Lmo7 - SNV Details



 Gene Information 
Gene Name Lmo7
Old Gene Names for Lmo7 C78582 , Gm914
Gene Description LIM domain only 7 [Source:MGI Symbol;Acc:MGI:1353586]
MGI phenotype Targeted mutations in this gene result in postnatal lethality, growth defects, skeletal muscle abnormalities and retinal defects reflective of retinal degeneration.
Uniprot Name
CCDS Name
Gene GO
zinc ion binding; protein binding
Homolog in other species LMO7
Omim http://omim.org/entry/604362
Immgen Expression
LOW(HIGH IN B1A.PC)
Gnf Expression
MEDIAN
MEDIAN(HIGH IN LUNG)
LOW/MEDIAN(HIGH IN C2C12, M1)
Novel Yes

 Mutation Information 
Mutation Type Splice
Ensembl ID ENSMUSG00000033060
Chromosome 14
Coordinate 101,902,371     (Assembly: GRCm38)    
Ref Base T
Var Base C
Zygosity Heterozygous
Read Depth 45
Allele Frequency
T:R0.51
C:V0.49
Amino Acid Change Disrupted splicing
Splice Position 2
Sample ID IGL01570
Median Base Quality 36
Backgrounds Balb/c:C57BL/6
Source Walter and Eliza Hall Institute (WEHI-G1)
Other variants in this mouse 28 Other Mutations

 Predictions 

 Availability Details 
Availability Cryopreserved