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Gene : CDH7 Homo sapiens

Name  ? cadherin 7 Cytological Location  18q22.1
Brief Description  cadherin 7
Description  This gene encodes a type II classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium dependent cell-cell adhesion molecule is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Type II (atypical) cadherins are defined based on their lack of a histidine-alanine-valine (HAV) cell adhesion recognition sequence specific to type I cadherins. Cadherins mediate cell-cell binding in a homophilic manner, contributing to the sorting of heterogeneous cell types. Mutations in this gene may be associated with bipolar disease in human patients. This gene is present in a gene cluster on chromosome 18. [provided by RefSeq, May 2016]
  • synonyms:
  • CDH7,
  • HGNC:1766,
  • NM_033646,
  • uc002lkb.4,
  • cadherin 7, type 2,
  • CDH7L1,
  • AB035301,
  • OTTHUMG00000132800
  • identifiers:
  • 1005,
  • ENSG00000081138,
  • CDH7

Genome feature

Region: gene ? Length: 140086  
Location: 18:65750252-65890337 Cyto location: 18q22.1


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

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SNPs

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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]

Homology

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Interactions

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Expression

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

Gene Ontology

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Other

626 SN Ps

5 Cross References

16 Data Sets

27 Homologues

0 Located Features

97 Rna Seq Results