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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 10576 - 10600 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080322 polycystic kidney disease SGD:S000000433 Saccharomyces cerevisiae S288C 852530 ROT2
  • MGI:6194238
DOID:0080322 polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:16943309
DOID:0080322 polycystic kidney disease Xenbase:XB-GENE-993408 Xenopus tropicalis (tropical clawed frog) 448400 xylt2
  • MGI:6194238
DOID:0080319 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia FB:FBgn0032015 Drosophila melanogaster (fruit fly) 34137 OstĪ³ CG7830
  • MGI:6194238
DOID:0080319 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia FB:FBgn0032015 Drosophila melanogaster (fruit fly) 34137 Ostgamma CG7830
  • MGI:6194238
DOID:0080319 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:0080283 developmental and epileptic encephalopathy 55 SGD:S000002845 Saccharomyces cerevisiae S288C 852047 GPI19
  • MGI:6194238
DOID:0080283 developmental and epileptic encephalopathy 55 MGI:1860433 Mus musculus (house mouse) 56176 Pigp
  • MGI:6194238
DOID:0080283 developmental and epileptic encephalopathy 55 HGNC:3046 Homo sapiens (human) 51227 PIGP
  • RGD:7240710
DOID:0080265 nephrotic syndrome type 14 HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • RGD:7240710
DOID:0080258 autosomal recessive congenital ichthyosis 14 HGNC:11459 Homo sapiens (human) 6820 SULT2B1
  • RGD:7240710
DOID:0080250 erythrokeratodermia variabilis et progressiva 4 HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
  • RGD:7240710
DOID:0080240 non-syndromic X-linked intellectual disability 106 Xenbase:XB-GENE-966153 Xenopus laevis (African clawed frog) 447694 ogt.L
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
  • RGD:7240710
DOID:0080240 non-syndromic X-linked intellectual disability 106 MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 Xenbase:XB-GENE-966145 Xenopus tropicalis (tropical clawed frog) 553157 ogt
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 RGD:62060 Rattus norvegicus (Norway rat) 26295 Ogt
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 ZFIN:ZDB-GENE-051128-1 Danio rerio (zebrafish) 652952 ogt.2
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 FB:FBgn0261403 Drosophila melanogaster (fruit fly) 35486 sxc CG10392
  • MGI:6194238
  • PMID:35500025
DOID:0080240 non-syndromic X-linked intellectual disability 106 ZFIN:ZDB-GENE-030131-9631 Danio rerio (zebrafish) 337685 ogt.1
  • MGI:6194238
DOID:0080217 lysosomal acid lipase deficiency HGNC:6617 Homo sapiens (human) 3988 LIPA
  • MGI:6194238
DOID:0080217 lysosomal acid lipase deficiency MGI:96789 Mus musculus (house mouse) 16889 Lipa
  • PMID:9700186
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:85 Homo sapiens (human) 32 ACACB
  • MGI:6194238

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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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