ENU mutagenesis induced a mutation in a 5' splice donor site in intron 29 that causes a thymine to guanine transversion at the second nucleotide of the downstream intron and converts the consensus donor sequence AGGT to AGGG. Analysis and sequencing of the transcript confirmed the deletion of exon 29. The skipping of exon 29 is predicted to result in an in-frame deletion of 73 amino acids resulting in a truncated protein lacking a critical part of the first ATP binding cassette beginning at amino acid 1388. (J:262458)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Intragenic deletion, Single point
Recessive
1
3
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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