Apbb1ip Gene Summary [Mouse]

Acts upstream of or within T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell and positive regulation of cell adhesion. Located in cytosol and plasma membrane. Part of T cell receptor complex. Is expressed in several structures, including brain; genitourinary system; hemolymphoid system; liver; and molar. Orthologous to human APBB1IP (amyloid beta precursor protein binding family B member 1 interacting protein). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Apbb1ip
Official Name
amyloid beta (A4) precursor protein-binding, family B, member 1 interacting protein [Source:MGI Symbol;Acc:MGI:1861354]
Ensembl ID
ENSMUSG00000026786
Bio databases IDs NCBI: 54519 Ensembl: ENSMUSG00000026786
Aliases amyloid beta (A4) precursor protein-binding, family B, member 1 interacting protein
Synonyms 9930118P07RIK, amyloid beta precursor protein binding family B member 1 interacting protein, amyloid β precursor protein binding family B member 1 interacting protein, INAG1, PREL1, Prp48, RARP1, RIAM
Species
Mouse, Mus musculus
OrthologiesHumanRat

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 mouse Apbb1ip often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Ubl1_cv_Nsp3_N-like
  • PH domain
  • protein binding
  • Pleckstrin homology-like domain
  • proline rich domain

Pathways

Biological processes and signaling networks where the Apbb1ip gene in mouse plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • colitis
  • Ullrich congenital muscular dystrophy
regulated by
regulates
role in cell
  • activation in
  • adhesion
  • number
  • development
  • replication in
  • reorganization

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
  • Plasma Membrane
  • cytosol
  • filopodia
  • lamellipodia

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Apbb1ip gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • signal transduction
  • T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell
  • positive regulation of cell adhesion

Cellular Component

Where in the cell the gene product is active
  • cytoskeleton
  • focal adhesion
  • cytosol
  • T cell receptor complex
  • plasma membrane
  • lamellipodium

Molecular Function

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

Gene-Specific Assays for Results You Can Trust

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