Variant position: 412 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 787 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 VGYKNYRYRAGFVLAPIGLV LIVGGYFLIRGVMTLFSIKSN
Mouse VGYKNYRYRAGFVLAPIGLV LIVGGYFLIRGVMTLFSIKSN
Rat VGYKNYRYRAGFVLAPIGLV LIVGGYFLIRGVMTLFSIKSN
Drosophila VGYINHSMRAGLLLGPLCGV ILIGGYFITRGMVMLFGLKHF
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.
A recurrent mosaic mutation in SMO, encoding the hedgehog signal transducer smoothened, is the major cause of Curry-Jones syndrome.
Twigg S.R.; Hufnagel R.B.; Miller K.A.; Zhou Y.; McGowan S.J.; Taylor J.; Craft J.; Taylor J.C.; Santoro S.L.; Huang T.; Hopkin R.J.; Brady A.F.; Clayton-Smith J.; Clericuzio C.L.; Grange D.K.; Groesser L.; Hafner C.; Horn D.; Temple I.K.; Dobyns W.B.; Curry C.J.; Jones M.C.; Wilkie A.O.;
Am. J. Hum. Genet. 98:1256-1265(2016)
Cited for: INVOLVEMENT IN CRJS; VARIANT CRJS PHE-412;
Identification of recurrent SMO and BRAF mutations in ameloblastomas.
Sweeney R.T.; McClary A.C.; Myers B.R.; Biscocho J.; Neahring L.; Kwei K.A.; Qu K.; Gong X.; Ng T.; Jones C.D.; Varma S.; Odegaard J.I.; Sugiyama T.; Koyota S.; Rubin B.P.; Troxell M.L.; Pelham R.J.; Zehnder J.L.; Beachy P.A.; Pollack J.R.; West R.B.;
Nat. Genet. 46:722-725(2014)
Cited for: VARIANT CRJS PHE-412; VARIANT LEU-535; CHARACTERIZATION OF VARIANT CRJS PHE-412; CHARACTERIZATION OF VARIANT LEU-535;
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.