Sequence information
Variant position: 813 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 920 The length of the canonical sequence.
Location on the sequence:
QEFGWLQITPQEFLCMKALL
L FSIIPVDGLKNQKFFDELRM
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 QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
Rhesus macaque QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
Chimpanzee QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
Mouse QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
Rat QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
Pig QEFGWLQITPQEFLCMKALLL FSIIPVDGLKNQKFFDELRM
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 – 920
Androgen receptor
Domain
669 – 900
NR LBD
Region
552 – 919
Interaction with LPXN
Region
592 – 919
Interaction with CCAR1
Region
625 – 919
Interaction with KAT7
Alternative sequence
645 – 920
Missing. In isoform 3.
Alternative sequence
649 – 920
Missing. In isoform 4.
Literature citations
Point mutations in the steroid-binding domain of the androgen receptor gene of five Japanese patients with androgen insensitivity syndrome.
Yaegashi N.; Uehara S.; Senoo M.; Sato J.; Fujiwara J.; Funato T.; Sasaki T.; Yajima A.;
Tohoku J. Exp. Med. 187:263-272(1999)
Cited for: VARIANTS AIS PHE-813 AND GLN-832;
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.