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Gene : CNTNAP4 Homo sapiens

Name  ? contactin associated protein family member 4 Cytological Location  16q23.1
Brief Description  contactin associated protein family member 4
Description  This gene encodes a member of the neurexin protein family. Members of this family function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. This protein may also play a role in proper neurotransmission in the dopaminergic and GABAergic systems and mutations in this gene may be associated with certain psychiatric illnesses. A polymorphism in an intron of this gene may be associated with longevity. [provided by RefSeq, Apr 2016]
  • synonyms:
  • CASPR4,
  • contactin associated protein-like 4,
  • HGNC:18747,
  • OTTHUMG00000137617,
  • KIAA1763,
  • CNTNAP4,
  • CASPR4,
  • AB051550,
  • NM_033401,
  • uc032efc.1
  • identifiers:
  • 85445,
  • ENSG00000152910,
  • CNTNAP4

Genome feature

Region: gene ? Length: 286235  
Location: 16:76277376-76563610 Cyto location: 16q23.1


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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 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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Expression

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

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Other

0 Pathways

3740 SNPs

5 Cross References

15 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results