about
P688
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationDisruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromeWdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeletonA transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.Disruption of a ciliary B9 protein complex causes Meckel syndromeA mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signalingAberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndromeCilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
P921
Q24337819-2CA73297-20D0-489B-A8E6-63F2EF146BDEQ24622660-0D2CCB2A-3A87-49E9-B6AC-36AB3FE83909Q27316402-F08F229B-DD60-46F6-91BC-0C6604701B0CQ28000057-31AAFBF4-DBDF-4F3B-B324-D86AA2A9F7C3Q28114969-DBC2FBCE-9165-4520-B107-50587B88A0D6Q28507443-9AB6FDB6-BC77-43FA-A88A-B0D5F1212EBFQ28591420-42BB0CAF-6E69-47DE-9723-EC5F51D7C3B4Q37530115-0F7A4567-2426-44BB-965E-AF783FF03BA2
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Meckel syndrome, type 1
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
MKS transition zone complex subunit 1
@en
Meckel syndrome, type 1
@nl
type
label
MKS transition zone complex subunit 1
@en
Meckel syndrome, type 1
@nl
altLabel
Meckel syndrome type 1 protein homolog
@en
Meckel syndrome, type 1
@en
Mks1
@en
prefLabel
MKS transition zone complex subunit 1
@en
Meckel syndrome, type 1
@nl
P681
P682
P352
P31
P352
P637
NP_001034773
XP_017170120
P680
P681
P682
P702
P703
P705
ENSMUSP00000043790