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Protein Coding Gene : Kctd17 potassium channel tetramerisation domain containing 17
Primary Identifier  MGI:1920094 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  72844
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable cullin family protein binding activity; identical protein binding activity; and ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in endoplasmic reticulum calcium ion homeostasis; positive regulation of cilium assembly; and proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul3-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. Human ortholog(s) of this gene implicated in myoclonic dystonia 26. Orthologous to human KCTD17 (potassium channel tetramerization domain containing 17).
  • synonyms:
  • AW742389,
  • expressed sequence N28155,
  • expressed sequence AW742389,
  • N28155,
  • MGI:2146244,
  • expressed sequence AA414907,
  • 2900008M13Rik,
  • Kctd17,
  • RIKEN cDNA 2900008M13 gene,
  • AA414907,
  • MGI:2146317,
  • MGI:2145906,
  • potassium channel tetramerisation domain containing 17
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Features --> Cross References

Genome

Sequence Feature Displayer

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3 Involved In Mutations

Trail: ProteinCodingGene

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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