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WormBase Tree Display for Gene: HGNC:1875

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Name Class

HGNC:1875IdentityNameCGC_nameCfl2Inferred_automaticallyAGR_import
Other_nameRGD:1315906
NEM7
cofilin 2 (muscle)
cofilin, muscle isoform
cofilin-2
nemaline myopathy type 7
Public_nameCfl2
DB_infoDatabaseHGNCid1875
AGRcURIHGNC:1875
EnsEMBLENSEMBL_geneIDENSG00000165410
UniProtUniProt_ACQ9Y281
OMIMgene601443
DOidDOID:0110934
SpeciesHomo sapiens
StatusLive
Gene_infoBiotypeSO:0001217
OrthologWBGene00006794Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
WBGene00302980Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
Structured_descriptionAutomated_descriptionThis gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH-dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]Inferred_automaticallyAGR_import