Hi Andrew,

I think what's happening is that there is more than one transcript for 
these genes, so when you query a single gene, e.g. Gvin1, you're getting 
multiple records since there are more than one transcript of that gene. 
Gvin1, for example, has two, e.g.,:

#name   chrom   strand  txStart txEnd   cdsStart        cdsEnd  exonCount       
exonStarts      exonEnds        proteinID       alignID
uc001meo.3      chr11   -       6734382 6743110 6735841 6741268 1       
6734382,        6743110,        Q7Z2Y8  uc001meo.3
uc010ras.1      chr11   -       6737526 6767670 6737527 6741268 2       
6737526,6767579,        6743113,6767670,        Q7Z2Y8  uc010ras.1


Please let us know if you have any additional questions: [email protected]

-
Greg Roe
UCSC Genome Bioinformatics Group


On 7/12/11 12:15 PM, Bissell, Andrew wrote:
> Greetings,
>
>
>
> I am utilizing your database for the acquisition of promoter regions of 
> various genes within the Mus musculus genome of the mm9 build, using the UCSC 
> Genes track.  My parameters are fairly basic, as I have only been searching 
> out the promoter region of each gene, to the extent of 1000 bp upstream and 
> 50 bp downstream, from the 5' side fo the transcription start site; and the 
> 'One FASTA record per gene' option is selected.
>
>
>
> My question is that, with the inclusion of only one known gene (e.g., Gvin1 
> or Lilrb3), why are multiple promoter region sequences provided along 
> different chromosomal coordinates for an single gene?
>
>
>
> Thank you kindly,
>
>
>
> Andrew
> _______________________________________________
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> https://lists.soe.ucsc.edu/mailman/listinfo/genome
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