Sequence information
Variant position: 446 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 567 The length of the canonical sequence.
Location on the sequence:
APEVLESRMNLENVESFKQT
D VYSMALVLWEMTSRCNAVGE
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 APEVLESRMNLENVESFKQTD VYSMALVLWEMTSRCNAVGE
Mouse APEVLESRMNLENVESFKQTD VYSMALVLWEMTSRCNAVGE
Rat APEVLESRMNLENMESFKQTD VYSMALVLWEMTSRCNAVGE
Chicken APEVLESRMNLENMESFKQTD VYSMALVLWEMTSRCNGVGE
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.
Literature citations
Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects.
Disabella E.; Grasso M.; Marziliano N.; Ansaldi S.; Lucchelli C.; Porcu E.; Tagliani M.; Pilotto A.; Diegoli M.; Lanzarini L.; Malattia C.; Pelliccia A.; Ficcadenti A.; Gabrielli O.; Arbustini E.;
Eur. J. Hum. Genet. 14:34-38(2006)
Cited for: VARIANT LDS2 ASN-446;
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.