about
P688
Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonUsher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activationLocalization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptors
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Clarin 1
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Clarin 1
@en
type
label
Clarin 1
@en
altLabel
Clrn1
@en
Usher syndrome 3A homolog
@en
clarin-1
@en
usher syndrome type-3 protein homolog
@en
prefLabel
Clarin 1
@en
P637
P681
P682
P705
P352
P31
P352
P637
P681
P682
P702
P703
P705
ENSMUSP00000051738
ENSMUSP00000052254
ENSMUSP00000072363