Variant position: 365 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 616 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 AGQDLAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Mouse AGQELAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Rat AGQELAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Pig AGQELAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Bovine AGQELAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Chicken AGQELAKQALQEIVILPSLR PELFTGLRAPARGLLLFGPPG
Xenopus laevis AGQDLAKQALQEIVILPSIR PELFTGLRAPARGLLLFGPPG
Xenopus tropicalis AGQDLAKQALQEIVILPSIR PELFTGLRAPARGLLLFGPPG
Zebrafish AGQDLAKQALQEIVILPALR PELFTGLRAPARGLLLFGPPG
Caenorhabditis elegans AGCHSAKAALEEAVILPALN PNLFKGLRQPVKGILLFGPPG
Drosophila AGQDVAKQALQEMVILPSVR PELFTGLRAPAKGLLLFGPPG
Slime mold VGLDKVKQSLMESVILPNLR PDVFTGLRAPPKGLLLFGPPG
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.
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.
de Bot S.T.; van den Elzen R.T.; Mensenkamp A.R.; Schelhaas H.J.; Willemsen M.A.; Knoers N.V.; Kremer H.P.; van de Warrenburg B.P.; Scheffer H.;
J. Neurol. Neurosurg. Psych. 81:1073-1078(2010)
Cited for: VARIANTS SPG4 ILE-162; LYS-356; SER-365; ARG-382; ILE-; PHE-422; ASN-445; SER-460; LEU-482; GLU-512 DEL; VAL-534 AND PRO-562; VARIANT LEU-44;
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.