Sequence information
Variant position: 214 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 452 The length of the canonical sequence.
Location on the sequence:
PDPEQRPLRSPLDNMIRRLS
P AERAQGPRPHQENNHQESYP
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 PDPEQ-RPLRSPLDNMIRRLSP AERAQGPRPHQENNHQESYP
Mouse PDPEQQRPQRSPLDNMSRRLSP VEKAQGPRLQQENNHQETY
Bovine PDPEQ-RPLRSPLDNMIRRLSP AERAQGPRLHQENNHQEPY
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 – 452
Transcription factor ETV6
Region
158 – 262
Disordered
Modified residue
213 – 213
Phosphoserine
Mutagenesis
213 – 213
S -> A. No effect.
Literature citations
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.
Zhang M.Y.; Churpek J.E.; Keel S.B.; Walsh T.; Lee M.K.; Loeb K.R.; Gulsuner S.; Pritchard C.C.; Sanchez-Bonilla M.; Delrow J.J.; Basom R.S.; Forouhar M.; Gyurkocza B.; Schwartz B.S.; Neistadt B.; Marquez R.; Mariani C.J.; Coats S.A.; Hofmann I.; Lindsley R.C.; Williams D.A.; Abkowitz J.L.; Horwitz M.S.; King M.C.; Godley L.A.; Shimamura A.;
Nat. Genet. 47:180-185(2015)
Cited for: FUNCTION; INVOLVEMENT IN THC5; VARIANTS THC5 LEU-214; GLN-369 AND CYS-399; CHARACTERIZATION OF VARIANTS THC5 LEU-214; GLN-369 AND CYS-399;
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.