Hi,
    I noticed some genes in UCSC has more than one chromosome locations.
    e.g. when I search DUX4 in human version 2006 genome browser. I can 
get the following position of this gene.
RefSeq Genes
DUX4 at chr4:191245841-191247457 - (NM_033178) double homeobox, 4
DUX4 at chr4:191232654-191234270 - (NM_033178) double homeobox, 4
DUX4 at chr4:191229361-191230977 - (NM_033178) double homeobox, 4
DUX4 at chr4:191239248-191240864 - (NM_033178) double homeobox, 4
DUX4 at chr4:191242541-191244157 - (NM_033178) double homeobox, 4
DUX4 at chr10:135330358-135335265 - (NM_033178) double homeobox, 4
DUX4 at chr10:135333669-135338574 - (NM_033178) double homeobox, 4

This gene has only one refseq accession number (NM_033178). But it was 
mapped on different chromosome (chr4 and chr10).
So what happened? I noticed that NCBI Entrez gene database only mapped 
this gene on a specific location on chr4.

Other genes like LOC728340, SULT1A3, XAGE1D etc. also have this problem.

I noticed many gene were mapped on both chrX and chrY. I saw the 
following assembly description at http://genome.ucsc.edu/cgi-bin/hgGateway
"The Y chromosome in this assembly contains two pseudoautosomal regions 
(PARs) at chrY:1-2709520 and chrY:57443438-57772954. These sequences 
were taken from the corresponding regions in the X chromosome and are 
exact duplications of the X chromosome sequences at chrX:1-2709520 and 
chrX:154584237-154913754, respectively."

Does this means those genes mapped on both ChrX and ChrY should be only 
mapped on ChrX?

Thanks.

Anyuan Guo
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Genome maillist  -  [email protected]
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