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Article

The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.

Genomics - 1 Apr 1998

Bartsch J W, Mukai H, Takahashi N, Ronsiek M, Fuchs S, Jockusch H, Ono Y

Abstract excerpt

Protein kinase N (PKN) is a fatty acid- and Rho-activated serine/threonine protein kinase involved in the regulation of cell motility by association with cytoskeletal components such as neurofilament and alpha-actinin. We determined the chromosomal location of the human PKN gene PRKCL1 by fluores...

Topics

Animals
Chromosome Mapping
Chromosomes, Human, Pair 19
Female
Genetic Linkage
Humans
In Situ Hybridization, Fluorescence
Male
Mice
Mice, Inbred C57BL
Muscular Dystrophy, Animal
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Protein Kinase C

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Identifiers

PMID: 9570957
DOI: 10.1006/geno.1997.5208

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9570957-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.PMID 9570957Read ↗

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