TP53TG3F
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:51817 |
| Approved symbol | TP53TG3F |
| Name | TP53 target 3 family member F |
| Location | 16p11.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000278848 |
| Ensembl biotype | protein_coding |
| Entrez | 102724127 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00003978343 | 33461213 | 33462249 |
| ENSE00003978344 | 33459612 | 33460041 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 84.47 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 82.32 | gold quality |
| testis | UBERON:0000473 | 60.91 | gold quality |
| right testis | UBERON:0004534 | 60.84 | gold quality |
| left testis | UBERON:0004533 | 60.50 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 56.48 | gold quality |
| placenta | UBERON:0001987 | 49.11 | gold quality |
| ventricular zone | UBERON:0003053 | 43.71 | silver quality |
| ganglionic eminence | UBERON:0004023 | 43.53 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 38.33 | gold quality |
| endometrium | UBERON:0001295 | 38.20 | silver quality |
| monocyte | CL:0000576 | 38.14 | gold quality |
| bone marrow cell | CL:0002092 | 37.97 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 37.92 | gold quality |
| leukocyte | CL:0000738 | 37.67 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| cerebellum | UBERON:0002037 | 36.68 | silver quality |
| cerebellar cortex | UBERON:0002129 | 36.62 | silver quality |
| cerebellar hemisphere | UBERON:0002245 | 36.56 | silver quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 36.02 | gold quality |
| bone marrow | UBERON:0002371 | 35.81 | gold quality |
| sural nerve | UBERON:0015488 | 35.11 | gold quality |
| frontal cortex | UBERON:0001870 | 34.90 | silver quality |
| smooth muscle tissue | UBERON:0001135 | 34.69 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 34.62 | gold quality |
| vermiform appendix | UBERON:0001154 | 34.56 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 34.33 | gold quality |
| islet of Langerhans | UBERON:0000006 | 33.81 | silver quality |
| duodenum | UBERON:0002114 | 32.33 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
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 protein — Q9ULZ0 (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 ID | Names | Canonical? |
|---|---|---|
| Q9ULZ0-2 | 2, TP53TG3a | yes |
| Q9ULZ0-1 | 1, TP53TG3b | |
| Q9ULZ0-3 | 3 |
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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9ULZ0-F1 | 40.37 | 0.00 |
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:
| Category | Terms |
|---|---|
| intracellular membrane-bounded organelle | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
268 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TP53TG3F | TP53I11 | O14683 | 400 |
| TP53TG3F | PGBD2 | Q6P3X8 | 398 |
| TP53TG3F | GLYATL3 | Q5SZD4 | 393 |
| TP53TG3F | ZNF672 | Q499Z4 | 370 |
| TP53TG3F | TP53TG5 | Q9Y2B4 | 352 |
| TP53TG3F | FAM174A | Q8TBP5 | 351 |
| TP53TG3F | ZNF595 | Q8IYB9 | 348 |
| TP53TG3F | ZNF280A | P59817 | 325 |
| TP53TG3F | HEATR5B | Q9P2D3 | 324 |
| TP53TG3F | VSIG10 | Q8N0Z9 | 323 |
| TP53TG3F | FAM72B | Q86X60 | 314 |
| TP53TG3F | DYDC2 | Q96IM9 | 310 |
| TP53TG3F | SLC6A8 | P48029 | 306 |
| TP53TG3F | TP53I13 | Q8NBR0 | 305 |
| TP53TG3F | SMIM3 | Q9BZL3 | 297 |
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):
| 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
764 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 16:33459953:T:C | F92L | 0.941 |
| 16:33459955:T:A | F92L | 0.941 |
| 16:33459955:T:G | F92L | 0.941 |
| 16:33459863:T:C | F62L | 0.935 |
| 16:33459865:C:A | F62L | 0.935 |
| 16:33459865:C:G | F62L | 0.935 |
| 16:33459818:T:C | F47L | 0.924 |
| 16:33459820:T:A | F47L | 0.924 |
| 16:33459820:T:G | F47L | 0.924 |
| 16:33459899:G:T | G74W | 0.910 |
| 16:33459899:G:A | G74R | 0.899 |
| 16:33459899:G:C | G74R | 0.899 |
| 16:33459900:G:T | G74V | 0.894 |
| 16:33459981:T:C | I101T | 0.887 |
| 16:33459923:T:A | C82S | 0.883 |
| 16:33459924:G:C | C82S | 0.883 |
| 16:33459900:G:A | G74E | 0.881 |
| 16:33459870:T:C | I64T | 0.876 |
| 16:33459964:T:G | C95W | 0.864 |
| 16:33459974:A:C | S99R | 0.863 |
| 16:33459976:T:A | S99R | 0.863 |
| 16:33459976:T:G | S99R | 0.863 |
| 16:33459962:T:C | C95R | 0.862 |
| 16:33459824:A:C | S49R | 0.859 |
| 16:33459826:C:A | S49R | 0.859 |
| 16:33459826:C:G | S49R | 0.859 |
| 16:33459860:T:C | C61R | 0.854 |
| 16:33460009:G:C | W110C | 0.851 |
| 16:33460009:G:T | W110C | 0.851 |
| 16:33459862:T:G | C61W | 0.846 |
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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| S-Nitrosoglutathione | increases expression | 1 |
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.