Gene

mffa

ID
ZDB-GENE-040426-1510
Name
mitochondrial fission factor a
Symbol
mffa Nomenclature History
Previous Names
  • mff
  • zgc:66022
Type
protein_coding_gene
Location
Chr: 15 Mapping Details/Browsers
Description
Predicted to have protein homodimerization activity. Predicted to be involved in mitochondrial fission; positive regulation of mitochondrial fission; and positive regulation of protein targeting to membrane. Predicted to localize to peroxisome. Human ortholog(s) of this gene implicated in brain disease. Is expressed in female organism. Orthologous to human MFF (mitochondrial fission factor).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With mffa Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Encephalopathy due to defective mitochondrial and peroxisomal fission 2 617086
Associated With mffa Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR039433 Mff-like domain
Family IPR008518 Mff/Tango-11
Domain Details Per Protein
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