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PMID: 10051327 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

PHF2, a novel PHD finger gene located on human chromosome 9q22.

Hasenpusch-Theil K, Chadwick BP, Theil T, Heath SK, Wilkinson DG, Frischauf AM

Abstract

We have isolated and characterized a novel PHD finger gene, PHF2, which maps to human Chromosome (Chr) 9q22 close to D9S196. Its mouse homolog was also characterized and mapped to the syntenic region on mouse Chr 13. The predicted human and mouse proteins are 98% identical and contain a PHD finger domain, eight possible nuclear localization signals, two potential PEST sequences, and a novel conserved hydrophobic domain. Northern analysis shows widespread expression of PHF2 in adult tissues, while in situ hybridization on mouse embryos reveals staining in the neural tube and dorsal root ganglia significantly above a ubiquitous low level expression signal. From its expression pattern and its chromosomal localization, PHF2 is a candidate gene for hereditary sensory neuropathy type I, HSN1.

MeSH Terms
Adult Amino Acid Sequence Animals Chromosome Mapping Chromosomes, Human, Pair 9 Cloning, Molecular DNA, Complementary Homeodomain Proteins Humans Mice Molecular Sequence Data Nuclear Localization Signals Proteins/genetics Sequence Homology, Amino Acid
Chemicals
DNA, Complementary Homeodomain Proteins Nuclear Localization Signals PHF2 protein, human Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hasenpusch-Theil K
Molecular Analysis of Mammalian Mutation, Imperial Cancer Research Fund, London WC2A 3PX, UK.
Chadwick B P
Theil T
Heath S K
Wilkinson D G
Frischauf A M
Article Info
Journal
Mammalian genome : official journal of the International Mammalian Genome Society
Abbr.
Mamm Genome
ISSN
0938-8990
Published
1999-03-00
Pages
294-8
Language
English
Region
United States
NLM ID
9100916
Subset
IM
Databases
GENBANK
AF043725, AF043726
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