Home  |  Contact

UniProtKB/Swiss-Prot O15294: Variant p.Leu254Phe

UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit
Gene: OGT
Variant information

Variant position:  254
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 Leucine (L) to Phenylalanine (F) at position 254 (L254F, p.Leu254Phe).
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 medium size and hydrophobic (L) to large size and aromatic (F)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  0
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 MRX106; decreased protein abundance; reduced protein stability.
Any additional useful information about the variant.

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



Sequence information

Variant position:  254
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  1046
The length of the canonical sequence.

Location on the sequence:   VLKEARIFDRAVAAYLRALS  L SPNHAVVHGNLACVYYEQGL
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                         VLKEARIFDRAVAAYLRALSLSPNHAVVHGNLACVYYEQGL

Mouse                         VLKEARIFDRAVAAYLRALSLSPNHAVVHGNLACVYYEQGL

Rat                           VLKEARIFDRAVAAYLRALSLSPNHAVVHGNLACVYYEQGL

Pig                           VLKEARIFDRAVAAYLRALSLSPNHAVVHGNLACVYYEQGL

Rabbit                        VLKEARIFDRAVAAYLRALSLSPNHAVVHGNLACVYYEQGL

Caenorhabditis elegans        VLKEARIFDRAVSAYLRALNLSGNHAVVHGNLACVYYEQGL

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 – 1046 UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit
Repeat 225 – 258 TPR 6
Alternative sequence 1 – 381 Missing. In isoform 4.
Helix 241 – 254


Literature citations

Identification and characterization of a missense mutation in the O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability.
Vaidyanathan K.; Niranjan T.; Selvan N.; Teo C.F.; May M.; Patel S.; Weatherly B.; Skinner C.; Opitz J.; Carey J.; Viskochil D.; Gecz J.; Shaw M.; Peng Y.; Alexov E.; Wang T.; Schwartz C.; Wells L.;
J. Biol. Chem. 292:8948-8963(2017)
Cited for: VARIANT MRX106 PHE-254; CHARACTERIZATION OF VARIANT MRX106 PHE-254; FUNCTION;

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.