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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 8126 - 8150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0111619 combined D-2- and L-2-hydroxyglutaric aciduria HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
  • RGD:7240710
DOID:700 mitochondrial metabolism disease HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
DOID:0060413 chromosome 22q11.2 deletion syndrome, distal HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
DOID:0070450 mitochondrial DNA depletion syndrome 19 HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • RGD:7240710
DOID:0070329 mitochondrial DNA depletion syndrome HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0060536 mitochondrial complex I deficiency HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0060475 myoclonic-atonic epilepsy HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0050773 paraganglioma HGNC:10981 Homo sapiens (human) 8402 SLC25A11
  • RGD:7240710
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:15056512
DOID:4137 common bile duct disease HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:24679184
DOID:0060041 autism spectrum disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:17151801
  • PMID:18180767
DOID:9273 citrullinemia HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:1852 intrahepatic cholestasis HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:0080349 developmental and epileptic encephalopathy 39 HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
  • RGD:7240710
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • RGD:7240710
DOID:9273 citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • MGI:6194238
DOID:4137 common bile duct disease HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • MGI:6194238
DOID:0070342 adult-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • PMID:10369257
  • PMID:11153906
  • RGD:7240710
DOID:1852 intrahepatic cholestasis HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • MGI:6194238
DOID:14687 diastrophic dysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • MGI:6194238
  • PMID:10482955
  • RGD:7240710
DOID:676 juvenile rheumatoid arthritis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:17393463
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:8571951

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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: August 19, 2024