Ush2a - SNV Details



 Human Rare Diseases 
Retinitis pigmentosa
Usher syndrome type 2

 Gene Information 
Gene Name Ush2a
Old Gene Names for Ush2a A930011d15rik , Gm983 , A930037m10rik , Gm676
Gene Description Usher syndrome 2A (autosomal recessive, mild) [Source:MGI Symbol;Acc:MGI:1341292]
MGI phenotype Mice homozygous for a knock-out allele display progressive retinal photoreceptor degeneration along with significantly reduced a- and b-wave amplitudes, and a moderate but nonprogressive high-frequency hearing loss associated with widespread loss of outer hair cells in the basal turn of the cochlea.
Uniprot Name
CCDS Name
Gene GO
basement membrane; myosin binding; stereocilia ankle link complex; response to stimulus; integral to membrane; apical plasma membrane; cytoplasm; photoreceptor cell maintenance; hair cell differentiation; protein binding; maintenance of organ identity; stereocilium membrane; sensory perception of sound; stereocilia ankle link; stereocilium bundle; sensory perception of light stimulus; inner ear receptor cell differentiation; collagen binding
Homolog in other species USH2A
Omim http://omim.org/entry/608400
Immgen Expression
MEDIAN(LOWER IN DC8+.TH, TGD.VG5+.ACT.IEL)
Gnf Expression
MEDIAN
MEDIAN
MEDIAN
HIGH
Novel Yes

 Mutation Information 
Mutation Type Splice
Ensembl ID ENSMUSG00000026609
Chromosome 1
Coordinate 188,743,687     (Assembly: GRCm38)    
Ref Base T
Var Base C
Zygosity Heterozygous
Read Depth 30
Allele Frequency
T:R0.60
C:V0.40
Amino Acid Change Disrupted splicing
Splice Position 2
Sample ID IGL02511
Median Base Quality 40
Backgrounds C57BL/6NCrl
Source Australian Phenomics Facility (APF-G1)
Other variants in this mouse 50 Other Mutations

 Predictions 

 Availability Details 
Availability Progeny Cryopreserved