Genes

Explore the normal functions of human genes and the health implications of genetic changes.

Find a specific gene:

MAGT1: magnesium transporter 1
MAN2B1: mannosidase alpha class 2B member 1
MANBA: mannosidase beta
MAP2K1: mitogen-activated protein kinase kinase 1
MAP2K2: mitogen-activated protein kinase kinase 2
MAP3K1: mitogen-activated protein kinase kinase kinase 1
MAPT: microtubule associated protein tau
MASP1: mannan binding lectin serine peptidase 1
MAT1A: methionine adenosyltransferase 1A
MATN3: matrilin 3
MATR3: matrin 3
MBL2: mannose binding lectin 2
MC1R: melanocortin 1 receptor
MC2R: melanocortin 2 receptor
MCCC1: methylcrotonoyl-CoA carboxylase 1
MCCC2: methylcrotonoyl-CoA carboxylase 2
MCEE: methylmalonyl-CoA epimerase
MCM6: minichromosome maintenance complex component 6
MCOLN1: mucolipin 1
MECP2: methyl-CpG binding protein 2
MED12: mediator complex subunit 12
MEFV: Mediterranean fever
MEGF8: multiple EGF like domains 8
MEN1: menin 1
MEOX1: mesenchyme homeobox 1
MESP2: mesoderm posterior bHLH transcription factor 2
MFN2: mitofusin 2
MFSD8: major facilitator superfamily domain containing 8
MID1: midline 1
MIR145: microRNA 145
MIR146A: microRNA 146a
MITF: melanogenesis associated transcription factor
MKKS: McKusick-Kaufman syndrome
MLC1: megalencephalic leukoencephalopathy with subcortical cysts 1
MLH1: mutL homolog 1
MLPH: melanophilin
MLYCD: malonyl-CoA decarboxylase
MMAA: methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB: methylmalonic aciduria (cobalamin deficiency) cblB type
MMACHC: methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC: methylmalonic aciduria and homocystinuria, cblD type
MMP2: matrix metallopeptidase 2
MMP14: matrix metallopeptidase 14
MMP20: matrix metallopeptidase 20
MOCOS: molybdenum cofactor sulfurase
MOCS1: molybdenum cofactor synthesis 1
MOCS2: molybdenum cofactor synthesis 2
MPL: MPL proto-oncogene, thrombopoietin receptor
MPLKIP: M-phase specific PLK1 interacting protein
MPV17: MPV17, mitochondrial inner membrane protein
MPZ: myelin protein zero
MRAP: melanocortin 2 receptor accessory protein
MSH2: mutS homolog 2
MSH6: mutS homolog 6
MSTN: myostatin
MSX1: msh homeobox 1
MSX2: msh homeobox 2
MT-ATP6: mitochondrially encoded ATP synthase 6
MT-CYB: mitochondrially encoded cytochrome b
MT-ND1: mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1
MT-ND4: mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4
MT-ND4L: mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L
MT-ND5: mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5
MT-ND6: mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6
MT-TE: mitochondrially encoded tRNA glutamic acid
MT-TH: mitochondrially encoded tRNA histidine
MT-TK: mitochondrially encoded tRNA lysine
MT-TL1: mitochondrially encoded tRNA leucine 1 (UUA/G)
MT-TS1: mitochondrially encoded tRNA serine 1 (UCN)
MT-TV: mitochondrially encoded tRNA valine
MTHFR: methylenetetrahydrofolate reductase (NAD(P)H)
MTM1: myotubularin 1
MTMR2: myotubularin related protein 2
MTR: 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR: 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MTTP: microsomal triglyceride transfer protein
MUC1: mucin 1, cell surface associated
MUT: methylmalonyl-CoA mutase
MUTYH: mutY DNA glycosylase
MVK: mevalonate kinase
MYBPC1: myosin binding protein C, slow type
MYBPC3: myosin binding protein C, cardiac
MYCN: v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
MYD88: myeloid differentiation primary response 88
MYH3: myosin, heavy chain 3, skeletal muscle, embryonic
MYH6: myosin, heavy chain 6, cardiac muscle, alpha
MYH7: myosin, heavy chain 7, cardiac muscle, beta
MYH9: myosin, heavy chain 9, non-muscle
MYH11: myosin, heavy chain 11, smooth muscle
MYO5A: myosin VA
MYO5B: myosin VB
MYO7A: myosin VIIA
MYOC: myocilin
MYOT: myotilin