TP53TG3B

gene
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Summary

TP53TG3B (TP53 target 3B, HGNC:37202) is a protein-coding gene on chromosome 16p11.2, encoding TP53-target gene 3 protein (Q9ULZ0). May play a significant role in p53/TP53-mediating signaling pathway.

Located in cytoplasm and nucleus.

Source: NCBI Gene 729355 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • MANE Select transcript: NM_001099687

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:37202
Approved symbolTP53TG3B
NameTP53 target 3B
Location16p11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000261509
Ensembl biotypeprotein_coding
Entrez729355

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 2 protein_coding, 2 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000341305, ENST00000563564, ENST00000563809, ENST00000567724, ENST00000569741

RefSeq mRNA: 1 — MANE Select: NM_001099687 NM_001099687

CCDS: CCDS45477

Canonical transcript exons

ENST00000341305 — 2 exons

ExonStartEnd
ENSE000036035923336244233363478
ENSE000039782273336084133361270

Expression profiles

Bgee: expression breadth broad, 58 present calls, max score 86.13.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047386.13gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.26gold quality
testisUBERON:000047370.09gold quality
left testisUBERON:000453368.39gold quality
right testisUBERON:000453466.74gold quality
lower esophagus mucosaUBERON:003583450.58gold quality
placentaUBERON:000198748.28gold quality
ganglionic eminenceUBERON:000402343.53gold quality
ventricular zoneUBERON:000305343.12gold quality
Brodmann (1909) area 9UBERON:001354040.89gold quality
skeletal muscle tissueUBERON:000113439.86gold quality
islet of LangerhansUBERON:000000639.25gold quality
stromal cell of endometriumCL:000225539.15gold quality
prefrontal cortexUBERON:000045139.04gold quality
cerebellumUBERON:000203738.84gold quality
cerebellar cortexUBERON:000212938.80gold quality
cerebellar hemisphereUBERON:000224538.73gold quality
right hemisphere of cerebellumUBERON:001489038.73gold quality
endometriumUBERON:000129538.67gold quality
C1 segment of cervical spinal cordUBERON:000646938.66gold quality
monocyteCL:000057638.33gold quality
hindlimb stylopod muscleUBERON:000425238.33gold quality
bone marrow cellCL:000209238.25gold quality
leukocyteCL:000073837.83gold quality
superior frontal gyrusUBERON:000266137.60silver quality
vermiform appendixUBERON:000115437.45gold quality
colonic epitheliumUBERON:000039737.20gold quality
muscle tissueUBERON:000238536.90gold quality
frontal cortexUBERON:000187036.78gold quality
cortical plateUBERON:000534336.47gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

68 targeting TP53TG3B, 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-3646100.0073.565283
HSA-MIR-548AW99.9972.573559
HSA-MIR-453199.9969.703181
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-548N99.9871.944170
HSA-MIR-314899.9775.066478
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-551B-5P99.9671.283493
HSA-MIR-539-5P99.9370.302855
HSA-MIR-627-3P99.9071.423316
HSA-MIR-380-3P99.8970.181978
HSA-MIR-153-5P99.8973.866317
HSA-MIR-1211999.8768.351653
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-3180-5P99.8269.122422
HSA-MIR-808099.8267.521342
HSA-MIR-4524A-3P99.7266.852406
HSA-MIR-371499.7170.742671
HSA-MIR-4690-5P99.6566.24813
HSA-MIR-612699.6268.09996
HSA-MIR-548AV-5P99.6070.842107
HSA-MIR-548K99.6070.842107
HSA-MIR-4649-3P99.5666.901783
HSA-MIR-1252-3P99.5567.712862
HSA-MIR-17-3P99.5566.771311
HSA-MIR-7159-5P99.5372.122472
HSA-MIR-805499.4870.812084
HSA-MIR-569599.4167.481047
HSA-MIR-425199.4069.193363
HSA-MIR-148A-5P99.3068.271141

Cross-species orthologs

0 orthologs

Paralogs (7): TP53TG3 (ENSG00000183632), TP53TG3D (ENSG00000205456), TP53TG3C (ENSG00000205457), (ENSG00000274175), TP53TG3E (ENSG00000275034), (ENSG00000275869), TP53TG3F (ENSG00000278848)

Protein

Protein identifiers

TP53-target gene 3 proteinQ9ULZ0 (reviewed: Q9ULZ0)

Alternative names: TP53-inducible gene 3 protein

All UniProt accessions (2): A0A1Y8EMM2, Q9ULZ0

UniProt curated annotations — full annotation on UniProt →

Function. May play a significant role in p53/TP53-mediating signaling pathway.

Subcellular location. Cytoplasm. Nucleus.

Tissue specificity. Strongly expressed in testis. Weakly expressed in heart, placenta and skeletal muscle.

Induction. By p53/TP53.

Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.

