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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 3001 - 3025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111626 D-glyceric aciduria HGNC:24247 Homo sapiens (human) 132158 GLYCTK
  • RGD:7240710
DOID:5679 retinal disease HGNC:24289 Homo sapiens (human) 10390 CEPT1
  • MGI:6194238
DOID:0060050 autoimmune disease of blood HGNC:24337 Homo sapiens (human) 56913 C1GALT1
  • MGI:6194238
DOID:0080520 Tn polyagglutination syndrome HGNC:24338 Homo sapiens (human) 29071 C1GALT1C1
  • RGD:7240710
DOID:12554 hemolytic-uremic syndrome HGNC:24338 Homo sapiens (human) 29071 C1GALT1C1
  • RGD:7240710
DOID:13564 aspergillosis HGNC:24355 Homo sapiens (human) 51267 CLEC1A
  • RGD:7240710
DOID:3571 liver cancer HGNC:24436 Homo sapiens (human) 134526 ACOT12
  • MGI:6194238
DOID:0080736 Ehlers-Danlos syndrome musculocontractural type 1 HGNC:24464 Homo sapiens (human) 113189 CHST14
  • PMID:20004762
  • PMID:26373698
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:24573 Homo sapiens (human) 55247 NEIL3
  • PMID:35693827
DOID:5844 myocardial infarction HGNC:2464 Homo sapiens (human) 1462 VCAN
  • MGI:6194238
DOID:10941 intracranial aneurysm HGNC:2464 Homo sapiens (human) 1462 VCAN
  • PMID:16917090
DOID:10907 microcephaly HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:10273 heart conduction disease HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:1826 epilepsy HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:2316 brain ischemia HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • MGI:6194238
DOID:2378 relapsing-remitting multiple sclerosis HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:10976643
DOID:9952 acute lymphoblastic leukemia HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:8562939
DOID:11725 Cornelia de Lange syndrome HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:29996118
DOID:1059 intellectual disability HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:25655089
DOID:0080507 Cornelia de Lange syndrome 3 HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
  • RGD:7240710
DOID:0050753 cerebellar ataxia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:1432 blindness HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:2476 hereditary spastic paraplegia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • 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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