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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 9751 - 9775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:162 cancer HGNC:20603 Homo sapiens (human) 79947 DHDDS
  • MGI:6194238
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:14692 Smith-Lemli-Opitz syndrome HGNC:2860 Homo sapiens (human) 1717 DHCR7
  • MGI:6194238
  • PMID:9683613
  • RGD:7240710
DOID:13241 Behcet's disease HGNC:2860 Homo sapiens (human) 1717 DHCR7
  • PMID:24184224
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24
  • PMID:11519011
DOID:4194 glucose metabolism disease HGNC:2853 Homo sapiens (human) 1608 DGKG
  • MGI:6194238
DOID:0080388 nephrotic syndrome type 7 HGNC:2852 Homo sapiens (human) 8526 DGKE
  • RGD:7240710
DOID:0050561 Lennox-Gastaut syndrome HGNC:2851 Homo sapiens (human) 8527 DGKD
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:2850 Homo sapiens (human) 1607 DGKB
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:2849 Homo sapiens (human) 1606 DGKA
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:10787 premature menopause HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
  • PMID:17618857
DOID:784 chronic kidney disease HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • PMID:21220706
DOID:9970 obesity HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • PMID:14569040
DOID:0060778 congenital diarrhea 7 with exudative enteropathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • RGD:7240710
DOID:784 chronic kidney disease SGD:S000005771 Saccharomyces cerevisiae S288C 854419 DGA1
  • MGI:6194238
DOID:9452 steatotic liver disease SGD:S000005771 Saccharomyces cerevisiae S288C 854419 DGA1
  • MGI:6194238
DOID:10787 premature menopause SGD:S000005771 Saccharomyces cerevisiae S288C 854419 DGA1
  • MGI:6194238
DOID:10140 dry eye syndrome SGD:S000005771 Saccharomyces cerevisiae S288C 854419 DGA1
  • MGI:6194238

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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