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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 11526 - 11550 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050812 spondyloepimetaphyseal dysplasia, Pakistani type HGNC:8604 Homo sapiens (human) 9060 PAPSS2
  • MGI:6194238
  • RGD:7240710
DOID:0050811 congenital adrenal hyperplasia HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:2026124
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
  • PMID:1430088
  • PMID:8964882
DOID:0050811 congenital adrenal hyperplasia HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
DOID:0050811 congenital adrenal hyperplasia HGNC:2600 Homo sapiens (human) 1589 CYP21A2
  • PMID:12930931
DOID:0050811 congenital adrenal hyperplasia HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • PMID:12161514
DOID:0050809 mucopolysaccharidosis IX HGNC:5320 Homo sapiens (human) 3373 HYAL1
  • MGI:6194238
  • RGD:7240710
DOID:0050809 mucopolysaccharidosis IX RGD:1303060 Rattus norvegicus (Norway rat) 367166 Hyal1
  • MGI:6194238
DOID:0050809 mucopolysaccharidosis IX MGI:96298 Mus musculus (house mouse) 15586 Hyal1
  • MGI:6194238
  • PMID:18344557
DOID:0050807 Kahrizi syndrome HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 WB:WBGene00005020 Caenorhabditis elegans 173635 sqv-2
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 ZFIN:ZDB-GENE-101104-13 Danio rerio (zebrafish) 572324 b3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 FB:FBgn0033315 Drosophila melanogaster (fruit fly) 35848 beta3GalTII CG8734
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-6488390 Xenopus laevis (African clawed frog) 108696563 b3galt6.L
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-17345196 Xenopus laevis (African clawed frog) 108697636 b3galt6.S
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 MGI:2152819 Mus musculus (house mouse) 117592 B3galt6
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 FB:FBgn0033315 Drosophila melanogaster (fruit fly) 35848 β3GalTII CG8734
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-974114 Xenopus tropicalis (tropical clawed frog) 548849 b3galt6
  • MGI:6194238
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency FB:FBgn0027572 Drosophila melanogaster (fruit fly) 37028 Acox1
  • MGI:6194238
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
  • RGD:7240710
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency FB:FBgn0027572 Drosophila melanogaster (fruit fly) 37028 ACOX1
  • MGI:6194238
DOID:0050793 short QT syndrome RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
DOID:0050793 short QT syndrome MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • 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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