FKTN Polyclonal Antibody, 100ul Pipette Filler and thus may mediate the

and thus may mediate the signaling processes that lead to the activation of JAK1

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

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

With 50 reactions and 1 reaction per μl

and adrenomyeloneuropathy due to defects in bile acid synthesis

FKTN Polyclonal Antibody, 100ul Pipette Filler and thus may mediate 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