Gene

lmod3

ID
ZDB-GENE-090313-353
Name
leiomodin 3 (fetal)
Symbol
lmod3 Nomenclature History
Previous Names
  • si:dkey-90a13.2
  • si:dkey-90a13.7 (1)
Type
protein_coding_gene
Location
Chr: 23 Mapping Details/Browsers
Description
Predicted to have tropomyosin binding activity. Involved in muscle contraction and skeletal muscle thin filament assembly. Predicted to localize to striated muscle thin filament. Human ortholog(s) of this gene implicated in nemaline myopathy 10. Orthologous to human LMOD3 (leiomodin 3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Berger et al., 2022
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
6 figures from 2 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With lmod3 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
nemaline myopathy 10 Alliance Nemaline myopathy 10 616165
Associated With lmod3 Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR004934 Tropomodulin
Homologous_superfamily IPR032675 Leucine-rich repeat domain superfamily
Domain Details Per Protein
Protein Length Leucine-rich repeat domain superfamily Tropomodulin
UniProtKB:A0A2R8QDE5 670
UniProtKB:A0A8M9QA08 670
UniProtKB:E7F7X0 670
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA lmod3-201 (1) Havana 2260 nt
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-lmod3 polyclonal IgG Rabbit
  • IHC
Proteintech
2
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations