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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 October 9, 2024
Displaying entries 67801 - 67825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0111933 phosphoglycerate kinase 1 deficiency HGNC:8896 Homo sapiens (human) 5230 PGK1
  • RGD:7240710
DOID:0081225 autosomal recessive intellectual developmental disorder 64 HGNC:21205 Homo sapiens (human) 84894 LINGO1
  • RGD:7240710
DOID:14115 toxic shock syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:28336767
DOID:1749 squamous cell carcinoma HGNC:2505 Homo sapiens (human) 1493 CTLA4
  • PMID:19622768
DOID:0080784 urinary tract infection HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19543401
DOID:0080162 lupus nephritis HGNC:4883 Homo sapiens (human) 3075 CFH
  • PMID:22171659
DOID:0070398 hypomyelinating leukodystrophy 15 HGNC:3418 Homo sapiens (human) 2058 EPRS1
  • RGD:7240710
DOID:10534 stomach cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17035401
DOID:0050741 alcohol dependence HGNC:3768 Homo sapiens (human) 342184 FMN1
  • PMID:27151647
DOID:809 cocaine abuse HGNC:15963 Homo sapiens (human) 8973 CHRNA6
  • PMID:24675634
DOID:2921 glomerulonephritis HGNC:1241 Homo sapiens (human) 712 C1QA
  • PMID:8840296
DOID:7148 rheumatoid arthritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:25311255
DOID:0110063 amelogenesis imperfecta hypomaturation type 2A5 HGNC:10978 Homo sapiens (human) 123041 SLC24A4
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:25941 Homo sapiens (human) 54790 TET2
  • PMID:32554069
DOID:2988 antiphospholipid syndrome HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:11157139
DOID:3443 mammary Paget's disease HGNC:3430 Homo sapiens (human) 2064 ERBB2
  • PMID:16932067
DOID:3526 cerebral infarction HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • PMID:28035729
DOID:13025 retinopathy of prematurity HGNC:5956 Homo sapiens (human) 3549 IHH
  • PMID:18787502
DOID:0112038 non-syndromic X-linked intellectual disability 1 HGNC:29059 Homo sapiens (human) 23096 IQSEC2
  • RGD:7240710
DOID:0111705 oculoectodermal syndrome HGNC:6407 Homo sapiens (human) 3845 KRAS
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:16217763
DOID:440 neuromuscular disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489
DOID:2986 IgA glomerulonephritis HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:21047277
DOID:1793 pancreatic cancer HGNC:7468 Homo sapiens (human) 4548 MTR
  • PMID:16737574
  • PMID:18843018
DOID:13241 Behcet's disease HGNC:11364 Homo sapiens (human) 6774 STAT3
  • PMID:22205606
  • PMID:23127549

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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: December 9, 2024