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 enable transcription coregulator activity. Acts upstream of or within neural crest cell migration. Predicted to be located in nucleus. Predicted to be part of mediator complex. Is expressed in blastomere; nervous system; pectoral fin; and pectoral fin bud. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder. Orthologous to human MED13 (mediator complex subunit 13).
- Genome Resources
- Note
- None
- Comparative Information
-
- 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
- All Phenotype Data
- 3 figures from Utami et al., 2014
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Intellectual developmental disorder, autosomal dominant 61 | 618009 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mediator complex subunit 13 | Mediator complex subunit Med13, C-terminal | MID domain of medPIWI |
|---|---|---|---|---|
|
UniProtKB:A2VCZ5
|
2102 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
med13b-201
(1)
|
Ensembl | 7,768 nt | ||
| ncRNA |
ottdart00000061411
(1)
|
Ensembl | 493 nt |
Interactions and Pathways
No data available
Plasmids
No data available