| 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.