Variant position: 210 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 346 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 KEVKDRIKSNVDGRYLVDGV PFSCCNPSSPRPCIQYQITNN
Mouse KEVKDRIKSNVDGRYLVDGV PFSCCNPSSPRPCIQYQLTNN
Rat KEVKDRIKSNVDGRYLVDGV PFSCCNPSSPRPCIQYQLTNN
Bovine KEVKDRIKSNVDGRYLVDGV PFSCCNPNSPRPCIQYQLTNN
Cat KEVKDRIKSNVDGRYLVDGV PFSCCNPNSPRPCIQYQLTNN
Chicken KEVKDRIKSNVDGRYLVDGV PFSCCNPSSPRPCIQYQVTNN
Xenopus laevis KEVKDRIQSNVDGKYLIDGV PFSCCNPSSPRPCIQLQVTNN
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
1 – 346 Peripherin-2
124 – 264 Lumenal
229 – 229 N-linked (GlcNAc...) asparagine
Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg).
Feist R.M.; White M.F. Jr.; Skalka H.; Stone E.M.;
Am. J. Ophthalmol. 118:259-260(1994)
Cited for: VARIANT FOVEOMACULAR DYSTROPHY ARG-210;
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration.
Gorin M.B.; Jackson K.E.; Ferrell R.E.; Sheffield V.C.; Jacobson S.G.; Gass J.D.; Mitchell E.; Stone E.M.;
Cited for: VARIANT RP7 ARG-210;
Founder effect, seen in the British population, of the 172 peripherin/RDS mutation- and further refinement of genetic positioning of the peripherin/RDS gene.
Payne A.M.; Downes S.M.; Bessant D.A.R.; Bird A.C.; Bhattacharya S.S.;
Am. J. Hum. Genet. 62:192-195(1998)
Cited for: VARIANTS MDPT1 ARG-210; ARG-213 AND TRP-220; VARIANTS MACULAR DYSTROPHY TRP-172 AND ARG-219;
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.