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MYH10 |
myosin heavy chain 10 |
- EPHA-mediated growth cone collapse
- Sema4D induced cell migration and growth-cone collapse
- RHO GTPases activate PKNs
- RHO GTPases activate CIT
- RHO GTPases Activate ROCKs
- RHO GTPases activate PAKs
- RHO GTPases activate PAKs
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MYO1B |
myosin IB |
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MYO1C |
myosin IC |
- Translocation of SLC2A4 (GLUT4) to the plasma membrane
- Regulation of actin dynamics for phagocytic cup formation
- FCGR3A-mediated phagocytosis
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MYO1D |
myosin ID |
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MYOF |
myoferlin |
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NACA |
nascent polypeptide associated complex subunit alpha |
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NCBP1 |
nuclear cap binding protein subunit 1 |
- SLBP independent Processing of Histone Pre-mRNAs
- Formation of RNA Pol II elongation complex
- Formation of the Early Elongation Complex
- Transport of the SLBP independent Mature mRNA
- Transport of the SLBP Dependant Mature mRNA
- Transport of Mature mRNA Derived from an Intronless Transcript
- Transport of Mature mRNA derived from an Intron-Containing Transcript
- Formation of HIV elongation complex in the absence of HIV Tat
- Formation of the HIV-1 Early Elongation Complex
- Formation of HIV-1 elongation complex containing HIV-1 Tat
- Abortive elongation of HIV-1 transcript in the absence of Tat
- snRNP Assembly
- RNA Polymerase II Pre-transcription Events
- FGFR2 alternative splicing
- RNA polymerase II transcribes snRNA genes
- mRNA Capping
- mRNA Splicing - Major Pathway
- mRNA Splicing - Minor Pathway
- mRNA 3'-end processing
- Processing of Capped Intron-Containing Pre-mRNA
- RNA Polymerase II Transcription Termination
- SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs
- Processing of Intronless Pre-mRNAs
- Signaling by FGFR2 IIIa TM
- Regulation of expression of SLITs and ROBOs
- Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
- Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
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NDFIP1 |
Nedd4 family interacting protein 1 |
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NGB |
neuroglobin |
- Intracellular oxygen transport
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NOP56 |
NOP56 ribonucleoprotein |
- Association of TriC/CCT with target proteins during biosynthesis
- rRNA modification in the nucleus and cytosol
- Major pathway of rRNA processing in the nucleolus and cytosol
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- Spinocerebellar ataxia (SCA); Machado-Joseph disease (SCA3)
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NOP58 |
NOP58 ribonucleoprotein |
- SUMOylation of RNA binding proteins
- rRNA modification in the nucleus and cytosol
- Major pathway of rRNA processing in the nucleolus and cytosol
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NPM3 |
nucleophosmin/nucleoplasmin 3 |
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NUMB |
NUMB endocytic adaptor protein |
- Activated NOTCH1 Transmits Signal to the Nucleus
- Recycling pathway of L1
- Degradation of GLI1 by the proteasome
- Hedgehog 'on' state
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OSGIN1 |
oxidative stress induced growth inhibitor 1 |
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OTUD3 |
OTU deubiquitinase 3 |
- Ovarian tumor domain proteases
- Regulation of PTEN stability and activity
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PBK |
PDZ binding kinase |
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PBRM1 |
polybromo 1 |
- RMTs methylate histone arginines
- RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
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PELO |
pelota mRNA surveillance and ribosome rescue factor |
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PELP1 |
proline, glutamate and leucine rich protein 1 |
- Major pathway of rRNA processing in the nucleolus and cytosol
- PTK6 Expression
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PLEC |
plectin |
- Assembly of collagen fibrils and other multimeric structures
- Caspase-mediated cleavage of cytoskeletal proteins
- Type I hemidesmosome assembly
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- Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy
- Epidermolysis bullosa, hemidesmosomal, including: Epidermolysis bullosa, generalized atrophic benign (GABEB); Epidermolysis bullosa simplex with pyloric atresia (EBS-PA); Epidermolysis bullosa simplex with muscular dystrophy (EBS-MD); Epidermolysis bullosa simplex, Ogna type (EBS-Ogna)
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