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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 63626 - 63650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6000 congestive heart failure HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21135513
DOID:7147 ankylosing spondylitis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21317434
DOID:5199 ureteral obstruction HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:37 skin disease MGI:1918605 Mus musculus (house mouse) 71355 Col24a1
  • MGI:6194238
DOID:299 adenocarcinoma HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:114 heart disease HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:0110313 hypertrophic cardiomyopathy 7 HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • RGD:7240710
DOID:0110460 dilated cardiomyopathy 2A HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:0110459 dilated cardiomyopathy 1FF HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • PMID:15698845
DOID:0111425 restrictive cardiomyopathy 1 HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:0050700 cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:397 restrictive cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • PMID:16288990
DOID:3393 coronary artery disease HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • PMID:12221049
DOID:12930 dilated cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • PMID:15070570
DOID:0050834 CHARGE syndrome MGI:1918639 Mus musculus (house mouse) 71389 Chd6
  • MGI:6194238
DOID:1682 congenital heart disease MGI:1918639 Mus musculus (house mouse) 71389 Chd6
  • MGI:6194238
DOID:0060041 autism spectrum disorder MGI:1918639 Mus musculus (house mouse) 71389 Chd6
  • MGI:6194238
DOID:0090093 hypogonadotropic hypogonadism 21 with or without anosmia MGI:1918686 Mus musculus (house mouse) 71436 Flrt3
  • MGI:6194238
DOID:216 dental caries MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • MGI:6194238
DOID:13207 proliferative diabetic retinopathy MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • MGI:6194238
DOID:83 cataract MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • MGI:6194238
DOID:5517 stomach carcinoma MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • MGI:6194238
DOID:9256 colorectal cancer MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • MGI:6194238
DOID:0111799 syndromic microphthalmia 1 MGI:1918708 Mus musculus (house mouse) 71458 Bcor
  • 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