Homo sapiens Protein: IFT88
Summary
InnateDB Protein IDBP-13476.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol IFT88
Protein Name intraflagellar transport 88 homolog (Chlamydomonas)
Synonyms D13S1056E; DAF19; hTg737; TG737; TTC10;
Species Homo sapiens
Ensembl Protein ENSP00000323580
InnateDB Gene IDBG-13468 (IFT88)
Protein Structure
UniProt Annotation
Function Involved in primary cilium biogenesis. Also involved in autophagy since it is required for trafficking of ATG16L and the expansion of the autophagic compartment (By similarity). {ECO:0000250}.
Subcellular Localization Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole {ECO:0000250}. Cytoplasm, cytoskeleton, cilium basal body {ECO:0000250}.
Disease Associations
Tissue Specificity Expressed in the heart, brain, liver, lung, kidney, skeletal muscle and pancreas. {ECO:0000269PubMed:7633404}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 11 interaction(s) predicted by orthology.
Experimentally validated
Total 5 [view]
Protein-Protein 4 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 11 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001654 eye development
GO:0001822 kidney development
GO:0001889 liver development
GO:0003382 epithelial cell morphogenesis
GO:0007219 Notch signaling pathway
GO:0007224 smoothened signaling pathway
GO:0007288 sperm axoneme assembly
GO:0007290 spermatid nucleus elongation
GO:0007368 determination of left/right symmetry
GO:0007399 nervous system development
GO:0007420 brain development
GO:0007507 heart development
GO:0008104 protein localization
GO:0008544 epidermis development
GO:0008589 regulation of smoothened signaling pathway
GO:0009887 organ morphogenesis
GO:0009952 anterior/posterior pattern specification
GO:0009953 dorsal/ventral pattern formation
GO:0021513 spinal cord dorsal/ventral patterning
GO:0021537 telencephalon development
GO:0030324 lung development
GO:0031016 pancreas development
GO:0031122 cytoplasmic microtubule organization
GO:0034405 response to fluid shear stress
GO:0036334 epidermal stem cell homeostasis
GO:0042384 cilium assembly
GO:0042487 regulation of odontogenesis of dentin-containing tooth
GO:0042733 embryonic digit morphogenesis
GO:0043568 positive regulation of insulin-like growth factor receptor signaling pathway
GO:0045598 regulation of fat cell differentiation
GO:0048853 forebrain morphogenesis
GO:0050680 negative regulation of epithelial cell proliferation
GO:0055007 cardiac muscle cell differentiation
GO:0060021 palate development
GO:0060122 inner ear receptor stereocilium organization
GO:0060173 limb development
GO:0060271 cilium morphogenesis
GO:0060411 cardiac septum morphogenesis
GO:0060426 lung vasculature development
GO:0060914 heart formation
GO:0070613 regulation of protein processing
GO:0090102 cochlea development
GO:1902017 regulation of cilium assembly
GO:2000785 regulation of autophagic vacuole assembly
Cellular Component
GO:0002080 acrosomal membrane
GO:0005813 centrosome
GO:0005814 centriole
GO:0005929 cilium
GO:0005930 axoneme
GO:0030992 intraciliary transport particle B
GO:0031512 motile primary cilium
GO:0031514 motile cilium
GO:0032391 photoreceptor connecting cilium
GO:0036064 ciliary basal body
GO:0045177 apical part of cell
GO:0060091 kinocilium
GO:0072372 primary cilium
GO:0097541 axonemal basal plate
GO:0097542 ciliary tip
GO:0097546 ciliary base
Protein Structure and Domains
PDB ID
InterPro IPR001440 Tetratricopeptide TPR1
IPR006597 Sel1-like
IPR013026 Tetratricopeptide repeat-containing domain
IPR013105 Tetratricopeptide TPR2
IPR019412 Outer membrane protein, IML2, mitochondrial/Tetratricopeptide repeat protein 39
IPR019734 Tetratricopeptide repeat
PFAM PF00515
PF08238
PF07719
PF10300
PF13174
PF13176
PF13181
PRINTS
PIRSF
SMART SM00671
SM00028
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q13099
PhosphoSite PhosphoSite-Q13099
TrEMBL F6SRW8
UniProt Splice Variant
Entrez Gene 8100
UniGene Hs.187376
RefSeq NP_783195
HUGO HGNC:20606
OMIM 600595
CCDS CCDS31944
HPRD 09000
IMGT
EMBL AK300769 AL161772 AL590096 BC030776 CH471075 U20362
GenPept AAA86720 AAH30776 BAG62434 CAH70874 CAI14390 CAM13405 CAM20430 EAX08272