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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 9626 - 9650 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111069 congenital bile acid synthesis defect 2 SGD:S000002776 Saccharomyces cerevisiae S288C 851974 YPR1
  • MGI:6194238
DOID:0111068 congenital bile acid synthesis defect 4 HGNC:451 Homo sapiens (human) 23600 AMACR
  • RGD:7240710
DOID:0111067 congenital bile acid synthesis defect 6 HGNC:120 Homo sapiens (human) 8309 ACOX2
  • RGD:7240710
DOID:0111063 hyperphosphatemic familial tumoral calcinosis HGNC:4125 Homo sapiens (human) 2591 GALNT3
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis FB:FBgn0034025 Drosophila melanogaster (fruit fly) 36717 Pgant1 CG8182
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis RGD:1306443 Rattus norvegicus (Norway rat) 366061 Galnt3
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis Xenbase:XB-GENE-954414 Xenopus tropicalis (tropical clawed frog) 100488466 galnt3
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis FB:FBgn0027558 Drosophila melanogaster (fruit fly) 35627 Pgant3 CG4445
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis ZFIN:ZDB-GENE-120313-1 Danio rerio (zebrafish) 100331984 galnt3
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis MGI:1101771 Mus musculus (house mouse) 16591 Kl
  • PMID:25860694
DOID:0111063 hyperphosphatemic familial tumoral calcinosis MGI:894695 Mus musculus (house mouse) 14425 Galnt3
  • PMID:19213845
  • PMID:22912827
DOID:0111061 familial hypobetalipoproteinemia 2 HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • RGD:7240710
DOID:0111061 familial hypobetalipoproteinemia 2 MGI:1353627 Mus musculus (house mouse) 30924 Angptl3
  • MGI:6194238
DOID:0111043 glycogen storage disease IXc HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • RGD:7240710
DOID:0111043 glycogen storage disease IXc MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:0111043 glycogen storage disease IXc RGD:620024 Rattus norvegicus (Norway rat) 140671 Phkg2
  • MGI:6194238
DOID:0111042 glycogen storage disease IXa WB:WBGene00015754 Caenorhabditis elegans 176149 C14B9.8
  • MGI:6194238
DOID:0111042 glycogen storage disease IXa MGI:97577 Mus musculus (house mouse) 110094 Phka2
  • MGI:6194238
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:0111042 glycogen storage disease IXa FB:FBgn0030087 Drosophila melanogaster (fruit fly) 31839 CG7766
  • MGI:6194238
DOID:0111041 glycogen storage disease IXb MGI:97578 Mus musculus (house mouse) 102093 Phkb
  • MGI:6194238
  • PMID:36077341
DOID:0111041 glycogen storage disease IXb HGNC:8927 Homo sapiens (human) 5257 PHKB
  • MGI:6194238
  • RGD:7240710
DOID:0111040 glycogen storage disease IXd FB:FBgn0030087 Drosophila melanogaster (fruit fly) 31839 CG7766
  • 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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