Ripor2 Gene Summary [Mouse]

Enables identical protein binding activity. Involved in several processes, including auditory receptor cell stereocilium organization; cellular response to mechanical stimulus; and positive regulation of neutrophil migration. Located in stereocilium. Is expressed in several structures, including brain; heart; inner ear; liver; and lung. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 21 and autosomal recessive nonsyndromic deafness 104. Orthologous to human RIPOR2 (RHO family interacting cell polarization regulator 2). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Ripor2
Official Name
RHO family interacting cell polarization regulator 2 [Source:MGI Symbol;Acc:MGI:2444879]
Ensembl ID
ENSMUSG00000036006
Bio databases IDs NCBI: 193385 Ensembl: ENSMUSG00000036006
Aliases RHO family interacting cell polarization regulator 2
Synonyms Ab2-162, Al225904, C6orf32, DFNA21, DFNB104, DIFF40, DIFF48, E430013J17Rik, FAM65B, LOC101928642, MYONAP, PL48, RGD1306939, RHO family interacting cell polarization regulator 2
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 Ripor2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Ferritin-like domain
  • protein binding
  • identical protein binding
  • Ferritin-like superfamily of diiron-containing four-helix-bundle proteins
  • Filopodia upregulated, FAM65

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • gout
  • survival
  • asthma
  • autosomal dominant deafness type 21
  • idiopathic scoliosis
  • non-insulin-dependent diabetes mellitus
  • insulin-dependent diabetes mellitus
  • androgenic alopecia
  • dementia
  • autosomal recessive deafness type 104
regulated by
regulates
role in cell
  • proliferation
  • migration
  • cell viability
  • assembly
  • adhesion
  • differentiation
  • response by
  • cell cycle progression
  • migration by
  • polarization

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
  • cytoskeleton
  • cytosol
  • stereocilia
  • apical membrane
  • neurites
  • filopodia

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Ripor2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • positive regulation of neutrophil extravasation
  • negative regulation of Rho protein signal transduction
  • positive regulation of neutrophil chemotaxis
  • negative regulation of cell adhesion
  • positive regulation of filopodium assembly
  • positive regulation of myoblast differentiation
  • cell adhesion
  • sensory perception of sound
  • muscle organ development
  • chemotaxis
  • negative regulation of T cell migration
  • cell differentiation
  • negative regulation of Rho guanyl-nucleotide exchange factor activity
  • regulation of establishment of cell polarity

Cellular Component

Where in the cell the gene product is active
  • cytoskeleton
  • cytoplasm
  • filopodium
  • stereocilium
  • stereocilium membrane
  • apical plasma membrane

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • 14-3-3 protein binding

Gene-Specific Assays for Results You Can Trust

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