TMSB15B

gene
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Also known as MGC39900

Summary

TMSB15B (thymosin beta 15B, HGNC:28612) is a protein-coding gene on chromosome Xq22.2, encoding Thymosin beta-15B (P0CG35). 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 286527 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 12 total — 1 pathogenic
  • MANE Select transcript: NM_194324

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28612
Approved symbolTMSB15B
Namethymosin beta 15B
LocationXq22.2
Locus typegene with protein product
StatusApproved
AliasesMGC39900
Ensembl geneENSG00000158427
Ensembl biotypeprotein_coding
OMIM301011
Entrez286527

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 11 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000419165, ENST00000436583, ENST00000455723, ENST00000540220, ENST00000563257, ENST00000569577, ENST00000877058, ENST00000940745, ENST00000940746, ENST00000940747, ENST00000940748, ENST00000944681

RefSeq mRNA: 3 — MANE Select: NM_194324 NM_001350211, NM_001350212, NM_194324

CCDS: CCDS59172

Canonical transcript exons

ENST00000540220 — 3 exons

ExonStartEnd
ENSE00002284321103962627103962723
ENSE00002323640103965539103965976
ENSE00003892701103964506103964622

Expression profiles

Bgee: expression breadth ubiquitous, 134 present calls, max score 95.10.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 2.1526 / max 100.8505, expressed in 972 samples.

FANTOM5 promoters (6 alternative TSS)

Promoter IDTPM avgSamples expressed
1971220.4598246
1971240.3844178
1971230.3565182
1971210.3238158
1971250.3187159
1971200.3094171

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
ganglionic eminenceUBERON:000402395.10gold quality
ventricular zoneUBERON:000305392.92gold quality
cortical plateUBERON:000534390.93gold quality
left ovaryUBERON:000211985.76gold quality
tibial arteryUBERON:000761085.58gold quality
popliteal arteryUBERON:000225085.56gold quality
ovaryUBERON:000099284.84gold quality
right ovaryUBERON:000211884.70gold quality
ascending aortaUBERON:000149684.60gold quality
thoracic aortaUBERON:000151584.58gold quality
descending thoracic aortaUBERON:000234583.42gold quality
right coronary arteryUBERON:000162583.33gold quality
left coronary arteryUBERON:000162682.91gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.60gold quality
body of uterusUBERON:000985382.18gold quality
endometriumUBERON:000129581.42gold quality
endocervixUBERON:000045881.28gold quality
ectocervixUBERON:001224980.90gold quality
smooth muscle tissueUBERON:000113580.01gold quality
mucosa of stomachUBERON:000119979.91gold quality
left uterine tubeUBERON:000130379.82gold quality
myometriumUBERON:000129679.69gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099179.45gold quality
uterine cervixUBERON:000000278.93gold quality
cerebellar hemisphereUBERON:000224578.81gold quality
cerebellar cortexUBERON:000212978.69gold quality
stromal cell of endometriumCL:000225578.64gold quality
islet of LangerhansUBERON:000000678.58gold quality
cerebellumUBERON:000203778.54gold quality
right hemisphere of cerebellumUBERON:001489078.14gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-MTAB-9388yes9.74
E-ANND-3no2.37

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

29 targeting TMSB15B, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-548AA99.9670.643753
HSA-MIR-548AP-3P99.9670.643753
HSA-MIR-548T-3P99.9670.643753
HSA-MIR-22-3P99.9368.13917
HSA-MIR-449699.8868.892236
HSA-MIR-137-3P99.8774.742401
HSA-MIR-221-3P99.8671.561329
HSA-MIR-222-3P99.8671.351337
HSA-MIR-7154-5P99.6970.521900
HSA-MIR-891B99.5969.811083
HSA-MIR-548G-3P99.4868.672159
HSA-MIR-6809-5P99.1368.451223
HSA-MIR-125399.1267.081688
HSA-MIR-10524-5P99.0566.08963
HSA-MIR-4699-5P98.9967.501210
HSA-MIR-806098.6166.931187
HSA-MIR-299-5P98.5671.141140
HSA-MIR-4684-5P98.2967.991650
HSA-MIR-1212098.0568.441768
HSA-MIR-4769-3P97.9568.171002
HSA-MIR-6817-5P97.9567.861026
HSA-MIR-7113-5P97.8867.331735
HSA-MIR-367497.0168.861171
HSA-MIR-6828-3P96.0667.611155
HSA-MIR-6821-3P95.2166.79578
HSA-MIR-6753-5P94.7064.08470
HSA-MIR-6800-5P94.5964.80525

