FHOD1 Rabbit Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene are

Mutations in this gene are associated with Pendred syndrome

Since this subunit shares identity with a subunit encoding the nuclear respiratory factor 2 gene

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The protein localizes to the cytoplasmic microtubule network and binds APCL

Pseudogenes of UBTF are located on the short arm of chromosomes 3

FHOD1 Rabbit Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene areThis gene encodes a protein which is a member of the formin diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled coil domain a collagen like domain two nuclear localization signals and several potential PKC and PKA phosphorylation sites. It is a