Variant position: 275 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1225 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 SSSTLPAPPRGGSPLAAPQG GSPTKLQRGGSAPEGATYAAP
Mouse SSSTLPAPPRGGSPLTTTQG GSPTKLQRGGSAPEGAAYAAP
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 – 1225 Catenin delta-2
264 – 264 Omega-N-methylarginine
267 – 267 Phosphoserine
276 – 276 Phosphoserine
282 – 282 Omega-N-methylarginine
NIEHS SNPs program;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS CYS-275; THR-482 AND ARG-810;
Loss of delta-catenin function in severe autism.
Turner T.N.; Sharma K.; Oh E.C.; Liu Y.P.; Collins R.L.; Sosa M.X.; Auer D.R.; Brand H.; Sanders S.J.; Moreno-De-Luca D.; Pihur V.; Plona T.; Pike K.; Soppet D.R.; Smith M.W.; Cheung S.W.; Martin C.L.; State M.W.; Talkowski M.E.; Cook E.; Huganir R.; Katsanis N.; Chakravarti A.;
Cited for: FUNCTION; TISSUE SPECIFICITY; INTERACTION WITH CTNNB1; INVOLVEMENT IN AUTISM; VARIANTS SER-34; LEU-189; LEU-224; CYS-275; HIS-330; HIS-454; ASN-465; THR-482; PRO-507; CYS-713 AND MET-862; CHARACTERIZATION OF VARIANTS SER-34; LEU-189; LEU-224; CYS-275; HIS-330; HIS-454; ASN-465; THR-482; PRO-507; CYS-713; ARG-810 AND MET-862;
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.