Sequence information
Variant position: 171 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 173 The length of the canonical sequence.
Location on the sequence:
AAGNMVHVKQKLYHNGHPSP
R HL
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 AAGNMVHVKQKLYHNGHPSPR HL
Mouse PTGNMVHVKQKLYHNGHPSPR HL
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
1 – 173
Transmembrane protein 240
Modified residue
169 – 169
Phosphoserine
Literature citations
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Delplanque J.; Devos D.; Huin V.; Genet A.; Sand O.; Moreau C.; Goizet C.; Charles P.; Anheim M.; Monin M.L.; Buee L.; Destee A.; Grolez G.; Delmaire C.; Dujardin K.; Dellacherie D.; Brice A.; Stevanin G.; Strubi-Vuillaume I.; Duerr A.; Sablonniere B.;
Brain 137:2657-2663(2014)
Cited for: INVOLVEMENT IN SCA21; VARIANTS SCA21 MET-80; CYS-116; LYS-149; LEU-170 AND TRP-171;
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.