×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GeneticVariation
disease
BEFREE
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation.
30705305
2019
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.
28719906
2017
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia.
28431631
2017
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Joubert syndrome: genotyping a Northern European patient cohort.
25920555
2016
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GeneticVariation
disease
CLINVAR
Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping.
26729329
2016
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping.
26729329
2016
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.
26092869
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
Biomarker
disease
BEFREE
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway.
26035863
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway.
26035863
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy.
23559409
2013
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy.
21068128
2011
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GermlineCausalMutation
disease
ORPHANET
Molecular genetics and pathogenic mechanisms for the severe ciliopathies: insights into neurodevelopment and pathogenesis of neural tube defects.
21110233
2011
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies.
21866095
2011
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.
20232449
2010
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
19574260
2010
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Polycystic kidney and hepatic disease with mental retardation is nephronophthisis 11 caused by MKS3/TMEM67 mutations.
20607301
2010
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
19540516
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
19508969
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GermlineCausalMutation
disease
ORPHANET
Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups?
19466712
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement.
19058225
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3.
17377820
2007
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GermlineCausalMutation
disease
ORPHANET
Meckel syndrome: genetics, perinatal findings, and differential diagnosis.
17389183
2007
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
CausalMutation
disease
CLINVAR
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
17397051
2007
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
GeneticVariation
disease
BEFREE
The transmembrane protein meckelin (MKS3 ) is mutated in Meckel-Gruber syndrome and the wpk rat.
16415887
2006
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
0.630
Biomarker
disease
RGD
The transmembrane protein meckelin (MKS3 ) is mutated in Meckel-Gruber syndrome and the wpk rat.
16415887
2006