×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
BARDET-BIEDL SYNDROME 14 (disorder)
0.600
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
BARDET-BIEDL SYNDROME 14 (disorder)
0.600
Biomarker
GENOMICS_ENGLAND
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
BARDET-BIEDL SYNDROME 14 (disorder)
0.600
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
BARDET-BIEDL SYNDROME 14 (disorder)
0.600
Biomarker
GENOMICS_ENGLAND
[Investigations on the stability of droplets from medical jet and ultrasound aerosol atomizers (author's transl)].
613550
1977
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Ciliopathies
0.390
Biomarker
GENOMICS_ENGLAND
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
18327255
2008
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
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
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
19508969
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
19508969
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
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
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
16415887
2006
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
[Investigations on the stability of droplets from medical jet and ultrasound aerosol atomizers (author's transl)].
613550
1977
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
COACH syndrome
0.740
Biomarker
GENOMICS_ENGLAND
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
Disorder of eye
0.300
Biomarker
GENOMICS_ENGLAND
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Disorder of eye
0.300
Biomarker
GENOMICS_ENGLAND
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Familial aplasia of the vermis
0.680
Biomarker
GENOMICS_ENGLAND
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
Familial aplasia of the vermis
0.680
Biomarker
GENOMICS_ENGLAND
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
18327255
2008
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Familial aplasia of the vermis
0.680
Biomarker
GENOMICS_ENGLAND
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
16415887
2006
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Familial aplasia of the vermis
0.680
Biomarker
GENOMICS_ENGLAND
Mutations of MKS3/TMEM67 , found recently in Meckel-Gruber syndrome (MKS) type 3 and Joubert syndrome (JBTS ) type 6, are predominantly truncating mutations.
19508969
2009
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Hepatic Fibrosis, Congenital
0.410
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Hepatic Fibrosis, Congenital
0.410
Biomarker
GENOMICS_ENGLAND
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.
26191240
2015
×
Entrez Id:
91147
Gene Symbol:
TMEM67
TMEM67
Hepatic Fibrosis, Congenital
0.410
Biomarker
GENOMICS_ENGLAND
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
JOUBERT SYNDROME 6
0.900
Biomarker
GENOMICS_ENGLAND
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
16415887
2006