Variant position: 449 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2321 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 ETDVNECLSGPCRNQATCLD RIGQFTCICMAGFTGTYCEVD
Mouse ETDVNECLSGPCRNQATCLD RIGQFTCICMAGFTGTYCEVD
Rat ETDVNECLSGPCRNQATCLD RIGQFTCICMAGFTGTFCEVD
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
40 – 2321 Neurogenic locus notch homolog protein 3
40 – 1643 Extracellular
431 – 467 EGF-like 11; calcium-binding
440 – 455
CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.
Kalimo H.; Ruchoux M.-M.; Viitanen M.; Kalaria R.N.;
Brain Pathol. 12:371-384(2002)
Cited for: VARIANTS CADASIL1 ARG-76; TYR-93; TYR-128; CYS-142; ARG-194; TYR-222; SER-233; ARG-251; CYS-420; GLY-440; CYS-449; CYS-953 AND CYS-1021;
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.