IFT122 and SLCO2A1

		IFT122	SLCO2A1
Description		intraflagellar transport 122	solute carrier organic anion transporter family member 2A1
Image		No pdb structure
GO Annotations	Cellular Component	Cytoplasm Cilium Membrane Intraciliary Transport Particle A Photoreceptor Connecting Cilium Ciliary Basal Body Ciliary Tip Non-motile Cilium	Plasma Membrane Integral Component Of Plasma Membrane Membrane
	Molecular Function	Protein Binding	Lipid Transporter Activity Prostaglandin Transmembrane Transporter Activity Sodium-independent Organic Anion Transmembrane Transporter Activity
	Biological Process	Neural Tube Closure Embryonic Body Morphogenesis Embryonic Heart Tube Development Intraciliary Retrograde Transport Intraciliary Transport Negative Regulation Of Smoothened Signaling Pathway Camera-type Eye Morphogenesis Limb Development Cilium Assembly Protein Localization To Cilium Non-motile Cilium Assembly	Lipid Transport Prostaglandin Transport Sodium-independent Organic Anion Transport Transmembrane Transport
Pathways		Hedgehog 'off' state Intraflagellar transport	Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2) Transport of organic anions
Drugs
Diseases
GWAS		Body shape index ( 34021172) Diisocyanate-induced asthma ( 25918132) Hip circumference adjusted for BMI ( 34021172) Hip index ( 34021172) Systemic sclerosis (anti-topoisomerase-positive) ( 29293537) Waist-to-hip ratio adjusted for BMI ( 26426971) Waist-to-hip ratio adjusted for BMI (age >50) ( 26426971) Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) ( 26426971)	Amyotrophic lateral sclerosis (sporadic) ( 24529757) Colorectal cancer ( 30529582) Height ( 31562340)
Interacting Genes		2 interacting genes: SLCO2A1 ZNF148	1 interacting genes: IFT122
Entrez ID		55764	6578
HPRD ID		06922	03269
Ensembl ID		ENSG00000163913	ENSG00000174640
Uniprot IDs		B3KUD1 B4DST2 Q9HBG6	Q92959
PDB IDs			3MRR
Enriched GO Terms of Interacting Partners?
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