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Gene : CNTN2 Homo sapiens

Name  ? contactin 2 Cytological Location  1q32.1
Brief Description  contactin 2
Description  This gene encodes a member of the contactin family of proteins, part of the immunoglobulin superfamily of cell adhesion molecules. The encoded glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein plays a role in the proliferation, migration, and axon guidance of neurons of the developing cerebellum. A mutation in this gene may be associated with adult myoclonic epilepsy. [provided by RefSeq, Sep 2016]
  • synonyms:
  • NM_005076,
  • X67734,
  • contactin 2 (axonal),
  • OTTHUMG00000037105,
  • AXT,
  • CNTN2,
  • TAX,
  • TAG-1,
  • FAME5,
  • TAX1,
  • HGNC:2172,
  • TAG-1,
  • TAX1,
  • TAX,
  • uc001hbr.4,
  • AXT
  • identifiers:
  • 6900,
  • ENSG00000184144,
  • CNTN2

Genome feature

Region: gene ? Length: 35353  
Location: 1:205042937-205078289 Cyto location: 1q32.1

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Gene -> HPO annotation (Human Phenotype Ontology)

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SN Ps

5 Cross References

19 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results