LongevityMap Gene

Gene details

HGNC symbol
MTTP 
Aliases
ABL; MTP 
Common name
microsomal triglyceride transfer protein 
Description
MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia. [provided by RefSeq, Jul 2008]
Cytogenetic Location
4q23
UCSC Genome Browser
View 4q23 on the UCSC genome browser
OMIM
157147
Ensembl
ENSG00000138823
UniProt/Swiss-Prot
B7Z7X3_HUMAN
Entrez Gene
4547
UniGene
195799
1000 Genomes
1000 Genomes

Homologs in model organisms

Danio rerio
mtp
Drosophila melanogaster
Mtp
Mus musculus
Mttp
Rattus norvegicus
Mttp

Studies (6)

Significant/Non-significant: 1/5

Study 1

Longevity Association
Non-significant
Population
German
Study Design
rs1800591, rs2866164, and Q/H 95 SNPs were examined in 1,039 unrelated individuals between 95 and 109 years of age (mean age, 98.2 years); 373 (36%) of the long-lived participants were centenarians or supercentenarians (mean age, 101.4 years). The sex ratio in the entire sample was 74% females vs. 26% males. A total of 540 control individuals aged between 60 and 75 years (mean age, 67.2 years) were used.
Conclusions
No evidence for association was detected between any of the tested SNPs at the allele or at the genotype level
Indentifier
rs1800591
Reference

    Study 2

    Longevity Association
    Non-significant
    Population
    Dutch
    Study Design
    -493G/T and Q95H allele and haplotype frequencies were examined in 379 nonagenarians, 525 of their offspring, and 251 partners of their offspring and in 655 octogenarians and 244 young controls
    Conclusions
    No association with longevity was found
    Indentifier
    -493G/T
    Reference

      Study 3

      Longevity Association
      Significant
      Population
      Ashkenazi Jewish
      Study Design
      205 centenarians (141 females, median age = 97 years and 64 males, median age = 97 years), their offspring (n = 145 total, 80 females, median age = 69 years and 65 males median age = 68 years), and 288 controls (167 females, median age = 74 years and 121 males, median age = 75 years) were examined for the association between genotype and longevity
      Conclusions
      A U-shape pattern of MTP CC genotype frequency with aging was observed. The CC was a buffered-deleterious genotype in the case group. In the control group without longevity genes, CC genotype included poorer survivorship.
      Indentifier
      rs2866164
      Reference

        Study 4

        Longevity Association
        Non-significant
        Population
        English (Oxford)
        Study Design
        11 SNPs in the MTTP gene were genotyped in 1451 old people (mean age: 77.9 ± 0.2 years) and 777 controls (30- 50 years, mean age: 40.6 ± 0.2 years) to study association with longevity
        Conclusions
        MTTP gene variants were not significant association with longevity
        Indentifier
        rs2866164
        Reference

          Study 5

          Longevity Association
          Non-significant
          Population
          American (Caucasian), French
          Study Design
          A haplotype-based fine-mapping study was performed in 653 individuals (456 females, >= 98 years, mean age = 100.8 years) and controls (< 50 years, mean age = 38.6 years). Then, the identified haplotype marker was tested in 564 French (472 females, >= 99 years, mean age = 103.1 years) and 564 controls (18- 70 years, mean age = 51.2 years).
          Conclusions
          Although the association was not replicated in French cohort, there was evidence for statistical distortion in the form of Hardy–Weinberg disequilibrium.
          Indentifier
          rs2866164
          Reference

            Study 6

            Longevity Association
            Non-significant
            Population
            Danish
            Study Design
            1651 participants in the Danish 1905 cohort study (aged 92-93 years) were genotyped for two SNPs (rs2866164 and Q95H). Furthermore, a group of 575 middle-aged Danish twins (mean age 53.7 years) were tested as a younger control group.
            Conclusions
            The risk haplotype had no significant survival disadvantage after 6.5 years of follow-up. The distributions of the suggested risk alleles and the resulting haplotypes were not statistically different between the two age cohorts.
            Indentifier
            rs2866164
            Reference