Variant position: 338 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 357 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 VELVFYVLSFCKSAVVPLAS VSVIPYCLAQVLGQPHKKSL
Mouse VELIFYILSFCKSATVPFAS VSLIPYCLARILGQTHKKSL
Rat IESIFYILSFCKSATVPFAS VSLIPYCLARLLGQTHKKSL
Bovine IELIFYVLSFCKSAAVPLAS VSLIPYCLAWVLGQPNKKTV
Cat IELIFYVLSFCKSAAVPLAS VSLIPYCLARVLGQPDKKSL
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 – 357 Glucose-6-phosphatase
321 – 341 Helical
176 – 356 Missing. In isoform 2.
353 – 353 H -> A. Partial loss of catalytic activity.
Glycogen storage disease type Ia: four novel mutations (175delGG, R170X, G266V and V338F) identified.
Rake J.P.; ten Berge A.M.; Verlind E.; Visser G.; Niezen-Koning K.E.; Buys C.H.C.M.; Smit G.P.; Scheffer H.;
Hum. Mutat. 13:173-173(1999)
Cited for: VARIANTS GSD1A VAL-266 AND PHE-338;
Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type Ia.
Stroppiano M.; Regis S.; DiRocco M.; Caroli F.; Gandullia P.; Gatti R.;
J. Inherit. Metab. Dis. 22:43-49(1999)
Cited for: VARIANTS GSD1A VAL-38; ARG-63; CYS-83; VAL-184; ARG-222; VAL-270; CYS-295; PRO-298 AND PHE-338;
Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patients.
Trioche P.; Francoual J.; Chalas J.; Capel L.; Lindenbaum A.; Odievre M.; Labrune P.;
Hum. Mutat. 16:444-444(2000)
Cited for: VARIANTS GSD1A ARG-5; VAL-38; PRO-54; CYS-83; ILE-108; LYS-110; ILE-111; GLU-184; ARG-188; THR-241; ARG-270; VAL-270; LEU-322; PHE-327 DEL AND PHE-338;
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