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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 65701 - 65725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4927 Klatskin's tumor HGNC:11110 Homo sapiens (human) 8289 ARID1A
  • PMID:33387086
DOID:4914 esophagus adenocarcinoma HGNC:11110 Homo sapiens (human) 8289 ARID1A
  • PMID:31906887
DOID:0050934 ovarian clear cell carcinoma HGNC:11110 Homo sapiens (human) 8289 ARID1A
  • PMID:21900401
DOID:0070042 Coffin-Siris syndrome 1 HGNC:11110 Homo sapiens (human) 8289 ARID1A
  • MGI:6194238
DOID:4928 intrahepatic cholangiocarcinoma HGNC:11110 Homo sapiens (human) 8289 ARID1A
  • PMID:27433094
  • PMID:30849962
  • PMID:31665232
DOID:0112368 Coffin-Siris syndrome 5 HGNC:11109 Homo sapiens (human) 6605 SMARCE1
  • RGD:7240710
DOID:3565 meningioma HGNC:11109 Homo sapiens (human) 6605 SMARCE1
  • PMID:29409008
DOID:1508 candidiasis HGNC:11109 Homo sapiens (human) 6605 SMARCE1
  • MGI:6194238
DOID:4586 familial meningioma HGNC:11109 Homo sapiens (human) 6605 SMARCE1
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:11107 Homo sapiens (human) 6603 SMARCD2
  • MGI:6194238
DOID:1925 Coffin-Siris syndrome HGNC:11107 Homo sapiens (human) 6603 SMARCD2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:11106 Homo sapiens (human) 6602 SMARCD1
  • MGI:6194238
DOID:1925 Coffin-Siris syndrome HGNC:11106 Homo sapiens (human) 6602 SMARCD1
  • MGI:6194238
DOID:0112372 Coffin-Siris syndrome 11 HGNC:11106 Homo sapiens (human) 6602 SMARCD1
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:11106 Homo sapiens (human) 6602 SMARCD1
  • MGI:6194238
DOID:0112367 Coffin-Siris syndrome 8 HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • RGD:7240710
DOID:162 cancer HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • MGI:6194238
DOID:1925 Coffin-Siris syndrome HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • MGI:6194238
DOID:0050340 opportunistic bacterial infectious disease HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:11104 Homo sapiens (human) 6599 SMARCC1
  • PMID:33532313
DOID:0050340 opportunistic bacterial infectious disease HGNC:11104 Homo sapiens (human) 6599 SMARCC1
  • MGI:6194238
DOID:162 cancer HGNC:11104 Homo sapiens (human) 6599 SMARCC1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:11104 Homo sapiens (human) 6599 SMARCC1
  • PMID:32514535
DOID:1574 alcohol use disorder HGNC:11104 Homo sapiens (human) 6599 SMARCC1
  • MGI:6194238

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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