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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 551 - 575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081180 autosomal recessive intellectual developmental disorder 12 Xenbase:XB-GENE-941057 Xenopus laevis (African clawed frog) 108715547 LOC108715547
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 Xenbase:XB-GENE-17331641 Xenopus laevis (African clawed frog) 108715652 alg14.S
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II Xenbase:XB-GENE-17346352 Xenopus laevis (African clawed frog) 108716128 galnt2.L
  • MGI:6194238
DOID:5419 schizophrenia Xenbase:XB-GENE-17334879 Xenopus laevis (African clawed frog) 108716933 b3gat2.L
  • MGI:6194238
DOID:9206 Barrett's esophagus Xenbase:XB-GENE-17334879 Xenopus laevis (African clawed frog) 108716933 b3gat2.L
  • MGI:6194238
DOID:1574 alcohol use disorder Xenbase:XB-GENE-6486698 Xenopus laevis (African clawed frog) 108717116 st6gal1.L
  • MGI:6194238
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia Xenbase:XB-GENE-17335472 Xenopus laevis (African clawed frog) 108717161 hs6st1.L
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 Xenbase:XB-GENE-17344746 Xenopus laevis (African clawed frog) 108717671 ppp1cb.S
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder Xenbase:XB-GENE-6486769 Xenopus laevis (African clawed frog) 108717884 ust.S
  • MGI:6194238
DOID:1574 alcohol use disorder Xenbase:XB-GENE-17330217 Xenopus laevis (African clawed frog) 108718183 st6gal1.S
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix Xenbase:XB-GENE-17341012 Xenopus laevis (African clawed frog) 108718938 stt3b.L
  • MGI:6194238
DOID:9256 colorectal cancer Xenbase:XB-GENE-17330127 Xenopus laevis (African clawed frog) 108719043 galnt12.L
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • PMID:23217742
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:22087236
DOID:332 amyotrophic lateral sclerosis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:22102466
  • PMID:23147503
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:1287 cardiovascular system disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:18162502
DOID:10376 amblyopia HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0050855 renal fibrosis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:114 heart disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:23269818
DOID:9970 obesity HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238

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International Collaboration

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: August 19, 2024