about
P688
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathwaysThe ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeThromboxane A2-induced signal transduction is negatively regulated by KIAA1005 that directly interacts with thromboxane A2 receptorTMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in RPGRIP1 like
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
RPGRIP1 like
@en
RPGRIP1 like
@nl
type
label
RPGRIP1 like
@en
RPGRIP1 like
@nl
altLabel
RPGR-interacting protein 1-like protein
@en
RPGRIP1-like protein
@en
RPGRIP1L
@en
fantom homolog
@en
nephrocystin-8
@en
protein fantom
@en
protein phosphatase 1, regulatory subunit 134
@en
prefLabel
RPGRIP1 like
@en
RPGRIP1 like
@nl
P637
P681
P682
P705
P352
P637
P638
P31
P352
P637
NP_001121369
NP_001295263
NP_001315351
NP_001315352
NP_001317467
XP_005255925
XP_011521272
XP_011521273
XP_011521275
P681
P682
P702
P703
P705
ENSP00000262135
ENSP00000455295
ENSP00000455451
ENSP00000456534
ENSP00000457889
ENSP00000458705
ENSP00000459817
ENSP00000463678
ENSP00000480698
ENSP00000493946