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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 70526 - 70550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:418 systemic scleroderma HGNC:16647 Homo sapiens (human) 10663 CXCR6
  • PMID:21303517
DOID:9256 colorectal cancer HGNC:1863 Homo sapiens (human) 1066 CES1
  • PMID:33878036
DOID:10534 stomach cancer HGNC:1863 Homo sapiens (human) 1066 CES1
  • PMID:28035468
DOID:3119 gastrointestinal system cancer HGNC:1863 Homo sapiens (human) 1066 CES1
  • PMID:33586000
DOID:684 hepatocellular carcinoma HGNC:1863 Homo sapiens (human) 1066 CES1
  • PMID:19658107
  • PMID:24259486
  • PMID:30901224
DOID:3571 liver cancer HGNC:1863 Homo sapiens (human) 1066 CES1
  • MGI:6194238
DOID:0070383 developmental and epileptic encephalopathy 97 HGNC:2550 Homo sapiens (human) 10659 CELF2
  • RGD:7240710
DOID:225 syndrome MGI:1925212 Mus musculus (house mouse) 106583 Scaf8
  • MGI:6194238
DOID:13608 biliary atresia HGNC:11247 Homo sapiens (human) 10653 SPINT2
  • PMID:21898507
DOID:0060781 congenital secretory sodium diarrhea 3 HGNC:11247 Homo sapiens (human) 10653 SPINT2
  • RGD:7240710
DOID:0050889 non-syndromic intellectual disability MGI:1915408 Mus musculus (house mouse) 106529 Tecr
  • MGI:6194238
DOID:0081188 autosomal recessive intellectual developmental disorder 14 MGI:1915408 Mus musculus (house mouse) 106529 Tecr
  • MGI:6194238
DOID:3070 high grade glioma HGNC:1470 Homo sapiens (human) 10645 CAMKK2
  • PMID:27012733
DOID:0060158 acquired metabolic disease HGNC:28868 Homo sapiens (human) 10643 IGF2BP3
  • MGI:6194238
DOID:0060158 acquired metabolic disease HGNC:28866 Homo sapiens (human) 10642 IGF2BP1
  • MGI:6194238
DOID:0070221 progressive familial intrahepatic cholestasis MGI:2146634 Mus musculus (house mouse) 106407 Slc51a
  • MGI:6194238
DOID:0060419 chromosome 3q29 microdeletion syndrome MGI:2146634 Mus musculus (house mouse) 106407 Slc51a
  • MGI:6194238
DOID:0110500 autosomal recessive nonsyndromic deafness 42 MGI:2146574 Mus musculus (house mouse) 106347 Ildr1
  • MGI:6194238
  • PMID:25217574
  • PMID:25819842
  • PMID:25822906
DOID:6000 congestive heart failure HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
  • PMID:16414453
DOID:1474 aggressive periodontitis HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
DOID:783 end stage renal disease HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
DOID:971 tendinitis HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
  • PMID:23453657
DOID:824 periodontitis HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:16953 Homo sapiens (human) 10631 POSTN
  • 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