MPRB Polyclonal Antibody, 100ul In vitro Assessment Mutations in this gene cause

Mutations in this gene cause ulnar-mammary syndrome

It constitutes approximately 12% of the noncollagenous proteins in human bone and is synthesized by skeletal-associated cell types

Diseases associated with RGAG1 include non-syndromic x-linked intellectual disability

It localizes primarily within subnuclear foci associated with the nuclear matrix

two nonphosphorylatable alkali light chains

MPRB Polyclonal Antibody, 100ul In vitro Assessment Mutations in this gene causeSteroid membrane receptor. Binds progesterone. May be involved in oocyte maturation.,Belongs to the ADIPOR family.,subcellular location: Colocalizes with a lysosomal protein cathepsin D.,tissue specificity: Expressed in brain and spinal cord.,