MTTP Chromosome 4

Microsomal triglyceride transfer protein
169 variants 169 Health Risk

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What This Gene Does
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]
Associated Conditions (5)
Abetalipoproteinaemia
Inborn genetic diseases
MTTP-related disorder
Ovarian cancer
Metabolic syndrome X
Key Variants
All Variants (169)
RSID Category Clinical Significance Conditions
RS1560627357 Health Risk Pathogenic
RS1717552752 Health Risk Pathogenic
RS1725126993 Health Risk Pathogenic
RS1725514012 Health Risk Pathogenic
RS1725671086 Health Risk Pathogenic
RS1725675795 Health Risk Pathogenic
RS1725827762 Health Risk Pathogenic
RS1725943334 Health Risk Pathogenic
RS1726221197 Health Risk Pathogenic
RS1726266741 Health Risk Pathogenic
RS1726269709 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS17599091 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS199422219 Health Risk Pathogenic Abetalipoproteinaemia, MTTP-related disorder, Abetalipoproteinaemia
RS199422221 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS199422222 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS2110211759 Health Risk Pathogenic
RS2110212658 Health Risk Pathogenic
RS2110212747 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS2110217058 Health Risk Pathogenic
RS2110217173 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS2110218614 Health Risk Pathogenic Abetalipoproteinaemia, Abetalipoproteinaemia
RS2110222141 Health Risk Pathogenic
RS2110222234 Health Risk Pathogenic
RS2110222265 Health Risk Pathogenic
RS2110228616 Health Risk Pathogenic
RS2110230118 Health Risk Pathogenic
RS2110230220 Health Risk Pathogenic
RS2110230260 Health Risk Pathogenic
RS2110231743 Health Risk Pathogenic
RS2110233238 Health Risk Pathogenic
RS2110237031 Health Risk Pathogenic
RS2110237126 Health Risk Pathogenic
RS2110238242 Health Risk Pathogenic
RS2476074113 Health Risk Pathogenic
RS2476086722 Health Risk Pathogenic
RS2476086913 Health Risk Pathogenic
RS2476090084 Health Risk Pathogenic
RS2476090164 Health Risk Pathogenic
RS2476102668 Health Risk Pathogenic
RS2476102752 Health Risk Pathogenic
RS2476106469 Health Risk Pathogenic
RS2476106633 Health Risk Pathogenic
RS2476118093 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2476118381 Health Risk Pathogenic
RS2476126352 Health Risk Pathogenic
RS2476134985 Health Risk Pathogenic
RS2476145104 Health Risk Pathogenic
RS2476145822 Health Risk Pathogenic
RS2476145911 Health Risk Pathogenic
RS2476161600 Health Risk Pathogenic
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