SH2D4A Polyclonal Antibody, 20ul Cytokines Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

Alternatively spliced transcript variants have been found for CBR1

Acrosin binding protein is located in the sperm acrosome and is thought to function as a binding protein to proacrosin for packaging and condensation of the acrosin zymogen in the acrosomal matrix

Ectopic expression of CDKN2C was shown to suppress the growth of human cells in a manner that appears to correlate with the presence of a wild-type RB1 function

as well as inhibiting polyamine uptake

SH2D4A Polyclonal Antibody, 20ul Cytokines Mutations in this gene haveSH2D4A (SH2 Domain Containing 4A) is a Protein Coding gene. GO annotations related to this gene include phosphatase binding. An important paralog of this gene is HSH2D.