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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 10701 - 10725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110352 retinitis pigmentosa 59 HGNC:20603 Homo sapiens (human) 79947 DHDDS
  • MGI:6194238
  • RGD:7240710
DOID:0080473 developmental delay and seizures with or without movement abnormalities HGNC:20603 Homo sapiens (human) 79947 DHDDS
  • RGD:7240710
DOID:0112160 autosomal dominant nonsyndromic deafness 79 HGNC:21088 Homo sapiens (human) 79966 SCD5
  • RGD:7240710
DOID:397 restrictive cardiomyopathy HGNC:21088 Homo sapiens (human) 79966 SCD5
  • MGI:6194238
DOID:0050589 inflammatory bowel disease ZFIN:ZDB-GENE-041014-161 Danio rerio (zebrafish) 799868 st6galnac1.2
  • MGI:6194238
DOID:10588 adrenoleukodystrophy HGNC:26292 Homo sapiens (human) 79993 ELOVL7
  • MGI:6194238
DOID:4621 holoprosencephaly HGNC:25712 Homo sapiens (human) 80055 PGAP1
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:13317 hyperinsulinemic hypoglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • RGD:7240710
DOID:162 cancer HGNC:30596 Homo sapiens (human) 80235 PIGZ
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:16787 Homo sapiens (human) 80267 EDEM3
  • RGD:7240710
DOID:1852 intrahepatic cholestasis HGNC:18324 Homo sapiens (human) 80270 HSD3B7
  • PMID:12679481
DOID:0111071 congenital bile acid synthesis defect 1 HGNC:18324 Homo sapiens (human) 80270 HSD3B7
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:14897 Homo sapiens (human) 80271 ITPKC
  • PMID:33470690
DOID:14250 Down syndrome MGI:1916863 Mus musculus (house mouse) 80294 Pofut2
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187
DOID:9352 type 2 diabetes mellitus HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187
DOID:9970 obesity HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:0050729 Chanarin-Dorfman syndrome HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:0060158 acquired metabolic disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:20648474
  • PMID:29674183
  • PMID:31377187

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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