TP53TG3F

gene
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Summary

TP53TG3F (TP53 target 3 family member F, HGNC:51817) 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 102724127 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001330066

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:51817
Approved symbolTP53TG3F
NameTP53 target 3 family member F
Location16p11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000278848
Ensembl biotypeprotein_coding
Entrez102724127

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000617705, ENST00000623042

RefSeq mRNA: 1 — MANE Select: NM_001330066 NM_001330066

CCDS: CCDS81976

Canonical transcript exons

ENST00000623042 — 2 exons

ExonStartEnd
ENSE000039783433346121333462249
ENSE000039783443345961233460041

Expression profiles

Bgee: expression breadth broad, 46 present calls, max score 84.47.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047384.47gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.32gold quality
testisUBERON:000047360.91gold quality
right testisUBERON:000453460.84gold quality
left testisUBERON:000453360.50gold quality
lower esophagus mucosaUBERON:003583456.48gold quality
placentaUBERON:000198749.11gold quality
ventricular zoneUBERON:000305343.71silver quality
ganglionic eminenceUBERON:000402343.53gold quality
hindlimb stylopod muscleUBERON:000425238.33gold quality
endometriumUBERON:000129538.20silver quality
monocyteCL:000057638.14gold quality
bone marrow cellCL:000209237.97gold quality
olfactory segment of nasal mucosaUBERON:000538637.92gold quality
leukocyteCL:000073837.67gold quality
colonic epitheliumUBERON:000039737.20gold quality
cerebellumUBERON:000203736.68silver quality
cerebellar cortexUBERON:000212936.62silver quality
cerebellar hemisphereUBERON:000224536.56silver quality
cortical plateUBERON:000534336.47gold quality
skeletal muscle tissueUBERON:000113436.02gold quality
bone marrowUBERON:000237135.81gold quality
sural nerveUBERON:001548835.11gold quality
frontal cortexUBERON:000187034.90silver quality
smooth muscle tissueUBERON:000113534.69silver quality
superior frontal gyrusUBERON:000266134.62gold quality
vermiform appendixUBERON:000115434.56gold quality
C1 segment of cervical spinal cordUBERON:000646934.33gold quality
islet of LangerhansUBERON:000000633.81silver quality
duodenumUBERON:000211432.33gold 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

Cross-species orthologs

0 orthologs

Paralogs (7): TP53TG3 (ENSG00000183632), TP53TG3D (ENSG00000205456), TP53TG3C (ENSG00000205457), TP53TG3B (ENSG00000261509), (ENSG00000274175), TP53TG3E (ENSG00000275034), (ENSG00000275869)

Protein

Protein identifiers

TP53-target gene 3 proteinQ9ULZ0 (reviewed: Q9ULZ0)

Alternative names: TP53-inducible gene 3 protein

All UniProt accessions (1): 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_001316995* (*=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: 1 (showing top): chr16p11

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
TP53TG3FTP53I11O14683400
TP53TG3FPGBD2Q6P3X8398
TP53TG3FGLYATL3Q5SZD4393
TP53TG3FZNF672Q499Z4370
TP53TG3FTP53TG5Q9Y2B4352
TP53TG3FFAM174AQ8TBP5351
TP53TG3FZNF595Q8IYB9348
TP53TG3FZNF280AP59817325
TP53TG3FHEATR5BQ9P2D3324
TP53TG3FVSIG10Q8N0Z9323
TP53TG3FFAM72BQ86X60314
TP53TG3FDYDC2Q96IM9310
TP53TG3FSLC6A8P48029306
TP53TG3FTP53I13Q8NBR0305
TP53TG3FSMIM3Q9BZL3297

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

0 predictions. Top by Δscore:

AlphaMissense

764 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:33459953:T:CF92L0.941
16:33459955:T:AF92L0.941
16:33459955:T:GF92L0.941
16:33459863:T:CF62L0.935
16:33459865:C:AF62L0.935
16:33459865:C:GF62L0.935
16:33459818:T:CF47L0.924
16:33459820:T:AF47L0.924
16:33459820:T:GF47L0.924
16:33459899:G:TG74W0.910
16:33459899:G:AG74R0.899
16:33459899:G:CG74R0.899
16:33459900:G:TG74V0.894
16:33459981:T:CI101T0.887
16:33459923:T:AC82S0.883
16:33459924:G:CC82S0.883
16:33459900:G:AG74E0.881
16:33459870:T:CI64T0.876
16:33459964:T:GC95W0.864
16:33459974:A:CS99R0.863
16:33459976:T:AS99R0.863
16:33459976:T:GS99R0.863
16:33459962:T:CC95R0.862
16:33459824:A:CS49R0.859
16:33459826:C:AS49R0.859
16:33459826:C:GS49R0.859
16:33459860:T:CC61R0.854
16:33460009:G:CW110C0.851
16:33460009:G:TW110C0.851
16:33459862:T:GC61W0.846

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)

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

ChemicalActions (top 5)PubMed papers
S-Nitrosoglutathioneincreases 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.