LMOD3

Identifiers

Aliases, NEM10, leiomodin 3

External IDsOMIM: ; MGI: ; HomoloGene: ; GeneCards: ; OMA:

Gene location ( Human )

Chr.Chromosome 3 (human)

Band 3p14.1 Start 69,106,065 bp

End69,123,032 bp

Gene location ( Mouse )

Chr.Chromosome 6 (mouse)

Band 6|6 D3 Start 97,215,495 bp

End97,229,720 bp

RNA expression pattern

HumanMouse (ortholog)biceps brachii vastus lateralis muscle skeletal muscle tissue Skeletal muscle tissue of rectus abdominis Skeletal muscle tissue of biceps brachii muscle of thigh deltoid muscle gastrocnemius muscle myocardium of left ventricle tibialis anterior musclesoleus muscle intercostal muscle tibialis anterior muscle sternocleidomastoid muscle medial head of gastrocnemius muscle temporal muscle quadriceps femoris muscle ankle digastric muscle vastus lateralis muscle

Human Mouse (ortholog)

biceps brachii vastus lateralis muscle skeletal muscle tissue Skeletal muscle tissue of rectus abdominis Skeletal muscle tissue of biceps brachii muscle of thigh deltoid muscle gastrocnemius muscle myocardium of left ventricle tibialis anterior musclesoleus muscle intercostal muscle tibialis anterior muscle sternocleidomastoid muscle medial head of gastrocnemius muscle temporal muscle quadriceps femoris muscle ankle digastric muscle vastus lateralis muscle

soleus muscle intercostal muscle tibialis anterior muscle sternocleidomastoid muscle medial head of gastrocnemius muscle temporal muscle quadriceps femoris muscle ankle digastric muscle vastus lateralis muscle

Gene ontologyMolecular functionCellular componentBiological processSources: /

Gene ontology

Molecular function

Cellular component

Biological process

Sources: /

OrthologsSpeciesHumanMouseEntrez Ensembl UniProtRefSeq (mRNA)RefSeq (protein)Location (UCSC)PubMed search

Orthologs

Species Human Mouse

Entrez

Ensembl

UniProt

RefSeq (mRNA)

RefSeq (protein)

Location (UCSC)

PubMed search

Wikidata

View/Edit HumanView/Edit Mouse

Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene. Leiomodin-3 is especially present at the pointed end of muscle thin filaments.

Clinical significance

Dysfunction is associated with thin filament disorganisation and nemaline myopathy.

LMOD3

Clinical significance

Further reading