Sequence information
Variant position: 264 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 375 The length of the canonical sequence.
Location on the sequence:
DGQVITIGNERFRCPEALFQ
P SFLGMESCGIHETTFNSIMK
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 DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Mouse DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Rat DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Bovine DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Chicken DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Xenopus laevis DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
Xenopus tropicalis DGQVITIGNERFRCPEALFQP SFLGMESCGIHETTFNSIMK
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 – 375
Actin, cytoplasmic 2
Chain
2 – 375
Actin, cytoplasmic 2, N-terminally processed
Cross
270 – 270
(Microbial infection) Isoglutamyl lysine isopeptide (Glu-Lys) (interchain with K-50); by Vibrio toxins RtxA and VgrG1
Literature citations
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
Zhu M.; Yang T.; Wei S.; DeWan A.T.; Morell R.J.; Elfenbein J.L.; Fisher R.A.; Leal S.M.; Smith R.J.H.; Friderici K.H.;
Am. J. Hum. Genet. 73:1082-1091(2003)
Cited for: VARIANTS DFNA20 ILE-89; MET-118; LEU-264 AND ALA-332;
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.