Variant position: 1890 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2155 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 YKNTLWIESANNTGNIITRD RTINVEFSCAYELDIKISLDS
Mouse YKNTIWIESANNTGNIITRD RTINVEFSCAYELDIKISLDS
Chicken YKNTVWIESANNTGNIITRD RTINVEVFCAYELDIKISLDS
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.
A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.
Plantinga R.F.; de Brouwer A.P.; Huygen P.L.; Kunst H.P.; Kremer H.; Cremers C.W.;
J. Assoc. Res. Otolaryngol. 7:173-181(2006)
Cited for: VARIANT DFNA12 CYS-1890;
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Hildebrand M.S.; Morin M.; Meyer N.C.; Mayo F.; Modamio-Hoybjor S.; Mencia A.; Olavarrieta L.; Morales-Angulo C.; Nishimura C.J.; Workman H.; DeLuca A.P.; del Castillo I.; Taylor K.R.; Tompkins B.; Goodman C.W.; Schrauwen I.; Wesemael M.V.; Lachlan K.; Shearer A.E.; Braun T.A.; Huygen P.L.; Kremer H.; Van Camp G.; Moreno F.; Casavant T.L.; Smith R.J.; Moreno-Pelayo M.A.;
Hum. Mutat. 32:825-834(2011)
Cited for: VARIANTS DFNA12 ASN-197; SER-211; CYS-362; LYS-465; MET-562; MET-815; SER-886; TYR-1036; VAL-1098; HIS-1136; LEU-1248; ARG-1517; ARG-1791; GLY-1837; MET-1866; ARG-1867; CYS-1890; ARG-1898; CYS-1947 AND THR-2009;
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.