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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 11676 - 11700 of 12216 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050559 Fukuyama congenital muscular dystrophy MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
  • PMID:15837576
  • PMID:19017726
  • PMID:22922256
DOID:0050559 Fukuyama congenital muscular dystrophy ZFIN:ZDB-GENE-070410-96 Danio rerio (zebrafish) 100006345 fktn
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy Xenbase:XB-GENE-971793 Xenopus laevis (African clawed frog) 495324 fktn.S
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00011554 Caenorhabditis elegans 188207 T07A5.1
  • MGI:6194238
DOID:0090001 Fraser syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:0050464 Farber lipogranulomatosis HGNC:735 Homo sapiens (human) 427 ASAH1
  • MGI:6194238
  • RGD:7240710
DOID:1062 Fanconi syndrome HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • RGD:7240710
DOID:1062 Fanconi syndrome HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
DOID:0080759 Fanconi renotubular syndrome 3 HGNC:3247 Homo sapiens (human) 1962 EHHADH
  • RGD:7240710
DOID:13636 Fanconi anemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:13636 Fanconi anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:24021704
  • PMID:8438880
DOID:13636 Fanconi anemia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:14499 Fabry disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
  • PMID:2539398
  • RGD:7240710
DOID:14499 Fabry disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20941593
DOID:14499 Fabry disease RGD:1306025 Rattus norvegicus (Norway rat) 315165 Naga
  • MGI:6194238
DOID:14499 Fabry disease MGI:1261422 Mus musculus (house mouse) 17939 Naga
  • MGI:6194238
DOID:14499 Fabry disease HGNC:7631 Homo sapiens (human) 4668 NAGA
  • MGI:6194238
DOID:2938 Epstein-Barr virus infectious disease HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:19339266
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 WB:WBGene00005020 Caenorhabditis elegans 173635 sqv-2
  • 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 FB:FBgn0033315 Drosophila melanogaster (fruit fly) 35848 beta3GalTII CG8734
  • MGI:6194238

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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