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Publication : Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17.

First Author  Ring HZ Year  1999
Journal  Genomics Volume  56
Issue  3 Pages  350-2
PubMed ID  10087204 Mgi Jnum  J:54030
Mgi Id  MGI:1334025 Doi  10.1006/geno.1998.5725
Citation  Ring HZ, et al. (1999) Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17. Genomics 56(3):350-2
abstractText  The K homology-type splicing regulatory protein, KSRP, activates splicing through intronic splicing enhancer sequences. It is highly expressed in neural cells and is required for the neural-specific splicing of the c-src N1 exon, In this study, we mapped the gene (gene symbols KHSRP and Khsrp) to human chromosome 19 by using radiation hybrid panels and to mouse chromosome 17 by studying an interspecific backcross panel. Human KHSRP is a positional candidate gene for familial febrile convulsion and Cayman type cerebellar ataxia, Comparative analysis of the human and mouse genomes indicates that the KHSRP gene is located in regions of conserved synteny between the two species. (C) 1999 Academic Press.
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