UBC - Wiki-MPM

Interactant Symbol	Name	Associated Pathways Hide	Binding Drugs Hide	Associated Diseases Hide
MRPS7	mitochondrial ribosomal protein S7	Mitochondrial translation initiation Mitochondrial translation elongation Mitochondrial translation elongation Mitochondrial translation termination Mitochondrial ribosome-associated quality control
MRPS9	mitochondrial ribosomal protein S9	Mitochondrial translation initiation Mitochondrial translation elongation Mitochondrial translation elongation Mitochondrial translation termination Mitochondrial ribosome-associated quality control
MSANTD4	Myb/SANT DNA binding domain containing 4 with coiled-coils
MTCH1	mitochondrial carrier 1
MTERF4	mitochondrial transcription termination factor 4	rRNA modification in the mitochondrion
MTMR14	myotubularin related protein 14	Macroautophagy Synthesis of PIPs at the plasma membrane
MTNAP1	mitochondrial nucleoid associated protein 1
MTO1	mitochondrial tRNA translation optimization 1	tRNA modification in the mitochondrion
MTURN	maturin, neural progenitor differentiation regulator homolog
MTUS2	microtubule associated scaffold protein 2
MUC16	mucin 16, cell surface associated	Defective GALNT3 causes HFTC Defective C1GALT1C1 causes TNPS Defective GALNT12 causes CRCS1 Dectin-2 family O-linked glycosylation of mucins Termination of O-glycan biosynthesis	Dimethyl sulfoxide Oregovomab
MUC5B	mucin 5B, oligomeric mucus/gel-forming	Defective GALNT3 causes HFTC Defective C1GALT1C1 causes TNPS Defective GALNT12 causes CRCS1 Dectin-2 family O-linked glycosylation of mucins Termination of O-glycan biosynthesis
MUL1	mitochondrial E3 ubiquitin protein ligase 1	Ub-specific processing proteases Neddylation KEAP1-NFE2L2 pathway
MVB12A	multivesicular body subunit 12A	Budding and maturation of HIV virion Membrane binding and targetting of GAG proteins Endosomal Sorting Complex Required For Transport (ESCRT) HCMV Late Events Late endosomal microautophagy
MVP	major vault protein	Neutrophil degranulation
MYCBP	MYC binding protein
MYL1	myosin light chain 1	Striated Muscle Contraction
MYL3	myosin light chain 3	Striated Muscle Contraction		Hypertrophic cardiomyopathy (HCM)
MYO6	myosin VI	Gap junction degradation Trafficking of AMPA receptors RHOBTB2 GTPase cycle RHOU GTPase cycle RHOBTB1 GTPase cycle		Deafness, autosomal recessive Deafness, autosomal dominant
N4BP1	NEDD4 binding protein 1	Regulation of NF-kappa B signaling

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