Gene Name: EMX2 proximal
Reference Genome: Human
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Click on individual and to
view eBLAT alignments.
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Score
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Total number of aligning bases.
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Start/End
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First and last aligning bases in reference sequence.
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Ns
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# of Sequence gap(s).
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View test species eBLAT to identify gap(s).
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R/D
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Sequence rearrangements and/or duplications.
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R
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Total # of aligning bases unique to the 2nd or 3rd eBLAT
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D
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Total # of common aligning bases
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Red
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Common to 1st, 2nd and 3rd eBLATs
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Brown
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Common to the 1st and 2nd eBLATs
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Magenta
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Common to the 1st and 3rd eBLATs
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