Variant position: 665 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1106 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 KQALMSELKIMSHLGPHLNV VNLLGACTKGGPIYIITEYCR
Mouse KQALMSELKIMSHLGPHLNV VNLLGACTKGGPIYIITEYCR
Rat KQALMSELKIMSHLGPHLNV VNLLGACTKGGPIYIITEYCR
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
33 – 1106 Platelet-derived growth factor receptor beta
554 – 1106 Cytoplasmic
600 – 962 Protein kinase
337 – 1106 Missing. In isoform 2.
A point mutation in PDGFRB causes autosomal-dominant Penttinen syndrome.
Johnston J.J.; Sanchez-Contreras M.Y.; Keppler-Noreuil K.M.; Sapp J.; Crenshaw M.; Finch N.A.; Cormier-Daire V.; Rademakers R.; Sybert V.P.; Biesecker L.G.;
Am. J. Hum. Genet. 97:465-474(2015)
Cited for: INVOLVEMENT IN PENTT; VARIANT PENTT ALA-665; CHARACTERIZATION OF VARIANT PENTT ALA-665;
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.