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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 10876 - 10900 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8947 diabetic retinopathy WB:WBGene00001685 Caenorhabditis elegans 180601 gpd-3
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:102851 Mus musculus (house mouse) 18609 Pdx1
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:8947 diabetic retinopathy ZFIN:ZDB-GENE-030115-1 Danio rerio (zebrafish) 317743 gapdh
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
DOID:8947 diabetic retinopathy WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:8955 sideroblastic anemia FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:8955 sideroblastic anemia HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24325359
DOID:8970 subacute sclerosing panencephalitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:16741935
DOID:898 autosomal dominant polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:21115670
  • PMID:22863349
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • PMID:21115670
  • PMID:8554072
DOID:898 autosomal dominant polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:898 autosomal dominant polycystic kidney disease MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:8986 narcolepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:18820697
DOID:8991 cervix uteri carcinoma in situ HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:17672936
DOID:8991 cervix uteri carcinoma in situ HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18565574
DOID:90 degenerative disc disease RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:29393545
DOID:90 degenerative disc disease HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:90 degenerative disc disease FB:FBgn0003371 Drosophila melanogaster (fruit fly) 31248 sgg
  • MGI:6194238
DOID:90 degenerative disc disease MGI:1861437 Mus musculus (house mouse) 56637 Gsk3b
  • MGI:6194238
DOID:900 hepatopulmonary syndrome MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:900 hepatopulmonary syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238

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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