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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 62351 - 62375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:0060675 catecholaminergic polymorphic ventricular tachycardia 1 RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:1574 alcohol use disorder RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:6000 congestive heart failure RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • PMID:16483256
DOID:6432 pulmonary hypertension RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • PMID:22962011
DOID:8545 malignant hyperthermia RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:11714 gestational diabetes RGD:620314 Rattus norvegicus (Norway rat) 689560 Ryr2
  • MGI:6194238
DOID:5082 liver cirrhosis MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:2747 glycogen storage disease MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:0111043 glycogen storage disease IXc MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:0111396 congenital dyserythropoietic anemia type I MGI:1916218 Mus musculus (house mouse) 68968 Cdan1
  • MGI:6194238
DOID:0111398 congenital dyserythropoietic anemia type Ia MGI:1916218 Mus musculus (house mouse) 68968 Cdan1
  • MGI:6194238
DOID:1338 congenital dyserythropoietic anemia MGI:1916218 Mus musculus (house mouse) 68968 Cdan1
  • MGI:6194238
DOID:0111870 nonphotosensitive trichothiodystrophy 7 HGNC:11572 Homo sapiens (human) 6897 TARS1
  • RGD:7240710
DOID:0111867 nonphotosensitive trichothiodystrophy HGNC:11572 Homo sapiens (human) 6897 TARS1
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:11572 Homo sapiens (human) 6897 TARS1
  • MGI:6194238
DOID:0080201 Peters plus syndrome RGD:1588723 Rattus norvegicus (Norway rat) 689765 B3glct
  • MGI:6194238
DOID:0070122 Meckel syndrome 8 RGD:1591895 Rattus norvegicus (Norway rat) 689779 Tctn2
  • MGI:6194238
DOID:0110993 Joubert syndrome 24 RGD:1591895 Rattus norvegicus (Norway rat) 689779 Tctn2
  • MGI:6194238
DOID:14227 azoospermia MGI:1916231 Mus musculus (house mouse) 68981 Snrpa1
  • MGI:6194238
DOID:65 connective tissue disease MGI:1916231 Mus musculus (house mouse) 68981 Snrpa1
  • MGI:6194238
DOID:5602 T-cell adult acute lymphocytic leukemia HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • MGI:6194238
DOID:0111691 familial adult myoclonic epilepsy 5 HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • RGD:7240710
DOID:3070 high grade glioma HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • PMID:11280781
DOID:850 lung disease HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • PMID:24292748

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International Collaboration

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