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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 63826 - 63850 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080750 erythema nodosum HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:2783924
DOID:2986 IgA glomerulonephritis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:11287758
DOID:8466 retinal degeneration HGNC:1318 Homo sapiens (human) 718 C3
  • MGI:6194238
DOID:10923 sickle cell anemia HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:3896597
  • PMID:7554454
DOID:9744 type 1 diabetes mellitus HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:3253105
DOID:0080162 lupus nephritis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:21888025
DOID:6195 conjunctivitis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:3875643
DOID:3310 atopic dermatitis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:3923750
DOID:5162 arteriolosclerosis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:22863782
DOID:3083 chronic obstructive pulmonary disease HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:17975205
DOID:11394 adult respiratory distress syndrome HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:2784515
  • PMID:3826891
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:20513133
  • RGD:7240710
DOID:3525 middle cerebral artery infarction HGNC:1318 Homo sapiens (human) 718 C3
  • MGI:6194238
DOID:526 human immunodeficiency virus infectious disease HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:7561187
DOID:0110019 age related macular degeneration 7 HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:19899988
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:6915939
DOID:321 tropical spastic paraparesis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:7561187
DOID:8354 complement component 3 deficiency HGNC:1318 Homo sapiens (human) 718 C3
  • MGI:6194238
  • RGD:7240710
DOID:12134 factor VIII deficiency HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:6912882
DOID:11555 Fuchs' endothelial dystrophy HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:21139973
DOID:0080600 COVID-19 HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:32434211
  • PMID:32747830
DOID:10652 Alzheimer's disease HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:22300950
DOID:10976 membranous glomerulonephritis HGNC:1318 Homo sapiens (human) 718 C3
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:1318 Homo sapiens (human) 718 C3
  • MGI:6194238
DOID:9408 acute myocardial infarction HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:26476955

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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