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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 65601 - 65625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3211 lysosomal storage disease HGNC:11753 Homo sapiens (human) 7942 TFEB
  • MGI:6194238
DOID:10763 hypertension RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:0110144 Bartter disease type 3 RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:0050450 Gitelman syndrome RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:445 Bartter disease RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:0110146 Bartter disease type 4b RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:423 myopathy RGD:628639 Rattus norvegicus (Norway rat) 79430 Clcnkb
  • MGI:6194238
DOID:0060870 isolated growth hormone deficiency RGD:68429 Rattus norvegicus (Norway rat) 79438 Igfals
  • MGI:6194238
DOID:1184 nephrotic syndrome RGD:68429 Rattus norvegicus (Norway rat) 79438 Igfals
  • MGI:6194238
DOID:3490 Noonan syndrome RGD:68429 Rattus norvegicus (Norway rat) 79438 Igfals
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia RGD:68429 Rattus norvegicus (Norway rat) 79438 Igfals
  • MGI:6194238
DOID:8689 anorexia nervosa RGD:68429 Rattus norvegicus (Norway rat) 79438 Igfals
  • MGI:6194238
DOID:0070515 chromosome 16p11.2 deletion syndrome, 593-kb HGNC:28707 Homo sapiens (human) 79447 PAGR1
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:28707 Homo sapiens (human) 79447 PAGR1
  • PMID:33833989
DOID:3635 congenital myasthenic syndrome RGD:69277 Rattus norvegicus (Norway rat) 79557 Chrna1
  • MGI:6194238
DOID:0110663 congenital myasthenic syndrome 1A RGD:69277 Rattus norvegicus (Norway rat) 79557 Chrna1
  • MGI:6194238
DOID:0110662 congenital myasthenic syndrome 1B RGD:69277 Rattus norvegicus (Norway rat) 79557 Chrna1
  • MGI:6194238
DOID:13374 fibrodysplasia ossificans progressiva RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:1405 primary angle-closure glaucoma RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:13641 exfoliation syndrome RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:13129 severe pre-eclampsia RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:1070 primary open angle glaucoma RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:1793 pancreatic cancer RGD:620200 Rattus norvegicus (Norway rat) 79558 Acvr1
  • MGI:6194238
DOID:891 progressive myoclonus epilepsy HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • PMID:9771710
DOID:3534 Lafora disease HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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