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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 1351 - 1375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:83 cataract MGI:104990 Mus musculus (house mouse) 14629 Gclc
  • PMID:23226398
DOID:5082 liver cirrhosis MGI:104990 Mus musculus (house mouse) 14629 Gclc
  • MGI:6194238
DOID:9256 colorectal cancer MGI:104990 Mus musculus (house mouse) 14629 Gclc
  • MGI:6194238
DOID:583 hemolytic anemia MGI:104990 Mus musculus (house mouse) 14629 Gclc
  • MGI:6194238
DOID:0111681 glutamate-cysteine ligase deficiency MGI:104990 Mus musculus (house mouse) 14629 Gclc
  • MGI:6194238
DOID:83 cataract MGI:95730 Mus musculus (house mouse) 14635 Galk1
  • MGI:6194238
DOID:14695 galactokinase deficiency MGI:95730 Mus musculus (house mouse) 14635 Galk1
  • 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:4795 GM2 gangliosidosis, AB variant MGI:95762 Mus musculus (house mouse) 14667 Gm2a
  • MGI:6194238
  • PMID:9223328
DOID:3321 GM2 gangliosidosis MGI:95762 Mus musculus (house mouse) 14667 Gm2a
  • MGI:6194238
DOID:0070450 mitochondrial DNA depletion syndrome 19 HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • RGD:7240710
DOID:0070329 mitochondrial DNA depletion syndrome HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0060536 mitochondrial complex I deficiency HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0060475 myoclonic-atonic epilepsy HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0070268 congenital disorder of glycosylation type IIp HGNC:18085 Homo sapiens (human) 147007 TMEM199
  • RGD:7240710
DOID:684 hepatocellular carcinoma MGI:1202304 Mus musculus (house mouse) 14711 Gnmt
  • PMID:19035462
DOID:0111037 glycine N-methyltransferase deficiency MGI:1202304 Mus musculus (house mouse) 14711 Gnmt
  • MGI:6194238
  • PMID:16779654
  • PMID:17937387
DOID:9120 amyloidosis MGI:95791 Mus musculus (house mouse) 14718 Got1
  • MGI:6194238
DOID:0050700 cardiomyopathy MGI:95791 Mus musculus (house mouse) 14718 Got1
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis MGI:95791 Mus musculus (house mouse) 14718 Got1
  • MGI:6194238
DOID:224 transient cerebral ischemia MGI:95791 Mus musculus (house mouse) 14718 Got1
  • MGI:6194238
DOID:3498 pancreatic ductal adenocarcinoma MGI:95791 Mus musculus (house mouse) 14718 Got1
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • 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: August 19, 2024