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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 276 - 300 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050563 nonsyndromic deafness Xenbase:XB-GENE-976267 Xenopus tropicalis (tropical clawed frog) 548946 alg10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness WB:WBGene00007043 Caenorhabditis elegans 172855 algn-10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness SGD:S000003459 Saccharomyces cerevisiae S288C 853142 DIE2
  • MGI:6194238
DOID:0050563 nonsyndromic deafness FB:FBgn0052076 Drosophila melanogaster (fruit fly) 326193 Alg10 CG32076
  • MGI:6194238
DOID:0050563 nonsyndromic deafness RGD:708500 Rattus norvegicus (Norway rat) 245960 Alg10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness ZFIN:ZDB-GENE-110310-8 Danio rerio (zebrafish) 100331575 alg10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness MGI:2146159 Mus musculus (house mouse) 380959 Alg10b
  • PMID:24303013
DOID:0050564 autosomal dominant nonsyndromic deafness HGNC:8984 Homo sapiens (human) 5298 PI4KB
  • RGD:7240710
DOID:0050565 autosomal recessive nonsyndromic deafness MGI:1921050 Mus musculus (house mouse) 70551 Tmtc4
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness WB:WBGene00018175 Caenorhabditis elegans 185454 F38B6.6
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness RGD:1560183 Rattus norvegicus (Norway rat) 290501 Tmtc4
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness Xenbase:XB-GENE-6488174 Xenopus laevis (African clawed frog) 108708472 tmtc4.L
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness FB:FBgn0038324 Drosophila melanogaster (fruit fly) 41867 Tmtc4
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness HGNC:25904 Homo sapiens (human) 84899 TMTC4
  • RGD:7240710
DOID:0050565 autosomal recessive nonsyndromic deafness ZFIN:ZDB-GENE-070912-148 Danio rerio (zebrafish) 560605 tmtc4
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness Xenbase:XB-GENE-5771787 Xenopus tropicalis (tropical clawed frog) 100158586 tmtc4
  • MGI:6194238
DOID:0050567 orofacial cleft HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:27229527
  • PMID:28543373
DOID:0050567 orofacial cleft FB:FBgn0026597 Drosophila melanogaster (fruit fly) 43565 Axn
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:2384774 Mus musculus (house mouse) 208211 Alg1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I Xenbase:XB-GENE-6036140 Xenopus tropicalis (tropical clawed frog) 100497477 alg9
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:19358 Homo sapiens (human) 79087 ALG12
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:3007 Homo sapiens (human) 54344 DPM3
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000005313 Saccharomyces cerevisiae S288C 855764 ALG12
  • PMID:12217961

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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