Gene

cplx2a

ID
ZDB-GENE-040718-160
Name
complexin 2a
Symbol
cplx2a Nomenclature History
Previous Names
  • cplx2
  • cplx2l (1)
  • fc97e10
  • wu:fc97e10 (1)
  • wu:fq40b06 (1)
  • zgc:92325
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Predicted to have SNARE binding activity. Predicted to be involved in regulation of neurotransmitter secretion and synaptic vesicle exocytosis. Predicted to localize to SNARE complex and terminal bouton. Human ortholog(s) of this gene implicated in early infantile epileptic encephalopathy 63. Is expressed in nervous system; neurons; and retina. Orthologous to human CPLX1 (complexin 1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
4 figures from Rauch et al., 2003
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With cplx2a Human Ortholog
No data available
Associated With cplx2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR008849 Synaphin
Domain Details Per Protein
Protein Length Synaphin
UniProtKB:Q6DHG4 133
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Note
Woods, et al. (2005. Genome Res. 15:1307-1914.) reported orthology to CPLX2 supported by amino acid sequence identity.
Citations