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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 2951 - 2975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050563 nonsyndromic deafness HGNC:23162 Homo sapiens (human) 84920 ALG10
  • MGI:6194238
DOID:0070432 hyperphosphatasia with impaired intellectual development syndrome 5 HGNC:23213 Homo sapiens (human) 284098 PIGW
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0090129 carnitine palmitoyltransferase I deficiency HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
  • RGD:7240710
DOID:9970 obesity HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • PMID:29885404
DOID:9352 type 2 diabetes mellitus HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:12351 alcoholic hepatitis HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:783 end stage renal disease HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • PMID:9691089
DOID:0080000 muscular disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:10873395
DOID:936 brain disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • RGD:7240710
DOID:3146 lipid metabolism disorder HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:1528846
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:0060732 chromosome 9p deletion syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
DOID:0090001 Fraser syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
  • PMID:23221805
DOID:0080565 congenital disorder of glycosylation Im HGNC:23406 Homo sapiens (human) 22845 DOLK
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:23406 Homo sapiens (human) 22845 DOLK
  • MGI:6194238
DOID:1612 breast cancer HGNC:23531 Homo sapiens (human) 196051 PLPP4
  • PMID:16818692

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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