rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function.
26224785
2015
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function.
26224785
2015
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function.
26224785
2015
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
In two patients with ABL , we identified in MTTP a novel frameshift mutation (K35Ffs*37), and four novel missense mutations, namely, G264R , Y528H, R540C, and N649S.
25108285
2014
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
These studies indicate that missense mutations Y528H , R540C, and N649S appear to cause ABL by reducing MTTP activity rather than by reducing binding of MTTP with protein disulfide isomerase or apoB.
25108285
2014
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
These studies indicate that missense mutations Y528H, R540C , and N649S appear to cause ABL by reducing MTTP activity rather than by reducing binding of MTTP with protein disulfide isomerase or apoB.
25108285
2014
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Loss of both phospholipid and triglyceride transfer activities of microsomal triglyceride transfer protein in abetalipoproteinemia.
23475612
2013
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Loss of both phospholipid and triglyceride transfer activities of microsomal triglyceride transfer protein in abetalipoproteinemia.
23475612
2013
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Loss of both phospholipid and triglyceride transfer activities of microsomal triglyceride transfer protein in abetalipoproteinemia.
23475612
2013
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
22236406
2012
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
22236406
2012
rs1560621495
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
A
0.700
CausalMutation
CLINVAR
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
22236406
2012
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
22236406
2012
rs755681036
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
A
0.700
GeneticVariation
CLINVAR
Abetalipoproteinemia: two case reports and literature review.
18611256
2008
rs146064714
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
T
0.700
CausalMutation
CLINVAR
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient.
17275380
2007
rs1560614646
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
T
0.700
GeneticVariation
CLINVAR
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient.
17275380
2007
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.
10679949
2000
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel mutations in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia.
10946006
2000
rs146064714
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
T
0.700
CausalMutation
CLINVAR
Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.
10679949
2000
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel mutations in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia.
10946006
2000
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.
10679949
2000
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.
10679949
2000
rs372321643
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
Novel mutations in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia.
10946006
2000
rs1367079155
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase.
8939939
1996
rs1485375137
×
Entrez Id:
4547
Gene Symbol:
MTTP
MTTP
Abetalipoproteinemia
0.700
GeneticVariation
UNIPROT
A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase.
8939939
1996