NCL RESOURCE - A GATEWAY FOR BATTEN DISEASE
No. of disease causing mutations: 1
| Identifier | Nucleotide change | Mutation | Amino acid change/ Predicted consequence | Location | Restriction site change | Reference |
|---|---|---|---|---|---|---|
| dcln6.001 | c.829T>C | Missense | p.Trp277Arg | exon 7 | Katz et al J Biomed Biotechnol. 2011;2011:198042. Epub 2010 Dec 22. | |
| dcln6.002 | c.668+7G>A | Polymophism | intron 6 | Katz et al J Biomed Biotechnol. 2011;2011:198042. Epub 2010 Dec 22. |
'NCL Resource' is maintained by Sara Mole.
MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London. WC1E 6BT. United Kingdom.
If you have comments or suggestions or details for inclusion, email ncl-www@ucl.ac.uk or telephone +44 207 679 7257.
Last updated 23/1/2013