Sh3pxd2b Gene Summary [Mouse]

Enables SH2 domain binding activity and phosphatidylinositol phosphate binding activity. Involved in several processes, including osteoblast fate commitment; podosome assembly; and skeletal system development. Located in cytoplasm and podosome. Is expressed in several structures, including branchial arch; central nervous system; heart; jaw; and skeleton. Used to study glaucoma and otitis media. Human ortholog(s) of this gene implicated in Frank-Ter Haar syndrome. Orthologous to human SH3PXD2B (SH3 and PX domains 2B). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Sh3pxd2b
Official Name
SH3 and PX domains 2B [Source:MGI Symbol;Acc:MGI:2442062]
Ensembl ID
ENSMUSG00000040711
Bio databases IDs NCBI: 268396 Ensembl: ENSMUSG00000040711
Aliases SH3 and PX domains 2B
Synonyms FAD49, FTHS, G431001E03Rik, HOFI, KIAA1295, LOC285590, RGD1309926, SH3 and PX domains 2B, TKS4, TSK4
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 Sh3pxd2b often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • binding protein
  • SH2-domain binding
  • The Phox Homology domain, a phosphoinositide binding module
  • protein binding
  • phosphatidylinositol binding
  • PX domain
  • Src Homology 3 domain superfamily

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
regulates
regulated by
disease
  • infertility condition
  • Frank-Ter Haar syndrome
  • multiple system atrophy
  • kyphosis
  • lung adenocarcinoma
  • lung adenocarcinoma formation
  • exophthalmos
  • lung squamous cell carcinoma
  • squamous cell lung cancer
  • lipodystrophy
role in cell
  • expression in
  • differentiation
  • migration
  • morphology
  • circularity
  • disassembly
  • assembly

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
  • podosomes

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Sh3pxd2b gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • heart development
  • eye development
  • superoxide metabolic process
  • skeletal system development
  • extracellular matrix disassembly
  • cell differentiation
  • protein localization in membrane
  • superoxide anion generation
  • podosome assembly
  • bone development
  • adipose tissue development

Cellular Component

Where in the cell the gene product is active
  • anchoring junction
  • cytoplasm
  • cell projection
  • podosome

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • phosphatidylinositol-5-phosphate binding
  • superoxide-generating NADPH oxidase activator activity
  • phosphatidylinositol-3,5-bisphosphate binding
  • phosphatidylinositol-3-phosphate binding
  • SH2 domain binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.