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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q08357: Variant p.Glu575Lys

Sodium-dependent phosphate transporter 2
Gene: SLC20A2
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Variant information Variant position: help 575 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 Glutamate (E) to Lysine (K) at position 575 (E575K, p.Glu575Lys). 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 medium size and acidic (E) to large size and basic (K) 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 IBGC1; substantially impaired phosphate transport. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 575 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 652 The length of the canonical sequence.
Location on the sequence: help VIQTMGKDLTPITPSSGFTI E LASAFTVVIASNIGLPVSTT 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                         VIQTMGKDLTPITPSSGFTIELASAFTVVIASNIGLPVSTT

Mouse                         VIQTMGKDLTPITPSSGFTIELASAFTVVIASNIGLPVSTT

Rat                           VIQTMGKDLTPITPSSGFTIELASAFTVVIASNIGLPVSTT

Bovine                        VIQTMGKDLTPITPSSGFTIELASAFTVVIASNIGLPVSTT

Cat                           VIQTMGKDLTPITPSSGFTIELASAFTVVIASNVGLPVSTT

Xenopus laevis                VIQTMGKDLTPITPSSGFTIELASAFTVVVASNIGLPISTT

Xenopus tropicalis            VIQTMGKDLTPITPSSGFTIELASAFTVVVASNIGLPISTT
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 – 652 Sodium-dependent phosphate transporter 2
Transmembrane 572 – 586 Helical
Mutagenesis 575 – 575 E -> DK. Abolishes sodium-dependent phosphate transport; no effect on retroviral receptor function.
Mutagenesis 575 – 575 E -> Q. Abolishes phosphate but not sodium uptake; when associated with Q-55 and Q-91.



Literature citations
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.
Wang C.; Li Y.; Shi L.; Ren J.; Patti M.; Wang T.; de Oliveira J.R.; Sobrido M.J.; Quintans B.; Baquero M.; Cui X.; Zhang X.Y.; Wang L.; Xu H.; Wang J.; Yao J.; Dai X.; Liu J.; Zhang L.; Ma H.; Gao Y.; Ma X.; Feng S.; Liu M.; Wang Q.K.; Forster I.C.; Zhang X.; Liu J.Y.;
Nat. Genet. 44:254-256(2012)
Cited for: VARIANTS IBGC1 VAL-42 DEL; ARG-498; LYS-575; MET-595; TRP-601 AND LEU-601; CHARACTERIZATION OF VARIANTS IBGC1 VAL-42 DEL; ARG-498; LYS-575; MET-595; TRP-601 AND LEU-601; FUNCTION AS SODIUM-PHOSPHATE SYMPORTER; TRANSPORTER ACTIVITY;
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.