about
sameAs
P688
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FThe giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking routeImpaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)Functional characterization of the human myosin-7a motor domainThe unconventional myosin-VIIa associates with lysosomesHuman Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cellsDefective myosin VIIA gene responsible for Usher syndrome type 1B
P921
Q24291312-F1A29E83-5DD1-4CC7-8C22-C7CBB308CAEAQ24293535-9F59A139-46F2-43E3-9664-62C0C3AFC0A0Q24300791-783C9926-1182-4D9D-968E-DE64E00F5EFAQ24306911-4034B18E-9DE6-4065-B2F6-964D6B99538CQ24307214-C51B9C7F-15D0-44B4-A612-4BEA5B728679Q24312049-8B928BB4-8104-48C6-B8A9-3288C8669846Q24314638-0B357AB6-26BA-46E8-9938-B5436ECFB6AB
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Myosin VIIA
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Myosin VIIA
@en
type
label
Myosin VIIA
@en
altLabel
MYO7A
@en
myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))
@en
unconventional myosin-VIIa
@en
prefLabel
Myosin VIIA
@en
P361
P527
P637
P680
P681
P682
P705
P352
P637
P638
P31
P352
P361
P527
P637
NP_001120652
NP_001356294
XP_011543346
XP_011543348
XP_011543352
XP_016873267
XP_016873268
XP_016873269
XP_016873270
P680
P681
P682
P702
P703
P705
ENSP00000386331
ENSP00000386635
ENSP00000386689
ENSP00000392185
ENSP00000417017
ENSP00000477640
ENSP00000499323
ENSP00000499401
ENSP00000499530