Variant position: 240 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1135 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 LERIGKKLNLFDSLYFCIVT FSTVGFGDVTPETWSSKLFVV
Rat LERIGKKLNLFDSLYFCIVT FSTVGFGDVTPETWSSKLFVV
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
1 – 1135 Potassium channel subfamily T member 2
229 – 249 Pore-forming
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy.
Gururaj S.; Palmer E.E.; Sheehan G.D.; Kandula T.; Macintosh R.; Ying K.; Morris P.; Tao J.; Dias K.R.; Zhu Y.; Dinger M.E.; Cowley M.J.; Kirk E.P.; Roscioli T.; Sachdev R.; Duffey M.E.; Bye A.; Bhattacharjee A.;
Cell Rep. 21:926-933(2017)
Cited for: FUNCTION; SUBCELLULAR LOCATION; INVOLVEMENT IN DEE57; VARIANT DEE57 LEU-240; CHARACTERIZATION OF VARIANT DEE57 LEU-240;
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.