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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 October 9, 2024
Displaying entries 62326 - 62350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9074 systemic lupus erythematosus HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:9014588
DOID:1580 diffuse scleroderma HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:16112028
DOID:8893 psoriasis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:11194890
DOID:4483 rhinitis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:12018331
  • PMID:17982230
DOID:6196 reactive arthritis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:7748224
DOID:4362 cervical cancer HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:12648582
  • PMID:18248301
DOID:1067 open-angle glaucoma HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:15887980
DOID:9744 type 1 diabetes mellitus HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:9129974
  • PMID:9458110
DOID:9563 bronchiectasis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:17245734
DOID:7147 ankylosing spondylitis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:19480848
DOID:5419 schizophrenia HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:19217216
DOID:2957 pulmonary tuberculosis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:21843574
DOID:0060009 MHC class I deficiency HGNC:43 Homo sapiens (human) 6890 TAP1
  • RGD:7240710
DOID:841 extrinsic allergic alveolitis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:18342853
DOID:9352 type 2 diabetes mellitus MGI:1921765 Mus musculus (house mouse) 68916 Cdkal1
  • MGI:6194238
  • PMID:21841312
DOID:9351 diabetes mellitus MGI:1921765 Mus musculus (house mouse) 68916 Cdkal1
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:1921765 Mus musculus (house mouse) 68916 Cdkal1
  • MGI:6194238
DOID:11714 gestational diabetes MGI:1921765 Mus musculus (house mouse) 68916 Cdkal1
  • MGI:6194238
DOID:627 severe combined immunodeficiency HGNC:11566 Homo sapiens (human) 6892 TAPBP
  • PMID:12149238
DOID:0050545 visceral heterotaxy MGI:1916172 Mus musculus (house mouse) 68922 Dnai1
  • MGI:5284969
DOID:0050144 Kartagener syndrome MGI:1916172 Mus musculus (house mouse) 68922 Dnai1
  • MGI:5284969
  • MGI:6194238
DOID:0110594 primary ciliary dyskinesia 1 MGI:1916172 Mus musculus (house mouse) 68922 Dnai1
  • MGI:5284969
  • MGI:6194238
  • PMID:19675306
DOID:3529 congenital myopathy 1A RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:10591 pre-eclampsia RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:114 heart disease RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • 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: December 9, 2024