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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 6426 - 6450 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:9975 cocaine dependence HGNC:8846 Homo sapiens (human) 8864 PER2
  • PMID:22832851
DOID:0050628 advanced sleep phase syndrome HGNC:8846 Homo sapiens (human) 8864 PER2
  • PMID:11232563
DOID:0014667 disease of metabolism SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1
  • MGI:6194238
DOID:2747 glycogen storage disease SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1
  • PMID:7825568
DOID:11721 glycogen storage disease VII SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1
  • MGI:6194238
DOID:11721 glycogen storage disease VII SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2
  • MGI:6194238
DOID:2747 glycogen storage disease SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2
  • PMID:7825568
DOID:0014667 disease of metabolism SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:8872 Homo sapiens (human) 5207 PFKFB1
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:8876 Homo sapiens (human) 5211 PFKL
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:8876 Homo sapiens (human) 5211 PFKL
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238
DOID:11721 glycogen storage disease VII HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238
  • PMID:1533013
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:8878 Homo sapiens (human) 5214 PFKP
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:8878 Homo sapiens (human) 5214 PFKP
  • MGI:6194238
DOID:0080108 myoglobinuria HGNC:8889 Homo sapiens (human) 5224 PGAM2
  • PMID:8447317
DOID:4621 holoprosencephaly FB:FBgn0029789 Drosophila melanogaster (fruit fly) 31487 PGAP1
  • MGI:6194238
DOID:4621 holoprosencephaly HGNC:25712 Homo sapiens (human) 80055 PGAP1
  • MGI:6194238
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 FB:FBgn0031284 Drosophila melanogaster (fruit fly) 33258 PGAP2
  • MGI:6194238
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2
  • RGD:7240710
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 FB:FBgn0033088 Drosophila melanogaster (fruit fly) 35570 PGAP3
  • MGI:6194238
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 HGNC:23719 Homo sapiens (human) 93210 PGAP3
  • RGD:7240710
DOID:14330 Parkinson's disease SGD:S000000400 Saccharomyces cerevisiae S288C 852495 PGI1
  • MGI:6194238
DOID:1059 intellectual disability SGD:S000000400 Saccharomyces cerevisiae S288C 852495 PGI1
  • 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