Alpl^Mhdabap32

This ENU-induced mutation was isolated in a screen for metabolic bone disease as part of the Munich ENU Mutagenesis Project. Missense mutation in exon 11 of the gene; an T-to-A point mutation at position 1217 of the cDNA is predicted to alter codon 406 in the encoded protein from a aspartate to glycine. (J:183993)