Clec3b - SNV Details



 Gene Information 
Gene Name Clec3b
Old Gene Names for Clec3b Tna
Gene Description C-type lectin domain family 3, member b [Source:MGI Symbol;Acc:MGI:104540]
MGI phenotype Homozygous null mice exhibit spinal deformities including kyphosis and abnormal morphology of the vertebrae.
Uniprot Name
CCDS Name
Gene GO
cellular response to organic substance; cytoplasm; cellular response to transforming growth factor beta stimulus; proteinaceous extracellular matrix; kringle domain binding; extracellular vesicular exosome; skeletal system development; carbohydrate binding; granular component; heparin binding; ossification; calcium ion binding; extracellular space; bone mineralization
Homolog in other species CLEC3B
Immgen Expression
MEDIAN(HIGHER IN NK GROUP, T.8MEM.LN, TGD.SPT.4NVE.PP, T.4FP3+25+.SP)
Gnf Expression
LOW/MEDIAN(HIGH IN RETINA, UMBLICALCORD, DIGIS, EPIDERMIS TISSUES,TRACHEA)
Novel Yes

 Mutation Information 
Mutation Type Splice
Ensembl ID ENSMUSG00000025784
Chromosome 9
Coordinate 123,151,035     (Assembly: GRCm38)    
Ref Base A
Var Base T
Zygosity Heterozygous
Read Depth 18
Allele Frequency
A:R0.56
T:V0.44
Amino Acid Change Disrupted splicing
Splice Position 9
Sample ID IGL03092
Median Base Quality 39.5
Backgrounds C57BL/6NCrl
Source Australian Phenomics Facility (APF-G1)
Other variants in this mouse 37 Other Mutations

 Predictions 

 Availability Details 
Availability Cryopreserved