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The genomic sequence extending from the 3' end of intron 1 through the 5' end of exon 3 was replaced with the missing portion of intron 1 through the 5' end of exon 3 following by a puromycin resistance cassette, loxP site, 3'Hprt mini-gene, and a duplication of the 3' end of intron 1 through the 5' end of exon 3. The absence of transcript expression was confirmed by northern blot analysis on brain extracts. (J:148467)
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
