Variant position: 2718 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2752 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 FEELPNVDRILKLCTDIFLV RETGELELEEDLYAKLIFLYR
Mouse FEELPNVDRILKLCTDIFLV RETGELELEEDLYAKLIFLYR
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 – 2752 Piezo-type mechanosensitive ion channel component 2
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
McMillin M.J.; Beck A.E.; Chong J.X.; Shively K.M.; Buckingham K.J.; Gildersleeve H.I.; Aracena M.I.; Aylsworth A.S.; Bitoun P.; Carey J.C.; Clericuzio C.L.; Crow Y.J.; Curry C.J.; Devriendt K.; Everman D.B.; Fryer A.; Gibson K.; Giovannucci Uzielli M.L.; Graham J.M. Jr.; Hall J.G.; Hecht J.T.; Heidenreich R.A.; Hurst J.A.; Irani S.; Krapels I.P.; Leroy J.G.; Mowat D.; Plant G.T.; Robertson S.P.; Schorry E.K.; Scott R.H.; Seaver L.H.; Sherr E.; Splitt M.; Stewart H.; Stumpel C.; Temel S.G.; Weaver D.D.; Whiteford M.; Williams M.S.; Tabor H.K.; Smith J.D.; Shendure J.; Nickerson D.A.; Bamshad M.J.;
Am. J. Hum. Genet. 94:734-744(2014)
Cited for: INVOLVEMENT IN DA3; DA5 AND MWKS; VARIANT MWKS CYS-2686; VARIANT DA3 HIS-2686; VARIANTS DA5 VAL-712; LEU-2718; PRO-2718 AND PRO-2739;
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.