Gene

kctd15b

ID
ZDB-GENE-040801-34
Name
potassium channel tetramerization domain containing 15b
Symbol
kctd15b Nomenclature History
Previous Names
  • kctd15
  • zgc:100865
Type
protein_coding_gene
Location
Unmapped
Description
Involved in brain development; canonical Wnt signaling pathway; and chordate embryonic development. Human ortholog(s) of this gene implicated in scalp-ear-nipple syndrome. Is expressed in neural plate. Orthologous to several human genes including KCTD15 (potassium channel tetramerization domain containing 15).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
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 kctd15b Human Ortholog
No data available
Associated With kctd15b 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
Domain IPR045904 KCTD15, tetramerisation-type BTB domain
Domain IPR048595 BTB/POZ domain-containing protein KCTD1/15-like, C-terminal domain
Homologous_superfamily IPR011333 SKP1/BTB/POZ domain superfamily
Domain Details Per Protein
Protein Length BTB/POZ domain BTB/POZ domain-containing protein KCTD1/15-like, C-terminal domain KCTD15, tetramerisation-type BTB domain Potassium channel tetramerisation-type BTB domain SKP1/BTB/POZ domain superfamily
UniProtKB:Q6DC02 257
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations