IPP2L Polyclonal Antibody, 50ul Miscellaneous Mutations in this gene cause

Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis

Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD)

The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation

This protein family is required for myocyte cytoskeletal development

Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum

IPP2L Polyclonal Antibody, 50ul Miscellaneous Mutations in this gene causePPP1R2P1 (Protein Phosphatase 1 Regulatory Inhibitor Subunit 2 Pseudogene 1) is a Pseudogene. GO annotations related to this gene include protein phosphatase inhibitor activity. Inhibitor of protein phosphatase 1.