Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7263
Citations
Scopus Web of ScienceĀ® Altmetric
?
?
Type: Journal article
Title: Location and structure of the human FHR-5 gene
Author: McRae, J.
Murphy, B.
Eyre, H.
Sutherland, G.
Crawford, J.
Cowan, P.
Citation: Genetica, 2002; 114(2):157-161
Publisher: Kluwer Academic Publ
Issue Date: 2002
ISSN: 0016-6707
1573-6857
Statement of
Responsibility: 
McRae, Jennifer ; Murphy, Brendan ; Eyre, Helen ; Sutherland, Grant ; Crawford, Joanna ; Cowan, Peter
Abstract: The factor H family of genes has been localised to human chromosome 1q32. This region encodes various proteins involved in complement regulation and is known as the regulators of complement activation (RCA) gene cluster. The factor H genes encode seven known plasma proteins. Using fluorescence in situ hybridisation (FISH), radiation hybrid (RH) mapping and BLAST alignment analysis, we have established that the factor H-related 5 (FHR-5) gene is closely linked to the other factor H gene family members. Analysis of the genomic sequence indicates that the FHR-5 gene is situated between FHR-2 and the non-complement protein factor XIIIb (Fl3B). Like all members of the factor H family. transcription of FHR-5 is in the telomeric direction. Furthermore, the short consensus repeats (SCRs) of FHR-5 are encoded by individual exons and splicing is of type 1. These data allow the generation of a more complete map of the factor H gene family.
Keywords: Chromosomes, Human, Pair 1; Humans; Blood Proteins; In Situ Hybridization, Fluorescence; Radiation Hybrid Mapping; Sequence Alignment; Base Sequence; Molecular Sequence Data; Complement System Proteins
RMID: 0020020573
DOI: 10.1023/A:1015114512924
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.