Variant position: 177 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 333 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 PYPLFVTWKIGRDKRLRGCI GTFSAMNLHSGLREYTLTSAL
Mouse PYPLFVTWKIGRDKRLRGCI GTFSAMNLHSGLREYTLTSAL
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 – 333 AMME syndrome candidate gene 1 protein
119 – 313 AMMECR1
158 – 333 Missing. In isoform 2.
159 – 195 Missing. In isoform 3.
AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis.
Andreoletti G.; Seaby E.G.; Dewing J.M.; O'Kelly I.; Lachlan K.; Gilbert R.D.; Ennis S.;
J. Med. Genet. 54:269-277(2017)
Cited for: VARIANT MFHIEN ASP-177; CHARACTERIZATION OF VARIANT MFHIEN ASP-177; INVOLVEMENT IN MFHIEN; SUBCELLULAR LOCATION;
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