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Gene Information
Gene symbol: CLDN16
Gene name: claudin 16
HGNC ID: 2037
Synonyms: PCLN1, HOMG3
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | CASR | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 18446382 | Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia. |