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Cntnap2 Gene Detail
Summary
  • Symbol
    Cntnap2
  • Name
    contactin associated protein-like 2
  • Synonyms
    5430425M22Rik, Caspr2, mKIAA0868
  • Feature Type
    protein coding gene
  • IDs
    MGI:1914047
    NCBI Gene: 66797
  • Gene Overview
    MyGene.info: CNTNAP2
  • Alliance
Location & Maps
more
  • Sequence Map
    Chr6:45059357-47304213 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      2244857 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 6, 21.81 cM, cytoband B2
  • Mapping Data
    3 experiments
Homology
more
  • Human Ortholog
    CNTNAP2, contactin associated protein like 2
  • Vertebrate Orthologs
    10
  • Human Ortholog
    CNTNAP2, contactin associated protein like 2
    Orthology source: HGNC, HomoloGene
  • Synonyms
    AUTS15, CASPR2, CDFE, NRXN4, PTHSL1
  • Links
    NCBI Gene ID: 26047
    neXtProt AC: NX_Q9UHC6
    UniProt: Q9UHC6

  • Chr Location
    7q35-q36.1; chr7:146116035-148420998 (+)  GRCh38.p7

Human Diseases
more
  • Diseases
    2 with Cntnap2 mouse models; 2 with human CNTNAP2 associations

Human Disease Mouse Models
      
IDs
View 1 model
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    23 phenotypes from 2 alleles in 3 genetic backgrounds
    26 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Inactivation of this gene results in molecular abnormalities within the central nervous system, but homozygous mutant mice show no overt phenotype.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
nucleic acid-templated transcription
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Interactions
    less
    Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic OTTMUSG00000022414 VEGA Gene Model | MGI Sequence Detail 2244857 C57BL/6J ±  kb
    transcript OTTMUST00000053586 VEGA | MGI Sequence Detail 9827 Not Applicable  
    polypeptide OTTMUSP00000025482 VEGA | MGI Sequence Detail 1332 Not Applicable  
    For the selected sequence
    Polymorphisms
    less
    • SNPs within 2kb
      13528 from dbSNP Build 142
    Protein
    Information
    less
    • UniProt
      6 Sequences
    • InterPro Domains
      IPR000421 Coagulation factor 5/8 C-terminal domain
      IPR013320 Concanavalin A-like lectin/glucanase domain superfamily
      IPR029831 Contactin-associated protein-like 2
      IPR000742 EGF-like domain
      IPR002181 Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain
      IPR036056 Fibrinogen-like, C-terminal
      IPR008979 Galactose-binding-like domain superfamily
      IPR001791 Laminin G domain
      IPR003585 Neurexin/syndecan/glycophorin C
    Molecular
    Reagents
    less
    • All nucleic 6
      cDNA 6

      Microarray probesets 5
    References
    more
    • Summaries
      All 72
      Developmental Gene Expression 10
      Diseases 1
      Gene Ontology 12
      Phenotypes 26
    • Earliest
      J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
    • Latest
      J:260424 Dawes JM, et al., Immune or Genetic-Mediated Disruption of CASPR2 Causes Pain Hypersensitivity Due to Enhanced Primary Afferent Excitability. Neuron. 2018 Feb 21;97(4):806-822.e10

    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
    Citing These Resources
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    last database update
    09/11/2018
    MGI 6.12
    The Jackson Laboratory