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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 8001 - 8025 of 12216 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:20476641
  • PMID:30052309
DOID:0080208 metabolic dysfunction-associated steatotic liver disease SGD:S000005185 Saccharomyces cerevisiae S288C 855480 ZWF1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:6194238
  • PMID:22118645
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3336 Rattus norvegicus (Norway rat) 24651 Pklr
  • PMID:26394137
DOID:0080208 metabolic dysfunction-associated steatotic liver disease Xenbase:XB-GENE-1017054 Xenopus tropicalis (tropical clawed frog) 395003 dgat2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:84 Homo sapiens (human) 31 ACACA
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:92 Homo sapiens (human) 37 ACADVL
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:18308829
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • MGI:6194238
  • PMID:18543254
  • PMID:21359922
DOID:10581 metachromatic leukodystrophy HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:10783 methemoglobinemia SGD:S000001305 Saccharomyces cerevisiae S288C 854768 CBR1
  • MGI:6194238
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:14749 methylmalonic acidemia HGNC:16732 Homo sapiens (human) 84693 MCEE
  • MGI:6194238
DOID:14749 methylmalonic acidemia HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
  • PMID:27167370
  • RGD:7240710
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:10907 microcephaly HGNC:25575 Homo sapiens (human) 55224 ETNK2
  • MGI:6194238
DOID:10907 microcephaly HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:10907 microcephaly HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:10907 microcephaly HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:10629 microphthalmia HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:28111184

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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