A 53bp segment of DNA containing the intron 2 5-prime splice site of endogenous mouse Sbds was replaced with 50 bp containing the intron 2 5-prime splice site found in human shwachman-diamond syndrome patients, c.258+2T>C. Assessment in MEFs shows that this is a hypomorph with aberrant splicing from a cryptic exon 2 splice site, and exon 2 skipping, with the residual wild type expression less than that found in the human samples. (J:335832)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Endonuclease-mediated
Insertion, Intragenic deletion, Nucleotide substitutions
Not Specified
1
8
--

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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