The mutation is a deletion of 27 nucleotides at the 3' terminus of exon 15 (nt 1754-1780, GenBank Accession ID XM_990099), including one copy of a duplicated 7-nucleotide sequence that occurs immediately upstream of the deleted bases and at the 3' end of the deletion; retention of a copy leaves the splice signal at the exon-intron boundary intact. The deletion results in loss of 9 amino acids (aa 506-514), 4 of them very highly conserved, within the DOCK homology region 1 (DRH1) domain of the protein. RT-PCR of mRNA from embryos/mice of various ages and from various organs of 3 week-old mice demonstrates identical expression patterns of wild-type and shorter mutant transcripts. Immunoblot analysis of eye, lung and kidney extracts detects much less immunoreactive protein in mutant than in wild-type tissues. The protein is barely detectable immunohistochemically in the anterior epithelium of the mutant lens, its predominant location in lenses of wild-type mice. (J:134025)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
CXSN/A
Spontaneous
Insertion, Intragenic deletion
Recessive
1
--
7

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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