Variant position: 292 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1023 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 RADP-GAPVSQEDMQAMVQLI RYMHTYCLPQRKLPPQTPEPL
Mouse TASPDSAQPPEEDVRAMVQLI RYMHTYCLPQRKLPQRAPEP
Rat TANPNSAQVPKDDVRAMVQLI RYMHTYCLPQRKLPQRASEP
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 – 1023 Peroxisome proliferator-activated receptor gamma coactivator 1-beta
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1); VARIANT SER-292;
Evidence of an association between genetic variation of the coactivator PGC-1beta and obesity.
Andersen G.; Wegner L.; Yanagisawa K.; Rose C.S.; Lin J.; Gluemer C.; Drivsholm T.; Borch-Johnsen K.; Jorgensen T.; Hansen T.; Spiegelman B.M.; Pedersen O.;
J. Med. Genet. 42:402-407(2005)
Cited for: POLYMORPHISM; VARIANTS PRO-203; ILE-279 AND SER-292;
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