Variant position: 60 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 133 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 MRHHYVDSISHPLYKCSSKM VLLARCEGHCSQASRSEPLVS
Mouse MRHHYVDSISHPLYKCSSKM VLLARCEGHCSQASRSEPLVS
Bovine MRHHYVDSISHPLYKCSSKM VLLARCEGHCSQASRSEPLVS
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.
Norrie disease protein (norrin) forms disulfide-linked oligomers associated with the extracellular matrix.
Perez-Vilar J.; Hill R.L.;
J. Biol. Chem. 272:33410-33415(1997)
Cited for: SUBCELLULAR LOCATION; OLIGOMERIZATION; MUTAGENESIS OF CYS-95; CHARACTERIZATION OF VARIANTS ND GLU-60 AND GLN-121;
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
Meindl A.; Berger W.; Meitinger T.; van de Pol D.; Achatz H.; Dorner C.; Haasemann M.; Hellebrand H.; Gal A.; Cremers F.P.M.; Ropers H.-H.;
Nat. Genet. 2:139-143(1992)
Cited for: VARIANTS ND CYS-44; GLU-60 AND TYR-96;
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.