18977 GENES FOUNDi
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Genei Gene descriptioni x Evidencei x Tissuei Celli Pathologyi Brain Blood
MISPMitotic spindle positioning
MISP3MISP family member 3
MITD1Microtubule interacting and trafficking domain containing 1
MITFMelanogenesis associated transcription factor
MIXL1Mix paired-like homeobox
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
MKRN2OSMKRN2 opposite strand
MKRN3Makorin ring finger protein 3
MKS1Meckel syndrome, type 1
MKXMohawk homeobox
MLANAMelan-A
MLC1Megalencephalic leukoencephalopathy with subcortical cysts 1
MLECMalectin
MLF1Myeloid leukemia factor 1
MLF2Myeloid leukemia factor 2
MLH1MutL homolog 1
MLH3MutL homolog 3
MLIPMuscular LMNA interacting protein
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
MLNMotilin
MLNRMotilin receptor
MLPHMelanophilin
MLST8MTOR associated protein, LST8 homolog
MLXMLX, MAX dimerization protein
MLXIPMLX interacting protein
MLXIPLMLX interacting protein like
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
MMD2Monocyte to macrophage differentiation associated 2
MMEMembrane metalloendopeptidase
MMEL1Membrane metalloendopeptidase like 1
MMGT1Membrane magnesium transporter 1
MMP1Matrix metallopeptidase 1
MMP10Matrix metallopeptidase 10
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