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CHRNE

  • CHRNE
  • Protein-coding gene

    receptor subunit epsilon is a protein that in humans is encoded by the CHRNE gene. Acetylcholine receptors at mature mammalian neuromuscular junctions

    CHRNE

    CHRNE

    CHRNE

  • Acetylcholine receptor
  • Integral membrane protein

    of the CHRNE gene with mutations encoding for the Alpha5 Nicotinic Acetylcholine Receptor cause increased susceptibility to addiction. The CHRNE gene codes

    Acetylcholine receptor

    Acetylcholine receptor

    Acetylcholine_receptor

  • Congenital myasthenic syndrome
  • Human disease

    deficiency. Most of the mutations of the AChR are mutations of the CHRNE gene. The CHRNE gene codes for the epsilon subunit of the AChR. Most mutations are

    Congenital myasthenic syndrome

    Congenital_myasthenic_syndrome

  • Nicotinic acetylcholine receptor
  • Acetylcholine receptors named for their selective binding of nicotine

    (muscle), CHRNB2 (neuronal), CHRNB3, CHRNB4 Other genes: CHRND (delta), CHRNE (epsilon), CHRNG (gamma) Neuronal nAChRs are transmembrane proteins that

    Nicotinic acetylcholine receptor

    Nicotinic acetylcholine receptor

    Nicotinic_acetylcholine_receptor

  • Ligand-gated ion channel
  • Type of ion channel transmembrane protein

    gamma γ CHRNG ACHRG delta δ CHRND ACHRD, CMS2A, FCCMS, SCCMS epsilon ε CHRNE ACHRE, CMS1D, CMS1E, CMS2A, FCCMS, SCCMS Zinc-activated ion channel (ZAC)

    Ligand-gated ion channel

    Ligand-gated ion channel

    Ligand-gated_ion_channel

  • Transient neonatal myasthenia gravis
  • Medical condition

    respiratory, head, and/or back skeletal muscles. Mutations in the COLQ, CHRNE, RAPSN, Dok-7, and CHAT genes were the most common mutations causing CMGS

    Transient neonatal myasthenia gravis

    Transient_neonatal_myasthenia_gravis

  • MINK1
  • Protein-coding gene in the species Homo sapiens

    Kajikawa E, Ishida T, Pandey A, Kusumi A (Jul 2002). "Overlapping of MINK and CHRNE gene loci in the course of mammalian evolution". Nucleic Acids Research

    MINK1

    MINK1

    MINK1

  • List of human protein-coding genes 2
  • Q05901 2999 CHRNB4 HGNC:1964; P30926 3000 CHRND HGNC:1965; Q07001 3001 CHRNE HGNC:1966; Q04844 3002 CHRNG HGNC:1967; P07510 3003 CHST1 HGNC:1969; O43916

    List of human protein-coding genes 2

    List_of_human_protein-coding_genes_2

  • List of OMIM disorder codes
  • congenital, associated with acetylcholine receptor deficiency; 608931; CHRNE Myasthenic syndrome, congenital, associated with acetylcholine receptor

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • Index of biophysics articles
  • Index of articles on biophysics

    CHRNA3 CHRNA4 CHRNA5 CHRNA6 CHRNA7 CHRNA9 CHRNB1 CHRNB2 CHRNB3 CHRNB4 CHRND CHRNE CHRNG CLCA1 CLCA2 CLCA3 CLCA4 CLCC1 CLCN1 CLCN2 CLCN3 CLCN4 CLCN5 CLCN6

    Index of biophysics articles

    Index_of_biophysics_articles

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