Variant position: 154 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 ATRARSRWVRVMPSLAYCTF LLAVGLSRIFILAHFPHQVLA
Mouse ASRSRSPWVRVIPGLAYCTF LLAVGLSRVFLLAHFPHQVLG
Rat ASQTRSPWVRVIPGLAYCTF LLAVGLSRVFLLAHFPHQVLA
Bovine ATRAHSRWVRVIPSLAYCTF LLAVGLSRVFLLAHFPHQVLA
Zebrafish QAYTGSKILSAVLYLLYAVF LGCVGLSRIFILAHFPHQVVA
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
147 – 164 Helical
167 – 167 Nucleophile
161 – 161 Substrate
167 – 167 H -> A. Loss of catalytic activity.
A novel G6PC3 gene mutation in a patient with severe congenital neutropenia.
Aytekin C.; Germeshausen M.; Tuygun N.; Dogu F.; Ikinciogullari A.;
J. Pediatr. Hematol. Oncol. 35:E81-E83(2013)
Cited for: VARIANT SCN4 PRO-154;
Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-beta deficiency.
Lin S.R.; Pan C.J.; Mansfield B.C.; Chou J.Y.;
Mol. Genet. Metab. 114:41-45(2015)
Cited for: CHARACTERIZATION OF VARIANTS SCN4 LEU-44; SER-44; ILE-116; LYS-116; THR-116; VAL-116; ARG-118; ILE-139; PRO-154; GLN-161; PRO-185; GLN-189; ARG-208; HIS-253; ARG-260 AND ASP-260;
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.