Isoforms (3)

UniProt IDNamesCanonical?
Q9ULZ0-22, TP53TG3ayes
Q9ULZ0-11, TP53TG3b
Q9ULZ0-33

RefSeq proteins (1): NP_001093157* (*=MANE)

Domains & families (InterPro)

UniProt features (6 total): splice variant 3, chain 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9ULZ0-F140.370.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 20 (showing top): chr16p11, MIR3646, MIR548AW, MIR551B_5P, MIR3065_5P, MIR539_5P, MIR4291, MIR1252_3P, MIR4801, MIR4731_3P, MIR509_5P, MIR509_3_5P, MIR4766_3P, MIR17_3P, MIR432_5P

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (2): nucleus (GO:0005634), cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
intracellular membrane-bounded organelle1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

268 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TP53TG3BTP53I11O14683400
TP53TG3BPGBD2Q6P3X8398
TP53TG3BGLYATL3Q5SZD4393
TP53TG3BZNF672Q499Z4370
TP53TG3BTP53TG5Q9Y2B4352
TP53TG3BFAM174AQ8TBP5351
TP53TG3BZNF595Q8IYB9348
TP53TG3BZNF280AP59817325
TP53TG3BHEATR5BQ9P2D3324
TP53TG3BVSIG10Q8N0Z9323
TP53TG3BFAM72BQ86X60314
TP53TG3BDYDC2Q96IM9310
TP53TG3BSLC6A8P48029306
TP53TG3BTP53I13Q8NBR0305
TP53TG3BSMIM3Q9BZL3297

IntAct

1 interactions, top by confidence:

BioGRID (5): TP53TG3C (Negative Genetic), TP53TG3C (Negative Genetic), TP53TG3B (Negative Genetic), TP53TG3 (Positive Genetic), TP53TG3 (Affinity Capture-RNA)

ESM2 similar proteins: A0A1B0GUT2, A0A3Q1LFG5, A1L4Q6, A2RUQ5, A8MQB3, A8MU10, B1ANY3, C0HM98, H3BQW9, J3KSC0, P0C092, P0DMU3, P0DPA3, P24026, P59020, P59021, P59052, P87743, Q06250, Q0IIN9, Q0VFX4, Q14695, Q4R3X9, Q4VX62, Q52M75, Q5SR53, Q6ZUF6, Q6ZWC4, Q71F78, Q7Z4H9, Q8JMY5, Q8JMZ5, Q8JN06, Q8N2C9, Q8N2X6, Q8N3U1, Q8N9X3, Q8NAA6, Q8NBC4, Q8NDY4

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

353 predictions. Top by Δscore:

VariantEffectΔscore
16:33362102:G:GTdonor_gain0.9900
16:33362109:C:Gdonor_gain0.9900
16:33362103:A:Tdonor_gain0.9700
16:33362193:GGTC:Gdonor_gain0.9700
16:33361266:TCAAG:Tdonor_loss0.9400
16:33361267:CAAG:Cdonor_loss0.9400
16:33361268:AAG:Adonor_loss0.9400
16:33361269:AG:Adonor_loss0.9400
16:33361270:GGTAA:Gdonor_loss0.9400
16:33361271:G:Adonor_loss0.9400
16:33361272:T:Gdonor_loss0.9400
16:33361560:G:GTdonor_gain0.9400
16:33362097:C:CGdonor_gain0.9300
16:33361018:TTG:Tdonor_gain0.8800
16:33361263:TTGTC:Tdonor_gain0.8800
16:33362072:G:GTdonor_gain0.8800
16:33361542:G:GAdonor_gain0.8700
16:33361265:GTCAA:Gdonor_loss0.8600
16:33361273:A:Cdonor_loss0.8600
16:33362276:T:TAdonor_gain0.8500
16:33362277:A:AAdonor_gain0.8500
16:33361125:C:Gdonor_gain0.8300
16:33362440:A:Gacceptor_gain0.8200
16:33362116:G:Tdonor_gain0.8100
16:33361655:T:TAdonor_gain0.7900
16:33361656:A:AAdonor_gain0.7900
16:33362440:A:ACacceptor_loss0.7900
16:33362441:GTTTT:Gacceptor_loss0.7900
16:33362441:GT:Gacceptor_gain0.7800
16:33362436:A:AGacceptor_loss0.7700

AlphaMissense

764 scored. Top likely-pathogenic:

dbSNP variants (sampled 20 via entrez): RS1555487202 (16:33360912 C>T), RS1555487203 (16:33361256 G>C), RS1555487204 (16:33361301 A>G), RS1555487205 (16:33361465 C>T), RS1555487207 (16:33361492 G>A), RS1555487208 (16:33361518 T>G), RS1555487209 (16:33361570 G>C), RS1555487211 (16:33361650 A>G), RS1555487212 (16:33361692 G>T), RS1555487213 (16:33361713 G>T), RS1555487214 (16:33361970 C>T), RS1555487218 (16:33361986 G>A), RS1555487219 (16:33362137 G>A), RS1555487220 (16:33362349 A>G), RS1555487221 (16:33362410 T>C)

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

1 associations (top):

StudyTraitp-value
GCST001762_296Obesity-related traits4.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0003939energy intake

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
2-palmitoylglycerolincreases expression1
Valproic Aciddecreases methylation1
Aflatoxin B1decreases methylation1

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.