Gene

myl13

ID
ZDB-GENE-040426-1593
Name
myosin, light chain 13
Symbol
myl13 Nomenclature History
Previous Names
  • zgc:66286
  • zgc:77943
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to have calcium ion binding activity. Human ortholog(s) of this gene implicated in hypertrophic cardiomyopathy 8. Is expressed in adaxial cell; heart; musculature system; and somite. Orthologous to human MYL3 (myosin light chain 3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
9 figures from 3 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 myl13 Human Ortholog
No data available
Associated With myl13 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR002048 EF-hand domain
Homologous_superfamily IPR011992 EF-hand domain pair
Domain Details Per Protein
Protein Length EF-hand domain EF-hand domain pair
UniProtKB:Q7ZUB0 186
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