FHOD1 Rabbit Polyclonal Antibody, 50ul Cellular Cultivation & Health Management A missense mutation in this

A missense mutation in this gene is associated with hypokalemic periodic paralysis

The DNA-binding motifs suggest this protein is involved in the regulation of transcription and chromatin remodeling

neuronal growth cone collapse and cell migration

Mutations in this gene are associated with Parkinson's disease

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FHOD1 Rabbit Polyclonal Antibody, 50ul Cellular Cultivation & Health Management A missense mutation in thisThis 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