Variant position: 698 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 714 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 NKKNWDKARERFTENFPETK PQKDDPGTMPWVKGTLE
Mouse SKKHWDKARERFAETFTENK PRKETPGAVPWVTGTAE
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
2 – 714 Angiogenic factor with G patch and FHA domains 1
655 – 714 Disordered
673 – 698 Basic and acidic residues
110 – 714 Missing. In isoform 2.
177 – 714 Missing. In isoform 3.
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome.
Tian X.-L.; Kadaba R.; You S.-A.; Liu M.; Timur A.A.; Yang L.; Chen Q.; Szafranski P.; Rao S.; Wu L.; Housman D.E.; DiCorleto P.E.; Driscoll D.J.; Borrow J.; Wang Q.;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORM 1); FUNCTION; SUBCELLULAR LOCATION; TISSUE SPECIFICITY; DISEASE; INTERACTION WITH TNFSF12; VARIANT THR-698; VARIANT KTS LYS-133;
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.