RGD Reference Report - Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis. - Rat Genome Database

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Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis.

Authors: Daoud, H  Belzil, V  Desjarlais, A  Camu, W  Dion, PA  Rouleau, GA 
Citation: Daoud H, etal., Arch Neurol. 2010 Apr;67(4):516-7.
RGD ID: 5686382
Pubmed: PMID:20385924   (View Abstract at PubMed)
DOI: DOI:10.1001/archneurol.2010.46   (Journal Full-text)

Abstract for this paper unavailable



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
UNC13AHumanamyotrophic lateral sclerosis no_associationIAGP DNA:SNP:intron:rs12608932 (human)RGD 
Unc13aRatamyotrophic lateral sclerosis no_associationISOUNC13A (Homo sapiens)DNA:SNP:intron:rs12608932 (human)RGD 
Unc13aMouseamyotrophic lateral sclerosis no_associationISOUNC13A (Homo sapiens)DNA:SNP:intron:rs12608932 (human)RGD 

Phenotype Annotations    Click to see Annotation Detail View

Manual Human Phenotype Annotations - RGD

Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
UNC13AHumanBulbar signs  IAGP DNA:SNP:intron:rs12608932 RGD 
Objects Annotated

Genes (Rattus norvegicus)
Unc13a  (unc-13 homolog A)

Genes (Mus musculus)
Unc13a  (unc-13 homolog A)

Genes (Homo sapiens)
UNC13A  (unc-13 homolog A)


Additional Information