TP53TG3B
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:37202 |
| Approved symbol | TP53TG3B |
| Name | TP53 target 3B |
| Location | 16p11.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000261509 |
| Ensembl biotype | protein_coding |
| Entrez | 729355 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00003603592 | 33362442 | 33363478 |
| ENSE00003978227 | 33360841 | 33361270 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 86.13 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 80.26 | gold quality |
| testis | UBERON:0000473 | 70.09 | gold quality |
| left testis | UBERON:0004533 | 68.39 | gold quality |
| right testis | UBERON:0004534 | 66.74 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 50.58 | gold quality |
| placenta | UBERON:0001987 | 48.28 | gold quality |
| ganglionic eminence | UBERON:0004023 | 43.53 | gold quality |
| ventricular zone | UBERON:0003053 | 43.12 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 40.89 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 39.86 | gold quality |
| islet of Langerhans | UBERON:0000006 | 39.25 | gold quality |
| stromal cell of endometrium | CL:0002255 | 39.15 | gold quality |
| prefrontal cortex | UBERON:0000451 | 39.04 | gold quality |
| cerebellum | UBERON:0002037 | 38.84 | gold quality |
| cerebellar cortex | UBERON:0002129 | 38.80 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 38.73 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 38.73 | gold quality |
| endometrium | UBERON:0001295 | 38.67 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 38.66 | gold quality |
| monocyte | CL:0000576 | 38.33 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 38.33 | gold quality |
| bone marrow cell | CL:0002092 | 38.25 | gold quality |
| leukocyte | CL:0000738 | 37.83 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 37.60 | silver quality |
| vermiform appendix | UBERON:0001154 | 37.45 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| muscle tissue | UBERON:0002385 | 36.90 | gold quality |
| frontal cortex | UBERON:0001870 | 36.78 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | 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
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):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-3646 | 100.00 | 73.56 | 5283 |
| HSA-MIR-548AW | 99.99 | 72.57 | 3559 |
| HSA-MIR-4531 | 99.99 | 69.70 | 3181 |
| HSA-MIR-548C-3P | 99.99 | 74.01 | 7587 |
| HSA-MIR-548N | 99.98 | 71.94 | 4170 |
| HSA-MIR-3148 | 99.97 | 75.06 | 6478 |
| HSA-MIR-3065-5P | 99.97 | 71.56 | 3281 |
| HSA-MIR-551B-5P | 99.96 | 71.28 | 3493 |
| HSA-MIR-539-5P | 99.93 | 70.30 | 2855 |
| HSA-MIR-627-3P | 99.90 | 71.42 | 3316 |
| HSA-MIR-380-3P | 99.89 | 70.18 | 1978 |
| HSA-MIR-153-5P | 99.89 | 73.86 | 6317 |
| HSA-MIR-12119 | 99.87 | 68.35 | 1653 |
| HSA-MIR-6875-3P | 99.82 | 70.26 | 2983 |
| HSA-MIR-3180-5P | 99.82 | 69.12 | 2422 |
| HSA-MIR-8080 | 99.82 | 67.52 | 1342 |
| HSA-MIR-4524A-3P | 99.72 | 66.85 | 2406 |
| HSA-MIR-3714 | 99.71 | 70.74 | 2671 |
| HSA-MIR-4690-5P | 99.65 | 66.24 | 813 |
| HSA-MIR-6126 | 99.62 | 68.09 | 996 |
| HSA-MIR-548AV-5P | 99.60 | 70.84 | 2107 |
| HSA-MIR-548K | 99.60 | 70.84 | 2107 |
| HSA-MIR-4649-3P | 99.56 | 66.90 | 1783 |
