ZO1 Polyclonal Antibody, 20ul Protein Post-translational Modification The interaction may be indirect

The interaction may be indirect

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

NDUFA3 (NADH: ubiquinone Oxidoreductase Subunit A3) is a Protein Coding gene

An important paralog of this gene is POLH

Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene

ZO1 Polyclonal Antibody, 20ul Protein Post-translational Modification The interaction may be indirectThis gene encodes a protein located on a cytoplasmic membrane surface of intercellular tight junctions. The encoded protein may be involved in signal transduction at cell cell junctions. Alternative splicing of this gene results in multiple transcript variants.