Sequence information
Variant position: 2312 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2897 The length of the canonical sequence.
Location on the sequence:
VASFYTTKLLDSPGAATEYS
D PSVPTPPGAGVKEEHDQSTQ
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 VASFYTTKLLDSPGAATEYSD PSVPTPPGAGVKEEHDQSTQ
Mouse VASFYTTKLLDSPGAATERGE PSVPTPPAVAVREEHEQSAQ
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
Chain
1 – 2897
Chromodomain-helicase-DNA-binding protein 9
Region
2305 – 2337
Disordered
Literature citations
Characterization and functional analysis of CReMM, a novel chromodomain helicase DNA-binding protein.
Shur I.; Benayahu D.;
J. Mol. Biol. 352:646-655(2005)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); FUNCTION; SUBCELLULAR LOCATION; TISSUE SPECIFICITY; PHOSPHORYLATION; VARIANT GLU-2312;
PRIC320, a transcription coactivator, isolated from peroxisome proliferator-binding protein complex.
Surapureddi S.; Viswakarma N.; Yu S.; Guo D.; Rao M.S.; Reddy J.K.;
Biochem. Biophys. Res. Commun. 343:535-543(2006)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2); FUNCTION; TISSUE SPECIFICITY; VARIANT GLU-2312; INTERACTION WITH PPARA; ESR1 AND NR1I3;
Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
Nagase T.; Ishikawa K.; Nakajima D.; Ohira M.; Seki N.; Miyajima N.; Tanaka A.; Kotani H.; Nomura N.; Ohara O.;
DNA Res. 4:141-150(1997)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 124-2897 (ISOFORM 3); VARIANT GLU-2312;
Disclaimer:
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.