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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 October 9, 2024
Displaying entries 68876 - 68900 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-6488390 Xenopus laevis (African clawed frog) 108696563 b3galt6.L
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 ZFIN:ZDB-GENE-101104-13 Danio rerio (zebrafish) 572324 b3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-17345196 Xenopus laevis (African clawed frog) 108697636 b3galt6.S
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 FB:FBgn0033315 Drosophila melanogaster (fruit fly) 35848 beta3GalTII CG8734
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 MGI:2152819 Mus musculus (house mouse) 117592 B3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:0050800 cerebral creatine deficiency syndrome 1 RGD:619711 Rattus norvegicus (Norway rat) 50690 Slc6a8
  • MGI:6194238
DOID:0050800 cerebral creatine deficiency syndrome 1 HGNC:11055 Homo sapiens (human) 6535 SLC6A8
  • MGI:6194238
  • RGD:7240710
DOID:0050800 cerebral creatine deficiency syndrome 1 MGI:2147834 Mus musculus (house mouse) 102857 Slc6a8
  • MGI:6194238
  • PMID:21249153
  • PMID:22751104
  • PMID:25485098
  • PMID:27466184
  • PMID:30013483
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency FB:FBgn0027572 Drosophila melanogaster (fruit fly) 37028 Acox1
  • MGI:6194238
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency SGD:S000003173 Saccharomyces cerevisiae S288C 852667 POX1
  • MGI:6194238
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
  • RGD:7240710
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency FB:FBgn0027572 Drosophila melanogaster (fruit fly) 37028 ACOX1
  • MGI:6194238
DOID:0050795 cone dystrophy HGNC:16262 Homo sapiens (human) 10413 YAP1
  • MGI:6194238
DOID:0050795 cone dystrophy MGI:103262 Mus musculus (house mouse) 22601 Yap1
  • PMID:32801350
DOID:0050794 multiple synostoses syndrome RGD:2610 Rattus norvegicus (Norway rat) 25444 Fgf9
  • MGI:6194238
DOID:0050794 multiple synostoses syndrome HGNC:3687 Homo sapiens (human) 2254 FGF9
  • MGI:6194238
DOID:0050794 multiple synostoses syndrome MGI:104723 Mus musculus (house mouse) 14180 Fgf9
  • PMID:28169396
DOID:0050794 multiple synostoses syndrome HGNC:4220 Homo sapiens (human) 8200 GDF5
  • MGI:6194238
DOID:0050794 multiple synostoses syndrome MGI:95688 Mus musculus (house mouse) 14563 Gdf5
  • MGI:5509308
DOID:0050793 short QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0050793 short QT syndrome WB:WBGene00006830 Caenorhabditis elegans 175527 unc-103
  • MGI:6194238
DOID:0050793 short QT syndrome RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
DOID:0050793 short QT syndrome WB:WBGene00019844 Caenorhabditis elegans 180943 abts-4
  • 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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Last updated: December 9, 2024