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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O43826: Variant p.Gly339Asp

Glucose-6-phosphate exchanger SLC37A4
Gene: SLC37A4
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Variant information Variant position: help 339 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Glycine (G) to Aspartate (D) at position 339 (G339D, p.Gly339Asp). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from glycine (G) to medium size and acidic (D) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In GSD1B. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 339 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 429 The length of the canonical sequence.
Location on the sequence: help RVTVTSDSPKLWILVLGAVF G FSSYGPIALFGVIANESAPP 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.
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 429 Glucose-6-phosphate exchanger SLC37A4
Transmembrane 329 – 349 Helical
Alternative sequence 328 – 328 K -> KDVAFWTLALHPLAELTGFTEHE. In isoform 2.



Literature citations
Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.
Chou J.Y.; Matern D.; Mansfield B.C.; Chen Y.-T.;
Curr. Mol. Med. 2:121-143(2002)
Cited for: REVIEW ON GSD1B VARIANTS; VARIANTS GSD1B HIS-28; PRO-85; ASN-278; ASP-339 AND ASP-373; Glycogen storage disease type Ib without neutropenia.
Kure S.; Hou D.-C.; Suzuki Y.; Yamagishi A.; Hiratsuka M.; Fukuda T.; Sugie H.; Kondo N.; Matsubara Y.; Narisawa K.;
J. Pediatr. 137:253-256(2000)
Cited for: VARIANT GSD1B ASP-339;
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.