Details for: Cldn10

Gene ID: 58187

Symbol: Cldn10

Ensembl ID: ENSMUSG00000022132

Description: claudin 10

Associated with

Other Information

Genular Protein ID: 1077529357

Symbol: CLD10_MOUSE

Name: Claudin-10

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 16804102

Title: Two splice variants of claudin-10 in the kidney create paracellular pores with different ion selectivities.

PubMed ID: 16804102

DOI: 10.1152/ajprenal.00138.2006

PubMed ID: 19383724

Title: Claudin-10 exists in six alternatively spliced isoforms that exhibit distinct localization and function.

PubMed ID: 19383724

DOI: 10.1242/jcs.040113

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 19468303

Title: Lineage-specific biology revealed by a finished genome assembly of the mouse.

PubMed ID: 19468303

DOI: 10.1371/journal.pbio.1000112

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 14698084

Title: Expression patterns of claudins, tight junction adhesion molecules, in the inner ear.

PubMed ID: 14698084

DOI: 10.1016/s0378-5955(03)00338-1

PubMed ID: 16520537

Title: Developmental changes in the expression of tight junction protein claudins in murine metanephroi and embryonic kidneys.

PubMed ID: 16520537

DOI: 10.1292/jvms.68.149

PubMed ID: 17075866

Title: Expression of claudins in murine tooth development.

PubMed ID: 17075866

DOI: 10.1002/dvdy.21001

PubMed ID: 21183079

Title: A tissue-specific atlas of mouse protein phosphorylation and expression.

PubMed ID: 21183079

DOI: 10.1016/j.cell.2010.12.001

PubMed ID: 22891322

Title: Deletion of claudin-10 (Cldn10) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis.

PubMed ID: 22891322

DOI: 10.1073/pnas.1203834109

PubMed ID: 28771254

Title: Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.

PubMed ID: 28771254

DOI: 10.1038/gim.2017.71

Sequence Information:

  • Length: 231
  • Mass: 24695
  • Checksum: 80A28863B258DED2
  • Sequence:
  • MASTALEIVA FVVSISGWVL VSSTLPTDYW KVSTIDGTVI TTATYFANLW KICVTDSTGV 
    ANCKEFPSML ALDGYIQACR GLMIAAVSLG FFGSIFALFG MKCTKVGGSD QAKAKIACLA 
    GIVFILSGLC SMTGCSLYAN KITTEFFDPL YMEQKYELGA ALFIGWAGAS LCIIGGVIFC 
    FSISDNNKTP RMGYTYNGPT SAMSSRTKYQ GGEGDFKTTG PSKQFDKNAY V

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.