The A SNP at this location results in an alternate splice site and the inclusion of a 138 bp cryptic exon (5'). QRT-PCR confirmed reduced transcript levels, likely due to nonsense mediated decay. Western blot analysis confirmed reduced protein levels in heterozygotes. This variant was identified in C57BL/6J and is present in multiple strains (determined by SNP analysis and confirmed by the lack of modifier of Aarssti phenotype activity in MOLF/Ei, DBA/2J, BALB/cJ and C3H/HeJ crosses). (J:262421)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
multiple strains
Not Applicable
Nucleotide substitutions
--
1
--
1

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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