RGPA1 Polyclonal Antibody, 20ul Serum & Sample Tubes Defects in this gene are

Defects in this gene are a cause of non-insulin-dependent diabetes mellitus (NIDDM)

This isozyme is predominantly expressed in the gastrointestinal tract (also in liver in human)| is localized in the cytoplasm| and whose preferred substrate is hydrogen peroxide

This protein may also play a role in early development

BCL7A (BCL tumor suppressor 7A) is directly involved

RGPA1 Polyclonal Antibody, 20ul Serum & Sample Tubes Defects in this gene areThis gene encodes a major subunit of the RAL GTPase activating protein. A similar protein in mouse binds E12, a transcriptional regulator of immunoglobulin genes. The mouse protein also functions in skeletal muscle by binding to the regulatory 14 3 3 proteins upon stimulation with insulin or muscle contraction. A pseudogene of this gene has been identified on chromosome 9.