Exon 1 was flanked by loxP sites and subsequently excised via in vitro cre mediated recombination. The resultant germline allele contained a single loxP site in place of exon 1, which included the 5' untranslated region and encoded the start codon, signal peptide, and part of the extracellular domain. RT-PCR indicated an absence of transcript in homozygous mutant embryos. (J:80043)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count