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KSR1 has a putative carboxy-terminal kinase domain that lacks a key Lys residue for phospho-group transfer

Diseases associated with MYBL1 include burkitt lymphoma

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a mutant defective in DNA double-strand break repair and in ability to undergo V(D)J recombination

BHE22 Rabbit Polyclonal Antibody, 100ul Monoclonal Antibodies Unleash your daring side withThis gene encodes a protein that belongs to the basic helix loop helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis.