Variant position: 59 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 346 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 FLFYFPAAYYASRRVGIAVL WISLITEWLNLIFKWFLFGDR
Mouse FQFCFPAAYYASRRLGISVL WITFIAEWLNLVFKWFLFGDR
Rat FQFYFPAVYYASRRLGISLF WIAFITEWLNLVFKWFLFGDR
Bovine FLFYFPAAYYASRRVGIAVL WISLITEWLNLVFKWFLFGDR
Zebrafish VLLVFPVVFYIHRRTGIAVL WVAALSEWLNLVFKWILFGER
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
1 – 346 Glucose-6-phosphatase 3
55 – 75 Helical
79 – 79 Substrate
79 – 79 R -> A. Loss of catalytic activity.
A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndrome.
Arikoglu T.; Kuyucu N.; Germeshausen M.; Kuyucu S.;
Eur. J. Haematol. 94:79-82(2015)
Cited for: VARIANT SCN4 ARG-59;
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.