GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
PMID:21149568
Formin follows function: a muscle-specific isoform of FHOD3 is regulated by CK2 phosphorylation and promotes myofibril maintenance.
PMID:15966898
Fhos2, a novel formin-related actin-organizing protein, probably associates with the nestin intermediate filament.
PMID:19706596
Mammalian formin fhod3 regulates actin assembly and sarcomere organization in striated muscles.
PMID:22509354
Expression and subcellular localization of mammalian formin Fhod3 in the embryonic and adult heart.
PMID:30442288
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
PMID:31742804
Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy.
PMID:16177791
DNA sequence and analysis of human chromosome 18.
file:human/FHOD3/FHOD3-evidence.yaml
FHOD3 source evidence and access boundaries