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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 67251 - 67275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14250 Down syndrome HGNC:10371 Homo sapiens (human) 6175 RPLP0
  • MGI:6194238
DOID:0080750 erythema nodosum HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:2783924
DOID:8893 psoriasis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:2609873
  • PMID:6559061
DOID:6195 conjunctivitis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:3875643
DOID:13241 Behcet's disease HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6900632
DOID:11400 pyelonephritis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:20218820
DOID:2986 IgA glomerulonephritis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:17385664
  • PMID:3118258
  • PMID:8567024
DOID:10887 lepromatous leprosy HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6342123
DOID:0080162 lupus nephritis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:21893562
DOID:418 systemic scleroderma HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:2803327
DOID:9952 acute lymphoblastic leukemia HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6958349
DOID:10976 membranous glomerulonephritis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:3272818
DOID:0110019 age related macular degeneration 7 HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:19899988
DOID:10923 sickle cell anemia HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:10440069
  • PMID:12793071
DOID:2920 membranoproliferative glomerulonephritis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:2329415
DOID:12134 factor VIII deficiency HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6912882
DOID:0080322 polycystic kidney disease HGNC:1037 Homo sapiens (human) 629 CFB
  • MGI:6194238
DOID:0110026 age related macular degeneration 14 HGNC:1037 Homo sapiens (human) 629 CFB
  • RGD:7240710
DOID:783 end stage renal disease HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:1837062
DOID:898 autosomal dominant polycystic kidney disease HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:24494798
DOID:0050127 sinusitis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:14510109
DOID:14095 boutonneuse fever HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:3361150
DOID:12662 paracoccidioidomycosis HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:7921333
DOID:12241 beta thalassemia HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6914868
DOID:1612 breast cancer HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:15274022

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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