Variant position: 540 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 806 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 SDLVSEMEMMKMIGKHKNII NLLGACTQGGPLYVLVEYAAK
Mouse SDLVSEMEMMKMIGKHKNII NLLGACTQGGPLYVLVEYAAK
Chicken SDLVSEMEMMKMIGKHKNII NLLGACTQDGPLYVLVEYASK
Xenopus laevis SDLVSEMEMMKMIGKHKNII NLLGACTQDGPLYVLVEYASK
Zebrafish SDLVSEMEMMKMIGKHKNII NLLGACTQDGPLYVLVEYASK
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
23 – 806 Fibroblast growth factor receptor 3
397 – 806 Cytoplasmic
472 – 761 Protein kinase
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.
Bellus G.A.; McIntosh I.; Smith E.A.; Aylsworth A.S.; Kaitila I.; Horton W.A.; Greenhaw G.A.; Hecht J.T.; Francomano C.A.;
Nat. Genet. 10:357-359(1995)
Cited for: VARIANT HYPOCHONDROPLASIA LYS-540;
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.