Gene

obscnb

ID
ZDB-GENE-070119-5
Name
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF b
Symbol
obscnb Nomenclature History
Previous Names
  • obscnl
  • obscurin A (1)
  • si:rp71-18a8.2
Type
protein_coding_gene
Location
Chr: 24 Mapping Details/Browsers
Description
Predicted to have guanyl-nucleotide exchange factor activity. Involved in myofibril assembly and retina development in camera-type eye. Localizes to M band. Is expressed in central nervous system; heart; retinal neural layer; skeletal muscle; and skeletal muscle cell. Orthologous to human OBSCN (obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
3 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
22 figures from 3 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With obscnb Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
{Rhabdomyolysis, susceptibility to, 1} 620235
Associated With obscnb Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-obscnl polyclonal IgG Rabbit
  • IHC
2
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations