Entity Details

Primary name COF2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y281
EntryNameCOF2_HUMAN
FullNameCofilin-2
TaxID9606
Evidenceevidence at protein level
Length166
SequenceStatuscomplete
DateCreated2000-05-30
DateModified2021-06-02

Ontological Relatives

GenesCFL2

GO terms

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GOName
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0007519 skeletal muscle tissue development
GO:0015629 actin cytoskeleton
GO:0016363 nuclear matrix
GO:0030018 Z disc
GO:0030042 actin filament depolymerization
GO:0030043 actin filament fragmentation
GO:0030836 positive regulation of actin filament depolymerization
GO:0031674 I band
GO:0045214 sarcomere organization
GO:0046716 muscle cell cellular homeostasis
GO:0048870 cell motility
GO:0051014 actin filament severing
GO:0051015 actin filament binding
GO:0070062 extracellular exosome

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus matrix

Domains

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DomainNameCategoryType
IPR002108 Actin-depolymerising factor homology domainDomainDomain
IPR017904 ADF/CofilinFamilyFamily
IPR029006 ADF-H/Gelsolin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
610687 OMIMNemaline myopathy 7 (NEM7)A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-like or rod-shaped structures in muscle fibers on histologic examination. Nemaline myopathy type 7 presents at birth with hypotonia and generalized weakness. Major motor milestones are delayed, but independent ambulation is achieved. The disease is caused by variants affecting the gene represented in this entry.