No coding sequence alterations were found, but a single G-to-A base pair change was identified in the first base of intron 4 that eliminates the exon 4 splice donor site by changing it from G-GT to G-AT. RT-PCR from samples derived from E10.5 embryos showed that in mutant homozygotes a 44 base pair extension of exon 4 into intron 4, was present that is predicted to result in an in-frame stop codon located immediately after exon 4 to be read and to terminate the translation of the encoded after 223 amino acids plus one altered amino acid. QRT-PCR confirmed reduced transcript expression at E10.5. (J:194385)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S5/SvEvBrd
Spontaneous
Single point
Recessive
1
2
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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