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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 1226 - 1250 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060713 autosomal recessive congenital ichthyosis 4B ZFIN:ZDB-GENE-040426-1086 Danio rerio (zebrafish) 791759 piga
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B MGI:99461 Mus musculus (house mouse) 18700 Piga
  • PMID:15304084
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:9491 Homo sapiens (human) 5652 PRSS8
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B Xenbase:XB-GENE-996765 Xenopus tropicalis (tropical clawed frog) 100158632 piga
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B RGD:1589723 Rattus norvegicus (Norway rat) 363464 Piga
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B SGD:S000006096 Saccharomyces cerevisiae S288C 855928 SPT14
  • MGI:6194238
DOID:0060718 autosomal recessive congenital ichthyosis 9 HGNC:23752 Homo sapiens (human) 204219 CERS3
  • RGD:7240710
DOID:0060728 NGLY1-deficiency HGNC:17646 Homo sapiens (human) 55768 NGLY1
  • MGI:6194238
  • RGD:7240710
DOID:0060732 chromosome 9p deletion syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
  • PMID:27167370
  • RGD:7240710
DOID:0060759 immunodeficiency with hyper IgM type 5 HGNC:12572 Homo sapiens (human) 7374 UNG
  • RGD:7240710
DOID:0060759 immunodeficiency with hyper IgM type 5 SGD:S000004483 Saccharomyces cerevisiae S288C 854987 UNG1
  • MGI:6194238
DOID:0060759 immunodeficiency with hyper IgM type 5 WB:WBGene00013241 Caenorhabditis elegans 176633 ung-1
  • MGI:6194238
DOID:0060759 immunodeficiency with hyper IgM type 5 MGI:109352 Mus musculus (house mouse) 22256 Ung
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries FB:FBgn0284408 Drosophila melanogaster (fruit fly) 45320 trol CG33950
  • MGI:6194238
DOID:0060774 congenital diarrhea HGNC:16526 Homo sapiens (human) 51703 ACSL5
  • RGD:7240710
DOID:0060778 congenital diarrhea 7 with exudative enteropathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • RGD:7240710
DOID:0060786 hypomyelinating leukodystrophy HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0060841 isolated microphthalmia 8 HGNC:409 Homo sapiens (human) 220 ALDH1A3
  • RGD:7240710
DOID:0060849 osteoporosis-pseudoglioma syndrome MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
  • PMID:11956231
  • PMID:24225945

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Supported by JST NBDC Grant Number JPMJND2204

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


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