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Gene : ANO5 Homo sapiens

Name  ? anoctamin 5 Cytological Location  11p14.3
Brief Description  anoctamin 5
Description  This gene encodes a member of the anoctamin family of transmembrane proteins. The encoded protein is likely a calcium activated chloride channel. Mutations in this gene have been associated with gnathodiaphyseal dysplasia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2009]
  • synonyms:
  • GDD1,
  • TMEM16E,
  • limb girdle muscular dystrophy 2L (autosomal recessive),
  • LGMD2L,
  • AL833271,
  • TMEM16E,
  • LGMDR12,
  • transmembrane protein 16E,
  • uc001mqi.3,
  • LGMD2L,
  • OTTHUMG00000166051,
  • HGNC:27337,
  • ANO5,
  • GDD1,
  • NM_213599
  • identifiers:
  • 203859,
  • ENSG00000171714,
  • ANO5

Genome feature

Region: gene ? Length: 90873  
Location: 11:22192485-22283357 Cyto location: 11p14.3

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


3 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 --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3740 SNPs

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results