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- Table of Contents
Facts about Claudin-10.
It functions as a paracellular ion channel probably forming permselective pores; isoform 1 seems to create pores preferentially permeable to cations and isoform 2 for anions. In sweat glands and in the thick ascending limb (TAL) of Henle's loop in kidney, it controls paracellular sodium permeability which is essential for proper sweat production and renal function (PubMed:19383724, PubMed:28771254, PubMed:28686597).
Human | |
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Gene Name: | CLDN10 |
Uniprot: | P78369 |
Entrez: | 9071 |
Belongs to: |
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claudin family |
claudin 10; claudin-10; CPETRL3; OSP-L; OSP-like protein
Mass (kDA):
24.488 kDA
Human | |
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Location: | 13q32.1 |
Sequence: | 13; NC_000013.11 (95433588..95579759) |
Expressed in the kidney, eccrine sweat glands and in all layers of the epidermis. In the kidney, it is detected in the thick ascending limb of Henle's loop (TAL) (PubMed:28771254, PubMed:28686597). In the sweat glands, it is expressed in cells from secretory portions, corresponding to the clear cells (PubMed:28686597).
Cell junction, tight junction. Cell membrane; Multi-pass membrane protein.
PMID: 19383724 by Gunzel D., et al. Claudin-10 exists in six alternatively spliced isoforms that exhibit distinct localization and function.
PMID: 28771254 by Hadj-Rabia S., et al. Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.