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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9NPI9: Variant p.Ile132Arg

Inward rectifier potassium channel 16
Gene: KCNJ16
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Variant information Variant position: help 132 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 Isoleucine (I) to Arginine (R) at position 132 (I132R, p.Ile132Arg). 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 hydrophobic (I) to large size and basic (R) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -3 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 HKTD; when coexpressed with KCNJ10 in Xenopus oocytes, it results in decreased channel expression at the surface and reduced potassium current amplitude compared to the wild-type. Any additional useful information about the variant.


Sequence information Variant position: help 132 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 418 The length of the canonical sequence.
Location on the sequence: help VDNVHSFTGAFLFSLETQTT I GYGYRCVTEECSVAVLMVIL 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                         VDNVHSFTGAFLFSLETQTTIGYGYRCVTEECSVAVLMVIL

Mouse                         VDNVHSFTAAFLFSLETQTTIGYGYRCVTEECSVAVLTVIL

Rat                           VDNVHSFTAAFLFSLETQTTIGYGYRCVTEECSVAVLTVIL
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 – 418 Inward rectifier potassium channel 16
Intramembrane 118 – 134 Helical; Pore-forming; Name=H5
Motif 131 – 136 Selectivity filter



Literature citations
Defects in KCNJ16 cause a novel tubulopathy with hypokalemia, salt wasting, disturbed acid-base homeostasis, and sensorineural deafness.
Schlingmann K.P.; Renigunta A.; Hoorn E.J.; Forst A.L.; Renigunta V.; Atanasov V.; Mahendran S.; Barakat T.S.; Gillion V.; Godefroid N.; Brooks A.S.; Lugtenberg D.; Lake J.; Debaix H.; Rudin C.; Knebelmann B.; Tellier S.; Rousset-Rouviere C.; Viering D.; de Baaij J.H.F.; Weber S.; Palygin O.; Staruschenko A.; Kleta R.; Houillier P.; Bockenhauer D.; Devuyst O.; Vargas-Poussou R.; Warth R.; Zdebik A.A.; Konrad M.;
J. Am. Soc. Nephrol. 32:1498-1512(2021)
Cited for: VARIANTS HKTD ILE-64; ARG-132; ALA-135; CYS-137; 176-ARG--MET-418 DEL AND LEU-250; INVOLVEMENT IN HKTD; CHARACTERIZATION OF VARIANTS HKTD ILE-64; ARG-132; CYS-137; 176-ARG--MET-418 DEL AND LEU-250;
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.