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UniProtKB/Swiss-Prot P46977: Variant p.Val626Ala

Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A
Gene: STT3A
Chromosomal location: 11q23.3
Variant information

Variant position:  626
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Disease [Disclaimer]
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 Valine (V) to Alanine (A) at position 626 (V626A, p.Val626Ala).
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 (V) to small size and hydrophobic (A)
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

Involvement in disease:  Congenital disorder of glycosylation 1W (CDG1W) [MIM:615596]: A form of congenital disorder of glycosylation, a multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269|PubMed:23842455}. Note=The disease is caused by mutations affecting the gene represented in this entry.
The name and a short description of the disease associated with the variant. For more information about the disease, the user can refer to OMIM, following the link provided after the disease acronym.

Variant description:  In CDG1W; affects activity resulting in hypoglycosylation of STT3A-specific substrates.
Any additional useful information about the variant.

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



Sequence information

Variant position:  626
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  705
The length of the canonical sequence.

Location on the sequence:   TDTGKHIKENDYYTPTGEFR  V DREGSPVLLNCLMYKMCYYR
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                         TDTGKHIKENDYYTPTGEFRVDREGSPVLLNCLMYKMCYYR

Mouse                         TETGRHIKENDYYTPTGEFRVDREGSPVLLNCLMYKMCYYR

Bovine                        TDTGKHIKEHDYYTPTGEFRVDREGSPVLLNCLMYKMCYYR

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 1 – 705 Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A
Topological domain 474 – 705 Lumenal


Literature citations

Mutations in STT3A and STT3B cause two congenital disorders of glycosylation.
Shrimal S.; Ng B.G.; Losfeld M.E.; Gilmore R.; Freeze H.H.;
Hum. Mol. Genet. 22:4638-4645(2013)
Cited for: VARIANT CDG1W ALA-626; CHARACTERIZATION OF VARIANT CDG1W ALA-626;

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.