Gene

cntnap2b

ID
ZDB-GENE-070912-26
Name
contactin associated protein 2b
Symbol
cntnap2b Nomenclature History
Previous Names
  • cntnap2 (1)
  • si:ch211-120f16.4
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to be involved in protein localization to juxtaparanode region of axon. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in several diseases, including Pitt-Hopkins syndrome; autism spectrum disorder (multiple); communication disorder (multiple); cortical dysplasia-focal epilepsy syndrome; and social phobia. Is expressed in telencephalon. Orthologous to human CNTNAP2 (contactin associated protein 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
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 cntnap2b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
cortical dysplasia-focal epilepsy syndrome Alliance Pitt-Hopkins like syndrome 1 610042
{Autism susceptibility 15} 612100
Associated With cntnap2b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein Length
UniProtKB:L7NKK5 1315
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-cntnap2
  • WB
1
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations