Gene

kctd7

ID
ZDB-GENE-060804-2
Name
potassium channel tetramerization domain containing 7
Symbol
kctd7 Nomenclature History
Previous Names
  • zgc:136884
Type
protein_coding_gene
Location
Chr: 10 Mapping Details/Browsers
Description
Predicted to be involved in membrane hyperpolarization and positive regulation of transporter activity. Predicted to act upstream of or within protein homooligomerization. Predicted to be located in cytosol and plasma membrane. Human ortholog(s) of this gene implicated in progressive myoclonus epilepsy 3. Orthologous to human KCTD7 (potassium channel tetramerization domain containing 7).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Burke et al., 2021
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With kctd7 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
progressive myoclonus epilepsy 3 Alliance Epilepsy, progressive myoclonic 3, with or without intracellular inclusions 611726
Associated With kctd7 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR000210 BTB/POZ domain
Domain IPR003131 Potassium channel tetramerisation-type BTB domain
Homologous_superfamily IPR011333 SKP1/BTB/POZ domain superfamily
Domain Details Per Protein
Protein Length BTB/POZ domain Potassium channel tetramerisation-type BTB domain SKP1/BTB/POZ domain superfamily
UniProtKB:F1R224 339
UniProtKB:Q0VFV7 292
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations