Gene

med23

ID
ZDB-GENE-040724-82
Name
mediator complex subunit 23
Symbol
med23 Nomenclature History
Previous Names
  • crsp3
  • si:ch211-272f15.2 (1)
  • zgc:91979 (1)
Type
protein_coding_gene
Location
Chr: 20 Mapping Details/Browsers
Description
Involved in circulatory system development; negative regulation of neurogenesis; and pigmentation. Predicted to localize to mediator complex and transcription regulator complex. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human MED23 (mediator complex subunit 23).
Genome Resources
Note
None
Expression
All Expression Data
3 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
4 figures from 3 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With med23 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive non-syndromic intellectual disability Alliance Mental retardation, autosomal recessive 18 614249
Associated With med23 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR021629 Mediator complex, subunit Med23
Domain Details Per Protein
Protein Length Mediator complex, subunit Med23
UniProtKB:Q5RIW8 1376
UniProtKB:B8A4G4 1387
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-med23 monoclonal IgG1 , k Mouse
  • WB
BD Biosciences
2
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Gene Tree
Ensembl
Citations