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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 6576 - 6600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:8778 Crohn's disease HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • MGI:6194238
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:162 cancer HGNC:8997 Homo sapiens (human) 5305 PIP4K2A
  • MGI:6194238
DOID:162 cancer HGNC:8998 Homo sapiens (human) 8396 PIP4K2B
  • MGI:6194238
DOID:162 cancer HGNC:23786 Homo sapiens (human) 79837 PIP4K2C
  • MGI:6194238
DOID:162 cancer HGNC:8994 Homo sapiens (human) 8394 PIP5K1A
  • MGI:6194238
DOID:162 cancer HGNC:8995 Homo sapiens (human) 8395 PIP5K1B
  • MGI:6194238
DOID:0060653 lethal congenital contracture syndrome 3 HGNC:8996 Homo sapiens (human) 23396 PIP5K1C
  • RGD:7240710
DOID:162 cancer HGNC:8996 Homo sapiens (human) 23396 PIP5K1C
  • MGI:6194238
DOID:5679 retinal disease HGNC:8999 Homo sapiens (human) 23761 PISD
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:8999 Homo sapiens (human) 23761 PISD
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
DOID:10941 intracranial aneurysm HGNC:9008 Homo sapiens (human) 5310 PKD1
  • PMID:12842373
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • PMID:21115670
  • PMID:8554072
DOID:0050770 polycystic liver disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
DOID:0110858 polycystic kidney disease 1 HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • RGD:7240710
DOID:0080322 polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
DOID:0060340 ciliopathy HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:21115670
  • PMID:22863349
DOID:3021 acute kidney failure HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
DOID:8466 retinal degeneration HGNC:9009 Homo sapiens (human) 5311 PKD2
  • PMID:16943309
DOID:0110859 polycystic kidney disease 2 HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • RGD:7240710
DOID:10941 intracranial aneurysm HGNC:9009 Homo sapiens (human) 5311 PKD2
  • PMID:12842373
DOID:0080322 polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:16943309

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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