Variant position: 442 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1294 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 ALAKTVYSHLFDHVVNRVNQ CFPFETSSYFIGVLDIAGFEY
Mouse ALAKTVYSHLFDHVVNRVNQ CFPFETSSYFIGVLDIAGFEY
Pig ALAKTVYSHLFDHVVNRVNQ CFPFETSSYFIGVLDIAGFEY
Bovine ALAKTVYSHLFDHVVNRVNQ CFPFETSSYFIGVLDIAGFEY
Chicken ALAKTVYSHLFDHVVNRVNQ CFPFETSSFFIGVLDIAGFEY
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 – 1294 Unconventional myosin-VI
57 – 771 Myosin motor
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.
Melchionda S.; Ahituv N.; Bisceglia L.; Sobe T.; Glaser F.; Rabionet R.; Arbones M.L.; Notarangelo A.; Di Iorio E.; Carella M.; Zelante L.; Estivill X.; Avraham K.B.; Gasparini P.;
Am. J. Hum. Genet. 69:635-640(2001)
Cited for: VARIANT DFNA22 TYR-442;
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