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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 1776 - 1800 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080552 congenital disorder of glycosylation Ia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19207313
DOID:0080552 congenital disorder of glycosylation Ia MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia MGI:1859214 Mus musculus (house mouse) 54128 Pmm2
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia MGI:1353418 Mus musculus (house mouse) 29858 Pmm1
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53
  • MGI:6194238
  • PMID:30530630
  • PMID:36214454
DOID:0080554 congenital disorder of glycosylation Ib WB:WBGene00014013 Caenorhabditis elegans 176388 ZK632.4
  • MGI:6194238
DOID:0080554 congenital disorder of glycosylation Ib RGD:3107 Rattus norvegicus (Norway rat) 300741 Mpi
  • MGI:6194238
DOID:0080554 congenital disorder of glycosylation Ib HGNC:7216 Homo sapiens (human) 4351 MPI
  • RGD:7240710
DOID:0080554 congenital disorder of glycosylation Ib SGD:S000000805 Saccharomyces cerevisiae S288C 856720 PMI40
  • MGI:6194238
DOID:0080554 congenital disorder of glycosylation Ib MGI:97075 Mus musculus (house mouse) 110119 Mpi
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic MGI:2444031 Mus musculus (house mouse) 320438 Alg6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic HGNC:23157 Homo sapiens (human) 29929 ALG6
  • RGD:7240710
DOID:0080555 congenital disorder of glycosylation Ic FB:FBgn0032234 Drosophila melanogaster (fruit fly) 34409 gny CG5091
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic RGD:1308815 Rattus norvegicus (Norway rat) 362547 Alg6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic Xenbase:XB-GENE-17342009 Xenopus laevis (African clawed frog) 446684 alg6.S
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic Xenbase:XB-GENE-998187 Xenopus tropicalis (tropical clawed frog) 496948 alg6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic WB:WBGene00007435 Caenorhabditis elegans 182392 algn-6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic Xenbase:XB-GENE-998193 Xenopus laevis (African clawed frog) 100049135 alg6.L
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic ZFIN:ZDB-GENE-040808-45 Danio rerio (zebrafish) 445327 alg6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic SGD:S000005528 Saccharomyces cerevisiae S288C 854163 ALG6
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id Xenbase:XB-GENE-986281 Xenopus laevis (African clawed frog) 100037243 alg3.S
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id RGD:1306004 Rattus norvegicus (Norway rat) 287983 Alg3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3
  • MGI:6194238
  • PMID:23038983

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Supported by JST NBDC Grant Number JPMJND2204

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


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