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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 9876 - 9900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1459 hypothyroidism WB:WBGene00015754 Caenorhabditis elegans 176149 C14B9.8
  • MGI:6194238
DOID:0111040 glycogen storage disease IXd WB:WBGene00015754 Caenorhabditis elegans 176149 C14B9.8
  • MGI:6194238
DOID:4079 heart valve disease WB:WBGene00001628 Caenorhabditis elegans 176112 gly-3
  • MGI:6194238
DOID:3525 middle cerebral artery infarction WB:WBGene00022817 Caenorhabditis elegans 176077 upp-1
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip WB:WBGene00015162 Caenorhabditis elegans 176032 algn-11
  • MGI:6194238
DOID:6000 congestive heart failure WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • MGI:6194238
DOID:9351 diabetes mellitus WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • PMID:31576392
DOID:0080240 non-syndromic X-linked intellectual disability 106 WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • MGI:6194238
DOID:1712 aortic valve stenosis WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1
  • PMID:16051707
  • PMID:16882729
DOID:8398 osteoarthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:11764092
DOID:6000 congestive heart failure HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:1824 status epilepticus HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:4480 achondroplasia HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16507130
DOID:0112282 spondyloepiphyseal dysplasia Kimberley type HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16080123
  • RGD:7240710
DOID:0080563 congenital disorder of glycosylation Ik WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix WB:WBGene00020437 Caenorhabditis elegans 175886 stt-3
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw WB:WBGene00020437 Caenorhabditis elegans 175886 stt-3
  • MGI:6194238
DOID:684 hepatocellular carcinoma WB:WBGene00017166 Caenorhabditis elegans 175827 aldo-2
  • MGI:6194238
DOID:5154 borna disease WB:WBGene00017166 Caenorhabditis elegans 175827 aldo-2
  • MGI:6194238

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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