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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 10476 - 10500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1024 leprosy HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:18177245
  • RGD:7240710
DOID:13241 Behcet's disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:18336589
  • PMID:19796535
  • PMID:23908180
  • PMID:24255044
DOID:6543 acne HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:18241264
  • PMID:20726329
  • PMID:20861605
DOID:9256 colorectal cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • RGD:7240710
DOID:10223 dermatomyositis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19953283
DOID:0050855 renal fibrosis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • MGI:6194238
DOID:8893 psoriasis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:23457721
DOID:0060224 atrial fibrillation HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19167648
DOID:4677 keratitis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • MGI:6194238
  • PMID:18398706
DOID:13564 aspergillosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:16461792
DOID:399 tuberculosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:18091991
DOID:2957 pulmonary tuberculosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:16493059
DOID:1024 leprosy HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:17548585
  • RGD:7240710
DOID:8677 perinatal necrotizing enterocolitis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • MGI:6194238
DOID:11400 pyelonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:19543401
DOID:2986 IgA glomerulonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:21108742
DOID:2841 asthma HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:18547625
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0111442 optic atrophy 9 HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0050883 infantile cerebellar-retinal degeneration HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:1891 optic nerve disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:4001 ovarian carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9066601
DOID:2871 endometrial carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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