Lentiviral human EVC2 sgRNA gene knockout kit

Human EVC2

Gene symbol: EVC2
Synonyms: LBN WAD
Species: HUMAN
Gene ID: 132884
Summary: This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_147127:8:8 NM_001166136:8:7