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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 1851 - 1875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19810822
  • PMID:22560646
  • PMID:23510418
DOID:6543 acne HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17033191
DOID:1273 respiratory syncytial virus infectious disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17264400
  • PMID:17449325
  • PMID:17709532
DOID:13141 uveitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:16157088
DOID:8677 perinatal necrotizing enterocolitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:2957 pulmonary tuberculosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:18008256
  • PMID:19575238
  • PMID:20403143
DOID:10140 dry eye syndrome HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:23372055
DOID:850 lung disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:10690 mastitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15864121
  • PMID:18549840
DOID:0080176 meningococcal meningitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:23691182
DOID:4194 glucose metabolism disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:854 collagen disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:1074 kidney failure HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:3310 atopic dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19764566
  • PMID:23821954
DOID:7147 ankylosing spondylitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20952467
DOID:12894 Sjogren's syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:22703762
DOID:8725 vascular dementia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11273064
DOID:10241 thalassemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11732868
DOID:9408 acute myocardial infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:0080750 erythema nodosum HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12198697
DOID:9588 encephalitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:8283 peritonitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:26601826

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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