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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 1426 - 1450 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:12930 dilated cardiomyopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:10652196
DOID:3083 chronic obstructive pulmonary disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20080081
DOID:8295 scabies HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17884035
DOID:850 lung disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:19897513
DOID:0002116 pterygium HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:18987486
DOID:2841 asthma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:16622028
  • PMID:18048809
  • PMID:19373626
  • PMID:19475625
DOID:1210 optic neuritis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:18055782
DOID:12306 vitiligo HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19439879
  • PMID:20613769
  • PMID:23868633
DOID:8741 seborrheic dermatitis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:24001414
DOID:0050853 chronic venous insufficiency HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:23182154
DOID:13580 cholestasis HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:3458 breast adenocarcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:25050522
DOID:3602 toxic encephalopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:1909 melanoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:9758419
DOID:9452 steatotic liver disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:2987 familial mediterranean fever HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22135646
DOID:9669 senile cataract HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:16129095
  • PMID:23781296
DOID:9111 cutaneous leishmaniasis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:9892499
DOID:9281 phenylketonuria HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:10003 sensorineural hearing loss HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22574884
DOID:10300 Raynaud disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17401513
DOID:9182 pemphigus HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22738420
DOID:8947 diabetic retinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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


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