about
P688
TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary ciliaMainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutationsCombined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseasePartial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome.Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.
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
Intraflagellar transport 140
@en
Intraflagellar transport 140
@nl
type
label
Intraflagellar transport 140
@en
Intraflagellar transport 140
@nl
altLabel
IFT140
@en
WD and tetratricopeptide repeats protein 2
@en
intraflagellar transport 140 homolog
@en
intraflagellar transport protein 140 homolog
@en
prefLabel
Intraflagellar transport 140
@en
Intraflagellar transport 140
@nl
P361
P637
P681
P682
P705
P352
P637
P31
P352
P361
P637
XP_005255782
XP_005255783
XP_006721053
XP_006721054
XP_006721055
XP_011521068
XP_011521069
XP_011521071
XP_011521073
P681
P682
P702
P703
P705
ENSP00000354895
ENSP00000380562
ENSP00000406012
ENSP00000454781
ENSP00000457092
ENSP00000458439