Literature-anchored findings (GeneRIF, showing 2)

  • TMSL8 is well conserved in many mammalian species. Two isoforms, thymosin beta15a and b, exist at different locations, 1.4Mb apart, on human chromosome X, with 98% identity across the coding sequences. (PMID:17567946)
  • Our data show that the TMSB15A and TMSB15B isoforms have distinct expression patterns in different tumor cell lines and tissues. (PMID:19296525)

Cross-species orthologs

0 orthologs

Paralogs (2): TMSB15A (ENSG00000158164), TMSB15C (ENSG00000269226)

Protein

Protein identifiers

Thymosin beta-15BP0CG35 (reviewed: P0CG35)

All UniProt accessions (2): P0CG35, H3BU88

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. May be involved in cell migration.

Subcellular location. Cytoplasm. Cytoskeleton.

Tissue specificity. Expressed in colon and colon cancer tissue.

Similarity. Belongs to the thymosin beta family.

RefSeq proteins (3): NP_001337140, NP_001337141, NP_919305* (*=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-P0CG35-F172.250.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 82 (showing top): GSE18804_SPLEEN_MACROPHAGE_VS_TUMORAL_MACROPHAGE_UP, BUYTAERT_PHOTODYNAMIC_THERAPY_STRESS_DN, GOBP_ACTIN_FILAMENT_ORGANIZATION, GOMF_ACTIN_BINDING, CUI_TCF21_TARGETS_2_UP, GOCC_FILAMENTOUS_ACTIN, GOMF_CYTOSKELETAL_PROTEIN_BINDING, GOMF_ACTIN_MONOMER_BINDING, chrXq22, JOHNSTONE_PARVB_TARGETS_3_DN, GOBERT_OLIGODENDROCYTE_DIFFERENTIATION_DN, PEDERSEN_METASTASIS_BY_ERBB2_ISOFORM_7, KRIEG_HYPOXIA_NOT_VIA_KDM3A, GOBP_SUPRAMOLECULAR_FIBER_ORGANIZATION, GOCC_SUPRAMOLECULAR_COMPLEX

GO Biological Process (3): actin filament organization (GO:0007015), regulation of cell migration (GO:0030334), positive regulation of cell migration (GO:0030335)

GO Molecular Function (3): actin monomer binding (GO:0003785), protein sequestering activity (GO:0140311), actin binding (GO:0003779)

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cell migration2
actin cytoskeleton organization1
supramolecular fiber organization1
regulation of cell motility1
regulation of cell migration1
positive regulation of cell motility1
actin binding1
protein binding1
molecular sequestering activity1
cytoskeletal protein binding1
actin filament1
protein-containing complex1
intracellular anatomical structure1
cellular anatomical structure1
intracellular membraneless organelle1

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

BioGRID (3): TMSB15B (Affinity Capture-RNA), TMSB15A (Affinity Capture-MS), TMSB15A (Cross-Linking-MS (XL-MS))

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

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

ClassificationCount (floor)
Pathogenic1
Likely pathogenic0
Uncertain significance6
Likely benign1
Benign1

Top pathogenic / likely-pathogenic (1)

Variant IDHGVSClassification
564879GRCh37/hg19 Xq22.2(chrX:102984836-103329001)x2Pathogenic

SpliceAI

974 predictions. Top by Δscore:

