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Gene : CNTN4 Homo sapiens

Name  ? contactin 4 Cytological Location  3p26.3-p26.2
Brief Description  contactin 4
description  This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]
  • synonyms:
  • uc003bpc.4,
  • AXCAM,
  • HGNC:2174,
  • BIG-2,
  • NM_001206955,
  • OTTHUMG00000119031,
  • BIG-2,
  • CNTN4,
  • AW665944
  • identifiers:
  • 152330,
  • ENSG00000144619,
  • CNTN4

Genome feature

Region: gene ? Length: 960278  
Location: 3:2098803-3059080 Cyto location: 3p26.3-p26.2


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Function

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Genomics

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Proteins

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SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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

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Other

384 SN Ps

5 Cross References

15 Data Sets

30 Homologues

0 Located Features

90 Rna Seq Results