Gene
eif3f
- ID
- ZDB-GENE-100215-2
- Name
- eukaryotic translation initiation factor 3, subunit F
- Symbol
- eif3f Nomenclature History
- Previous Names
-
- si:dkey-58j19.2
- Type
- protein_coding_gene
- Location
- Chr: 1 Mapping Details/Browsers
- Description
- Predicted to enable translation initiation factor binding activity. Predicted to contribute to translation initiation factor activity. Acts upstream of or within cranial skeletal system development. Predicted to be located in cytoplasm. Predicted to be part of eukaryotic translation initiation factor 3 complex, eIF3m. Is expressed in female organism. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 67. Orthologous to human EIF3F (eukaryotic translation initiation factor 3 subunit F).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Newman et al., 2019
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal recessive intellectual developmental disorder 67 | Alliance | Intellectual developmental disorder, autosomal recessive 67 | 618295 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | EIF3F/CSN6-like, C-terminal | Eukaryotic translation initiation factor 3 subunit F | JAB1/MPN/MOV34 metalloenzyme domain | MPN domain |
|---|---|---|---|---|---|
|
UniProtKB:A0A8M1NXK7
|
273 |
Interactions and Pathways
No data available
Plasmids
No data available