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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 October 9, 2024
Displaying entries 64851 - 64875 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060787 hypomyelinating leukodystrophy 2 HGNC:17494 Homo sapiens (human) 57165 GJC2
  • MGI:6194238
  • PMID:15192806
  • PMID:16707726
  • PMID:18094336
  • PMID:21959080
  • RGD:7240710
DOID:0060786 hypomyelinating leukodystrophy HGNC:30348 Homo sapiens (human) 55703 POLR3B
  • MGI:6194238
DOID:0060786 hypomyelinating leukodystrophy HGNC:30074 Homo sapiens (human) 11128 POLR3A
  • MGI:6194238
DOID:0060786 hypomyelinating leukodystrophy HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:0060785 adult-onset autosomal dominant demyelinating leukodystrophy HGNC:6637 Homo sapiens (human) 4001 LMNB1
  • MGI:6194238
  • PMID:16951681
  • RGD:7240710
DOID:0060785 adult-onset autosomal dominant demyelinating leukodystrophy RGD:620522 Rattus norvegicus (Norway rat) 116685 Lmnb1
  • MGI:6194238
DOID:0060785 adult-onset autosomal dominant demyelinating leukodystrophy MGI:96795 Mus musculus (house mouse) 16906 Lmnb1
  • MGI:6194238
  • PMID:23676464
DOID:0060781 congenital secretory sodium diarrhea 3 MGI:1338031 Mus musculus (house mouse) 20733 Spint2
  • MGI:6194238
DOID:0060781 congenital secretory sodium diarrhea 3 HGNC:11247 Homo sapiens (human) 10653 SPINT2
  • RGD:7240710
DOID:0060780 congenital diarrhea 6 HGNC:4688 Homo sapiens (human) 2984 GUCY2C
  • RGD:7240710
DOID:0060780 congenital diarrhea 6 MGI:106903 Mus musculus (house mouse) 14917 Gucy2c
  • MGI:6194238
DOID:0060780 congenital diarrhea 6 RGD:2771 Rattus norvegicus (Norway rat) 25711 Gucy2c
  • MGI:6194238
DOID:0060780 congenital diarrhea 6 WB:WBGene00001550 Caenorhabditis elegans 191654 gcy-27
  • MGI:6194238
DOID:0060778 congenital diarrhea 7 with exudative enteropathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • RGD:7240710
DOID:0060777 congenital secretory sodium diarrhea 8 HGNC:11073 Homo sapiens (human) 6550 SLC9A3
  • RGD:7240710
DOID:0060777 congenital secretory sodium diarrhea 8 WB:WBGene00003731 Caenorhabditis elegans 183811 nhx-3
  • MGI:6194238
DOID:0060777 congenital secretory sodium diarrhea 8 WB:WBGene00003736 Caenorhabditis elegans 178126 nhx-9
  • MGI:6194238
DOID:0060776 congenital diarrhea 5 with tufting enteropathy MGI:106653 Mus musculus (house mouse) 17075 Epcam
  • MGI:6194238
  • PMID:23209569
DOID:0060776 congenital diarrhea 5 with tufting enteropathy RGD:621365 Rattus norvegicus (Norway rat) 171577 Epcam
  • MGI:6194238
DOID:0060776 congenital diarrhea 5 with tufting enteropathy HGNC:11529 Homo sapiens (human) 4072 EPCAM
  • MGI:6194238
  • RGD:7240710
DOID:0060775 microvillus inclusion disease HGNC:1736 Homo sapiens (human) 998 CDC42
  • MGI:6194238
DOID:0060774 congenital diarrhea Xenbase:XB-GENE-960151 Xenopus laevis (African clawed frog) 378566 wnt2b.L
  • MGI:6194238
DOID:0060774 congenital diarrhea MGI:1261834 Mus musculus (house mouse) 22414 Wnt2b
  • MGI:6194238
DOID:0060774 congenital diarrhea MGI:1919129 Mus musculus (house mouse) 433256 Acsl5
  • MGI:6194238
DOID:0060774 congenital diarrhea HGNC:13635 Homo sapiens (human) 83483 PLVAP
  • 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: December 9, 2024