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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 11701 - 11725 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050663 Bethlem myopathy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • PMID:8782832
  • RGD:7240710
DOID:0050663 Bethlem myopathy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:14625552
  • PMID:9817932
DOID:0050657 Bannayan-Riley-Ruvalcaba syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • RGD:7240710
DOID:0050650 familial atrial fibrillation MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • MGI:6194238
DOID:0050650 familial atrial fibrillation RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • RGD:7240710
DOID:0050647 Arts syndrome HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • RGD:7240710
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10
  • RGD:7240710
DOID:0050644 arterial calcification of infancy MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:23798568
  • PMID:25479107
DOID:0050644 arterial calcification of infancy HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:12881724
  • PMID:15940697
  • PMID:20016754
  • RGD:7240710
DOID:0050644 arterial calcification of infancy RGD:628825 Rattus norvegicus (Norway rat) 85496 Enpp1
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18205195
DOID:0050636 familial visceral amyloidosis HGNC:6740 Homo sapiens (human) 4069 LYZ
  • RGD:7240710
DOID:0050636 familial visceral amyloidosis FB:FBgn0004430 Drosophila melanogaster (fruit fly) 38130 LysS CG1165
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004428 Drosophila melanogaster (fruit fly) 38128 LysE CG1180
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004429 Drosophila melanogaster (fruit fly) 38129 LysP CG9116
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004431 Drosophila melanogaster (fruit fly) 38122 LysX CG9120
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004425 Drosophila melanogaster (fruit fly) 38125 LysB CG1179
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis MGI:96902 Mus musculus (house mouse) 17110 Lyz1
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis MGI:96897 Mus musculus (house mouse) 17105 Lyz2
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004427 Drosophila melanogaster (fruit fly) 38127 LysD CG9118
  • MGI:6194238
DOID:0050635 alternating hemiplegia of childhood HGNC:800 Homo sapiens (human) 477 ATP1A2
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024