TRIM43B

gene
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Summary

TRIM43B (tripartite motif containing 43B, HGNC:37146) is a protein-coding gene on chromosome 2q11.1, encoding Tripartite motif-containing protein 43B (A6NCK2).

Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response and regulation of gene expression. Predicted to be active in cytoplasm.

Source: NCBI Gene 653192 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 7 total
  • MANE Select transcript: NM_001164464

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:37146
Approved symbolTRIM43B
Nametripartite motif containing 43B
Location2q11.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000144010
Ensembl biotypeprotein_coding
Entrez653192

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000639673

RefSeq mRNA: 1 — MANE Select: NM_001164464 NM_001164464

CCDS: CCDS92808

Canonical transcript exons

ENST00000639673 — 7 exons

ExonStartEnd
ENSE000024371379547700895477645
ENSE000034845159548030595480535
ENSE000035053239548159595481690
ENSE000035525409547876095478857
ENSE000036647169547938695479408
ENSE000038044789548460695484754
ENSE000038082839548230495482718

Expression profiles

Bgee: expression breadth tissue_specific, 8 present calls, max score 85.60.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.60gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.00gold quality
ganglionic eminenceUBERON:000402339.57silver quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
hindlimb stylopod muscleUBERON:000425236.39gold quality
bone marrow cellCL:000209236.16gold quality
apex of heartUBERON:000209836.11gold quality
skeletal muscle tissueUBERON:000113435.40gold quality
sural nerveUBERON:001548835.22gold quality
muscle tissueUBERON:000238533.79gold quality
bone marrowUBERON:000237131.74gold quality
olfactory segment of nasal mucosaUBERON:000538629.91gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.37gold quality
liverUBERON:000210728.69gold quality
cerebellumUBERON:000203728.64gold quality
monocyteCL:000057628.61gold quality
cerebellar hemisphereUBERON:000224528.60gold quality
cerebellar cortexUBERON:000212928.59gold quality
leukocyteCL:000073828.51gold quality
duodenumUBERON:000211428.14gold quality
smooth muscle tissueUBERON:000113528.09gold quality
islet of LangerhansUBERON:000000628.01gold quality
right hemisphere of cerebellumUBERON:001489027.95gold quality
calcaneal tendonUBERON:000370127.92gold quality
lymph nodeUBERON:000002927.57gold quality
placentaUBERON:000198727.45gold quality
tonsilUBERON:000237227.05gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.30

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

19 targeting TRIM43B, 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-366299.9973.825684
HSA-LET-7C-3P99.9573.422862
HSA-MIR-95-5P99.8972.173973
HSA-MIR-684499.8270.692423
HSA-MIR-807699.7868.521170
HSA-MIR-548AV-5P99.6070.842107
HSA-MIR-548K99.6070.842107
HSA-MIR-3616-5P99.5567.02989
HSA-MIR-57399.5567.44955
HSA-MIR-805499.4870.812084
HSA-MIR-429399.2265.461263
HSA-MIR-6780B-3P99.1367.18622
HSA-MIR-3117-5P99.0467.93618
HSA-MIR-4703-5P98.5370.131645
HSA-MIR-3942-5P98.5269.511517
HSA-MIR-4709-5P98.5167.251335
HSA-MIR-4766-3P98.4867.941347
HSA-MIR-10398-5P97.1264.941051
HSA-MIR-6514-5P95.0766.02655

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
mus_musculusTrim43cENSMUSG00000067399
mus_musculusTrim43bENSMUSG00000079162
mus_musculusTrim43aENSMUSG00000090693
rattus_norvegicusTrim43aENSRNOG00000010699

