Homo sapiens Protein: IFT52
Summary
InnateDB Protein IDBP-76123.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol IFT52
Protein Name intraflagellar transport 52 homolog (Chlamydomonas)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000362121
InnateDB Gene IDBG-76119 (IFT52)
Protein Structure
UniProt Annotation
Function Forms part of a complex involved in intraflagellar transport (IFT), the bi-directional movement of particles required for the assembly, maintenance and functioning of primary cilia. {ECO:0000250}.
Subcellular Localization Cell projection, cilium.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008022 protein C-terminus binding
Biological Process
GO:0001841 neural tube formation
GO:0001947 heart looping
GO:0007224 smoothened signaling pathway
GO:0007368 determination of left/right symmetry
GO:0009953 dorsal/ventral pattern formation
GO:0042733 embryonic digit morphogenesis
GO:0050680 negative regulation of epithelial cell proliferation
GO:0060271 cilium morphogenesis
GO:0070613 regulation of protein processing
Cellular Component
GO:0005813 centrosome
GO:0005929 cilium
GO:0030992 intraciliary transport particle B
GO:0031514 motile cilium
GO:0032391 photoreceptor connecting cilium
GO:0044292 dendrite terminus
GO:0097542 ciliary tip
GO:0097546 ciliary base
Protein Structure and Domains
PDB ID
InterPro IPR019196 ABC-type uncharacterised transport system
PFAM PF09822
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y366
PhosphoSite PhosphoSite-Q9Y366
TrEMBL
UniProt Splice Variant
Entrez Gene 51098
UniGene Hs.444332
RefSeq NP_057088
HUGO HGNC:15901
OMIM
CCDS CCDS33470
HPRD 12789
IMGT
EMBL AF151811 AK001436 AL121886 BC039831 CH471077 Z98752
GenPept AAD34048 AAH39831 BAG50913 CAI18925 CAI42316 EAW75953 EAW75954