Basic Information

Symbol
TUSC3
RNA class
mRNA
Alias
Tumor Suppressor Candidate 3 N33 Magnesium Uptake/Transporter TUSC3 SLC58A2 OST3A MagT2 MRT7 Dolichyl-Diphosphooligosaccharide--Protein Glycosyltransferase Subunit TUSC3 Oligosaccharyl Transferase Subunit TUSC3 MGC13453 MRT22 Mental Retardation, Non-Syndromic, Autosomal Recessive, 22 Oligosaccharyltransferase 3 Homolog A (S. Cerevisiae) Putative Prostate Cancer Tumor Suppressor Oligosaccharyltransferase 3 Homolog A Protein N33 D8S1992 M33
Location (GRCh38)
Forensic tag(s)
Drug abuse diagnoses

MANE select

Transcript ID
NM_006765.4
Sequence length
3697.0 nt
GC content
0.3808

Transcripts

ID Sequence Length GC content
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 1494 nt 0.4652
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 1399 nt 0.4911
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 4615 nt 0.3764
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 4540 nt 0.3756
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 1284 nt 0.4883
AGUCUCCUCCUCUGCGUCCUCGGCCGCGGCCCGGGUCCCUCGCAAAGCC… 3697 nt 0.3808
AGAUUGAGGUCCCAGGGCCAAAGGACCACUCCUCUCCUCAGCGCUGGUC… 3823 nt 0.3950
Showing 21 to 27 of 27 entries
Summary

This gene encodes a protein that has been associated with several biological functions including cellular magnesium uptake, protein glycosylation and embryonic development. This protein localizes to the endoplasmic reticulum and acts as a component of the oligosaccharyl transferase complex which is responsible for N-linked protein glycosylation. This gene is a candidate tumor suppressor gene. Homozygous mutations in this gene are associated with autosomal recessive nonsyndromic mental retardation-7 and in the proliferation and invasiveness of several cancers including metastatic pancreatic cancer, ovarian cancer and glioblastoma multiform. [provided by RefSeq, Oct 2017]

Forensic Context

A study in mice demonstrated that chronic methamphetamine administration significantly dysregulates the TUSC3 in microglia, where it is involved in the protein processing of endoplasmic reticulum pathway [Oladapo et al. DOI:10.3390/Ijms26020649].