Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | CLDN14 | contributors: npt/mct - updated : 16-01-2010 |
HGNC name | claudin 14 |
HGNC id | 2035 |
|
DNA |
TYPE | functioning gene |
SPECIAL FEATURE | arranged in tandem |
STRUCTURE | 19.47 kb 3 Exon(s) |
10 Kb 5' upstream gene genomic sequence study |
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MAPPING | cloned | Y | linked | N | status | provisional |
Map | cen - D21S1445 - D21S1920 - D21S2074 - D21S1895 - D21S1921 - D21S2075 - D21S2076 - [D21S2017 - D21S2078 - D21S1252 - CLDN14 - D21S2079 - D21S2080 ] - D21S2081 - D21S167 - D21S267 - qter |
Authors | Wilcox (01) |
RNA |
TRANSCRIPTS | type | messenger |
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EXPRESSION |
Type |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||
organ(s) |
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tissue |
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cells |
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cell lineage
cell lines
| fluid/secretion
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at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
| |
motifs/domains
| |
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HOMOLOGY |
interspecies | ortholog to murine Cldn14 |
Homologene |
FAMILY |
CATEGORY | adhesion , structural protein |
SUBCELLULAR LOCALIZATION | plasma membrane,junction,tight |
basic FUNCTION | |
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CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling | sensory transduction/hearing |
a component |
INTERACTION |
DNA |
RNA |
small molecule | other, |
protein |
cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | DFNB29 |
related resource | Hereditary Hearing Loss Homepage |
Susceptibility | to kidney stones |
Variant & Polymorphism SNP | common, synonymous variants in the CLDN14 gene that associate with kidney stones (Thorleifsson 2009) |
Candidate gene
Marker
| Therapy target
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ANIMAL & CELL MODELS |