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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 October 9, 2024
Displaying entries 63626 - 63650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0060572 Ritscher-Schinzel syndrome 2 HGNC:28909 Homo sapiens (human) 28952 CCDC22
  • RGD:7240710
DOID:12347 osteogenesis imperfecta HGNC:26185 Homo sapiens (human) 79879 CCDC134
  • RGD:7240710
DOID:1324 lung cancer HGNC:26688 Homo sapiens (human) 164592 CCDC116
  • PMID:29193083
DOID:0070267 congenital disorder of glycosylation type IIo HGNC:28178 Homo sapiens (human) 84317 CCDC115
  • RGD:7240710
DOID:0060366 Hennekam syndrome HGNC:29426 Homo sapiens (human) 147372 CCBE1
  • RGD:7240710
DOID:7148 rheumatoid arthritis FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:2560 morphine dependence FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:0050589 inflammatory bowel disease FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:535 sleep disorder FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:2841 asthma FB:FBgn0039396 Drosophila melanogaster (fruit fly) 2768688 CCAP-R
  • MGI:6194238
DOID:0060340 ciliopathy HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • MGI:6194238
DOID:0111004 Joubert syndrome 9 HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • PMID:19068953
  • PMID:22241855
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • RGD:7240710
DOID:0050778 Meckel syndrome HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • MGI:6194238
DOID:0050545 visceral heterotaxy HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • MGI:6194238
DOID:0050777 Joubert syndrome HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • MGI:6194238
DOID:0070120 Meckel syndrome 6 HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • RGD:7240710
DOID:1059 intellectual disability HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • PMID:22023432
DOID:1059 intellectual disability HGNC:30237 Homo sapiens (human) 54862 CC2D1A
  • PMID:22023432
DOID:0081179 autosomal recessive intellectual developmental disorder 3 HGNC:30237 Homo sapiens (human) 54862 CC2D1A
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:30237 Homo sapiens (human) 54862 CC2D1A
  • MGI:6194238
DOID:0060340 ciliopathy HGNC:30237 Homo sapiens (human) 54862 CC2D1A
  • MGI:6194238
DOID:162 cancer HGNC:15962 Homo sapiens (human) 57332 CBX8
  • MGI:6194238
DOID:3068 glioblastoma HGNC:15962 Homo sapiens (human) 57332 CBX8
  • PMID:24260522

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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: December 9, 2024