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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 7251 - 7275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:573 nerve compression syndrome HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG
  • RGD:7240710
DOID:0050636 familial visceral amyloidosis HGNC:6740 Homo sapiens (human) 4069 LYZ
  • RGD:7240710
DOID:2921 glomerulonephritis HGNC:6719 Homo sapiens (human) 4056 LTC4S
  • MGI:6194238
DOID:574 peripheral nervous system disease HGNC:6719 Homo sapiens (human) 4056 LTC4S
  • MGI:6194238
DOID:2841 asthma HGNC:6710 Homo sapiens (human) 4048 LTA4H
  • MGI:6194238
DOID:1749 squamous cell carcinoma HGNC:6710 Homo sapiens (human) 4048 LTA4H
  • MGI:6194238
DOID:299 adenocarcinoma HGNC:6710 Homo sapiens (human) 4048 LTA4H
  • MGI:6194238
DOID:0080582 hypotrichosis 14 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0080950 alopecia-mental retardation syndrome 4 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:83 cataract HGNC:6708 Homo sapiens (human) 4047 LSS
  • MGI:6194238
  • PMID:26200341
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:15346351
DOID:0110937 autosomal dominant osteopetrosis 1 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:10629 microphthalmia HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:28111184
DOID:0050770 polycystic liver disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:24706814
  • RGD:7240710
DOID:971 tendinitis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:12559 idiopathic juvenile osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:22487062
DOID:0111411 exudative vitreoretinopathy 4 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0050535 exudative vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:0050563 nonsyndromic deafness HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:4079 heart valve disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:16631011
DOID:0060849 osteoporosis-pseudoglioma syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:11719191
  • PMID:16679074
  • RGD:7240710
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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