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FKTN Polyclonal Antibody, 20ul Variant Libraries The protein encoded by this

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FKTN Polyclonal Antibody, 20ul Variant Libraries The protein encoded by thisThe 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

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Description

The protein encoded by this gene contains a Src homology-3 (SH3) domain and a sterile alpha motif (SAM)

This protein is thought to function in matrix maturation during wound healing

Mutations in this gene have been associated with Pfeiffer syndrome| Jackson-Weiss syndrome|

maturation of spliceosomal snRNPs

FKTN Polyclonal Antibody, 20ul Variant Libraries The protein encoded by thisThe 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

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