Sequence information
Variant position: 513 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:
GIDKDRAAKPVTVAVKMLKD
D ATDKDLSDLVSEMEMMKMIG
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 GIDKDRAAKPVTVAVKMLKDD ATDKDLSDLVSEMEMMKMIG
Mouse GIDKDRTAKPVTVAVKMLKDD ATDKDLSDLVSEMEMMKMIG
Chicken GIDKDKPNKAITVAVKMLKDD ATDKDLSDLVSEMEMMKMIG
Xenopus laevis GIDKERPNKPATVAVKMLKDD ATDKDLSDLVSEMEMMKMIG
Zebrafish GIDKEKPNKPLTVAVKMLKDD GTDKDLSDLVSEMEMMKMIG
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
Chain
23 – 806
Fibroblast growth factor receptor 3
Topological domain
397 – 806
Cytoplasmic
Domain
472 – 761
Protein kinase
Binding site
508 – 508
Mutagenesis
508 – 508
K -> A. Loss of kinase activity. Abolishes ubiquitination.
Literature citations
Mutations in different components of FGF signaling in LADD syndrome.
Rohmann E.; Brunner H.G.; Kayserili H.; Uyguner O.; Nuernberg G.; Lew E.D.; Dobbie A.; Eswarakumar V.P.; Uzumcu A.; Ulubil-Emeroglu M.; Leroy J.G.; Li Y.; Becker C.; Lehnerdt K.; Cremers C.W.R.J.; Yueksel-Apak M.; Nuernberg P.; Kubisch C.; Schlessinger J.; van Bokhoven H.; Wollnik B.;
Nat. Genet. 38:414-417(2006)
Cited for: VARIANT LADDS ASN-513;
Disclaimer:
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.