Gene

med27

ID
ZDB-GENE-040426-1601
Name
mediator complex subunit 27
Symbol
med27 Nomenclature History
Previous Names
  • crsp34
  • crsp8
  • trap37 (1)
  • zgc:66302 (1)
Type
protein_coding_gene
Location
Chr: 8 Mapping Details/Browsers
Description
Involved in retinal cone cell development. Predicted to localize to mediator complex. Orthologous to human MED27 (mediator complex subunit 27).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
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 med27 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia 619286
Associated With med27 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR021627 Mediator complex, subunit Med27
Domain Details Per Protein
Protein Length Mediator complex, subunit Med27
UniProtKB:Q6PFL0 311
UniProtKB:A0A8M9QDN3 253
UniProtKB:B2GNU2 311
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