Dear mailing list,

I was using to Ensembl Biomart web interface to retrieve the chromsome locations of my genes of interest (gene symbols). I chose Ensembl Genes 66 and Homo Sapiens genes (GRCh37.p6) as dataset. For filters I chose to limit to genes with HGNC IDs, and gave a few HGNC genes symbols. For Attributes I chose Ensembl Gene ID, Ensembl Transcript ID, Chromosome Name, Gene Start (bp), Gene End (bp), Transcript Start (bp) and Transcript End (bp). In the results table I have many transcripts with different start and stop positions corresponding to one gene. This is fine. It looks like the Gene Start is the minimum of all Transcript Start and the Gene Stop is the maximum of all Transcript End. Could anyone confirm this? This is important to me because in the next step I need to find the SNPs in these chromosome regions.

Thank you in advance!

Yong

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Dr. Yong Li
AG PD Dr. Anna Koettgen, MPH
Universitaetsklinikum Freiburg
Innere Medizin IV

Tel +49 761 270-78210 / Fax -78040
Berliner Allee 29, 79110 Freiburg
[email protected]
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