neurofilament heavy chain

Summary
Gene Symbol
  • NEFH
Organism
Homo sapiens (human)
NCBI Gene
4744
PubChem
4744
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Amyotrophic lateral sclerosis
  • Cell projection
  • Charcot-Marie-Tooth disease
  • Coiled coil
  • Cytoskeleton
  • Disease variant
  • Intermediate filament
  • Phosphoprotein
  • Reference proteome
  • Repeat
Proteins
Displaying 1 entry
UniProt Protein Name
P12036
  • 200 kDa neurofilament protein
  • Neurofilament triplet H protein
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Keratin
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 16 in total
DO ID Disease Name Source
DOID:0040089 autoimmune optic neuritis
DOID:0050328 congenital hypothyroidism
DOID:0060193 amyotrophic lateral sclerosis type 1
DOID:0110180 Charcot-Marie-Tooth disease axonal type 2CC
DOID:11446 sciatic neuropathy
DOID:11949 Creutzfeldt-Jakob disease
DOID:1210 optic neuritis
DOID:1459 hypothyroidism
DOID:1686 glaucoma
DOID:224 transient cerebral ischemia

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024