Trappc2 Gene Summary [Rat]

Predicted to enable transcription corepressor binding activity; transcription regulator inhibitor activity; and transmembrane transporter binding activity. Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport; positive regulation of gene expression; and skeletal system development. Predicted to be located in endoplasmic reticulum; nucleus; and perinuclear region of cytoplasm. Predicted to be part of TRAPP complex. Predicted to be active in cytoplasm and nucleus. Human ortholog(s) of this gene implicated in X-linked spondyloepiphyseal dysplasia tarda. Orthologous to human TRAPPC2 (trafficking protein particle complex subunit 2). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Trappc2
Official Name
trafficking protein particle complex 2 [Source:RGD Symbol;Acc:1306925]
Ensembl ID
ENSRNOG00000042276
Bio databases IDs NCBI: 501550 Ensembl: ENSRNOG00000042276
Aliases trafficking protein particle complex 2
Synonyms 1110066L09Rik, 1810064C02Rik, hYP38334, MIP-2A, RGD1306925, SEDL, SEDT, trafficking protein particle complex 2, trafficking protein particle complex subunit 2, TRAPPC2P1, TRS20, ZNF547L
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Trappc2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • ion channel binding
  • transcription factor binding
  • Sedlin, N-terminal conserved region
  • protein binding
  • Longin-like domains

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • hereditary disorder
  • diabetic nephropathy
  • X-linked spondyloepiphyseal dysplasia tarda
  • spondyloepiphyseal dysplasia tarda
  • connective tissue disorder
  • autosomal dominant spastic paraplegia type 4
regulated by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • intracellular membrane-bounded organelle
  • perinuclear region
  • Nucleus
  • Endoplasmic Reticulum
  • granules
  • cytosol
  • nucleoplasm
  • outer nuclear membrane

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Trappc2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • vesicle coating
  • ER to Golgi vesicle-mediated transport
  • skeletal system development
  • COPII vesicle coating

Cellular Component

Where in the cell the gene product is active
  • TRAPP complex
  • nucleus
  • perinuclear region of cytoplasm
  • cytoplasm
  • intracellular membrane-bounded organelle
  • cytosol
  • endoplasmic reticulum
  • endoplasmic reticulum-Golgi intermediate compartment
  • nucleoplasm

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • ion channel binding

Gene-Specific Assays for Results You Can Trust

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