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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 2501 - 2525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3407 carotid artery disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:15640605
  • PMID:16873708
DOID:552 pneumonia HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20302606
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518
DOID:1205 allergic disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19222419
DOID:13580 cholestasis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:10608 celiac disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18728522
DOID:2945 severe acute respiratory syndrome HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19635508
DOID:11335 sarcoidosis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20430603
DOID:5844 myocardial infarction HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10195920
  • PMID:14587643
  • PMID:17436151
DOID:9744 type 1 diabetes mellitus HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10831941
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:10487 Hirschsprung's disease HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:824 periodontitis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:13603 obstructive jaundice HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:1394 urinary schistosomiasis HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:22347409
DOID:2957 pulmonary tuberculosis HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:30972222
DOID:10534 stomach cancer HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:26119195
DOID:12206 dengue hemorrhagic fever HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:24945350
DOID:0110480 autosomal recessive nonsyndromic deafness 22 HGNC:16378 Homo sapiens (human) 146183 OTOA
  • MGI:6194238
  • RGD:7240710
DOID:635 acquired immunodeficiency syndrome HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:17530998
DOID:0050598 extrapulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:24874302
DOID:6432 pulmonary hypertension HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:17107989
DOID:11650 bronchopulmonary dysplasia HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20050784
DOID:2957 pulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:19126442
  • PMID:24874302

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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