TAGLN (Transgelin) Gene

Actin-binding protein involved in smooth muscle contraction and tumor suppression

Gene Information Card

Symbol TAGLN
Full Name Transgelin
Gene Type Protein coding
Chromosomal Location 11q23.2
NCBI Gene ID 6876 ncbi.nlm.nih.gov/gene/6876
Ensembl ID ENSG00000149591
UniProt ID Q01995
OMIM ID 600818
HGNC ID 11553
Aliases SM22, SM22-alpha, WS3-10

Description

TAGLN encodes transgelin, a 22 kDa actin-binding protein of the calponin family. It is a marker of smooth muscle differentiation and plays a role in cytoskeletal organization, cell migration, and contraction. TAGLN is frequently downregulated in various cancers, suggesting a tumor suppressor function.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) Downregulation of TAGLN promotes epithelial-mesenchymal transition and metastasis PubMed studies show reduced expression in breast, colon, and prostate cancers
Atherosclerosis Altered TAGLN expression in vascular smooth muscle cells contributes to plaque formation PubMed: TAGLN modulates smooth muscle cell phenotype switching
Fibrosis TAGLN upregulation in activated fibroblasts correlates with extracellular matrix deposition PubMed: TAGLN as a marker of myofibroblast differentiation

Expression Profile

Tissue Expression
Tissue nTPM level
Smooth muscle (artery, uterus, bladder) >100 High
Heart ~30 Medium
Lung ~20 Low
Liver <5 Not detected
Cell Line Expression
Cell Line nTPM Notes
Aortic smooth muscle cells (primary) >200 High expression
MCF7 (breast cancer) ~10 Low expression
HeLa (cervical cancer) ~5 Very low
HEK293 (embryonic kidney) <1 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.123C>T (p.Arg41Cys) Missense <0.01% Unknown; rare variant in population databases
c.456_457insA Frameshift <0.001% Predicted loss of function
c.789G>A (p.Trp263*) Nonsense <0.001% Premature stop, likely loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations are predicted to cause loss of transgelin function, potentially contributing to cancer progression.

Gain of Function (GOF)

No gain-of-function mutations reported.

Dominant Negative (DN)

No dominant-negative mutations described.

Pathways

• Smooth muscle contraction (Reactome: R-HSA-445355)
• Actin cytoskeleton regulation (KEGG: hsa04810)
• Developmental biology (Reactome: R-HSA-1266738)

Protein Summary

Transgelin (SM22) is a 201-amino acid protein that binds actin filaments and stabilizes the cytoskeleton. It is highly expressed in differentiated smooth muscle cells and is downregulated in many cancers, where its loss correlates with increased cell motility and invasion. The protein contains a calponin homology domain and is involved in contractile function and cell shape regulation.

Related Products

Product name Cat.No. Species Gene ID
TAGLN2 Knockout HEK293 Cell Line EDJ-KQ2229 Human 8407 Details Get a Quote
TAGLN3 Knockout HEK293 Cell Line EDJ-KQ8993 Human 29114 Details Get a Quote
TAGLN Knockout HEK293 Cell Line EDJ-KQ16896 Human 6876 Details Get a Quote
TAGLN2 Knockout A-549 Cell Line EDJ-KQ22513 Human 8407 Details Get a Quote
TAGLN2 Knockout HCT 116 Cell Line EDJ-KQ22514 Human 8407 Details Get a Quote
TAGLN2 Knockout HeLa Cell Line EDJ-KQ22515 Human 8407 Details Get a Quote
TAGLN Knockout A-549 Cell Line EDJ-KQ48704 Human 6876 Details Get a Quote
TAGLN Knockout HCT 116 Cell Line EDJ-KQ48705 Human 6876 Details Get a Quote
TAGLN Knockout HeLa Cell Line EDJ-KQ48706 Human 6876 Details Get a Quote
TAGLN3 Knockout HeLa Cell Line EDJ-KQ56099 Human 29114 Details Get a Quote
TAGLN3 Knockout A-549 Cell Line EDJ-KQ64585 Human 29114 Details Get a Quote
TAGLN3 Knockout HCT 116 Cell Line EDJ-KQ73039 Human 29114 Details Get a Quote
Contact Us
*
*
*
How did you hear about us: