Homo sapiens Protein: DNAAF1
Summary
InnateDB Protein IDBP-44268.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DNAAF1
Protein Name dynein, axonemal, assembly factor 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000367815
InnateDB Gene IDBG-44266 (DNAAF1)
Protein Structure
UniProt Annotation
Function Cilium-specific protein required for the stability of the ciliary architecture. Plays a role in cytoplasmic preassembly of dynein arms. Involved in regulation of microtubule-based cilia and actin-based brush border microvilli. {ECO:0000269PubMed:18385425, ECO:0000269PubMed:19944400, ECO:0000269PubMed:19944405}.
Subcellular Localization Cell projection, cilium {ECO:0000269PubMed:18385425}. Cytoplasm {ECO:0000269PubMed:18385425}. Cytoplasm, cytoskeleton, spindle pole {ECO:0000269PubMed:18385425}. Note=In HEK293T cells, it is diffusely cytoplasmic and concentrates at the mitotic spindle poles, while in MDCK cells, it localizes in the cilium. In vivo, this protein is probably restricted to the cilium.
Disease Associations Ciliary dyskinesia, primary, 13 (CILD13) [MIM:613193]: A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. At ultrastructural level, CILD13 is characterized by a marked reduction or absence of both dynein arms from the patients cilia. {ECO:0000269PubMed:19944400, ECO:0000269PubMed:19944405}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Mainly expressed in trachea and testis. {ECO:0000269PubMed:19944405}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0045502 dynein binding
Biological Process
GO:0001947 heart looping
GO:0003341 cilium movement
GO:0003356 regulation of cilium beat frequency
GO:0030324 lung development
GO:0035469 determination of pancreatic left/right asymmetry
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0044458 motile cilium assembly
GO:0060271 cilium morphogenesis
GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry
GO:0060972 left/right pattern formation
GO:0070286 axonemal dynein complex assembly
GO:0071907 determination of digestive tract left/right asymmetry
GO:0071910 determination of liver left/right asymmetry
Cellular Component
GO:0000922 spindle pole
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005930 axoneme
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8NEP3
PhosphoSite PhosphoSite-Q8NEP3
TrEMBL H3BP51
UniProt Splice Variant
Entrez Gene 123872
UniGene Hs.703315
RefSeq NP_848547
HUGO HGNC:30539
OMIM 613190
CCDS CCDS10943
HPRD 14023
IMGT
EMBL AC009123 AC040169 AK057238 AK058059 AK295990 AL137334 AL833328 AL833336 BC024009
GenPept AAH24009 BAB71392 BAB71645 BAG58765 CAH10390 CAH10394 CAH10706