Mutation details: A 1.1 kb sequence containing 365 bp upstream of the predicted translational start site of exon 1 and 696 bp downstream of the exon 1 splice donor site was replaced with a PGKneo selection cassette. The deleted sequence was common to both known transcripts. Northern blot of mutant brains suggested that the allele may not have been a null as overexposure to probes demonstrated transcripts at ~7% of wild-type levels.
(J:72166)
Phenotypes
View phenotypes and curated references for all genotypes (concatenated display).
J:72166 Clark RM, et al., Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting lmbr1. Genetics. 2001 Oct;159(2):715-26
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