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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 70601 - 70625 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050574 L-2-hydroxyglutaric aciduria HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • MGI:6194238
  • PMID:24573090
  • RGD:7240710
DOID:0050574 L-2-hydroxyglutaric aciduria FB:FBgn0032729 Drosophila melanogaster (fruit fly) 35156 L2HGDH
  • MGI:6194238
DOID:0050573 2-hydroxyglutaric aciduria FB:FBgn0032729 Drosophila melanogaster (fruit fly) 35156 L2HGDH
  • MGI:6194238
DOID:0050573 2-hydroxyglutaric aciduria HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24894778
  • PMID:26208971
DOID:0050572 cone-rod dystrophy FB:FBgn0259685 Drosophila melanogaster (fruit fly) 42896 crb
  • MGI:6194238
DOID:0050572 cone-rod dystrophy HGNC:21555 Homo sapiens (human) 346007 EYS
  • MGI:6194238
DOID:0050572 cone-rod dystrophy ZFIN:ZDB-GENE-130530-959 Danio rerio (zebrafish) 557044 eys
  • PMID:28378834
DOID:0050572 cone-rod dystrophy MGI:2136343 Mus musculus (house mouse) 170788 Crb1
  • MGI:6194238
DOID:0050572 cone-rod dystrophy FB:FBgn0031414 Drosophila melanogaster (fruit fly) 3771890 eys
  • MGI:6194238
DOID:0050572 cone-rod dystrophy HGNC:2343 Homo sapiens (human) 23418 CRB1
  • PMID:23767994
DOID:0050571 congenital disorder of glycosylation type II MGI:1914217 Mus musculus (house mouse) 66967 Edem3
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II Xenbase:XB-GENE-17346352 Xenopus laevis (African clawed frog) 108716128 galnt2.L
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II RGD:1310692 Rattus norvegicus (Norway rat) 292090 Galnt2
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II MGI:1928483 Mus musculus (house mouse) 56389 Stx5a
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II FB:FBgn0265351 Drosophila melanogaster (fruit fly) 40981 nac CG9620
  • PMID:16344471
DOID:0050571 congenital disorder of glycosylation type II HGNC:18619 Homo sapiens (human) 83548 COG3
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:16787 Homo sapiens (human) 80267 EDEM3
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II FB:FBgn0031530 Drosophila melanogaster (fruit fly) 33556 Pgant2 CG3254
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II WB:WBGene00013919 Caenorhabditis elegans 181210 ZC506.1
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:20197 Homo sapiens (human) 55343 SLC35C1
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II Xenbase:XB-GENE-5811512 Xenopus laevis (African clawed frog) 443907 edem3.L
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II Xenbase:XB-GENE-980077 Xenopus tropicalis (tropical clawed frog) 100488284 galnt2
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II Xenbase:XB-GENE-6486521 Xenopus laevis (African clawed frog) 101027298 galnt2.S
  • 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: December 9, 2024