about
P688
Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variabilityClarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonSerial audiometry and speech recognition findings in Finnish Usher syndrome type III patients
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Clarin 1
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Clarin 1
@en
type
label
Clarin 1
@en
altLabel
CLRN1
@en
Usher syndrome type-3 protein
@en
clarin-1
@en
prefLabel
Clarin 1
@en
P637
P681
P682
P705
P352
P31
P352
P637
NP_001182723
NP_001243748
P681
P682
P702
P703
P705
ENSP00000295911
ENSP00000322280
ENSP00000329158
ENSP00000419892
ENSP00000494762
ENSP00000496637
P7260
9.A.46.1.1