Abstract:
:Employing the mouse homologue of the human choroideremia cDNA as a probe, we have identified a homologous human gene. The consensus cDNA of this gene, designated human choroideremia-like (hCHML) gene, encompasses an open reading frame of 1968 base pairs. The deduced polypeptide of hCHML displays several regions of homology to smg p25A GDI, a bovine protein known to regulate the GDP/GTP exchange of the GTP-binding protein smg p25A. hCHML is located at 1q31-qter, a chromosomal region which, by means of linkage analysis, was previously shown to carry a gene locus for Usher syndrome type II. The colocalization of hCHML and Usher syndrome type II, as well as the clinical similarities between choroideremia and Usher syndrome type II, make hCHML a candidate gene for this disorder.
journal_name
Hum Mol Genetjournal_title
Human molecular geneticsauthors
Cremers FP,Molloy CM,van de Pol DJ,van den Hurk JA,Bach I,Geurts van Kessel AH,Ropers HHdoi
10.1093/hmg/1.2.71subject
Has Abstractpub_date
1992-05-01 00:00:00pages
71-5issue
2eissn
0964-6906issn
1460-2083journal_volume
1pub_type
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