SH2D5 Polyclonal Antibody, 50ul Protein Expression Mutations in this gene result

Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency

suggesting that it plays a regulatory role in the translation apparatus

Both the human and orthologous mouse genes have been reported to encode two isoforms (with preferential cellular localization) resulting from the use of alternative in-frame translation initiation codons

Protein phosphatase 2A holoenzymes are heterotrimeric proteins composed of a structural subunit A

SH2D5 Polyclonal Antibody, 50ul Protein Expression Mutations in this gene resultSH2D5 (SH2 Domain Containing 5) is a Protein Coding gene. May be involved in synaptic plasticity regulation through the control of Rac GTP levels.