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 protein homooligomerization. Predicted to localize to 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

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

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