about
P688
Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteinsCiliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
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
MKS transition zone complex subunit 1
@en
MKS transition zone complex subunit 1
@nl
type
label
MKS transition zone complex subunit 1
@en
MKS transition zone complex subunit 1
@nl
altLabel
MKS1
@en
Meckel syndrome type 1 protein
@en
POC12 centriolar protein homolog
@en
prefLabel
MKS transition zone complex subunit 1
@en
MKS transition zone complex subunit 1
@nl
P637
P681
P682
P705
P352
P637
P31
P352
P361
P637
NP_001159399
NP_001308197
NP_001308198
NP_001317326
XP_005257542
XP_006722028
XP_011523259
XP_011523260
XP_011523261
P680
P681
P682
P702
P703
P705
ENSP00000316631
ENSP00000376827
ENSP00000376828
ENSP00000442096
ENSP00000462129
ENSP00000462179
ENSP00000462411
ENSP00000462423
ENSP00000462460
ENSP00000463826