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

First Author  Hasenpusch-Theil K Year  1999
Journal  Mamm Genome Volume  10
Issue  3 Pages  294-8
PubMed ID  10051327 Mgi Jnum  J:53817
Mgi Id  MGI:1333442 Doi  10.1007/s003359900989
Citation  Hasenpusch-Theil K, et al. (1999) PHF2, a novel PHD finger gene located on human chromosome 9q22. Mamm Genome 10(3):294-8
abstractText  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.
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