Paralogs (80): MID2 (ENSG00000080561), TRIM9 (ENSG00000100505), MID1 (ENSG00000101871), MEFV (ENSG00000103313), TRIM35 (ENSG00000104228), TRIM14 (ENSG00000106785), TRIM37 (ENSG00000108395), TRIM2 (ENSG00000109654), TRIM3 (ENSG00000110171), TRIM38 (ENSG00000112343), TRIM62 (ENSG00000116525), TRIM67 (ENSG00000119283), TRIM32 (ENSG00000119401), BSPRY (ENSG00000119411), TRIM25 (ENSG00000121060), TRIM6 (ENSG00000121236), TRIM24 (ENSG00000122779), TRIM51 (ENSG00000124900), TRIM28 (ENSG00000130726), TRIM21 (ENSG00000132109), TRIM5 (ENSG00000132256), TRIM22 (ENSG00000132274), TRIM47 (ENSG00000132481), TRIM45 (ENSG00000134253), TRIM29 (ENSG00000137699), TRIM54 (ENSG00000138100), PML (ENSG00000140464), TRIM65 (ENSG00000141569), TRIM43 (ENSG00000144015), TRIM7 (ENSG00000146054), TRIM41 (ENSG00000146063), TRIM50 (ENSG00000146755), TRIM4 (ENSG00000146833), TRIM55 (ENSG00000147573), TRIM48 (ENSG00000150244), TRIM36 (ENSG00000152503), TRIM11 (ENSG00000154370), TRIM74 (ENSG00000155428), TRIM42 (ENSG00000155890), TRIM63 (ENSG00000158022)

Protein

Protein identifiers

Tripartite motif-containing protein 43BA6NCK2 (reviewed: A6NCK2)

All UniProt accessions (1): A6NCK2

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the TRIM/RBCC family.

RefSeq proteins (1): NP_001157936* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000315Znf_B-boxDomain
IPR001841Znf_RINGDomain
IPR001870B30.2/SPRYDomain
IPR003877SPRY_domDomain
IPR003879Butyrophylin_SPRYDomain
IPR013083Znf_RING/FYVE/PHDHomologous_superfamily
IPR013320ConA-like_dom_sfHomologous_superfamily
IPR017907Znf_RING_CSConserved_site
IPR043136B30.2/SPRY_sfHomologous_superfamily
IPR050143TRIM/RBCCFamily

Pfam: PF00622, PF00643, PF15227

UniProt features (10 total): binding site 4, zinc finger region 2, coiled-coil region 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NCK2-F188.470.64

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Ligand- & substrate-binding residues (4): 93; 96; 115; 121

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 15 (showing top): GOBP_DEFENSE_RESPONSE_TO_OTHER_ORGANISM, GOMF_ACYLTRANSFERASE_ACTIVITY, GOMF_AMINOACYLTRANSFERASE_ACTIVITY, GOMF_UBIQUITIN_LIKE_PROTEIN_LIGASE_ACTIVITY, chr2q11, ESC_V6.5_UP_EARLY.V1_UP, ESC_V6.5_UP_LATE.V1_UP, LET_7C_3P, MIR548AV_5P_MIR548K, MIR8054, MIR4703_5P, MIR3942_5P, MIR4766_3P, MIR6780B_3P, GOBP_BIOLOGICAL_PROCESS_INVOLVED_IN_INTERSPECIES_INTERACTION_BETWEEN_ORGANISMS

GO Biological Process (2): regulation of gene expression (GO:0010468), innate immune response (GO:0045087)

GO Molecular Function (4): zinc ion binding (GO:0008270), ubiquitin protein ligase activity (GO:0061630), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (1): cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
gene expression1
regulation of macromolecule biosynthetic process1
immune response1
defense response to symbiont1
transition metal ion binding1
ubiquitin-protein transferase activity1
ubiquitin-like protein ligase activity1
binding1
cation binding1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

150 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TRIM43BPRAMEF25A6NGN4507
TRIM43BA0A096LNW4A0A096LNW4480
TRIM43BPRAMEF15P0DUQ1478
TRIM43BMBD3L3A6NE82447
TRIM43BKCTD1Q719H9431
TRIM43BMBD3L5A6NJ08418
TRIM43BKHDC1LQ5JSQ8394
TRIM43BPTPRRQ15256348
TRIM43BZSCAN4Q8NAM6323
TRIM43BLEUTXA8MZ59323
TRIM43BAK8Q96MA6322
TRIM43BZNF407Q9C0G0314
TRIM43BKHDC1Q4VXA5307
TRIM43BMBD3L2Q8NHZ7285
TRIM43BDUX4L2P0CJ85272

