Sequence information
Variant position: 123 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 265 The length of the canonical sequence.
Location on the sequence:
GILYGVAPLNARGNLAVNAL
N NNTTQGQAMVVELILTFQLA
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 GILYGVAPLNARGNLAVNALN NNTTQGQAMVVELILTFQLA
Mouse GILYWLAPGNARGNLAVNALS NNTTPGKAVVVELILTFQLA
Rat GILYWLAPLNARGNLAVNALN NNTTPGKAMVVELILTFQLA
Pig GILYGLAPGNARGNLAVNSLN NNTTPGQAVVVEMILTFQLA
Sheep AILYGLAPYNARSNLAVNALN NNTTAGQAVVAEMILTFQLA
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 – 265
Aquaporin-5
Topological domain
109 – 126
Extracellular
Glycosylation
124 – 124
N-linked (GlcNAc...) asparagine
Glycosylation
125 – 125
N-linked (GlcNAc...) asparagine
Literature citations
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.
Blaydon D.C.; Lind L.K.; Plagnol V.; Linton K.J.; Smith F.J.; Wilson N.J.; McLean W.H.; Munro C.S.; South A.P.; Leigh I.M.; O'Toole E.A.; Lundstroem A.; Kelsell D.P.;
Am. J. Hum. Genet. 93:330-335(2013)
Cited for: VARIANTS PPKB GLU-38; SER-45; ASP-123; PHE-177 AND CYS-188; CHARACTERIZATION OF VARIANTS GLU-38; SER-45; ASP-123; PHE-177 AND CYS-188; SUBCELLULAR LOCATION;
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.