Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Combined Automated Annotation using Multiple IEA Methods
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.
A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
Large protein assemblies formed by multivalent interactions between cadherin23 and harmonin suggest a stable anchorage structure at the tip link of stereocilia.
Cadherin-23 mediates heterotypic cell-cell adhesion between breast cancer epithelial cells and fibroblasts.
The strong propensity of Cadherin-23 for aggregation inhibits cell migration.
Structural basis of the strong cell-cell junction formed by cadherin-23.
CDH23: catenin, neuronal and calcium process scope
PTHR24026 PAINT ancestral assertions