Sequence information
Variant position: 739 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1367 The length of the canonical sequence.
Location on the sequence:
RKVFENFLHNSIFVPRPERK
R RDVMQVANTTMSSRSRNTTA
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 RKVFENFLHNSIFVPRPERKR RDVMQVANTTMSSRSRNTTA
Mouse RKVFENFLHNSIFVPRPERRR RDVMQVANTTMSSRSRNTTV
Rat RKVFENFLHNSIFVPRPERRR RDVLQVANTTMSSRSRNTTV
Xenopus laevis RKVFENFLHNSIFVPRPNRRR RDVLAVGNSTVTSYEKNSTT
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
Domain
735 – 828
Fibronectin type-III 3
Glycosylation
747 – 747
N-linked (GlcNAc...) asparagine
Glycosylation
756 – 756
N-linked (GlcNAc...) asparagine
Literature citations
Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardation.
Kawashima Y.; Kanzaki S.; Yang F.; Kinoshita T.; Hanaki K.; Nagaishi J.; Ohtsuka Y.; Hisatome I.; Ninomoya H.; Nanba E.; Fukushima T.; Takahashi S.;
J. Clin. Endocrinol. Metab. 90:4679-4687(2005)
Cited for: VARIANT IGF1RES GLN-739; CHARACTERIZATION OF VARIANT IGF1RES GLN-739;
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.