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MIRAGE
SH3 and PX domains 2B

Summary
Gene Symbol
  • SH3PXD2B
Organism
Homo sapiens (human)
NCBI Gene
285590
KEGG Gene ID
PubChem
285590
Alliance of Genome Resources
Annotation
Keyword
  • Cell junction
  • Cell projection
  • Cytoplasm
  • Differentiation
  • Disease variant
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Repeat
  • SH3 domain
Proteins
Displaying all 2 entries
UniProt Protein Name
A1X283
  • Adapter protein HOFI
  • Factor for adipocyte differentiation 49
  • Tyrosine kinase substrate with four SH3 domains
G3V144
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 28 in total
GO Term Evidence Code PMID
skeletal system development
skeletal system development
eye development
eye development
osteoblast fate commitment
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
sh3 and px domain-containing
Functional Category
  • G: Carbohydrate transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Displaying all 3 entries
Gene Ontology
phosphatidylinositol binding
superoxide anion generation
superoxide-generating NADPH oxidase activator activity
Displaying all 8 entries
InterPro
PX domain superfamily
Phox homology
SH3 domain
SH3-like domain superfamily
SH3PXD2B, SH3 domain 1
SH3PXD2B, SH3 domain 2
SH3PXD2B, SH3 domain 3
SH3PXD2B, SH3 domain 4
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0111789 Frank-Ter Haar syndrome
Ortholog
Displaying 1 entry
Species Gene ID Alliance of Genome Resources
268396 MGI:2442062
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 6, 2026