Gene

svilb

ID
ZDB-GENE-081104-411
Name
supervillin b
Symbol
svilb Nomenclature History
Previous Names
  • si:dkey-42d18.3
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to enable actin filament binding activity. Predicted to act upstream of or within cytoskeleton organization. Is expressed in macula. Human ortholog(s) of this gene implicated in myofibrillar myopathy 10. Orthologous to human SVIL (supervillin).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Pollock et al., 2016
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 svilb Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
myofibrillar myopathy 10 Alliance Myofibrillar myopathy 10 619040
Associated With svilb Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR007122 Villin/Gelsolin
Family IPR015628 Supervillin
Domain Details Per Protein
Protein Length Supervillin Villin/Gelsolin
UniProtKB:F1QU62 179
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