Identity
HGNC
LOCATION
11q24.2
LOCUSID
ALIAS
ITM1,STT3-A,TMC
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 3703
MIM: 601134
HGNC: 6172
Ensembl: ENSG00000134910
Variants:
dbSNP: 3703
ClinVar: 3703
TCGA: ENSG00000134910
COSMIC: STT3A
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37864032 | 2023 | STT3A-mediated viral N-glycosylation underlies the tumor selectivity of oncolytic virus M1. | 0 |
| 37864032 | 2023 | STT3A-mediated viral N-glycosylation underlies the tumor selectivity of oncolytic virus M1. | 0 |
| 36139350 | 2022 | Proteome and Glycoproteome Analyses Reveal the Protein N-Linked Glycosylation Specificity of STT3A and STT3B. | 4 |
| 36139350 | 2022 | Proteome and Glycoproteome Analyses Reveal the Protein N-Linked Glycosylation Specificity of STT3A and STT3B. | 4 |
| 34653363 | 2021 | Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings. | 6 |
| 34653363 | 2021 | Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings. | 6 |
| 31296534 | 2019 | Quantitative glycoproteomics reveals new classes of STT3A- and STT3B-dependent N-glycosylation sites. | 33 |
| 31296534 | 2019 | Quantitative glycoproteomics reveals new classes of STT3A- and STT3B-dependent N-glycosylation sites. | 33 |
| 30181269 | 2018 | Mammalian STT3A/B oligosaccharyltransferases segregate N-glycosylation at the translocon from lipid-linked oligosaccharide hydrolysis. | 13 |
| 30181269 | 2018 | Mammalian STT3A/B oligosaccharyltransferases segregate N-glycosylation at the translocon from lipid-linked oligosaccharide hydrolysis. | 13 |
| 28424003 | 2017 | Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A. | 6 |
| 28860277 | 2017 | DC2 and KCP2 mediate the interaction between the oligosaccharyltransferase and the ER translocon. | 24 |
| 28424003 | 2017 | Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A. | 6 |
| 28860277 | 2017 | DC2 and KCP2 mediate the interaction between the oligosaccharyltransferase and the ER translocon. | 24 |
| 25029371 | 2014 | The middle X residue influences cotranslational N-glycosylation consensus site skipping. | 22 |
Citation
Dessen P
STT3A (STT3 oligosaccharyltransferase complex catalytic subunit A)
Atlas Genet Cytogenet Oncol Haematol. 2011-07-01
Online version: http://atlasgeneticsoncology.org/gene/52275/stt3a
