Sequence information
Variant position: 121 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 447 The length of the canonical sequence.
Location on the sequence:
ACSLETKELWDKFHELGTEM
I ITKSGRRMFPTIRVSFSGVD
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 ACSLETKELWDKFHELGTEMI ITKSGRRMFPTIRVSFSGVD
Mouse ACSLETKELWDKFHELGTEMI ITKSGRRMFPTIRVSFSGVD
Chicken SCSLETKELWDKFHELGTEMI ITKSGRRMFPTIRVSFSGVD
Xenopus laevis SCSLETKELWDKFHDLGTEMI ITKSGRRMFPTIRVSFSGVD
Xenopus tropicalis SCSLETKELWDKFHDLGTEMI ITKSGRRMFPTIRVSFSGVD
Zebrafish SCSLETKELWDKFHELGTEMI ITKSGRRMFPTIRVSFSGVD
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
1 – 447
T-box transcription factor TBX20
DNA binding
109 – 288
T-box
Literature citations
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects.
Posch M.G.; Gramlich M.; Sunde M.; Schmitt K.R.; Lee S.H.; Richter S.; Kersten A.; Perrot A.; Panek A.N.; Al Khatib I.H.; Nemer G.; Megarbane A.; Dietz R.; Stiller B.; Berger F.; Harvey R.P.; Ozcelik C.;
J. Med. Genet. 47:230-235(2010)
Cited for: VARIANTS ASD4 MET-121 AND MET-152; CHARACTERIZATION OF VARIANTS ASD4 MET-121 AND MET-152;
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.