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UniProtKB/Swiss-Prot P09471: Variant p.Gly203Arg

Guanine nucleotide-binding protein G(o) subunit alpha
Gene: GNAO1
Variant information

Variant position:  203
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  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:  From Glycine (G) to Arginine (R) at position 203 (G203R, p.Gly203Arg).
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 glycine (G) to large size and basic (R)
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

Variant description:  In DEE17; the mutant protein localizes normally to the cell periphery.
Any additional useful information about the variant.

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  203
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  354
The length of the canonical sequence.

Location on the sequence:   TGIVETHFTFKNLHFRLFDV  G GQRSERKKWIHCFEDVTAII
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                         TGIVETHFTFKNLHFRLFDVGGQRSERKKWIHCFEDVTAII

Mouse                         TGIVETHFTFKNLHFRLFDVGGQRSERKKWIHCFEDVTAII

Rat                           TGIVETHFTFKNLHFRLFDVGGQRSERKKWIHCFEDVTAII

Bovine                        TGIVETHFTFKNLHFRLFDVGGQRSERKKWIHCFEDVTAII

Xenopus laevis                TGIVETHFTFKNLHFRLFDVGGQRSERKKWWHCFEDVTAII

Caenorhabditis elegans        TGIVEVHFTFKNLNFKLFDVGGQRSERKKWIHCFEDVTAII

Drosophila                    TGIVEVHFSFKNLNFKLFDVGGQRSERKKWIHCFEDVTAII

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.

TypePositionsDescription
Chain 2 – 354 Guanine nucleotide-binding protein G(o) subunit alpha
Domain 32 – 354 G-alpha
Nucleotide binding 201 – 205 GTP
Region 197 – 206 G3 motif
Modified residue 205 – 205 5-glutamyl histamine


Literature citations

De Novo mutations in GNAO1, encoding a Galphao subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
Nakamura K.; Kodera H.; Akita T.; Shiina M.; Kato M.; Hoshino H.; Terashima H.; Osaka H.; Nakamura S.; Tohyama J.; Kumada T.; Furukawa T.; Iwata S.; Shiihara T.; Kubota M.; Miyatake S.; Koshimizu E.; Nishiyama K.; Nakashima M.; Tsurusaki Y.; Miyake N.; Hayasaka K.; Ogata K.; Fukuda A.; Matsumoto N.; Saitsu H.;
Am. J. Hum. Genet. 93:496-505(2013)
Cited for: VARIANTS DEE17 GLY-174; 191-THR--PHE-197 DEL; ARG-203 AND ASN-279; CHARACTERIZATION OF VARIANTS DEE17 GLY-174; 191-THR--PHE-197 DEL; ARG-203 AND ASN-279; INVOLVEMENT IN DEE17;

Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
Saitsu H.; Fukai R.; Ben-Zeev B.; Sakai Y.; Mimaki M.; Okamoto N.; Suzuki Y.; Monden Y.; Saito H.; Tziperman B.; Torio M.; Akamine S.; Takahashi N.; Osaka H.; Yamagata T.; Nakamura K.; Tsurusaki Y.; Nakashima M.; Miyake N.; Shiina M.; Ogata K.; Matsumoto N.;
Eur. J. Hum. Genet. 24:129-134(2016)
Cited for: INVOLVEMENT IN NEDIM; VARIANTS NEDIM CYS-209; VAL-227 AND LYS-246; VARIANT DEE17 ARG-203;

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.