Variant position: 485 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 758 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 IYFDIWVSINDRFQQRIFDP RVDIVQAAWSPFQRTSWVQPL
Mouse IYFDIWVSINDRFQQRLFDP RVDIVQAVWSPFQRTPWVQPL
Rat IYFDIWVSINDRFQQRLFDP RVDIVQAVWSPFRRTPWVQPL
Bovine IYFDIWVSINDRFQQRIFDP RVDIVQAAWSPFQRTPWLQPL
Sheep IYFDIWVSINDRFQQRIFDP RVDIVQAAWSPFQRTPWLQPL
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 – 758 Vitamin K-dependent gamma-carboxylase
383 – 758 Lumenal
Compound heterozygous mutations in the gamma-glutamyl carboxylase gene cause combined deficiency of all vitamin K-dependent blood coagulation factors.
Rost S.; Fregin A.; Koch D.; Compes M.; Mueller C.R.; Oldenburg J.;
Br. J. Haematol. 126:546-549(2004)
Cited for: VARIANT VKCFD1 PRO-485;
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.