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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9UL51: Variant p.Glu515Lys

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2
Gene: HCN2
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Variant information Variant position: help 515 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 515 (E515K, p.Glu515Lys). 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 EIG17; causes a large negative shift of the activation curve; homomeric mutant channels transfected into rat cortical neurons lower the threshold of action potential firing and strongly increase cell excitability when compared with wild-type channels. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 515 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 889 The length of the canonical sequence.
Location on the sequence: help DFRQKIHDYYEHRYQGKMFD E DSILGELNGPLREEIVNFNC 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                         DFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNC

Mouse                         DFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNC

Rat                           DFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNC
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 – 889 Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2
Topological domain 462 – 889 Cytoplasmic
Helix 515 – 520



Literature citations
Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy.
DiFrancesco J.C.; Barbuti A.; Milanesi R.; Coco S.; Bucchi A.; Bottelli G.; Ferrarese C.; Franceschetti S.; Terragni B.; Baruscotti M.; DiFrancesco D.;
J. Neurosci. 31:17327-17337(2011)
Cited for: VARIANT EIG17 LYS-515; CHARACTERIZATION OF VARIANT EIG17 LYS-515; INVOLVEMENT IN EIG17;
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.