MME Chromosome 3

Membrane metalloendopeptidase
92 variants 92 Health Risk

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

What This Gene Does
The protein encoded by this gene is a type II transmembrane glycoprotein and a common acute lymphocytic leukemia antigen that is an important cell surface marker in the diagnosis of human acute lymphocytic leukemia (ALL). The encoded protein is present on leukemic cells of pre-B phenotype, which represent 85% of cases of ALL. This protein is not restricted to leukemic cells, however, and is found on a variety of normal tissues. The protein is a neutral endopeptidase that cleaves peptides at the amino side of hydrophobic residues and inactivates several peptide hormones including glucagon, enkephalins, substance P, neurotensin, oxytocin, and bradykinin. [provided by RefSeq, Aug 2017]
Gene Info
Gene Group
"CD molecules|M13 metallopeptidases|Elastases"
Locus Type
gene with protein product
Location
3q25.2
Ensembl
ENSG00000196549
Associated Conditions (14)
Charcot-Marie-Tooth disease axonal type 2T
Spinocerebellar ataxia 43
Peripheral neuropathy
Inborn genetic diseases
Familial cancer of breast
Early-onset dementia of unclear type
Distal myopathy
MME-related disorder
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
MME-related distal hereditary motor neuropathies
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease type 2T
See cases
Ovarian serous cystadenocarcinoma
Key Variants
RS1003705057
Conflicting classifications of pathogenicity
Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
Health Risk
RS1060499935
Conflicting classifications of pathogenicity
Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
Health Risk
RS1158932542
Conflicting classifications of pathogenicity
Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
Health Risk
RS1209332250
Conflicting classifications of pathogenicity
Health Risk
RS1284714866
Conflicting classifications of pathogenicity
Spinocerebellar ataxia 43, Spinocerebellar ataxia 43
Health Risk
RS182602615
Conflicting classifications of pathogenicity
Peripheral neuropathy, Peripheral neuropathy
Health Risk
RS184666602
Conflicting classifications of pathogenicity
Spinocerebellar ataxia 43, Spinocerebellar ataxia 43
Health Risk
RS200157166
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200308077
Conflicting classifications of pathogenicity
Health Risk
RS201002280
Conflicting classifications of pathogenicity
Inborn genetic diseases, Spinocerebellar ataxia 43, Charcot-Marie-Tooth disease axonal type 2T
Health Risk
RS201494121
Conflicting classifications of pathogenicity
Familial cancer of breast, Familial cancer of breast
Health Risk
RS202095767
Conflicting classifications of pathogenicity
Early-onset dementia of unclear type, Early-onset dementia of unclear type
Health Risk
All Variants (92)
RSID Category Clinical Significance Conditions
RS1003705057 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1060499935 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1158932542 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1209332250 Health Risk Conflicting classifications of pathogenicity
RS1284714866 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia 43, Spinocerebellar ataxia 43
RS182602615 Health Risk Conflicting classifications of pathogenicity Peripheral neuropathy, Peripheral neuropathy
RS184666602 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia 43, Spinocerebellar ataxia 43
RS200157166 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200308077 Health Risk Conflicting classifications of pathogenicity
RS201002280 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Spinocerebellar ataxia 43, Charcot-Marie-Tooth disease axonal type 2T
RS201494121 Health Risk Conflicting classifications of pathogenicity Familial cancer of breast, Familial cancer of breast
RS202095767 Health Risk Conflicting classifications of pathogenicity Early-onset dementia of unclear type, Early-onset dementia of unclear type
RS2473156355 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS767841325 Health Risk Conflicting classifications of pathogenicity
RS1170321638 Health Risk Likely pathogenic
RS1281943901 Health Risk Likely pathogenic
RS1395068713 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1403042622 Health Risk Likely pathogenic
RS1446583831 Health Risk Likely pathogenic
RS1559961997 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1559963660 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1712967888 Health Risk Likely pathogenic
RS1718622890 Health Risk Likely pathogenic
RS199987860 Health Risk Likely pathogenic
RS201533045 Health Risk Likely pathogenic Peripheral neuropathy, Distal myopathy, Peripheral neuropathy
RS2108311839 Health Risk Likely pathogenic
RS2108312675 Health Risk Likely pathogenic Spinocerebellar ataxia 43, Spinocerebellar ataxia 43
RS2472967212 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS2472973234 Health Risk Likely pathogenic
RS2472974805 Health Risk Likely pathogenic
RS2473057222 Health Risk Likely pathogenic MME-related disorder, MME-related disorder
RS2473065142 Health Risk Likely pathogenic
RS2473072963 Health Risk Likely pathogenic
RS2473073824 Health Risk Likely pathogenic
RS2473075038 Health Risk Likely pathogenic
RS2473082304 Health Risk Likely pathogenic
RS2473093626 Health Risk Likely pathogenic
RS2473161755 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS2473162385 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS879253752 Health Risk Likely pathogenic Charcot-Marie-Tooth disease axonal type 2T, Peripheral neuropathy, Charcot-Marie-Tooth disease axonal type 2T
RS1057519023 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1057519024 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS1165784045 Health Risk Pathogenic
RS1190163112 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
RS149905705 Health Risk Pathogenic Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization, Spinocerebellar ataxia 43, MME-related disorder
RS1553765316 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, Spinocerebellar ataxia 43, Charcot-Marie-Tooth disease axonal type 2T
RS1711573891 Health Risk Pathogenic
RS1722635259 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, MME-related disorder, Charcot-Marie-Tooth disease axonal type 2T
RS200698972 Health Risk Pathogenic
RS2108261555 Health Risk Pathogenic Charcot-Marie-Tooth disease axonal type 2T, Charcot-Marie-Tooth disease axonal type 2T
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