Gene

myl1

ID
ZDB-GENE-030131-8109
Name
myosin, light chain 1, alkali; skeletal, fast
Symbol
myl1 Nomenclature History
Previous Names
  • fj53a11
  • wu:fj53a11
  • zgc:77231 (1)
Type
protein_coding_gene
Location
Chr: 9 Mapping Details/Browsers
Description
Predicted to have calcium ion binding activity. Is expressed in adaxial cell; fin; musculature system; and somite. Orthologous to human MYL1 (myosin light chain 1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
22 figures from 6 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Ravenscroft et al., 2018
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With myl1 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Myopathy, congenital, with fast-twitch (type II) fiber atrophy 618414
Associated With myl1 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:Q6P0G6 190
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