Sequence information
Variant position: 385 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 470 The length of the canonical sequence.
Location on the sequence:
DNIARLEEEIRHLKDEMARH
L REYQDLLNVKMALDVEIATY
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 DNIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Mouse DNIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Rat DNIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Pig DNIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Bovine DNIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Chicken DTIARLEEEIRHLKDEMARHL REYQDLLNVKMALDVEIATY
Xenopus laevis DTIGRLEEEIRNMKDEMARHL REYQDLLNVKMALDMEIATY
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.
Literature citations
A novel de novo mutation in the desmin gene causes desmin myopathy with toxic aggregates.
Sugawara M.; Kato K.; Komatsu M.; Wada C.; Kawamura K.; Shindo P.S.; Yoshioka P.N.; Tanaka K.; Watanabe S.; Toyoshima I.;
Neurology 55:986-990(2000)
Cited for: VARIANT MFM1 PRO-385;
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.