Sequence information
Variant position: 331 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:
VMVVATLIVMNCVIVLNVSQ
R TPTTHAMSPRLRHVLLELLP
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 VMVVATLIVMNCVIVLNVSQR TPTTHAMSPRLRHVLLELLP
Mouse VMVVATLIVMNCVIVLNVSLR TPTTHATSPRLRQILLELLP
Rat VMVVATLIVMNCVIVLNVSLR TPTTHATSPRLRQILLELLP
Bovine VMVVATLIVMNCVIVLNVSLR TPTTHAMSPRLRYVLLELLP
Xenopus laevis VMFVSTLIVLSCVIVLNVSLR SPSTHNLSTKVKHMLLEVLP
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
Chain
21 – 493
Acetylcholine receptor subunit epsilon
Topological domain
329 – 456
Cytoplasmic
Literature citations
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations.
Ohno K.; Quiram P.A.; Milone M.; Wang H.-L.; Harper M.C.; Pruitt J.N. II; Brengman J.M.; Pao L.; Fischbeck K.H.; Crawford T.O.; Sine S.M.; Engel A.G.;
Hum. Mol. Genet. 6:753-766(1997)
Cited for: VARIANTS CMS4C LEU-167; LEU-265 AND TRP-331; CHARACTERIZATION OF VARIANTS CMS4C LEU-167; LEU-265 AND TRP-331;
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.