Abstract: The FXYD gene family has seven members in mammals and others in fish. Five of these (FXYD1, FXYD2, FXYD4, FXYD7, and PLMS from shark) have been shown to alter the activity of the Na,K‐ATPase, as described by other papers in this volume. The gene structure of FXYD family members suggests assembly from protein domain modules and gene duplication. The γ subunit is unique in the family for having alternative splice variants in the coding region and can be posttranslationally modified with different final consequences for enzyme properties. The nonoverlapping distribution of γ and CHIF (FXYD4) in kidney helps to explain physiological differences in Na+ affinity among nephron segments. We also detected phospholemman (FXYD1) in kidney. By immunofluorescence, it was found in extraglomerular mesangial cells (EM cells) of the juxtaglomerular apparatus and in the afferent arteriole. Contrary to many reports that only α1 and β1 are expressed in the kidney, we found that α2 and β2 are present, although not in any nephron segment. Both were detected in arterioles, and β2 was found in the EM cells. In contrast, α1, β1, and γ were found in adjacent macula densa. Phospholemman, α2, and β2 are proposed to have distinct roles in regulating the sodium pump in structures involved in tubuloglomerular feedback.