SGTA: Small Glutamine Rich Tetratricopeptide Repeat Co-Chaperone Alpha

A comprehensive biomedical overview of SGTA gene, including genomic context, expression, mutations, and clinical relevance.

Gene Information Card

Symbol SGTA
Full Name Small glutamine rich tetratricopeptide repeat co-chaperone alpha
Gene Type Protein coding
Chromosomal Location 19p13.3
NCBI Gene ID 6449 ncbi.nlm.nih.gov/gene/6449
Ensembl ID ENSG00000104973
UniProt ID O43765
OMIM ID 601117
HGNC ID 10819
Aliases SGT, SGT1, hSGT, Vpu-binding protein

Description

SGTA encodes a co-chaperone protein that contains tetratricopeptide repeats (TPR) and a glutamine-rich region. It interacts with Hsp70 and Hsp90, participating in protein quality control, steroid hormone receptor assembly, and viral protein trafficking. The gene is located on chromosome 19p13.3 and is ubiquitously expressed.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Prostate cancer SGTA overexpression may modulate androgen receptor signaling via Hsp90 interaction PMID: 19160496
Hepatocellular carcinoma SGTA upregulation associated with poor prognosis; promotes cell proliferation PMID: 25605247
HIV-1 infection SGTA binds HIV-1 Vpu protein, influencing viral release PMID: 12504017

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 18.2 Medium
Brain 12.5 Medium
Liver 10.8 Medium
Heart 9.3 Low
Lung 8.7 Low
Cell Line Expression
Cell Line nTPM Notes
HEK 293 22.1 High expression
HeLa 19.4 High expression
HepG2 15.6 Medium expression
K562 11.3 Medium expression
A549 9.8 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.344C>T (p.Pro115Leu) Missense <0.01% Unknown functional effect
c.487G>A (p.Gly163Ser) Missense <0.01% Unknown functional effect
c.1A>G (p.Met1?) Start loss <0.01% Likely loss of function
Mutation functional classification

Loss of Function (LOF)

Start loss mutations (e.g., p.Met1?) are predicted to abolish protein translation.

Gain of Function (GOF)

No gain-of-function mutations reported in COSMIC or ClinVar.

Dominant Negative (DN)

No dominant-negative mutations described.

Pathways

• Hsp90 chaperone cycle for steroid hormone receptors (Reactome: R-HSA-3371497)
• Protein processing in endoplasmic reticulum (KEGG: hsa04141)

Protein Summary

SGTA is a 313-amino acid co-chaperone with three TPR domains and a glutamine-rich region. It facilitates Hsp70/Hsp90-mediated protein folding, particularly for steroid receptors. It also participates in retrotranslocation of misfolded proteins from the endoplasmic reticulum and modulates viral protein trafficking. The protein is predominantly cytoplasmic but can shuttle to the nucleus.

Related Products

Product name Cat.No. Species Gene ID
SGTA Knockout HEK293 Cell Line EDJ-KQ2417 Human 6449 Details Get a Quote
SGTA Knockout A-549 Cell Line EDJ-KQ22924 Human 6449 Details Get a Quote
SGTA Knockout HeLa Cell Line EDJ-KQ22925 Human 6449 Details Get a Quote
SGTA Knockout HCT 116 Cell Line EDJ-KQ21600 Human 6449 Details Get a Quote
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