IntAct

0 interactions, top by confidence:

BioGRID (3): TRIM43B (Affinity Capture-MS), SSR3 (Cross-Linking-MS (XL-MS)), PARP1 (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, C9J1S8, I1YAP6, K7N6K2, P0CI25, P0CI26, P15533, Q0PF16, Q1ACD5, Q1ACD6, Q1ACD7, Q1ACD8, Q2YEM8, Q2YEM9, Q2YEN0, Q2YEN2, Q3ZEE5, Q587N6, Q587N7, Q5BN31, Q5C8T6, Q5C8T8, Q5C8U1, Q5C8U3, Q5C8U4, Q5D7H7, Q5D7H8, Q5D7I0, Q5D7I1, Q5D7I2, Q5D7I3, Q5D7I5, Q5D7I6, Q5D7I9, Q5D7J0

Diamond homologs: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, B0BLU1, C9J1S8, I1YAP6, O00478, O00481, O15344, O75677, O75678, O75679, O76064, P0CI25, P0CI26, P18892, P19474, P62603, P86448, P86449, Q13410, Q2HJ46, Q3C1V9, Q3TL54, Q4KLN8, Q5EBN2, Q5PQN2, Q5R4I2, Q5R996, Q61510, Q62556, Q6INS5, Q6MFY8, Q6UX41, Q6UXE8, Q6ZWI9, Q7T308

SIGNOR signaling

1 interactions.

AEffectBMechanism
Ub:E2“up-regulates activity”TRIM43Bubiquitination

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance5
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

3004 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:95477257:A:CF416L0.978
2:95477257:A:TF416L0.978
2:95477259:A:GF416L0.978
2:95477460:A:GW349R0.961
2:95477460:A:TW349R0.961
2:95477490:A:GW339R0.956
2:95477490:A:TW339R0.956
2:95477258:A:GF416S0.947
2:95477488:C:AW339C0.947
2:95477488:C:GW339C0.947
2:95482613:G:CF34L0.946
2:95482613:G:TF34L0.946
2:95482615:A:GF34L0.946
2:95478764:G:CF285L0.943
2:95478764:G:TF285L0.943
2:95478766:A:GF285L0.943
2:95477287:A:CF406L0.941
2:95477287:A:TF406L0.941
2:95477289:A:GF406L0.941
2:95477185:G:CF440L0.932
2:95477185:G:TF440L0.932
2:95477187:A:GF440L0.932
2:95477450:C:TG352E0.928
2:95477457:C:GA350P0.925
2:95482406:G:CF103L0.923
2:95482406:G:TF103L0.923
2:95482408:A:GF103L0.923
2:95477451:C:GG352R0.907
2:95477451:C:TG352R0.907
2:95477458:C:AW349C0.904

dbSNP variants (sampled 300 via entrez): RS1000033358 (2:95482061 G>A), RS1000933828 (2:95486071 C>T), RS1000978434 (2:95486226 G>A,C), RS1000987048 (2:95480191 A>G), RS1002330513 (2:95484101 T>G), RS1002984883 (2:95480038 A>G), RS1003374182 (2:95484348 A>G), RS1004046934 (2:95486716 G>A,T), RS1005001503 (2:95485395 G>A,T), RS1005054303 (2:95485701 G>A), RS1006352568 (2:95483072 T>C), RS1006553526 (2:95485072 C>A,T), RS1007968057 (2:95483931 A>C,G), RS1008795735 (2:95481015 A>G), RS1010412935 (2:95482199 G>T)

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

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
methylmercuric chlorideincreases expression1
ethyl-p-hydroxybenzoateincreases expression1
Benzo(a)pyreneaffects methylation, increases methylation1
Estradioldecreases expression1
Thiramincreases expression1
Genisteindecreases 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.