Gene

med13b

ID
ZDB-GENE-030131-3529
Name
mediator complex subunit 13b
Symbol
med13b Nomenclature History
Previous Names
  • fc43h07
  • fc43h08
  • wu:fb66c06
  • wu:fc43h07
  • wu:fc43h08
  • zgc:153454 (1)
Type
protein_coding_gene
Location
Chr: 15 Mapping Details/Browsers
Description
Predicted to have transcription coregulator activity. Involved in neural crest cell migration. Predicted to localize to mediator complex. Human ortholog(s) of this gene implicated in autosomal dominant non-syndromic intellectual disability. Is expressed in blastomere; nervous system; pectoral fin; and pectoral fin bud. Orthologous to human MED13 (mediator complex subunit 13).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Utami et al., 2014
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
3 figures from Utami et al., 2014
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With med13b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Intellectual developmental disorder, autosomal dominant 61 618009
Associated With med13b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR009401 Mediator complex subunit Med13, C-terminal
Domain IPR041285 MID domain of medPIWI
Domain Details Per Protein
Protein Length Mediator complex subunit Med13, C-terminal MID domain of medPIWI
UniProtKB:R4GE16 2103
UniProtKB:A2VCZ5 2102
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