Gene

cux2a

ID
ZDB-GENE-031204-9
Name
cut-like homeobox 2a
Symbol
cux2a Nomenclature History
Previous Names
  • sb:cb1008
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in early infantile epileptic encephalopathy. Is expressed in hindbrain neural plate; nervous system; neural tube; otic vesicle; and somite. Orthologous to human CUX2 (cut like homeobox 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
5 figures from Thisse et al., 2001
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
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 cux2a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
developmental and epileptic encephalopathy 67 Alliance Developmental and epileptic encephalopathy 67 618141
Associated With cux2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Transcripts
Genome Browsers
No data available
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