| HSA-MIR-1252-3P | 99.55 | 67.71 | 2862 |
| HSA-MIR-17-3P | 99.55 | 66.77 | 1311 |
| HSA-MIR-7159-5P | 99.53 | 72.12 | 2472 |
| HSA-MIR-8054 | 99.48 | 70.81 | 2084 |
| HSA-MIR-5695 | 99.41 | 67.48 | 1047 |
| HSA-MIR-4251 | 99.40 | 69.19 | 3363 |
| HSA-MIR-148A-5P | 99.30 | 68.27 | 1141 |
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 protein — Q9ULZ0 (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 ID | Names | Canonical? |
|---|---|---|
| Q9ULZ0-2 | 2, TP53TG3a | yes |
| Q9ULZ0-1 | 1, TP53TG3b | |
| Q9ULZ0-3 | 3 |
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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9ULZ0-F1 | 40.37 | 0.00 |
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:
| 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 |
|---|---|---|---|
| TP53TG3B | TP53I11 | O14683 | 400 |
| TP53TG3B | PGBD2 | Q6P3X8 | 398 |
| TP53TG3B | GLYATL3 | Q5SZD4 | 393 |
| TP53TG3B | ZNF672 | Q499Z4 | 370 |
| TP53TG3B | TP53TG5 | Q9Y2B4 | 352 |
| TP53TG3B | FAM174A | Q8TBP5 | 351 |
| TP53TG3B | ZNF595 | Q8IYB9 | 348 |
| TP53TG3B | ZNF280A | P59817 | 325 |
| TP53TG3B | HEATR5B | Q9P2D3 | 324 |
| TP53TG3B | VSIG10 | Q8N0Z9 | 323 |
| TP53TG3B | FAM72B | Q86X60 | 314 |
| TP53TG3B | DYDC2 | Q96IM9 | 310 |
| TP53TG3B | SLC6A8 | P48029 | 306 |
| TP53TG3B | TP53I13 | Q8NBR0 | 305 |
| TP53TG3B | 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
353 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 16:33362102:G:GT | donor_gain | 0.9900 |
| 16:33362109:C:G | donor_gain | 0.9900 |
| 16:33362103:A:T | donor_gain | 0.9700 |
| 16:33362193:GGTC:G | donor_gain | 0.9700 |
| 16:33361266:TCAAG:T | donor_loss | 0.9400 |
| 16:33361267:CAAG:C | donor_loss | 0.9400 |
| 16:33361268:AAG:A | donor_loss | 0.9400 |
| 16:33361269:AG:A | donor_loss | 0.9400 |
| 16:33361270:GGTAA:G | donor_loss | 0.9400 |
| 16:33361271:G:A | donor_loss | 0.9400 |
| 16:33361272:T:G | donor_loss | 0.9400 |
| 16:33361560:G:GT | donor_gain | 0.9400 |
| 16:33362097:C:CG | donor_gain | 0.9300 |
| 16:33361018:TTG:T | donor_gain | 0.8800 |
| 16:33361263:TTGTC:T | donor_gain | 0.8800 |
| 16:33362072:G:GT | donor_gain | 0.8800 |
| 16:33361542:G:GA | donor_gain | 0.8700 |
| 16:33361265:GTCAA:G | donor_loss | 0.8600 |
| 16:33361273:A:C | donor_loss | 0.8600 |
| 16:33362276:T:TA | donor_gain | 0.8500 |
| 16:33362277:A:AA | donor_gain | 0.8500 |
| 16:33361125:C:G | donor_gain | 0.8300 |
| 16:33362440:A:G | acceptor_gain | 0.8200 |
| 16:33362116:G:T | donor_gain | 0.8100 |
| 16:33361655:T:TA | donor_gain | 0.7900 |
| 16:33361656:A:AA | donor_gain | 0.7900 |
| 16:33362440:A:AC | acceptor_loss | 0.7900 |
| 16:33362441:GTTTT:G | acceptor_loss | 0.7900 |
| 16:33362441:GT:G | acceptor_gain | 0.7800 |
| 16:33362436:A:AG | acceptor_loss | 0.7700 |
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):
| Study | Trait | p-value |
|---|---|---|
| GCST001762_296 | Obesity-related traits | 4.000000e-06 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0003939 | energy 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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| 2-palmitoylglycerol | increases expression | 1 |
| Valproic Acid | decreases methylation | 1 |
| Aflatoxin B1 | decreases methylation | 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.