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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 69476 - 69500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1826 epilepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:8619 recurrent hypersomnia HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:19404393
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:0060558 lethal congenital contracture syndrome HGNC:237 Homo sapiens (human) 112 ADCY6
  • RGD:7240710
DOID:5199 ureteral obstruction HGNC:237 Homo sapiens (human) 112 ADCY6
  • MGI:6194238
DOID:0070469 neurodevelopmental disorder with dysmorphic facies and thin corpus callosum HGNC:11465 Homo sapiens (human) 11198 SUPT16H
  • MGI:6194238
  • RGD:7240710
DOID:1612 breast cancer HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:16501252
DOID:10283 prostate cancer HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:14517837
DOID:3008 invasive ductal carcinoma HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:14517837
DOID:11054 urinary bladder cancer HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:14517837
  • PMID:18325051
DOID:2154 nephroblastoma HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:16575872
DOID:0050685 small cell carcinoma HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:14517837
DOID:4450 renal cell carcinoma HGNC:18081 Homo sapiens (human) 11197 WIF1
  • PMID:17145819
DOID:2476 hereditary spastic paraplegia HGNC:17018 Homo sapiens (human) 11196 SEC23IP
  • MGI:6194238
DOID:0110779 hereditary spastic paraplegia 28 HGNC:17018 Homo sapiens (human) 11196 SEC23IP
  • MGI:6194238
DOID:0110806 hereditary spastic paraplegia 54 HGNC:17018 Homo sapiens (human) 11196 SEC23IP
  • MGI:6194238
DOID:10907 microcephaly HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:1826 epilepsy HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:219 colon cancer HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:0050912 colon adenoma HGNC:1937 Homo sapiens (human) 1119 CHKA
  • PMID:10363580
DOID:3748 esophagus squamous cell carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1
  • RGD:7240710
DOID:5041 esophageal cancer HGNC:13861 Homo sapiens (human) 11178 LZTS1
  • PMID:10097140
DOID:3459 breast carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1
  • PMID:18686028
DOID:1749 squamous cell carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1
  • PMID:10097140

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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