ERMAP Polyclonal Antibody, 50ul Cryopreservation Loss of function mutations in

Loss of function mutations in SLC16A2 are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes

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This gene encodes a member of the adaptor complexes large subunit protein family

Rechargeable Battery: The DLAB pipette can be recharged via a desktop or power cord

ERMAP Polyclonal Antibody, 50ul Cryopreservation Loss of function mutations inThe protein encoded by this gene is a cell surface transmembrane protein that may act as an erythroid cell receptor, possibly as a mediator of cell adhesion. Polymorphisms in this gene are responsible for the Scianna Radin blood group system. Two transcript variants encoding the same protein have been found for this gene.