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Gene : KCTD7 Homo sapiens

Name  ? potassium channel tetramerization domain containing 7 Cytological Location  7q11.21
Brief Description  potassium channel tetramerization domain containing 7
Description  This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]
  • synonyms:
  • AK056631,
  • CLN14,
  • KCTD7,
  • uc003tve.4,
  • HGNC:21957,
  • NM_153033,
  • OTTHUMG00000129543,
  • FLJ32069,
  • potassium channel tetramerisation domain containing 7,
  • CLN14,
  • EPM3,
  • EPM3
  • identifiers:
  • 154881,
  • ENSG00000243335,
  • KCTD7

Genome feature

Region: gene ? Length: 14349  
Location: 7:66628881-66643229 Cyto location: 7q11.21


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Genomics

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Proteins

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SNPs

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Disease

1 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Expression

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Other

3756 SN Ps

5 Cross References

16 Data Sets

19 Homologues

0 Located Features

97 Rna Seq Results