MMP20 Chromosome 11

Matrix metallopeptidase 20
19 variants 19 Health Risk

Upload your DNA to see your personal genotypes for variants in MMP20.

What This Gene Does
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The protein encoded by this gene degrades amelogenin, the major protein component of dental enamel matrix, and thus thought to play a role in tooth enamel formation. A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta. This gene is part of a cluster of MMP genes located on chromosome 11q22.3. [provided by RefSeq, Aug 2011]
Gene Info
Gene Group
M10 matrix metallopeptidases
Locus Type
gene with protein product
Location
11q22.2
Ensembl
ENSG00000137674
Associated Conditions (4)
Amelogenesis imperfecta hypomaturation type 2A2
MMP20-related disorder
Inborn genetic diseases
Gastric cancer
Key Variants
RS148818720
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS149589493
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS17098831
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS61730847
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS61730848
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, MMP20-related disorder, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS61730849
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, MMP20-related disorder, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS61751462
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Inborn genetic diseases, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS61753770
Conflicting classifications of pathogenicity
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS199788797
Likely pathogenic
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS759614533
Likely pathogenic
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS761478767
Likely pathogenic
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
RS781178683
Likely pathogenic
Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
Health Risk
All Variants (19)
RSID Category Clinical Significance Conditions
RS148818720 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS149589493 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS17098831 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS61730847 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS61730848 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, MMP20-related disorder, Amelogenesis imperfecta hypomaturation type 2A2
RS61730849 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, MMP20-related disorder, Amelogenesis imperfecta hypomaturation type 2A2
RS61751462 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Inborn genetic diseases, Amelogenesis imperfecta hypomaturation type 2A2
RS61753770 Health Risk Conflicting classifications of pathogenicity Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS199788797 Health Risk Likely pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS759614533 Health Risk Likely pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS761478767 Health Risk Likely pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS781178683 Health Risk Likely pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS140213840 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, MMP20-related disorder, Inborn genetic diseases
RS1565397250 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS1859555583 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS587777515 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS587777516 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS786204826 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
RS916966344 Health Risk Pathogenic Amelogenesis imperfecta hypomaturation type 2A2, Amelogenesis imperfecta hypomaturation type 2A2
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