Gene

cfap418

ID
ZDB-GENE-100921-86
Name
cilia and flagella associated protein 418
Symbol
cfap418 Nomenclature History
Previous Names
  • si:dkey-242e21.4
Type
protein_coding_gene
Location
Chr: 16 Mapping Details/Browsers
Description
Involved in Kupffer's vesicle development and melanosome transport. Predicted to localize to cytoplasm. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome and cone-rod dystrophy 16. Is expressed in brain; eye; heart; liver; and pleuroperitoneal region. Orthologous to human C8orf37 (chromosome 8 open reading frame 37).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Heon et al., 2016
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
2 figures from Heon et al., 2016
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With cfap418 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Bardet-Biedl syndrome 21 Alliance Bardet-Biedl syndrome 21 617406
cone-rod dystrophy 16 Alliance Cone-rod dystrophy 16 614500
cone-rod dystrophy 16 Alliance Retinitis pigmentosa 64 614500
Associated With cfap418 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR029239 Cilia- and flagella-associated protein 418
Domain Details Per Protein
Protein Length Cilia- and flagella-associated protein 418
UniProtKB:P0DOC8
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