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FLASH GENE
Symbol NRXN2 contributors: mct/pgu - updated : 06-04-2016
HGNC name neurexin 2
HGNC id 8009
EXPRESSION
Type widely
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Nervousbrain   predominantly
 nervecranial nerve  highly
Reproductivefemale systemovary  lowly
 male systemtestis  lowly
Urinarykidney   lowly
Visualeye   highly
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Nervouscentral   
Nervousperipherous   
cells
SystemCellPubmedSpeciesStageRna symbol
Nervousneuron
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period fetal
Text brain lowly
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • N terminal signal peptide
  • three overall repeats, each composed of two similar domains LNS (laminin A/neurexin/sex hormone-binding globulin) separated from each other by an EGF-like sequence
  • an O-glycosylation site
  • a single TM segment
  • a short cytoplasmic tail
  • HOMOLOGY
    interspecies homolog to rattus Neurexin II alpha
    Homologene
    FAMILY
  • neurexin family
  • CATEGORY adhesion , signaling
    SUBCELLULAR LOCALIZATION     plasma membrane
    text type I membrane protein
    basic FUNCTION
  • neuronal cell surface protein involved in cell recognition and cell adhesion
  • mediating intracellular signaling
  • play an essential role in synapse function, and its alterations are linked to autistic spectrum disorder
  • polymorphic presynaptic proteins that are implicated in synaptic plasticity and memory processing
  • NRXN2 may play a part in early cortical synaptogenesis, but NRXNs could have diverse roles in development including axon guidance, and intercellular communication between proliferating cells and/or migrating neurons
  • CELLULAR PROCESS cell communication
    PHYSIOLOGICAL PROCESS
    text putative
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule other,
  • binding to alpha-dystroglycan
  • protein
  • neuroxophilin 1 (by laminin g-like domain 2)
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility to autism spectrum disorders (ASD)
    Variant & Polymorphism other
  • NRXN2 rs12273892 polymorphism T allele and AT genotype were significantly associated with increased risk of ASD
  • Candidate gene for autism
    Marker
    Therapy target
    ANIMAL & CELL MODELS