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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 326 - 350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4608 common bile duct neoplasm HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:16416732
DOID:26 pancreas disease HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:19843662
DOID:2394 ovarian cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17581599
  • PMID:17785569
DOID:3587 pancreatic ductal carcinoma HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:12874021
  • PMID:19818733
DOID:1793 pancreatic cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17019794
  • PMID:17785569
  • PMID:18281514
  • PMID:19843662
DOID:4897 bile duct carcinoma HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17276942
DOID:0080564 congenital disorder of glycosylation Il MGI:1924753 Mus musculus (house mouse) 102580 Alg9
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:1924753 Mus musculus (house mouse) 102580 Alg9
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:920 Homo sapiens (human) 10317 B3GALT5
  • PMID:14555842
DOID:3910 lung adenocarcinoma HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:30727821
DOID:1612 breast cancer HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:25526449
DOID:0050560 Walker-Warburg syndrome HGNC:13530 Homo sapiens (human) 10329 RXYLT1
  • MGI:6194238
DOID:0111239 congenital muscular dystrophy-dystroglycanopathy type A10 HGNC:13530 Homo sapiens (human) 10329 RXYLT1
  • RGD:7240710
DOID:2841 asthma HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:15266299
  • PMID:18547625
DOID:8677 perinatal necrotizing enterocolitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:399 tuberculosis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:18091991
DOID:13564 aspergillosis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:16461792
DOID:0060000 infective endocarditis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:25213166
DOID:874 bacterial pneumonia HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:5679 retinal disease HGNC:24289 Homo sapiens (human) 10390 CEPT1
  • MGI:6194238
DOID:4195 hyperglycemia MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
DOID:0111100 maturity-onset diabetes of the young type 2 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:15102714
  • PMID:15161764
  • PMID:15569412
  • PMID:17353190
  • PMID:19952346
  • PMID:24447392
  • PMID:7553875
  • PMID:7665557
  • PMID:8530440
  • PMID:9867845
DOID:2018 hyperinsulinism MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
DOID:10763 hypertension MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • 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: August 19, 2024