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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 12076 - 12100 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050453 lissencephaly Xenbase:XB-GENE-6489079 Xenopus laevis (African clawed frog) 108698684 pomt2.L
  • MGI:6194238
DOID:0050453 lissencephaly FB:FBgn0086368 Drosophila melanogaster (fruit fly) 31024 tw CG12311
  • MGI:6194238
DOID:0050453 lissencephaly HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17559086
DOID:0050452 mevalonic aciduria HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7780142
DOID:0050452 mevalonic aciduria MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050452 mevalonic aciduria RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050441 mucosulfatidosis HGNC:20376 Homo sapiens (human) 285362 SUMF1
  • MGI:6194238
  • RGD:7240710
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG
  • RGD:7240710
DOID:0050433 fatal familial insomnia HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • RGD:7240710
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:24679184
DOID:0050432 Asperger syndrome FB:FBgn0028646 Drosophila melanogaster (fruit fly) 43616 aralar1
  • MGI:6194238
DOID:0050426 Stevens-Johnson syndrome MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050426 Stevens-Johnson syndrome RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050426 Stevens-Johnson syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9852250
DOID:0050424 familial adenomatous polyposis MGI:1917853 Mus musculus (house mouse) 70603 Mutyh
  • MGI:6194238
DOID:0050424 familial adenomatous polyposis RGD:620045 Rattus norvegicus (Norway rat) 170841 Mutyh
  • MGI:6194238
DOID:0050424 familial adenomatous polyposis FB:FBgn0026597 Drosophila melanogaster (fruit fly) 43565 Axn
  • MGI:6194238
DOID:0050424 familial adenomatous polyposis HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:11818965
DOID:0050424 familial adenomatous polyposis HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8174133
DOID:0050328 congenital hypothyroidism FB:FBgn0004057 Drosophila melanogaster (fruit fly) 32974 Zw
  • MGI:6194238
DOID:0050328 congenital hypothyroidism WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:0050328 congenital hypothyroidism MGI:105977 Mus musculus (house mouse) 14380 G6pd2
  • MGI:6194238
DOID:0050328 congenital hypothyroidism HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0050328 congenital hypothyroidism MGI:105979 Mus musculus (house mouse) 14381 G6pdx
  • MGI:6194238
DOID:0050328 congenital hypothyroidism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238

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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