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EN
Genomic sequence spanning part of exon 1 through exon 3 was replaced with (from 5' to 3'): a loxP site, lacZ gene, frt-flanked neo cassette, loxP site, and polyadenylation site. The absence of full-length protein expression was confirmed by western blot analysis on brain extracts. Small amounts of a truncated peptide is detected. (J:158427)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
