| NEFH | 
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| Identifiers | 
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| Aliases | NEFH, NFH, CMT2CC, neurofilament, heavy polypeptide, neurofilament heavy, neurofilament heavy chain | 
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| External IDs | OMIM: 162230; MGI: 97309; HomoloGene: 40755; GeneCards: NEFH; OMA:NEFH - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 11 (mouse) | 
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 |  |  | Band | 11 A1|11 3.12 cM | Start | 4,888,754 bp | 
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 | End | 4,898,064 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | spinal ganglia
 Pons
 lateral nuclear group of thalamus
 Brodmann area 23
 pars compacta
 pars reticulata
 superior vestibular nucleus
 external globus pallidus
 trigeminal ganglion
 endothelial cell
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 | | Top expressed in |  | anterior horn of spinal cord
 facial motor nucleus
 motor neuron
 pontine nuclei
 deep cerebellar nuclei
 medial vestibular nucleus
 lateral geniculate nucleus
 dorsal tegmental nucleus
 medial geniculate nucleus
 central gray substance of midbrain
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Neurofilament, heavy polypeptide (NEFH) is a protein that in humans is encoded by the NEFH gene.
It is the gene for a heavy protein subunit that is combined with medium and light subunits to make neurofilaments, which form the framework for nerve cells.
Mutations in the NEFH gene are associated with Charcot-Marie-Tooth disease.