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 contribute to translation initiation factor activity. Involved in cranial skeletal system development. Predicted to localize to eukaryotic translation initiation factor 3 complex, eIF3m. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Is expressed in female organism. Orthologous to human EIF3F (eukaryotic translation initiation factor 3 subunit F).
Genome Resources
Note
None
Comparative Information
Expression
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
All Phenotype Data
2 figures from 2 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With eif3f Human Ortholog
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
Associated With eif3f Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein Length
UniProtKB:A0A8M1NXK7 273
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