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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 501 - 525 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050636 familial visceral amyloidosis FB:FBgn0004427 Drosophila melanogaster (fruit fly) 38127 LysD CG9118
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18205195
DOID:0050644 arterial calcification of infancy MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:23798568
  • PMID:25479107
DOID:0050644 arterial calcification of infancy HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:12881724
  • PMID:15940697
  • PMID:20016754
  • RGD:7240710
DOID:0050644 arterial calcification of infancy RGD:628825 Rattus norvegicus (Norway rat) 85496 Enpp1
  • MGI:6194238
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10
  • RGD:7240710
DOID:0050647 Arts syndrome HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • RGD:7240710
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • RGD:7240710
DOID:0050650 familial atrial fibrillation MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • MGI:6194238
DOID:0050650 familial atrial fibrillation RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0050657 Bannayan-Riley-Ruvalcaba syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • RGD:7240710
DOID:0050663 Bethlem myopathy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • PMID:8782832
  • RGD:7240710
DOID:0050663 Bethlem myopathy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:14625552
  • PMID:9817932
DOID:0050665 fetal alcohol syndrome SGD:S000006369 Saccharomyces cerevisiae S288C 856294 RHO1
  • MGI:6194238
DOID:0050669 spastic cerebral palsy HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
DOID:0050669 spastic cerebral palsy HGNC:4093 Homo sapiens (human) 2572 GAD2
  • MGI:6194238
DOID:0050685 small cell carcinoma FB:FBgn0026415 Drosophila melanogaster (fruit fly) 31926 Idgf4 CG1780
  • MGI:6194238
DOID:0050685 small cell carcinoma FB:FBgn0013763 Drosophila melanogaster (fruit fly) 36868 Idgf6
  • MGI:6194238
DOID:0050685 small cell carcinoma MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050685 small cell carcinoma MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:0050685 small cell carcinoma WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:0050685 small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15541818

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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