1. Gene
  2. TRIM43 - tripartite motif containing 43 Gene

TRIM43 - tripartite motif containing 43 Gene

Homo sapiens

Also known as TRIM43A

Gene ID: 129868 | Gene type: protein coding

About TRIM43

This gene has 1 transcript (splice variant), 93 orthologues and 80 paralogues. Low expression observed in reference dataset.

Summary

Predicted to enable ubiquitin protein Ligase activity. Predicted to be involved in innate immune response; protein ubiquitination; and regulation of gene expression. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

TRIM43 Products(1)

mRNA Protein Name
NM_138800.3 NP_620155.1 tripartite motif-containing protein 43
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TRIM43 Protein Structure

zf-C3HC4_4

zf-C3HC4_4: zinc finger of C3HC4-type, RING (15 - 55)

SPRY

SPRY: SPRY domain (335 - 443)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 446 a.a.
Protein Preferred Names Protein Names

tripartite motif-containing protein 43

TRIM43 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TRIM43 Q96BQ3 GRB7 Homo sapiens Q14451-3
Y2H Array
32296183
Intra
TRIM43 Q96BQ3 GRB7 Homo sapiens Q14451-3
Y2H Prey Pooling
32296183
Intra
TRIM43 Q96BQ3 TGFBR2 Homo sapiens P37173
Validated Y2H
32814053
Intra
TRIM43 Q96BQ3 TGFBR2 Homo sapiens P37173
Y2H Pooling
32814053
Intra
TRIM43 Q96BQ3 TGFBR2 Homo sapiens P37173
Y2H Array
32814053
Intra
TRIM43 Q96BQ3 UBE2K Homo sapiens P61086
Validated Y2H
32814053
Intra
TRIM43 Q96BQ3 UBE2K Homo sapiens P61086
Y2H Array
32814053
Intra
TRIM43 Q96BQ3 UBE2K Homo sapiens P61086
Y2H Pooling
32814053
Intra
TRIM43 Q96BQ3 ENOX1 Homo sapiens Q8TC92
Validated Y2H
25416956
Intra
TRIM43 Q96BQ3 ENOX1 Homo sapiens Q8TC92
Y2H Prey Pooling
32296183
Intra
TRIM43 Q96BQ3 ENOX1 Homo sapiens Q8TC92
Y2H Array
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Facioscapulohumeral Muscular Dystrophy 1

Facioscapulohumeral Muscular Dystrophy

Fshd

Landouzy-Dejerine Muscular Dystrophy

Muscular Dystrophy, Facioscapulohumeral

FSHD1

Fshd1a

Muscular Dystrophy, Facioscapulohumeral, Type 1a

Facioscapulohumeral Muscular Dystrophy Type 1a

Fsh Muscular Dystrophy

Facioscapulohumeral Muscular Dystrophy 1a

Facioscapulohumeral Atrophy

Facioscapulohumeral Myopathy

Muscular Dystrophy, Facioscapulohumeral, Type 1

Facioscapulohumeral Muscular Dystrophy Type 1

Landouzy Dejerine Muscular Dystrophy

Muscular Dystrophy, Landouzy-Dejerine

Fshmd1a

Facio-Scapulo-Humeral Dystrophy

Facioscapulohumeral Type Progressive Muscular Dystrophy

Facioscapuloperoneal Muscular Dystrophy

Facioscapulohumeral Dystrophy

Fsh Dystrophy

Landouzy-Dejerine Dystrophy

Landouzy-Dejerine Myopathy

Fmd

Facioscapulohumeral Muscular Dystrophy-1a

Muscular Dystrophy Facioscapulohumeral

Dystrophy, Muscular, Facioscapulohumeral

Dystrophy, Muscular, Facioscapulohumeral, Type 1

Landouzy-Dejerine Disease

Landouzy-Déjerine Atrophy

Facioscapulohumeral Muscle Dystrophy

Fmd - [Facioscapulohumeral Muscular Dystrophy]

Fsh - [Facioscapulohumeral Muscular Dystrophy]

Fshd - [Facioscapulohumeral Muscular Dystrophy]

Landouzy-Déjerine Dystrophy Or Facioscapulohumeral Atrophy

Landouzy-Déjérine Muscular Dystrophy

Facioscapulohumeral Muscular Dystrophy 2, Digenic

Facioscapulohumeral Muscular Dystrophy 2

FSHD2

Fshd1b

Facioscapulohumeral Muscular Dystrophy 1b

Fshd2, Digenic

Muscular Dystrophy, Facioscapulohumeral, Type 2

Muscular Dystrophy, Facioscapulohumeral, Type 1b

Fascioscapulohumeral Muscular Dystrophy 2, Digenic

Facioscapulohumeral Muscular Dystrophy Type 2

Digenic Facioscapulohumeral Muscular Dystrophy

Digenic Fshd2

Facioscapulohumeral Muscular Dystrophy Type 1b

Dystrophy, Muscular, Facioscapulohumeral, Type 2

Digenic Disease
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus TRIM43 RGD RGD:1561074