Browse our CDH23 (CDH23) ELISA Kits

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Cadherin-Like 23 ELISA Kits (CDH23)
On are 0 Cadherin-Like 23 (CDH23) ELISA Kits from different suppliers available. Additionally we are shipping CDH23 Antibodies (14) and many more products for this protein. A total of 16 CDH23 products are currently listed.
list all ELISA KIts Gene Name GeneID UniProt
Human CDH23 CDH23 64072 Q9H251

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More ELISA Kits for CDH23 Interaction Partners

Human Cadherin-Like 23 (CDH23) interaction partners

  1. We have identified CDH23 mutations as a genetic risk factor for both familial and sporadic pituitary adenoma.

  2. an important contribution of CDH23 mutations to poslingual Sensorineural Hearing Loss

  3. A new diagnosis of sector retinitis pigmentosa was found to have two novel compound heterozygous mutations in CDH23, including one missense (c.8530C > A; p.Pro2844Thr) and one splice-site (c.5820 + 5G > A) mutation.

  4. Four (3.1 %) of 128 children carried two CDH23 mutant alleles, and SLC26A4 (show SLC26A4 ELISA Kits) and GJB2 (show GJB2 ELISA Kits) accounted for 18.0 and 17.2 %, respectively and showed profound nonsyndromic sensorineural hearing loss with minimal residual hearing.

  5. The results revealed that CDH23 mutations are highly prevalent in patients with congenital high-frequency sporadic or recessively inherited hearing loss

  6. Description of the spectrum of mutations in CDH23 in 374 families with autosomal recessive, non-syndromic hearing loss from India.

  7. The results of this study confirm that CDH23 genetic variant may modify the susceptibility to noise-induced hearing loss development in humans

  8. mutations in the CDH23 gene are one of the most important causes of non-syndromic hearing loss in East Asians.

  9. Hearing loss was found to co-segregate with locus-specific STR (show STATH ELISA Kits) markers for CDH23 in 1 Pakistani family.

  10. mutations of the CDH23 gene are an important cause of non-syndromic hearing loss.

Zebrafish Cadherin-Like 23 (CDH23) interaction partners

  1. Unlike other vertebrates, cdh23 is not detectable in zebrafish photoreceptors but instead expressed by a small subset of GABAergic amacrine cells.

  2. Cdh23 is an essential tip link component required for hair-cell mechanotransduction

CDH23 Antigen Profile

Antigen Summary

This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.

Alternative names and synonyms associated with CDH23

  • cadherin-related 23 (CDH23) Elisa Kit
  • cadherin-like 23 (cdh23) Elisa Kit
  • cadherin-like 23 (CDH23) Elisa Kit
  • cadherin-like 23 (LOC100337921) Elisa Kit
  • CDH23 Elisa Kit
  • CDHR23 Elisa Kit
  • USH1D Elisa Kit

Protein level used designations for Cadherin-Like 23 (CDH23) ELISA Kits

cadherin-23 , cadherin-like 23 , cadherin-related family member 23 , otocadherin , cadherin 23 , cadherin related 23 , spu , sputnik , ush1d

64072 Homo sapiens
407978 Danio rerio
423718 Gallus gallus
450516 Pan troglodytes
784716 Bos taurus
100337921 Oryctolagus cuniculus
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