Neb - SNV Details



 Human Rare Diseases 
Mild nemaline myopathy
Typical nemaline myopathy
Severe congenital nemaline myopathy
Intermediate nemaline myopathy

 Gene Information 
Gene Name Neb
Old Gene Names for Neb Ai595938
Gene Description nebulin [Source:MGI Symbol;Acc:MGI:97292]
Uniprot Name
CCDS Name
Gene GO
sarcomere organization; protein complex; protein binding; Z disc; striated muscle thin filament; contractile fiber; regulation of actin filament length; actin binding
Homolog in other species NEB
Omim http://omim.org/entry/161650
Immgen Expression
MEDIAN(HIGH IN TGD GROUP, ABT GROUP, TACTIVATION GROUP)
Novel Yes

 Mutation Information 
Mutation Type Non-synonymous
Ensembl ID ENSMUSG00000026950
Chromosome 2
Coordinate 52,319,705     (Assembly: GRCm38)    
Ref Base T
Var Base C
Zygosity Heterozygous
Read Depth 33
Allele Frequency
T:R0.48
C:V0.52
Amino Acid Change T->A (Threonine -> Alanine)
Sample ID IGL03410
Median Base Quality 39
Backgrounds C57BL/6NCrl
Source Australian Phenomics Facility (APF-G1)
Other variants in this mouse 53 Other Mutations

 Predictions 
Polyphen Score 0.04
Polyphen Prediction Benign

 Availability Details 
Availability Cryopreserved