about
P688
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DA functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafnessDigenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansSurvey 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%Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Cadherin related 23
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Cadherin related 23
@en
Cadherin related 23
@nl
type
label
Cadherin related 23
@en
Cadherin related 23
@nl
altLabel
CDH23
@en
cadherin-23
@en
cadherin-like 23
@en
cadherin-related family member 23
@en
otocadherin
@en
prefLabel
Cadherin related 23
@en
Cadherin related 23
@nl
P637
P638
P680
P681
P682
P705
P352
P637
P31
P352
P637
NP_001165401
NP_001165402
NP_001165403
NP_001165404
NP_001165405
NP_001165406
NP_001165407
P638
P682
P702
P703
P705
ENSP00000224721
ENSP00000299366
ENSP00000381768
ENSP00000381789
ENSP00000381822
ENSP00000388894
ENSP00000473454
ENSP00000473539
ENSP00000478374
ENSP00000480146