Claudin-11 is a membrane protein in the claudin family that contributes to specialized tight junction strands. It occurs in central-nervous-system myelin and at contacts between Sertoli cells in the testis. A protein shared by those locations can contribute to different tissue functions without making the two tissues anatomically equivalent.[ref]
In the 1999 null-mouse experiment, freeze-fracture electron microscopy showed loss of the normal strands in myelin and between Sertoli cells. The mice also had slowed nerve conduction, conspicuous hindlimb weakness and male sterility. This connected a defined molecular change with both structural and physiological observations.[ref]
The comparison separates contact from a functional junction. Two membranes can remain close in an image without possessing the normal strand organization. Conversely, seeing a strand does not supply a direct numerical measurement of permeability to every solute. Structural imaging, tracer passage and nerve conduction ask complementary questions; the knockout results should not be rewritten as if all three measurements were identical.

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