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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 2526 - 2550 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12205 dengue disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:16274635
  • RGD:7240710
DOID:12206 dengue hemorrhagic fever HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:15838506
  • PMID:21245921
DOID:2841 asthma HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21471959
DOID:399 tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:18167547
  • PMID:21454357
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • RGD:7240710
DOID:13564 aspergillosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21381282
DOID:0050827 rheumatic heart disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:30261069
DOID:0080599 Coronavirus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20864747
DOID:0050745 diffuse large B-cell lymphoma HGNC:1643 Homo sapiens (human) 933 CD22
  • PMID:25708834
DOID:1240 leukemia HGNC:16496 Homo sapiens (human) 23305 ACSL6
  • PMID:10502316
DOID:9119 acute myeloid leukemia HGNC:16496 Homo sapiens (human) 23305 ACSL6
  • PMID:10502316
DOID:0060774 congenital diarrhea HGNC:16526 Homo sapiens (human) 51703 ACSL5
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38
  • MGI:6194238
  • PMID:12488956
  • PMID:16459468
DOID:9352 type 2 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38
  • MGI:6194238
  • PMID:12242463
  • PMID:9754820
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:14749 methylmalonic acidemia HGNC:16732 Homo sapiens (human) 84693 MCEE
  • MGI:6194238
DOID:423 myopathy HGNC:16781 Homo sapiens (human) 80896 NPL
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:16787 Homo sapiens (human) 80267 EDEM3
  • RGD:7240710
DOID:10283 prostate cancer HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:17998819

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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