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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 70376 - 70400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:11243954
DOID:9563 bronchiectasis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:12123489
  • PMID:7543317
DOID:1793 pancreatic cancer HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:16227367
  • PMID:17072959
DOID:5733 salpingitis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
  • PMID:19012687
DOID:0050127 sinusitis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:11773581
DOID:0080526 bronchiectasis 1 HGNC:1884 Homo sapiens (human) 1080 CFTR
  • RGD:7240710
DOID:4988 alcoholic pancreatitis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:26089335
DOID:13258 typhoid fever HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:16078047
DOID:11132 prostatic hypertrophy HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:25546515
DOID:10652 Alzheimer's disease HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:14757935
DOID:0111864 autosomal recessive congenital bilateral absence of vas deferens HGNC:1884 Homo sapiens (human) 1080 CFTR
  • RGD:7240710
DOID:1724 duodenal ulcer HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
DOID:10808 gastric ulcer HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
DOID:0111862 congenital bilateral absence of vas deferens HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
  • PMID:10653141
  • PMID:11119745
DOID:10211 cholelithiasis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:12184527
DOID:2841 asthma HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:20298391
DOID:1682 congenital heart disease HGNC:233 Homo sapiens (human) 108 ADCY2
  • MGI:6194238
DOID:0070047 Schuurs-Hoeijmakers Syndrome MGI:1277113 Mus musculus (house mouse) 107975 Pacs1
  • MGI:6194238
DOID:1324 lung cancer MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • MGI:6194238
DOID:684 hepatocellular carcinoma MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • MGI:6194238
DOID:0060058 lymphoma MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • MGI:6194238
DOID:0060480 left ventricular noncompaction MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • PMID:37254794
DOID:9256 colorectal cancer MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • MGI:6194238
DOID:1993 rectum cancer MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • MGI:6194238
DOID:234 colon adenocarcinoma MGI:1344380 Mus musculus (house mouse) 107932 Chd4
  • 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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Last updated: December 9, 2024