:3005 Homo sapiens (human) 8813 DPM1
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I SGD:S000006387 Saccharomyces cerevisiae S288C 856313 DPM1
  • MGI:6194238
DOID:0080557 congenital disorder of glycosylation Ie SGD:S000006387 Saccharomyces cerevisiae S288C 856313 DPM1
  • MGI:6194238
DOID:1612 breast cancer SGD:S000006387 Saccharomyces cerevisiae S288C 856313 DPM1
  • PMID:30637701
DOID:0080571 congenital disorder of glycosylation Iu HGNC:3006 Homo sapiens (human) 8818 DPM2
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:3007 Homo sapiens (human) 54344 DPM3
  • RGD:7240710
DOID:0112376 muscular dystrophy-dystroglycanopathy type B15 HGNC:3007 Homo sapiens (human) 54344 DPM3
  • RGD:7240710
DOID:0111156 spermatogenic failure 9 HGNC:19414 Homo sapiens (human) 283417 DPY19L2
  • RGD:7240710
DOID:0080737 Ehlers-Danlos syndrome musculocontractural type 2 HGNC:21144 Homo sapiens (human) 29940 DSE
  • RGD:7240710
DOID:0111258 pentosuria MGI:1915130 Mus musculus (house mouse) 67880 Dcxr
  • MGI:6194238
DOID:0111258 pentosuria RGD:620031 Rattus norvegicus (Norway rat) 171408 Dcxr
  • MGI:6194238
DOID:5844 myocardial infarction FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:9884 muscular dystrophy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • PMID:17215867
  • PMID:21256839
  • PMID:21943192
  • PMID:23107381
  • PMID:33620318
  • PMID:36594281
DOID:12930 dilated cardiomyopathy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0110293 autosomal recessive limb-girdle muscular dystrophy type 2P FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:3429 inclusion body myositis FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:767 muscular atrophy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:12236 primary biliary cholangitis FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238

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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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