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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 2251 - 2275 of 12216 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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:0110474 autosomal recessive nonsyndromic deafness 18B HGNC:8516 Homo sapiens (human) 340990 OTOG
  • MGI:6194238
  • RGD:7240710
DOID:0110474 autosomal recessive nonsyndromic deafness 18B MGI:1202064 Mus musculus (house mouse) 18419 Otog
  • MGI:6194238
  • PMID:26636018
DOID:0110479 autosomal recessive nonsyndromic deafness 21 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • RGD:7240710
DOID:0110480 autosomal recessive nonsyndromic deafness 22 HGNC:16378 Homo sapiens (human) 146183 OTOA
  • MGI:6194238
  • RGD:7240710
DOID:0110515 autosomal recessive nonsyndromic deafness 63 HGNC:25033 Homo sapiens (human) 220074 LRTOMT
  • MGI:6194238
  • RGD:7240710
DOID:0110530 autosomal recessive nonsyndromic deafness 84B MGI:3647600 Mus musculus (house mouse) 628870 Otogl
  • MGI:6194238
DOID:0110942 autosomal recessive osteopetrosis 1 HGNC:18481 Homo sapiens (human) 23545 ATP6V0A2
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease RGD:620916 Rattus norvegicus (Norway rat) 170911 Pik3ca
  • PMID:24498161
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:20575 Homo sapiens (human) 284541 CYP4A22
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:0110861 autosomal recessive polycystic kidney disease RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:24498161
DOID:0110861 autosomal recessive polycystic kidney disease MGI:87986 Mus musculus (house mouse) 11651 Akt1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
DOID:4492 avian influenza HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18613795
DOID:14227 azoospermia HGNC:20779 Homo sapiens (human) 64579 NDST4
  • 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