Gene
fancf
- ID
- ZDB-GENE-060306-3
- Name
- FA complementation group F
- Symbol
- fancf Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Predicted to be involved in cellular response to DNA damage stimulus. Predicted to localize to Fanconi anaemia nuclear complex. Human ortholog(s) of this gene implicated in Fanconi anemia complementation group F; adenocarcinoma in situ; and granulosa cell tumor. Is expressed in brain; central nervous system; and lens. Orthologous to human FANCF (FA complementation group F).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from Titus et al., 2009
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Ramanagoudr-Bhojappa et al., 2018
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Fanconi anemia complementation group F | Alliance | Fanconi anemia, complementation group F | 603467 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | FANCF, C-terminal domain superfamily | Fanconi anemia group F protein |
|---|---|---|---|
|
UniProtKB:A4QNZ2
|
333 |
Interactions and Pathways
No data available
Plasmids
No data available