11362 GENES FOUNDi
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Genei Gene descriptioni x Evidencei x Tissuei Celli Pathologyi Brain Blood
MIOSMeiosis regulator for oocyte development
MIPEPMitochondrial intermediate peptidase
MIPOL1Mirror-image polydactyly 1
MIS12MIS12, kinetochore complex component
MIS18AMIS18 kinetochore protein A
MIS18BP1MIS18 binding protein 1
MITD1Microtubule interacting and trafficking domain containing 1
MKI67Marker of proliferation Ki-67
MKKSMcKusick-Kaufman syndrome
MKL1Megakaryoblastic leukemia (translocation) 1
MKL2MKL1/myocardin like 2
MKLN1Muskelin 1
MKNK1MAP kinase interacting serine/threonine kinase 1
MKNK2MAP kinase interacting serine/threonine kinase 2
MKRN1Makorin ring finger protein 1
MKRN2Makorin ring finger protein 2
MKS1Meckel syndrome, type 1
MLECMalectin
MLF1Myeloid leukemia factor 1
MLF2Myeloid leukemia factor 2
MLH1MutL homolog 1
MLH3MutL homolog 3
MLKLMixed lineage kinase domain like pseudokinase
MLLT1MLLT1, super elongation complex subunit
MLLT10MLLT10, histone lysine methyltransferase DOT1L cofactor
MLLT11MLLT11, transcription factor 7 cofactor
MLLT3MLLT3, super elongation complex subunit
MLLT6MLLT6, PHD finger containing
MLNMotilin
MLPHMelanophilin
MLST8MTOR associated protein, LST8 homolog
MLXMLX, MAX dimerization protein
MLXIPMLX interacting protein
MLYCDMalonyl-CoA decarboxylase
MMAAMethylmalonic aciduria (cobalamin deficiency) cblA type
MMABMethylmalonic aciduria (cobalamin deficiency) cblB type
MMACHCMethylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHCMethylmalonic aciduria and homocystinuria, cblD type
MMDMonocyte to macrophage differentiation associated
MMEMembrane metalloendopeptidase
MMGT1Membrane magnesium transporter 1
MMP1Matrix metallopeptidase 1
MMP10Matrix metallopeptidase 10
MMP11Matrix metallopeptidase 11
MMP14Matrix metallopeptidase 14
MMP15Matrix metallopeptidase 15
MMP16Matrix metallopeptidase 16
MMP17Matrix metallopeptidase 17
MMP19Matrix metallopeptidase 19
MMP2Matrix metallopeptidase 2
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