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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 8001 - 8025 of 12216 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2861 congenital nonspherocytic hemolytic anemia FB:FBgn0004057 Drosophila melanogaster (fruit fly) 32974 Zw
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:7655856
DOID:2861 congenital nonspherocytic hemolytic anemia SGD:S000000400 Saccharomyces cerevisiae S288C 852495 PGI1
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766
DOID:2861 congenital nonspherocytic hemolytic anemia SGD:S000005185 Saccharomyces cerevisiae S288C 855480 ZWF1
  • MGI:6194238
  • PMID:14757426
DOID:2861 congenital nonspherocytic hemolytic anemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
  • PMID:8417789
DOID:0081337 congenital myopathy HGNC:9639 Homo sapiens (human) 9200 HACD1
  • RGD:7240710
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN
  • MGI:6194238
  • RGD:7240710
DOID:0110671 congenital myasthenic syndrome 6 HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
  • PMID:11172068
  • RGD:7240710
DOID:0110658 congenital myasthenic syndrome 15 SGD:S000000274 Saccharomyces cerevisiae S288C 852362 ALG14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 WB:WBGene00019725 Caenorhabditis elegans 187398 algn-14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 ZFIN:ZDB-GENE-041010-195 Danio rerio (zebrafish) 450072 alg14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 HGNC:28287 Homo sapiens (human) 199857 ALG14
  • RGD:7240710
DOID:0110658 congenital myasthenic syndrome 15 Xenbase:XB-GENE-6487844 Xenopus laevis (African clawed frog) 108714370 alg14.L
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 FB:FBgn0030645 Drosophila melanogaster (fruit fly) 32479 Alg14 CG6308
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 Xenbase:XB-GENE-17331641 Xenopus laevis (African clawed frog) 108715652 alg14.S
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 Xenbase:XB-GENE-983948 Xenopus tropicalis (tropical clawed frog) 100379745 alg14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 RGD:1312003 Rattus norvegicus (Norway rat) 362031 Alg14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 MGI:1914039 Mus musculus (house mouse) 66789 Alg14
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 MGI:1914731 Mus musculus (house mouse) 56737 Alg2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 RGD:1309940 Rattus norvegicus (Norway rat) 313231 Alg2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 WB:WBGene00017282 Caenorhabditis elegans 173912 algn-2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 FB:FBgn0035401 Drosophila melanogaster (fruit fly) 38374 Alg2 CG1291
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 Xenbase:XB-GENE-494533 Xenopus laevis (African clawed frog) 446622 alg2.L
  • 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: August 19, 2024