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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 8101 - 8125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0111395 mucopolysaccharidosis type IIIA HGNC:10818 Homo sapiens (human) 6448 SGSH
  • MGI:6194238
  • RGD:7240710
DOID:162 cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • PMID:17031801
DOID:1574 alcohol use disorder HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • MGI:6194238
DOID:1612 breast cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • PMID:17896178
DOID:162 cancer HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:5419 schizophrenia HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:0060180 colitis HGNC:10856 Homo sapiens (human) 6476 SI
  • MGI:6194238
DOID:0111633 congenital sucrase-isomaltase deficiency HGNC:10856 Homo sapiens (human) 6476 SI
  • RGD:7240710
DOID:417 autoimmune disease HGNC:18187 Homo sapiens (human) 54414 SIAE
  • RGD:7240710
DOID:9975 cocaine dependence HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3070 high grade glioma HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:14932 Homo sapiens (human) 23409 SIRT4
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:14934 Homo sapiens (human) 51548 SIRT6
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:14934 Homo sapiens (human) 51548 SIRT6
  • MGI:6194238
DOID:3911 progeria HGNC:14934 Homo sapiens (human) 51548 SIRT6
  • MGI:6194238
DOID:9970 obesity HGNC:14934 Homo sapiens (human) 51548 SIRT6
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:3635 congenital myasthenic syndrome HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • RGD:7240710
DOID:0050573 2-hydroxyglutaric aciduria HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • PMID:23561848
DOID:11198 DiGeorge syndrome HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • 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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