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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 9626 - 9650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0112313 brain small vessel disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20885295
DOID:526 human immunodeficiency virus infectious disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:22156911
DOID:6000 congestive heart failure HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
  • PMID:12165563
  • PMID:17391113
  • PMID:21162967
DOID:9970 obesity HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:19228864
DOID:2754 glycogen storage disease VI RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
DOID:2747 glycogen storage disease RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:0060480 left ventricular noncompaction HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:0060250 idiopathic scoliosis HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:557 kidney disease HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • PMID:16759312
DOID:0080322 polycystic kidney disease HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum RGD:620093 Rattus norvegicus (Norway rat) 64133 Xylt1
  • MGI:6194238
DOID:557 kidney disease RGD:620093 Rattus norvegicus (Norway rat) 64133 Xylt1
  • PMID:18095597
DOID:9744 type 1 diabetes mellitus RGD:620093 Rattus norvegicus (Norway rat) 64133 Xylt1
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia RGD:620093 Rattus norvegicus (Norway rat) 64133 Xylt1
  • MGI:6194238
DOID:0080322 polycystic kidney disease RGD:619765 Rattus norvegicus (Norway rat) 64134 Xylt2
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum RGD:619765 Rattus norvegicus (Norway rat) 64134 Xylt2
  • MGI:6194238
DOID:0080762 autosomal recessive limb-girdle muscular dystrophy type 2Z ZFIN:ZDB-GENE-051120-24 Danio rerio (zebrafish) 641495 poglut1
  • MGI:6194238
DOID:0060256 Dowling-Degos disease ZFIN:ZDB-GENE-051120-24 Danio rerio (zebrafish) 641495 poglut1
  • 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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Last updated: August 19, 2024