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IGF2 Polyclonal Antibody, 100ul Centrifugal Filter Mutations in this gene have

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IGF2 Polyclonal Antibody, 100ul Centrifugal Filter Mutations in this gene haveThis gene encodes a member of the insulin family of polypeptide growth factors which are involved in development and growth. It is an imprinted gene expressed only from the paternal allele and epigenetic changes at this locus are associated with Wilms tumour Beckwith Wiedemann syndrome rhabdomyosarcoma and Silver Russell syndrome. A read through INS IGF2 gene exists whose 5' region overlaps the INS gene and the 3' region overlaps this gene.

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Description

Mutations in this gene have been found in somatic sebaceous tumors

The encoded protein regulates the Catalytic activity of protein phosphatase 1 delta and assembly of the actin cytoskeleton

Required for collagen VII (COL7A1) secretion by loading COL7A1 into transport carriers

This gene encodes a cytokine distantly related to type I interferons and the IL-10 family

This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins

IGF2 Polyclonal Antibody, 100ul Centrifugal Filter Mutations in this gene haveThis gene encodes a member of the insulin family of polypeptide growth factors which are involved in development and growth. It is an imprinted gene expressed only from the paternal allele and epigenetic changes at this locus are associated with Wilms tumour Beckwith Wiedemann syndrome rhabdomyosarcoma and Silver Russell syndrome. A read through INS IGF2 gene exists whose 5' region overlaps the INS gene and the 3' region overlaps this gene.

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