Variant position: 22 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1164 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 AQQANVGELLAMLDSPMLGV RDDVTAVFKENLNSDRGPMLV
Mouse AQLANIGELLSMLDSSTLGV RDDVTAIFKESLNSERGPMLV
Rat AQLANIGELLSMLDSSTLGV RDDVTTIFKESLNSERGPMLV
Fission yeast PLQSLVKALWNVLHEEESEG YPDLTELIAE----------V
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 – 1164 Hamartin
Somatic mutations in TSC1 and TSC2 cause focal cortical dysplasia.
Lim J.S.; Gopalappa R.; Kim S.H.; Ramakrishna S.; Lee M.; Kim W.I.; Kim J.; Park S.M.; Lee J.; Oh J.H.; Kim H.D.; Park C.H.; Lee J.S.; Kim S.; Kim D.S.; Han J.M.; Kang H.C.; Kim H.H.; Lee J.H.;
Am. J. Hum. Genet. 100:454-472(2017)
Cited for: FUNCTION; INTERACTION WITH TSC2; INVOLVEMENT IN FCORD2; VARIANTS FCORD2 TRP-22 AND CYS-204; CHARACTERIZATION OF VARIANTS FCORD2 TRP-22 AND CYS-204;
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.