VariantEffectΔscore
X:103919293:G:GGdonor_gain1.0000
X:103919290:TCT:Tdonor_gain0.9900
X:103919290:TCTGT:Tdonor_loss0.9900
X:103919292:TGT:Tdonor_loss0.9900
X:103919293:G:GAdonor_loss0.9900
X:103919294:TGAG:Tdonor_loss0.9900
X:103919295:GAGT:Gdonor_loss0.9900
X:103928162:A:Tdonor_gain0.9900
X:103928184:GCC:Gdonor_gain0.9900
X:103947974:G:GGdonor_gain0.9900
X:103964618:GGAAA:Gdonor_gain0.9900
X:103964619:GAAAG:Gdonor_gain0.9900
X:103919296:AGTT:Adonor_loss0.9800
X:103919297:G:Cdonor_loss0.9800
X:103931208:G:GTdonor_gain0.9800
X:103964620:A:Tdonor_gain0.9800
X:103919288:CATCT:Cdonor_gain0.9700
X:103919291:CT:Cdonor_gain0.9700
X:103964623:G:GGdonor_gain0.9700
X:103919289:ATCT:Adonor_gain0.9600
X:103947973:A:AGdonor_gain0.9600
X:103919413:A:Tdonor_gain0.9500
X:103928161:G:GTdonor_gain0.9400
X:103962721:CAGG:Cdonor_loss0.9400
X:103962722:AGG:Adonor_loss0.9400
X:103962724:GTGA:Gdonor_loss0.9400
X:103962725:T:Adonor_loss0.9400
X:103931236:A:Tdonor_gain0.9200
X:103947970:A:AGdonor_gain0.9200
X:103964619:GAAA:Gdonor_gain0.9200

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS10046954 (X:103939406 A>C,T), RS1008559233 (X:103917759 G>A), RS10127145 (X:103942294 A>G), RS1024386530 (X:103918031 T>C), RS1027742681 (X:103917364 A>T), RS1027881848 (X:103917908 T>C), RS1050168713 (X:103917721 A>C), RS1053716173 (X:103917580 T>C), RS10681462 (X:103930725 GATAATAATAATAATAATAATA>G,GATA,GATAATA,GATAATAATA,GATAATAATAATA,GATAATAATAATAATA,GATAATAATAATAATAATA,GATAATAATAATAATAATAATAATA,GATAATAATAATAATAATAATAATAATA,GATAATAATAATAATAATAATAATAATAATA,GATAATAATAATAATAATAATAATAATAATAATA), RS11092466 (X:103944008 C>G,T), RS11092467 (X:103955544 A>C,G,T), RS111305533 (X:103962328 T>C), RS111481418 (X:103918598 C>G), RS111506375 (X:103964184 GT>G), RS111755550 (X:103928177 C>T)

Disease associations

OMIM: gene MIM:301011 | 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)

CTD chemical–gene interactions

31 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, increases expression3
Valproic Aciddecreases expression, increases expression3
Estradioldecreases expression, increases expression, affects cotreatment2
beta-lapachonedecreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
sodium arsenitedecreases expression1
butyraldehydeincreases expression1
potassium chromate(VI)decreases expression1
nickel sulfatedecreases expression1
pentanalincreases expression1
entinostatdecreases expression1
ICG 001decreases expression1
Resveratrolaffects cotreatment, increases expression1
Zoledronic Aciddecreases expression1
Air Pollutantsincreases abundance, decreases expression1
Cytarabineincreases expression1
Dichlorodiphenyl Dichloroethylenedecreases expression1
Plant Extractsaffects cotreatment, increases expression1
Progesteroneaffects cotreatment, decreases expression1
Seleniumdecreases expression1
Silicon Dioxidedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Tunicamycindecreases expression1
Vitamin Edecreases expression1
Cyclosporinedecreases expression1
Aflatoxin B1decreases methylation1
Antirheumatic Agentsincreases expression1
Thapsigargindecreases expression1
Okadaic Acidincreases expression1
beta-Naphthoflavonedecreases expression1

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.