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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P78562: Variant p.Gly579Arg

Phosphate-regulating neutral endopeptidase PHEX
Gene: PHEX
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Variant information Variant position: help 579 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 Arginine (R) at position 579 (G579R, p.Gly579Arg). 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 large size and basic (R) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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 XLHRD. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 579 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 749 The length of the canonical sequence.
Location on the sequence: help FFWGTEYPRSLSYGAIGVIV G HEFTHGFDNNGRKYDKNGNL 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         FFWGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNL

Mouse                         FFWGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNL
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 – 749 Phosphate-regulating neutral endopeptidase PHEX
Topological domain 42 – 641 Extracellular
Domain 53 – 749 Peptidase M13
Active site 581 – 581
Binding site 580 – 580
Binding site 584 – 584
Disulfide bond 77 – 733
Disulfide bond 85 – 693



Literature citations
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.
Francis F.; Strom T.M.; Hennig S.; Boeddrich A.; Lorenz B.; Brandau O.; Mohnike K.L.; Cagnoli M.; Steffens C.; Klages S.; Borzym K.; Pohl T.; Oudet C.L.; Econs M.J.; Rowe P.S.N.; Reinhardt R.; Meitinger T.; Lehrach H.;
Genome Res. 7:573-585(1997)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS XLHRD ARG-85; LEU-534; ARG-579 AND PRO-651; Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).
Rowe P.S.N.; Oudet C.L.; Francis F.; Sinding C.; Pannetier S.; Econs M.J.; Strom T.M.; Meitinger T.; Garabedian M.; David A.; Macher M.-A.; Questiaux E.; Popowska E.; Pronicka E.; Read A.P.; Mokrzycki A.; Glorieux F.H.; Drezner M.K.; Hanauer A.; Lehrach H.; Goulding J.N.; O'Riordan J.L.H.;
Hum. Mol. Genet. 6:539-549(1997)
Cited for: VARIANTS XLHRD SER-77; PRO-138; LEU-534 AND ARG-579; Mutational analysis of PHEX gene in X-linked hypophosphatemia.
Dixon P.H.; Christie P.T.; Wooding C.; Trump D.; Grieff M.; Holm I.A.; Gertner J.M.; Schmidtke J.; Shah B.; Shaw N.; Smith C.; Tau C.; Schlessinger D.; Whyte M.P.; Thakker R.V.;
J. Clin. Endocrinol. Metab. 83:3615-3623(1998)
Cited for: VARIANTS XLHRD PHE-317; LEU-534; ARG-579; ARG-621; ASN-680 DEL; THR-720; TYR-731 AND ARG-749;
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.