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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 8851 - 8875 of 12216 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:26899 Homo sapiens (human) 160418 TMTC3
  • MGI:6194238
DOID:0112233 lissencephaly 8 HGNC:26899 Homo sapiens (human) 160418 TMTC3
  • RGD:7240710
DOID:1936 atherosclerosis HGNC:26876 Homo sapiens (human) 165631 PARP15
  • PMID:33381146
DOID:676 juvenile rheumatoid arthritis HGNC:26789 Homo sapiens (human) 144811 LACC1
  • RGD:7240710
DOID:0111232 congenital muscular dystrophy-dystroglycanopathy type A9 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • RGD:7240710
DOID:0050453 lissencephaly HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:11723 Duchenne muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
  • PMID:15833425
  • PMID:7630355
DOID:12236 primary biliary cholangitis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
DOID:11650 bronchopulmonary dysplasia HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:17196572
DOID:3429 inclusion body myositis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:14972325
DOID:12930 dilated cardiomyopathy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110293 autosomal recessive limb-girdle muscular dystrophy type 2P HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
  • RGD:7240710
DOID:767 muscular atrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:9884 muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:15833425
DOID:769 neuroblastoma HGNC:2665 Homo sapiens (human) 1604 CD55
  • MGI:6194238
DOID:4362 cervical cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:9358772
DOID:1612 breast cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:15102687
  • PMID:18676748
DOID:2870 endometrial adenocarcinoma HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:11506079
DOID:576 proteinuria HGNC:2665 Homo sapiens (human) 1604 CD55
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: August 19, 2024