Sequence Detail

ID/Version

E9QA62 A0JP45 A0AUN8 (UniProt | EBI)

Last sequence update: 2011-04-05
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=Leiomodin-3;

Provider

SWISS-PROT

Sequence

Polypeptide 571 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Lmod3	leiomodin 3 (fetal)	26	103	3	6

Sequence references in MGI

J:213780 Garg A, et al., KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy. J Clin Invest. 2014 Aug 1;124(8):3529-39
J:222174 Cenik BK, et al., Severe myopathy in mice lacking the MEF2/SRF-dependent gene leiomodin-3. J Clin Invest. 2015 Apr;125(4):1569-78
J:223382 Tian L, et al., Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy. Dis Model Mech. 2015 Jun;8(6):635-41