Skip to main content

Table 3 Multiple sequence alignment of the exon 3 splice acceptor site of SLC26A5.

From: High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss

Species

Intron 2/EXON 3*

Ensembl Gene ID

Human

cccctag/TGACACT

ENSG00000170615

Chimp

cccctag/TGACACT

ENSPTRG00000019554

Rat

cctgcag/GCTTAGC

ENSRNOG00000011616

Mouse

cccttag/TGGCCAT

ENSMUSG00000029015

Zebrafish

ttttcag/CTGTTCG

ENSDARG00000022424

Fruit fly

ttttcag/CTCCTAA

CG5485

  1. *The invariant AG dinucleotide at the intron 2/exon 3 splice acceptor site is shown in bold and underlined.
Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us