SELENOF: Selenoprotein F (Sep15) - Gene Information and Function

Comprehensive biomedical overview of SELENOF, a selenoprotein involved in redox regulation and protein folding in the endoplasmic reticulum.

Gene Information Card

Symbol SELENOF
Full Name Selenoprotein F
Gene Type protein-coding
Chromosomal Location 1p22.3
NCBI Gene ID 6415 ncbi.nlm.nih.gov/gene/6415
Ensembl ID ENSG00000162433
UniProt ID O60613
OMIM ID 601291
HGNC ID 10712
Aliases SELENOF, Sep15, 15 kDa selenoprotein

Description

SELENOF (selenoprotein F, also known as Sep15) encodes a selenoprotein containing a selenocysteine residue. It is localized in the endoplasmic reticulum (ER) and functions as a thiol-disulfide oxidoreductase involved in redox regulation, protein folding, and protection against oxidative stress. SELENOF is highly expressed in the prostate, thyroid, and liver, and its expression is regulated by selenium levels. Polymorphisms and altered expression have been associated with cancer risk and progression.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Prostate cancer Reduced SELENOF expression may impair antioxidant defense, promoting oxidative damage and tumorigenesis. PMID: 15642720; COSMIC
Breast cancer Loss of SELENOF expression correlates with poor prognosis; potential tumor suppressor role. PMID: 19177216; ClinVar
Colorectal cancer SELENOF polymorphisms (e.g., rs5845) associated with increased risk. PMID: 16951129; NCBI Gene
Thyroid cancer SELENOF downregulation observed in thyroid tumors; linked to altered redox balance. PMID: 20068074; OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Prostate 12.5 Medium
Thyroid 10.8 Medium
Liver 8.2 Medium
Kidney 6.4 Low
Lung 5.1 Low
Cell Line Expression
Cell Line nTPM Notes
PC-3 (prostate cancer) 8.9 Androgen-independent line
MCF-7 (breast cancer) 7.2 ER-positive line
HepG2 (liver cancer) 6.5 Hepatocellular carcinoma
HEK293 (embryonic kidney) 5.0 Normal transformed line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.112G>A (p.Gly38Arg) Missense <0.01% rs5845; associated with altered selenium metabolism
c.200C>T (p.Thr67Met) Missense <0.01% Reported in COSMIC; functional impact unknown
c.311G>A (p.Arg104Gln) Missense <0.01% ClinVar; uncertain significance
Mutation functional classification

Loss of Function (LOF)

Missense variants (e.g., p.Gly38Arg) may reduce selenoprotein stability or redox activity, leading to impaired ER stress response.

Gain of Function (GOF)

No known gain-of-function mutations reported.

Dominant Negative (DN)

No evidence for dominant-negative effects.

Pathways

Endoplasmic reticulum protein processing (KEGG: hsa04141)
Selenocysteine synthesis and incorporation (Reactome: R-HSA-2408522)

Protein Summary

SELENOF is a 15 kDa selenoprotein localized to the endoplasmic reticulum lumen. It contains a thioredoxin-like fold and a selenocysteine residue at its active site, enabling redox activity. The protein participates in disulfide bond formation and isomerization during protein folding, and protects cells from ER stress-induced apoptosis. SELENOF expression is selenium-dependent and tissue-specific, with highest levels in prostate, thyroid, and liver.

Related Products

Product name Cat.No. Species Gene ID
SELENOF Knockout HEK293 Cell Line EDJ-KQ6575 Human 9403 Details Get a Quote
SELENOF Knockout A-549 Cell Line EDJ-KQ30788 Human 9403 Details Get a Quote
SELENOF Knockout HCT 116 Cell Line EDJ-KQ30789 Human 9403 Details Get a Quote
SELENOF Knockout HeLa Cell Line EDJ-KQ30790 Human 9403 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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