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
-
- 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