Variant position: 163 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:
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 IYRSVCAVEVTYFPFDWQNC SLIFRSQTYNAEEVEFTFAVD
Mouse IYRSTCAVEVTYFPFDWQNC SLIFRSQTYNAEEVEFIFAVD
Rat IYRSTCAVEVTYFPFDWQNC SLIFRSQTYNAEEVELIFAVD
Bovine IYRSTCAVEVTYFPFDWQNC SLVFRSQTYNAEEVEFVFAVD
Xenopus laevis IFRSTCNIEITYFPFDWQNC SLVFRSKTYSANEIDLQLVTD
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.
Type Positions Description
21 – 493 Acetylcholine receptor subunit epsilon
21 – 239 Extracellular
161 – 161 N-linked (GlcNAc...) asparagine
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.;
Cited for: VARIANTS CMS4B ARG-13; LEU-141 AND LEU-163; CHARACTERIZATION OF VARIANTS CMS4B ARG-13; LEU-141 AND LEU-163;
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