Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
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
Electronic Gene Ontology annotations created by transferring manual GO annotations between related proteins based on shared sequence features
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
Combined Automated Annotation using Multiple IEA Methods
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.
DYX1C1 is required for axonemal dynein assembly and ciliary motility.
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects.
C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.
The RPAP3-Cterminal domain identifies R2TP-like quaternary chaperones.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Multimodal cell maps as a foundation for structural and functional genomics.
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.
A liquid-like organelle at the root of motile ciliopathy.
Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins.
The establishment of rotational polarity in the airway and ependymal cilia: analysis with a novel cilium motility mutant mouse.
Systematic studies of all PIH proteins in zebrafish reveal their distinct roles in axonemal dynein assembly.
Human PIH1 associates with histone H4 to mediate the glucose-dependent enhancement of pre-rRNA synthesis.
Dynein axonemal assembly factor 2 (DNAAF2), Homo sapiens
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The reviewed sequence record defines two alternative products of 837 and 789 residues, with an internal 48-residue deletion in product 2.
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The curated subunit comment records CFAP300 association with experimental support attributed to PMID:29727693.
Human Protein Atlas DNAAF2 record, ENSG00000165506, retrieved 2026-10-17