Gene

fbxo38

ID
ZDB-GENE-030131-2797
Name
F-box protein 38
Symbol
fbxo38 Nomenclature History
Previous Names
  • fc18a08
  • wu:fc18a08
Type
protein_coding_gene
Location
Chr: 14 Mapping Details/Browsers
Description
Predicted to be involved in SCF-dependent proteasomal ubiquitin-dependent protein catabolic process. Human ortholog(s) of this gene implicated in distal hereditary motor neuronopathy type 2D. Orthologous to human FBXO38 (F-box protein 38).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
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 fbxo38 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant distal hereditary motor neuronopathy 6 Alliance Neuronopathy, distal hereditary motor, autosomal dominant 6 615575
Associated With fbxo38 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR001810 F-box domain
Family IPR042354 F-box only protein 38
Homologous_superfamily IPR032675 Leucine-rich repeat domain superfamily
Homologous_superfamily IPR036047 F-box-like domain superfamily
Domain Details Per Protein
Protein Length F-box domain F-box-like domain superfamily F-box only protein 38 Leucine-rich repeat domain superfamily
UniProtKB:A0A8M2BH07 1119
UniProtKB:A0A8M9Q5D2 1119
UniProtKB:E7F2P7 1120
UniProtKB:A0A8M9PUM2 1120
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA fbxo38-201 (1) Havana 5147 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations