FKTN Polyclonal Antibody, 100ul Pipette Filler IGSF8 encodes a member the

IGSF8 encodes a member the EWI subfamily of the immunoglobulin protein superfamily

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A mutation in this gene was associated with microphthalmia| syndromic 13

MIM 601912) is required for many cellular processes

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FKTN Polyclonal Antibody, 100ul Pipette Filler IGSF8 encodes a member theThe protein encoded by this gene is a putative transmembrane protein that is localized to the cis Golgi compartment, where it may be involved in the glycosylation of alpha dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama type congenital muscular dystrophy (FCMD), Walker Warburg syndrome (WWS), limb girdle muscular