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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 66301 - 66325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4001 ovarian carcinoma HGNC:10887 Homo sapiens (human) 6495 SIX1
  • PMID:17409410
DOID:3192 neurilemmoma HGNC:10887 Homo sapiens (human) 6495 SIX1
  • PMID:19901965
DOID:1612 breast cancer HGNC:10887 Homo sapiens (human) 6495 SIX1
  • PMID:9770533
DOID:14702 branchiootorenal syndrome HGNC:10887 Homo sapiens (human) 6495 SIX1
  • MGI:6194238
  • PMID:15141091
  • PMID:17637804
  • PMID:18330911
  • PMID:21280147
DOID:684 hepatocellular carcinoma HGNC:10887 Homo sapiens (human) 6495 SIX1
  • PMID:17008870
DOID:9975 cocaine dependence HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3070 high grade glioma HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:8552 chronic myeloid leukemia HGNC:10885 Homo sapiens (human) 6494 SIPA1
  • MGI:6194238
DOID:0060470 salt and pepper syndrome HGNC:10872 Homo sapiens (human) 8869 ST3GAL5
  • RGD:7240710
DOID:0080414 developmental and epileptic encephalopathy 15 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:0081180 autosomal recessive intellectual developmental disorder 12 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • PMID:17697868
DOID:3070 high grade glioma HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • MGI:6194238
DOID:0060180 colitis HGNC:10856 Homo sapiens (human) 6476 SI
  • MGI:6194238
DOID:0111633 congenital sucrase-isomaltase deficiency HGNC:10856 Homo sapiens (human) 6476 SI
  • RGD:7240710
DOID:5419 schizophrenia HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:162 cancer HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:1612 breast cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • PMID:17896178
DOID:162 cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • PMID:17031801

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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