Gene Ontology annotation through association of InterPro records with GO terms
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin.
Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.
The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins.
Unusual splicing events result in distinct Xin isoforms that associate differentially with filamin c and Mena/VASP.
Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening.
Nebulette interacts with filamin C.
Novel interactions of ankyrins-G at the costameres: the muscle-specific Obscurin/Titin-Binding-related Domain (OTBD) binds plectin and filamin C.
Analysis of the myosin-II-responsive focal adhesion proteome reveals a role for β-Pix in negative regulation of focal adhesion maturation.
F-box and leucine-rich repeat protein 22 is a cardiac-enriched F-box protein that regulates sarcomeric protein turnover and is essential for maintenance of contractile function in vivo.
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
MigFilin associates with Filamin and F-actin
Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure.
FLNC source evidence, context projection and natural-product boundaries