Variant position: 67 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 160 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 SGNVHHCFSSSPNEWLQSVQ ATMILSIIFSILSLFLFFCQL
Mouse LGAVQHCYSSSVSEWLQSVQ ATMILSVIFSVLALFLFFCQL
Rat LGAVQHCYSSSVSEWLQSVQ ATMILSVIFSVLSLFLFFCQL
Bovine MGSVQHCFSSSANEWLQSVQ ATMILSIIFSVLSLFLFFCQL
Horse -GNVQHCLSSSANEWLQSVQ ATMILSIIFSVLSLFLFFCQL
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 – 160 Peripheral myelin protein 22
65 – 91 Helical
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.
Kovach M.J.; Lin J.-P.; Boyadjiev S.; Campbell K.; Mazzeo L.; Herman K.; Rimer L.A.; Frank W.; Llewellyn B.; Wang Jabs E.; Gelber D.; Kimonis V.E.;
Am. J. Hum. Genet. 64:1580-1593(1999)
Cited for: VARIANT CMT1E PRO-67;
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.