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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 201 - 225 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050548 hereditary sensory neuropathy HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
DOID:0050557 congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
DOID:0050557 congenital muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
DOID:0050558 Ullrich congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • RGD:7240710
DOID:0050558 Ullrich congenital muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:28043812
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy Xenbase:XB-GENE-971788 Xenopus tropicalis (tropical clawed frog) 100124956 fktn
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:3622 Homo sapiens (human) 2218 FKTN
  • MGI:6194238
  • PMID:11445638
  • RGD:7240710
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:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1007367 Xenopus tropicalis (tropical clawed frog) 100170600 b4gat1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-944435 Xenopus tropicalis (tropical clawed frog) 448433 pomt1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1006906 Xenopus tropicalis (tropical clawed frog) 100490100 pomt2
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome HGNC:15685 Homo sapiens (human) 11041 B4GAT1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-17338998 Xenopus laevis (African clawed frog) 108698503 fkrp.L
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome ZFIN:ZDB-GENE-070410-96 Danio rerio (zebrafish) 100006345 fktn
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-971793 Xenopus laevis (African clawed frog) 495324 fktn.S
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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


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