about
P688
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisTULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary ciliaIntraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis.
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
WD repeat domain 35
@en
WD repeat domain 35
@nl
type
label
WD repeat domain 35
@en
WD repeat domain 35
@nl
altLabel
WD repeat-containing protein 35
@en
WDR35
@en
intraflagellar transport protein 121 homolog
@en
naofen
@en
prefLabel
WD repeat domain 35
@en
WD repeat domain 35
@nl
P361
P527
P637
P681
P682
P705
P352
P31
P352
P361
P637
NP_001006658
XP_011531309
P681
P682
P702
P703
P705
ENSP00000281405
ENSP00000314444
ENSP00000390105
ENSP00000390802
ENSP00000404409