PLC Beta2 Polyclonal Antibody, 50ul Drug Development and Evaluation Loss of function compound heterozygous

Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype

Mutations in RPS19 cause Diamond-Blackfan anemia (DBA)

This motif is involved in modulation of cellular responses

that associates with a variety of regulatory subunits

and ovalbumin(ov)-serpin subfamily

PLC Beta2 Polyclonal Antibody, 50ul Drug Development and Evaluation Loss of function compound heterozygousPLCB2 (Phospholipase C Beta 2) is a Protein Coding gene. Diseases associated with PLCB2 include prostate leiomyosarcoma. Among its related pathways are cGMP PKG signaling pathway and African trypanosomiasis. GO annotations related to this gene include calcium ion binding and phosphoric diester hydrolase activity. An important paralog of this gene is PLCB3.