TMF1 (TATA Element Modulatory Factor 1)

A Golgin Protein Involved in Golgi Structure, Androgen Receptor Signaling, and Potential Tumor Suppression

Gene Information Card

Symbol TMF1
Full Name TATA element modulatory factor 1
Gene Type protein-coding
Chromosomal Location 3p13
NCBI Gene ID 7110 ncbi.nlm.nih.gov/gene/7110
Ensembl ID ENSG00000144747
UniProt ID P82094
OMIM ID 603019
HGNC ID 11870
Aliases ARA160, TMF, TMF1_HUMAN

Description

TMF1 (TATA element modulatory factor 1) encodes a Golgi-associated protein (golgin) that plays a role in maintaining Golgi structure and vesicle trafficking. It also functions as a coactivator of the androgen receptor (AR) and has been implicated in transcriptional regulation. TMF1 is considered a potential tumor suppressor in certain cancers, with loss or downregulation observed in prostate and other malignancies.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Prostate cancer TMF1 (ARA160) acts as an androgen receptor coactivator; altered expression may influence AR signaling and tumor progression. PMID: 10887107; NCBI Gene
Breast cancer Reduced TMF1 expression has been reported in breast cancer cell lines, suggesting a possible tumor suppressor role. COSMIC; PMID: 23382219
Colorectal cancer Somatic mutations and copy number loss of TMF1 have been identified in colorectal tumors. COSMIC; ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 12.5 Medium
Prostate 8.2 Medium
Breast 6.1 Low
Colon 5.8 Low
Liver 4.3 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 7.0 Cervical cancer cell line
MCF7 5.2 Breast cancer cell line
LNCaP 9.1 Prostate cancer cell line
HCT116 6.5 Colorectal cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234C>T (p.Arg412*) Nonsense <0.1% Loss of function; predicted to cause nonsense-mediated decay
c.567_568insA (p.Glu190fs) Frameshift <0.1% Loss of function; truncated protein
c.2101G>A (p.Gly701Arg) Missense <0.1% Unknown significance; may affect Golgi localization
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations in TMF1 are predicted to result in loss of function, potentially disrupting Golgi integrity and AR coactivation.

Gain of Function (GOF)

No gain-of-function mutations have been reported for TMF1.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for TMF1.

Gene Ontology (GO)

• Golgi apparatus • Golgi membrane
• protein binding • androgen receptor binding
• Golgi organization • vesicle-mediated transport
• intracellular protein transport

Pathways

• Androgen receptor signaling pathway
• Golgi vesicle transport

Protein Summary

TMF1 is a 1098-amino acid golgin protein localized to the Golgi apparatus. It contains a coiled-coil domain and a TATA element modulatory domain. TMF1 is involved in maintaining Golgi ribbon structure, retrograde transport, and acts as a coactivator of the androgen receptor. Its loss is associated with Golgi fragmentation and altered AR signaling.

Related Products

Product name Cat.No. Species Gene ID
TMF1 Knockout HEK293 Cell Line EDJ-KQ5942 Human 7110 Details Get a Quote
TMF1 Knockout A-549 Cell Line EDJ-KQ29494 Human 7110 Details Get a Quote
TMF1 Knockout HCT 116 Cell Line EDJ-KQ29495 Human 7110 Details Get a Quote
TMF1 Knockout HeLa Cell Line EDJ-KQ29496 Human 7110 Details Get a Quote
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