TMSB15C
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:55173 |
| Approved symbol | TMSB15C |
| Name | thymosin beta 15C |
| Location | Xq22.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000269226 |
| Ensembl biotype | protein_coding |
| Entrez | 122394733 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00003006043 | 104074241 | 104074357 |
| ENSE00003978335 | 104076140 | 104076236 |
| ENSE00003978336 | 104072887 | 104073324 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| ganglionic eminence | UBERON:0004023 | 85.89 | gold quality |
| cortical plate | UBERON:0005343 | 85.10 | gold quality |
| ventricular zone | UBERON:0003053 | 79.91 | gold quality |
| right ovary | UBERON:0002118 | 79.30 | gold quality |
| left ovary | UBERON:0002119 | 78.78 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 78.58 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 78.53 | gold quality |
| cerebellar cortex | UBERON:0002129 | 78.34 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 75.97 | gold quality |
| cerebellum | UBERON:0002037 | 75.65 | gold quality |
| stromal cell of endometrium | CL:0002255 | 74.27 | gold quality |
| right coronary artery | UBERON:0001625 | 74.01 | gold quality |
| body of uterus | UBERON:0009853 | 73.82 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 73.00 | gold quality |
| tibial artery | UBERON:0007610 | 72.98 | gold quality |
| popliteal artery | UBERON:0002250 | 72.97 | gold quality |
| ovary | UBERON:0000992 | 72.55 | gold quality |
| aorta | UBERON:0000947 | 72.48 | gold quality |
| thoracic aorta | UBERON:0001515 | 72.27 | gold quality |
| ascending aorta | UBERON:0001496 | 72.23 | gold quality |
| mucosa of stomach | UBERON:0001199 | 71.91 | gold quality |
| endocervix | UBERON:0000458 | 71.42 | gold quality |
| left coronary artery | UBERON:0001626 | 70.57 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 70.45 | gold quality |
| left uterine tube | UBERON:0001303 | 70.27 | gold quality |
| islet of Langerhans | UBERON:0000006 | 69.55 | gold quality |
| coronary artery | UBERON:0001621 | 69.20 | gold quality |
| ectocervix | UBERON:0012249 | 69.00 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 68.28 | gold quality |
| calcaneal tendon | UBERON:0003701 | 67.95 | gold quality |
Single-cell (SCXA)
Detected in 4 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-109979 | yes | 104.44 |
| E-MTAB-7606 | no | 26.60 |
| E-HCAD-5 | no | 14.20 |
| E-ANND-3 | no | 1.21 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Paralogs (2): TMSB15A (ENSG00000158164), TMSB15B (ENSG00000158427)
Protein
Protein identifiers
Thymosin beta-15C — P0DX04 (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)
| ID | Name | Type |
|---|---|---|
| IPR001152 | Beta-thymosin | Family |
| IPR038386 | Beta-thymosin_sf | Homologous_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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DX04-F1 | 72.00 | 0.00 |
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:
| Category | Terms |
|---|---|
| actin cytoskeleton organization | 1 |
| supramolecular fiber organization | 1 |
| cell migration | 1 |
| regulation of cell motility | 1 |
| actin binding | 1 |
| protein binding | 1 |
| molecular sequestering activity | 1 |
| intracellular membraneless organelle | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
| actin filament | 1 |
| protein-containing complex | 1 |
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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
291 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| X:104074302:A:C | F13L | 0.971 |
| X:104074302:A:T | F13L | 0.971 |
| X:104074304:A:G | F13L | 0.971 |
| X:104073315:T:G | Q37P | 0.912 |
| X:104073321:A:T | I35N | 0.901 |
| X:104074284:C:A | K19N | 0.899 |
| X:104074284:C:G | K19N | 0.899 |
| X:104073321:A:C | I35S | 0.892 |
| X:104073311:C:A | E38D | 0.864 |
| X:104073311:C:G | E38D | 0.864 |
| X:104073321:A:G | I35T | 0.860 |
| X:104073318:T:G | Q36P | 0.845 |
| X:104074288:A:G | L18P | 0.836 |
| X:104073312:T:A | E38V | 0.815 |
| X:104073313:C:T | E38K | 0.805 |
| X:104074303:A:G | F13S | 0.784 |
| X:104073312:T:G | E38A | 0.776 |
| X:104074263:T:A | K26N | 0.769 |
| X:104074263:T:G | K26N | 0.769 |
| X:104074303:A:C | F13C | 0.767 |
| X:104073308:T:A | K39N | 0.756 |
| X:104073308:T:G | K39N | 0.756 |
| X:104073312:T:C | E38G | 0.742 |
| X:104074288:A:T | L18Q | 0.692 |
| X:104074285:T:G | K19T | 0.672 |
| X:104074264:T:A | K26I | 0.659 |
| X:104074312:A:T | V10E | 0.659 |
| X:104074273:G:A | T23I | 0.658 |
| X:104074286:T:C | K19E | 0.635 |
| X:104074281:T:A | K20N | 0.623 |
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.