Identifying unique protein alterations caused by SPTLC1 mutations in a transfected neuronal cell model

Biochemistry, Genetics and Molecular Biology

• Synapsin I 100%
• SPTLC1 100%
• Mitochondrion 100%
• Serine 100%
• Cell Mutant 50%
• Autosomal Dominant Inheritance 50%
• Channel Protein 50%
• Sensory Neuron 50%
• Missense Mutation 50%
• Protein Expression Level 50%
• Cytochrome C 50%
• Ribosomal Protein 50%

Neuroscience

• Neuropathy 100%
• Mitochondrion 66%
• Synapsin I 66%
• Serine Palmitoyltransferase 66%
• Cell Line 33%
• Protein Expression 33%
• Dorsal Root Ganglion 33%
• Missense Mutation 33%
• Sensory Neuron 33%
• Endoplasmic Reticulum 33%
• Cytochrome C 33%
• Autosomal Dominant Disorder 33%
• Ribosome Protein 33%