TMSB15C

gene
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Summary

TMSB15C (thymosin beta 15C, HGNC:55173) is a protein-coding gene on chromosome Xq22.2, encoding Thymosin beta-15C (P0DX04). Plays an important role in the organization of the cytoskeleton.

Predicted to enable actin monomer binding activity. Involved in positive regulation of cell migration. Predicted to be located in cytoskeleton. Predicted to be active in cytoplasm.

Source: NCBI Gene 122394733 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001395930

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:55173
Approved symbolTMSB15C
Namethymosin beta 15C
LocationXq22.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000269226
Ensembl biotypeprotein_coding
Entrez122394733

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 6 protein_coding

ENST00000598087, ENST00000620307, ENST00000881651, ENST00000913430, ENST00000913431, ENST00000913432

RefSeq mRNA: 1 — MANE Select: NM_001395930 NM_001395930

CCDS: CCDS94644

Canonical transcript exons

ENST00000598087 — 3 exons

ExonStartEnd
ENSE00003006043104074241104074357
ENSE00003978335104076140104076236
ENSE00003978336104072887104073324

Expression profiles

Bgee: expression breadth ubiquitous, 154 present calls, max score 85.89.

Top tissues by expression

244 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
ganglionic eminenceUBERON:000402385.89gold quality
cortical plateUBERON:000534385.10gold quality
ventricular zoneUBERON:000305379.91gold quality
right ovaryUBERON:000211879.30gold quality
left ovaryUBERON:000211978.78gold quality
right hemisphere of cerebellumUBERON:001489078.58gold quality
cerebellar hemisphereUBERON:000224578.53gold quality
cerebellar cortexUBERON:000212978.34gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047375.97gold quality
cerebellumUBERON:000203775.65gold quality
stromal cell of endometriumCL:000225574.27gold quality
right coronary arteryUBERON:000162574.01gold quality
body of uterusUBERON:000985373.82gold quality
descending thoracic aortaUBERON:000234573.00gold quality
tibial arteryUBERON:000761072.98gold quality
popliteal arteryUBERON:000225072.97gold quality
ovaryUBERON:000099272.55gold quality
aortaUBERON:000094772.48gold quality
thoracic aortaUBERON:000151572.27gold quality
ascending aortaUBERON:000149672.23gold quality
mucosa of stomachUBERON:000119971.91gold quality
endocervixUBERON:000045871.42gold quality
left coronary arteryUBERON:000162670.57gold quality
smooth muscle tissueUBERON:000113570.45gold quality
left uterine tubeUBERON:000130370.27gold quality
islet of LangerhansUBERON:000000669.55gold quality
coronary arteryUBERON:000162169.20gold quality
ectocervixUBERON:001224969.00gold quality
esophagogastric junction muscularis propriaUBERON:003584168.28gold quality
calcaneal tendonUBERON:000370167.95gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-GEOD-109979yes104.44
E-MTAB-7606no26.60
E-HCAD-5no14.20
E-ANND-3no1.21

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Paralogs (2): TMSB15A (ENSG00000158164), TMSB15B (ENSG00000158427)

Protein

Protein identifiers

Thymosin beta-15CP0DX04 (reviewed: P0DX04)

All UniProt accessions (2): A0A087X1C1, P0DX04

UniProt curated annotations — full annotation on UniProt →

Function. Plays an important role in the organization of the cytoskeleton. Binds to and sequesters actin monomers (G-actin) and therefore inhibits actin polymerization.

Subcellular location. Cytoplasm. Cytoskeleton.

Similarity. Belongs to the thymosin beta family.

RefSeq proteins (2): NP_001337142, NP_001382859* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001152Beta-thymosinFamily
IPR038386Beta-thymosin_sfHomologous_superfamily

Pfam: PF01290

UniProt features (5 total): compositionally biased region 2, initiator methionine 1, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0DX04-F172.000.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 21 (showing top): GOBP_ACTIN_FILAMENT_ORGANIZATION, GOMF_ACTIN_BINDING, GOCC_FILAMENTOUS_ACTIN, GOMF_CYTOSKELETAL_PROTEIN_BINDING, GOMF_ACTIN_MONOMER_BINDING, chrXq22, GOBP_SUPRAMOLECULAR_FIBER_ORGANIZATION, GOCC_SUPRAMOLECULAR_COMPLEX, GOCC_POLYMERIC_CYTOSKELETAL_FIBER, GOCC_SUPRAMOLECULAR_POLYMER, GOBP_LOCOMOTION, GOBP_POSITIVE_REGULATION_OF_LOCOMOTION, GOMF_PROTEIN_SEQUESTERING_ACTIVITY, GOMF_MOLECULAR_SEQUESTERING_ACTIVITY, GOBP_REGULATION_OF_LOCOMOTION

GO Biological Process (2): actin filament organization (GO:0007015), regulation of cell migration (GO:0030334)

GO Molecular Function (2): actin monomer binding (GO:0003785), protein sequestering activity (GO:0140311)

GO Cellular Component (3): cytoskeleton (GO:0005856), cytoplasm (GO:0005737), filamentous actin (GO:0031941)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
actin cytoskeleton organization1
supramolecular fiber organization1
cell migration1
regulation of cell motility1
actin binding1
protein binding1
molecular sequestering activity1
intracellular membraneless organelle1
intracellular anatomical structure1
cellular anatomical structure1
actin filament1
protein-containing complex1

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A097SRV6, A0A0J1BDH3, O41801, P04605, P0C1K3, P0C766, P0CG34, P0CG35, P0DX04, P12692, P15633, P15835, P18758, P20065, P21113, P21117, P21752, P21753, P26351, P26352, P33248, P33735, P33736, P33737, P34338, P34493, P53768, P60743, P75605, Q12026, Q4UKT5, Q54CC7, Q55GR5, Q5MJ07, Q5MJ08, Q5VSR9, Q66H17, Q6I7R5, Q6SJ84, Q6SJ91

Diamond homologs: O14604, P0CG34, P0CG35, P0DX04, P18758, P20065, P21752, P21753, P26351, P26352, P33248, P34032, P62326, P62327, P62328, P62329, P63312, P63313, P63314, Q5R7H8, Q6S9C5, Q6ZWY8, Q7YRC3, Q8T697, Q95274, Q9DET5, Q9DFJ9, Q9I954, Q9I955, Q9I980, Q9W7M8

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

291 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:104074302:A:CF13L0.971
X:104074302:A:TF13L0.971
X:104074304:A:GF13L0.971
X:104073315:T:GQ37P0.912
X:104073321:A:TI35N0.901
X:104074284:C:AK19N0.899
X:104074284:C:GK19N0.899
X:104073321:A:CI35S0.892
X:104073311:C:AE38D0.864
X:104073311:C:GE38D0.864
X:104073321:A:GI35T0.860
X:104073318:T:GQ36P0.845
X:104074288:A:GL18P0.836
X:104073312:T:AE38V0.815
X:104073313:C:TE38K0.805
X:104074303:A:GF13S0.784
X:104073312:T:GE38A0.776
X:104074263:T:AK26N0.769
X:104074263:T:GK26N0.769
X:104074303:A:CF13C0.767
X:104073308:T:AK39N0.756
X:104073308:T:GK39N0.756
X:104073312:T:CE38G0.742
X:104074288:A:TL18Q0.692
X:104074285:T:GK19T0.672
X:104074264:T:AK26I0.659
X:104074312:A:TV10E0.659
X:104074273:G:AT23I0.658
X:104074286:T:CK19E0.635
X:104074281:T:AK20N0.623

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.