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Gene : ANO6 Homo sapiens

Name  ? anoctamin 6 Cytological Location  12q12
Brief Description  anoctamin 6
Description  This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]
  • synonyms:
  • TMEM16F,
  • transmembrane protein 16F,
  • HGNC:25240,
  • TMEM16F,
  • ANO6,
  • NM_001025356,
  • OTTHUMG00000169564,
  • SCTS,
  • uc001roo.4,
  • AL832340,
  • DKFZp313M0720,
  • BDPLT7
  • identifiers:
  • 196527,
  • ENSG00000177119,
  • ANO6

Genome feature

Region: gene ? Length: 224372  
Location: 12:45216033-45440404 Cyto location: 12q12

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Report --> GWAS hit


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.



534 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results