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Sequences in exon 1 between nucleotides +119 and +164 were replaced with a neomycin selection cassette. The deleted sequences include the translation initiation site and the first 5 codons. RNase protection assays on E13.5 embryos demonstrated that an abnormal transcript was expressed from this allele, but no signal was detected in western blots in extracts derived from E13.5 homozygous embryos. (J:23139)
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
