synaptic Ras GTPase activating protein 1

Summary
Gene Symbol
  • SYNGAP1
Organism
Homo sapiens (human)
NCBI Gene
8831
PubChem
8831
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Autism
  • Coiled coil
  • Disease variant
  • GTPase activation
  • Intellectual disability
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • SH3-binding
Proteins
Displaying all 3 entries
UniProt Protein Name
A0A1U9X8L0
B7ZCA0
Q96PV0
  • Neuronal RasGAP
  • Synaptic Ras GTPase-activating protein 1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
disabled homolog 2-interacting protein
Functional Category
  • O: Posttranslational modification, protein turnover, chaperones
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0070035 autosomal dominant intellectual developmental disorder 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: April 7, 2025