Gene

myl9b

ID
ZDB-GENE-040426-2296
Name
myosin, light chain 9b, regulatory
Symbol
myl9b Nomenclature History
Previous Names
  • myl9
  • myl9l
  • zgc:77916
Type
protein_coding_gene
Location
Chr: 6 Mapping Details/Browsers
Description
Predicted to have calcium ion binding activity. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy. Is expressed in smooth muscle cell. Orthologous to human MYL9 (myosin light chain 9).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
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 myl9b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
?Megacystis-microcolon-intestinal hypoperistalsis syndrome 4 619365
Associated With myl9b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Binding_site IPR018247 EF-Hand 1, calcium-binding site
Domain IPR002048 EF-hand domain
Homologous_superfamily IPR011992 EF-hand domain pair
Domain Details Per Protein
Protein Length EF-Hand 1, calcium-binding site EF-hand domain EF-hand domain pair
UniProtKB:Q6NVA6 173
Transcripts
Genome Browsers
No data available
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