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Publication : Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4.

First Author  Jackson T Year  2002
Journal  Biochem Biophys Res Commun Volume  296
Issue  5 Pages  1143-7
PubMed ID  12207892 Mgi Jnum  J:79101
Mgi Id  MGI:2387226 Doi  10.1016/s0006-291x(02)02023-5
Citation  Jackson T, et al. (2002) Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4. Biochem Biophys Res Commun 296(5):1143-7
abstractText  The jerker mutation causes degeneration of cochlea and vestibular sensory hair cells in mice. A frame-shift mutation in the actin bundling gene Espin (Espn) leads to hair bundle defects by disrupting the actin filament assembly in stereocilia. Previously, jerker was mapped to distal mouse chromosome 4. Here, analyzing 2536 informative meioses derived from two intersubspecific intercrosses, we localize jerker to a 0.51+/-0.14cM interval on chromosome 4. The following order and distances of genes and markers were determined: D4Mit180-0.44+/-0.13cM-Hes2, Espn(je)-0.08+/-0.06cM-D4Mit356-0.28+/-0.1cM-D4Mit208. A 300kb physical bacterial artificial chromosome (BAC) contig was generated containing the Espn(je) locus. The human homologous region maps to 1p36.31. We present a detailed high-resolution genetic and physical map of markers located at distal chromosome 4 and demonstrate concordance of Espn with jerker.
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