PITPNM family member 3

Summary
Gene Symbol
  • PITPNM3
Organism
Homo sapiens (human)
NCBI Gene
83394
PubChem
83394
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Calcium
  • Cone-rod dystrophy
  • Disease variant
  • Lipid-binding
  • Membrane
  • Metal-binding
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
Proteins
Displaying all 2 entries
UniProt Protein Name
Q9BZ71
  • Phosphatidylinositol transfer protein, membrane-associated 3
  • Pyk2 N-terminal domain-interacting receptor 1
A1A5C9
  • Phosphatidylinositol transfer protein, membrane-associated 3
  • Pyk2 N-terminal domain-interacting receptor 1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
phosphatidylinositol transfer
Functional Category
  • E: Amino acid transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0111010 cone-rod dystrophy 5

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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: December 8, 2025