I've found some things in refFlat that I don't understand.  Perhaps somebody 
can help shed some light on this.

Intuitively it seemed to me that in most circumstances, all of the records with 
the same geneName should be in about the same place, and certainly in the same 
orientation on the same chromosome. However, I have found several situations 
where this is not the case.  Some of these make sense to me, for example, genes 
in the PARs have records on both chrX and chrY.  Also, there are several that 
have some records on the "hap" sequences.  These I can understand.  Others 
truly puzzle me.  Maybe somebody can help me interpret.

First example is MAGEA2.  This gene has two locations on chrX:

MAGEA2  chrX    -      151918388       151922364       3
MAGEA2  chrX    +       151883119       151887095       3

I don't understand how the same gene could be in two different places?

In some cases they are even on different chromosomes.

In many cases, there seem to be duplicates with different geneName/names.  For 
example:

MIR4509-1       NR_039732       chr15   -       22675147        22675241
MIR4509-2       NR_039733       chr15   -       22675147        22675241
MIR4509-3       NR_039734       chr15   -       22675147        22675241
MIR4509-1       NR_039732       chr15   +       28671636        28671730
MIR4509-2       NR_039733       chr15   +       28671636        28671730
MIR4509-3       NR_039734       chr15   +       28671636        28671730
MIR4509-1       NR_039732       chr15   -       28735897        28735991
MIR4509-2       NR_039733       chr15   -       28735897        28735991
MIR4509-3       NR_039734       chr15   -       28735897        28735991

In this case, there are three geneName/name combinations, and three loci, and 
each geneName/name has a record in each locus.

There are hundreds of these that I've found.

I get the impression that I'm not using this data correctly, and perhaps there 
would be a better table to be using for the purpose of locating genes and 
annotated transcripts on the genome.  Can anybody explain this to me?

Michael

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