SHAN3 Polyclonal Antibody, 20ul Dry Bath This gene is located within

This gene is located within a cluster of keratin family members on chromosome 17q21

Mutations in this gene are associated with autosomal dominant progressive external ophthalmoplegia-6 (PEOA6) and Seckel syndrome 8

Cytochrome c oxidase I is the main subunit of the cytochrome c oxidase complex

subunit:Interacts with LMNB1

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SHAN3 Polyclonal Antibody, 20ul Dry Bath This gene is located withinThis gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G protein coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized