The Val342Asp mutation of human cardiac Myosin-Binding Protein C

SEQUENCE
exon 13
nucleotide change T>A
nucleotide pos. in gene 7408
UCSC Golden Path position 47324399
charge change  
codon change  
transcript change  
translation change  


mutated amplimer sequence:
tccccagcccctcttcagctcccttggcccccagtcctgcctggcctggg
acccagagcagctccagctgccccaccagaagggaaggggcagagggaca
ggggtggctacagctccttggtcctgggcccaggaagccccgcccagggg
gctgcagtcttgcccccggccacagcctagactgcgggacacagggactc
gaagctggaggcaccagcagaggaggacgtgtgggagatcctacggcagg
cacccccatctgagtacgagcgcatcgccttccagtacggcgAcactgac
ctgcgcggcatgctaaagaggctcaagggcatgaggcgcgatgagaagaa
gagcacaggttagcccttcctcagaggggagaggagagggcacaggctag
cccttccctacacaggagaggagagggcataggttagcccttccccacag
ggagaggagagggcacaggttagccccccacctcgtccacatacatggaa
agagcggagtccggc


RESTRICTION ENZYME
no information

 
disease HCM

 
    References and comments
  1. Garcia-Castro M, Reguero JR, Alvarez V, Batalla A, Soto MI, Albaladejo V, Coto E.
    Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect.
    Int J Cardiol 2005 Jul 20;102(3):501-7. Epub 2004 Sep 23. (PubMed:16004897)
 

Last modified: April 24, 2006