Dmwd - SNV Details



 Gene Information 
Gene Name Dmwd
Old Gene Names for Dmwd Dm9
Gene Description dystrophia myotonica-containing WD repeat motif [Source:MGI Symbol;Acc:MGI:94907]
Uniprot Name
CCDS Name
Gene GO
protein binding; cellular_component; biological_process; molecular_function
Homolog in other species DMWD
Omim http://omim.org/entry/609857
Immgen Expression
MEDIAN(HIGH IN GN.BM)
Gnf Expression
HIGH(HIGHER IN IMM GROUP, NS GROUPS)
Novel Yes

 Mutation Information 
Mutation Type Non-synonymous
Ensembl ID ENSMUSG00000030410
Chromosome 7
Coordinate 19,081,234     (Assembly: GRCm38)    
Ref Base T
Codon Change cTg/cAg
Var Base A
Zygosity Heterozygous
Read Depth 22
Allele Frequency
T:R0.50
A:V0.50
Amino Acid Position 603
Amino Acid Change L->Q (Leucine -> Glutamine)
Sample ID IGL01620
Median Base Quality 36
Backgrounds Balb/c:C57BL/6
Source Walter and Eliza Hall Institute (WEHI-G1)
Other variants in this mouse 48 Other Mutations

 Predictions 
Polyphen Score 1
Polyphen Prediction Probably damaging
Sift Score 0.04
Sift Prediction deleterious

 Availability Details 
Availability Cryopreserved