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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 69801 - 69825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3748 esophagus squamous cell carcinoma MGI:96704 Mus musculus (house mouse) 110310 Krt7
  • MGI:6194238
DOID:4947 cholangiocarcinoma MGI:96704 Mus musculus (house mouse) 110310 Krt7
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma MGI:96704 Mus musculus (house mouse) 110310 Krt7
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome HGNC:9771 Homo sapiens (human) 11031 RAB31
  • PMID:19635508
DOID:0060735 epidermolysis bullosa simplex Dowling-Meara type MGI:96702 Mus musculus (house mouse) 110308 Krt5
  • PMID:11408584
DOID:11054 urinary bladder cancer MGI:96702 Mus musculus (house mouse) 110308 Krt5
  • MGI:6194238
DOID:0060256 Dowling-Degos disease MGI:96702 Mus musculus (house mouse) 110308 Krt5
  • MGI:6194238
DOID:0111346 epidermolysis bullosa simplex with mottled pigmentation MGI:96702 Mus musculus (house mouse) 110308 Krt5
  • MGI:6194238
DOID:4644 epidermolysis bullosa simplex MGI:96702 Mus musculus (house mouse) 110308 Krt5
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
  • PMID:12401548
DOID:1596 depressive disorder HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
DOID:0110671 congenital myasthenic syndrome 6 HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
  • PMID:11172068
  • RGD:7240710
DOID:2841 asthma HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
DOID:8552 chronic myeloid leukemia MGI:88141 Mus musculus (house mouse) 110279 Bcr
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia MGI:88141 Mus musculus (house mouse) 110279 Bcr
  • MGI:6194238
DOID:1240 leukemia MGI:88141 Mus musculus (house mouse) 110279 Bcr
  • MGI:6194238
DOID:0110486 autosomal recessive nonsyndromic deafness 28 MGI:1349410 Mus musculus (house mouse) 110253 Triobp
  • MGI:6194238
  • PMID:20510926
DOID:3633 beta-mannosidosis MGI:88175 Mus musculus (house mouse) 110173 Manba
  • MGI:6194238
  • PMID:16377659
DOID:9256 colorectal cancer HGNC:792 Homo sapiens (human) 11016 ATF7
  • PMID:26148593
DOID:3393 coronary artery disease MGI:99501 Mus musculus (house mouse) 110135 Fgb
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:99501 Mus musculus (house mouse) 110135 Fgb
  • MGI:6194238
DOID:1574 alcohol use disorder MGI:99501 Mus musculus (house mouse) 110135 Fgb
  • MGI:6194238
DOID:0060903 thrombosis MGI:99501 Mus musculus (house mouse) 110135 Fgb
  • MGI:6194238
DOID:783 end stage renal disease MGI:99501 Mus musculus (house mouse) 110135 Fgb
  • 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