TMEM176A

Transmembrane Protein 176A: A Potential Tumor Suppressor and Immune Modulator

Gene Information Card

Symbol TMEM176A
Full Name Transmembrane Protein 176A
Gene Type Protein-coding
Chromosomal Location 7q36.1
NCBI Gene ID 55365 ncbi.nlm.nih.gov/gene/55365
Ensembl ID ENSG00000106031
UniProt ID Q96HP0
OMIM ID 613334
HGNC ID 28838
Aliases FLJ20457, MGC117188, MGC117189, TMEM176A

Description

TMEM176A (Transmembrane Protein 176A) is a protein-coding gene located on chromosome 7q36.1. It encodes a multi-pass transmembrane protein of unknown function, but evidence suggests it may act as a tumor suppressor and modulator of immune responses. The gene is frequently downregulated in various cancers, and its expression is associated with dendritic cell maturation and T-cell activation. TMEM176A is also implicated in the regulation of calcium signaling and cell adhesion.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer Downregulation of TMEM176A may promote tumor progression and immune evasion NCBI Gene, COSMIC
Breast Cancer Reduced expression correlates with poor prognosis and metastasis NCBI Gene, COSMIC
Lung Cancer Epigenetic silencing of TMEM176A observed in non-small cell lung cancer NCBI Gene, COSMIC
Gastric Cancer Loss of TMEM176A expression associated with aggressive tumor phenotype NCBI Gene, COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Lymph node 12.5 Medium
Spleen 10.8 Medium
Bone marrow 8.2 Low
Lung 6.1 Low
Colon 4.3 Low
Breast 2.7 Not detected
Cell Line Expression
Cell Line nTPM Notes
HEK 293 15.2 Embryonic kidney, high expression
HeLa 8.9 Cervical cancer, moderate expression
A549 5.4 Lung cancer, low expression
MCF7 3.1 Breast cancer, low expression
HCT116 2.8 Colorectal cancer, low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G Missense <0.1% Unknown, likely benign
c.100C>T Nonsense <0.1% Predicted loss of function
c.200_201del Frameshift <0.1% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations are predicted to cause loss of function, potentially contributing to tumor progression.

Gain of Function (GOF)

No gain-of-function mutations reported.

Dominant Negative (DN)

No dominant-negative mutations reported.

Gene Ontology (GO)

• integral component of membrane • protein binding
• calcium ion binding • cell adhesion
• immune response

Pathways

Calcium signaling pathway
Cell adhesion molecules (CAMs)
Immune system

Protein Summary

TMEM176A is a 244-amino acid multi-pass transmembrane protein with four predicted transmembrane domains. It is localized to the plasma membrane and endoplasmic reticulum. The protein contains a conserved domain of unknown function (DUF) and is thought to interact with other membrane proteins to regulate calcium homeostasis and cell-cell adhesion. Its expression is enriched in immune tissues, suggesting a role in antigen presentation and T-cell activation.

Related Products

Product name Cat.No. Species Gene ID
TMEM176A Knockout HeLa Cell Line EDJ-KQ17946 Human 55365 Details Get a Quote
TMEM176A Knockout HEK293 Cell Line EDJ-KQ51450 Human 55365 Details Get a Quote
TMEM176A Knockout A-549 Cell Line EDJ-KQ65081 Human 55365 Details Get a Quote
TMEM176A Knockout HCT 116 Cell Line EDJ-KQ73527 Human 55365 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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