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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 7401 - 7425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma ZFIN:ZDB-GENE-040718-68 Danio rerio (zebrafish) 403070 rgn
  • MGI:6194238
DOID:6432 pulmonary hypertension ZFIN:ZDB-GENE-040218-2 Danio rerio (zebrafish) 403130 has1
  • MGI:6194238
DOID:0112361 spondylocostal dysostosis 3 FB:FBgn0011591 Drosophila melanogaster (fruit fly) 40314 fng CG10580
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis ZFIN:ZDB-GENE-040219-1 Danio rerio (zebrafish) 403143 sarm1
  • MGI:6194238
DOID:1289 neurodegenerative disease ZFIN:ZDB-GENE-040219-1 Danio rerio (zebrafish) 403143 sarm1
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q Xenbase:XB-GENE-980614 Xenopus laevis (African clawed frog) 403360 dhtkd1.L
  • MGI:6194238
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria Xenbase:XB-GENE-980614 Xenopus laevis (African clawed frog) 403360 dhtkd1.L
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip FB:FBgn0037108 Drosophila melanogaster (fruit fly) 40402 Alg11 CG11306
  • MGI:6194238
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:15346351
DOID:0110937 autosomal dominant osteopetrosis 1 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:10629 microphthalmia HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:28111184
DOID:0050770 polycystic liver disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:24706814
  • RGD:7240710
DOID:971 tendinitis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:12559 idiopathic juvenile osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:22487062
DOID:0111411 exudative vitreoretinopathy 4 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0050535 exudative vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:0050563 nonsyndromic deafness HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:4079 heart valve disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:16631011
DOID:0060849 osteoporosis-pseudoglioma syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:11719191
  • PMID:16679074
  • RGD:7240710
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554
DOID:0080037 Worth syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:11476 osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:17002564
DOID:10159 osteonecrosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:0080582 hypotrichosis 14 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: August 19, 2024