The molecular lesion is an 11-bp missense deletion in exon 2 causing an out-of-frame mutation following 34 amino-acids and a premature stop codon in a highly conserved region of the gene. Homology-Independent Targeted Integration (HITI) labeling revealed loss of puncta staining in hippocampal neurons from homozygous mutant mice, thus confirming absence of protein expression. (J:284536)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Endonuclease-mediated
Intragenic deletion
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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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