UniProtKB/SwissProt variant VAR

Variant information

Variant position:

867

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:

Polymorphism

The variants are classified into three categories: Disease, Polymorphism and Unclassified.

Disease: Variants implicated in disease according to literature reports.
Polymorphism: Variants not reported to be implicated in disease.
Unclassified: Variants with uncertain implication in disease according to literature reports. Evidence against or in favor of a pathogenic role is limited and/or conflicting.

Residue change:

From Arginine (R) to Glycine (G) at position 867 (R867G, p.Arg867Gly).

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:

Change from large size and basic (R) to glycine (G)

The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:

-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

Other resources:

Links to websites of interest for the variant.

Variant rs61306957 [ dbSNP | Ensembl ]

Sequence information

Variant position:

867

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:

933

The length of the canonical sequence.

Location on the sequence:

LELKLTPSAIFDRNRKDELP R LQLEWIDSICMPLYQALVKV

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:

The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         LELKLTPSAIFDRNRKDELPRLQLEWIDSICMPLYQALVKV

Mouse                         SELKLTPSAIFDRNRKDELPRLQLEWIDSICMPLYQALVKV

Rat                           SELKLTPSAIFDRNRKDELPRLQLEWIDSICMPLYQALVKV

Drosophila                    QELNITPIDIMNREKEDELPMMQVNFIDSICLPIYEAFATL

Sequence annotation in neighborhood:

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.

Type	Positions	Description
Chain	1 – 933	Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A
Domain	588 – 912	PDEase
Binding site	869 – 869	cAMP or cGMP

Literature citations

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia.
Horvath A.; Boikos S.; Giatzakis C.; Robinson-White A.; Groussin L.; Griffin K.J.; Stein E.; Levine E.; Delimpasi G.; Hsiao H.P.; Keil M.; Heyerdahl S.; Matyakhina L.; Libe R.; Fratticci A.; Kirschner L.S.; Cramer K.; Gaillard R.C.; Bertagna X.; Carney J.A.; Bertherat J.; Bossis I.; Stratakis C.A.;
Nat. Genet. 38:794-800(2006)
Cited for: INVOLVEMENT IN PPNAD2; TISSUE SPECIFICITY; VARIANTS HIS-804 AND GLY-867;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9HCR9: Variant p.Arg867Gly