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
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