UniProtKB/Swiss-Prot Q04844: Variant p.Gly13Arg

Acetylcholine receptor subunit epsilon
Gene: CHRNE
Chromosomal location: 17p13.1
Variant information

Variant position:  13
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Disease [Disclaimer]
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants have been found in patients and disease-association is reported in literature. However, this classification is not a definitive assessment of variant pathogenicity.
  • Polymorphism: No disease-association has been reported.
  • Unclassified: Variants have been found in patients but disease-association remains unclear.

Residue change:  From Glycine (G) to Arginine (R) at position 13 (G13R, p.Gly13Arg).
Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.

Physico-chemical properties:  Change from glycine (G) to large size and basic (R)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  -2
The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Involvement in disease:  Myasthenic syndrome, congenital, fast-channel (FCCMS) [MIM:608930]: A congenital myasthenic syndrome characterized by kinetic abnormalities of the AChR. Due in most cases to mutations that decrease activity of the AChR by slowing the rate of opening of the receptor channel, speeding the rate of closure of the channel, or decreasing the number of openings of the channel during ACh occupancy. The result is failure to achieve threshold depolarization of the endplate and consequent failure to fire an action potential. Note=The disease is caused by mutations affecting the gene represented in this entry.
The name and a short description of the disease associated with the variant. For more information about the disease, the user can refer to OMIM, following the link provided after the disease acronym.

Variant description:  In FCCMS; impaired association with alpha CHRNA1 subunit of AChR.
Any additional useful information about the variant.



Sequence information

Variant position:  13
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  493
The length of the canonical sequence.

Location on the sequence:   MARAPLGVLLLL  G LLGRGVGKNEELRLYHHLFN
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.

Residue conservation: 
The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         MARAPLGVLLLLGLLGRGVGKNEELRLYHHLFN

Mouse                         MAGALLGALLLLTLFGRSQGKNEELSLYHHLFD

Rat                           MTMALLGTLLLLALFGRSQGKNEELSLYHHLFD

Bovine                        MAGALLCALLLLQLLGRGEGKNEELRLYHYLFD

Xenopus laevis                MESGVRILSLLILLHNSLASESEESRLIKHLFT

Sequence annotation in neighborhood:  
The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.

TypePositionsDescription
Signal peptide 1 – 20


Literature citations

Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit.
Ohno K.; Wang H.-L.; Milone M.; Bren N.; Brengman J.M.; Nakano S.; Quiram P.; Pruitt J.N. II; Sine S.M.; Engel A.G.;
Neuron 17:157-170(1996)
Cited for: VARIANTS FCCMS ARG-13; LEU-141 AND LEU-163; CHARACTERIZATION OF VARIANTS FCCMS ARG-13; LEU-141 AND LEU-163;

Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.