A c.164C>T point mutation changes serine codon 55 (TCA) to leucine codon TTA (p.S55L) in exon 3. This mutation is the equivalent of the p.S59L mutation found in some FTD-ALS (frontotemporal dementia-amyotrophic lateral sclerosis) patients. The self-excising loxP site flanked cre gene neomycin resistance gene cassette that was inserted into intron 3 was removed through cre-mediated recombination in male germinal cells. (J:293836)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6N
Targeted
Single point
--
1
6
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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