The UMD-DMD France mutations database
Record ID: 1826

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.6439_6614delp.Glu2147AlafsX17HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel176aFs.Stop at 2163Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #17 

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

On isoforms (a blue cell indicates that the corresponding isoform is affected by the mutation)
Dp 427cDp 427mDp 427pDp 260Dp 140Dp 116Dp 71
       
Immunofluorescence
dys 1 dys 2 dys 3
 No signal with Revertant fibers No signal with Revertant fibers No signal with Revertant fibers
Western Blot
dys 1 dys 2 dys 3
  No signal 

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---035-1-71ProbandMaleUnknownFRANCE

Phenotypic group
 DMD

Comments


WB Dys1 : very low expression (size?)

Reference


Reference IDReference
115Unpublished data