The UMD-DMD France mutations database
Record ID: 3114

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.2281_2285delGAAAAp.Glu761SerfsX10HemizygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel5aFs.Stop at 770Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
CRD-repeat #4 Yes, non coding strand

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): Dde I, Fnu4H I

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
   
Western Blot
dys 1 dys 2 dys 3
   

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
---727-0-1ProbandMaleFamilial

Phenotypic group
 DMD

Comments


+ Mental retardation

Reference


Reference IDReference
1Unpublished data