NPHP1 and NPHP3

Number of citations of the paper that reports this interaction (PubMedID 12872122)
104

Data Source:
BioGRID (affinity chromatography technology)
HPRD (in vivo, in vitro)

		NPHP1	NPHP3
Description		nephrocystin 1	nephrocystin 3
Image
GO Annotations	Cellular Component	Cytosol Cytoskeleton Cell-cell Junction Adherens Junction Bicellular Tight Junction Membrane Motile Cilium Photoreceptor Connecting Cilium	Extracellular Region Cytosol Cilium
	Molecular Function	Structural Molecule Activity Protein Binding	Protein Binding
	Biological Process	Signal Transduction Excretion Visual Behavior Cell Projection Organization Actin Cytoskeleton Organization Spermatid Differentiation Retina Development In Camera-type Eye Ciliary Basal Body-plasma Membrane Docking Cell-cell Adhesion Positive Regulation Of Bicellular Tight Junction Assembly	Kidney Development Heart Looping Atrial Septum Development Determination Of Left/right Symmetry Wnt Signaling Pathway Lung Development Determination Of Pancreatic Left/right Asymmetry Photoreceptor Cell Maintenance Maintenance Of Animal Organ Identity Convergent Extension Involved In Gastrulation Cilium Assembly Epithelial Cilium Movement Involved In Determination Of Left/right Asymmetry Kidney Morphogenesis Determination Of Intestine Left/right Asymmetry Determination Of Stomach Left/right Asymmetry Determination Of Liver Left/right Asymmetry Ureter Development Negative Regulation Of Canonical Wnt Signaling Pathway Regulation Of Wnt Signaling Pathway, Planar Cell Polarity Pathway Regulation Of Planar Cell Polarity Pathway Involved In Neural Tube Closure
Pathways		Anchoring of the basal body to the plasma membrane	Trafficking of myristoylated proteins to the cilium
Drugs
Diseases		Joubert syndrome Nephronophthisis-medullary cystic kidney disease, including; Nephronophthisis (NPH) ; Nephronophthisis-like nephropathy 1; Medullary cystic kidney disease 1; Medullary cystic kidney disease 2 (MSKD2) Senior-Loken syndrome	Senior-Loken syndrome Renal-hepatic-pancreatic dysplasia Nephronophthisis-medullary cystic kidney disease, including; Nephronophthisis (NPH) ; Nephronophthisis-like nephropathy 1; Medullary cystic kidney disease 1; Medullary cystic kidney disease 2 (MSKD2) Meckel syndrome (MKS); Meckel-Gruber syndrome
GWAS			Blood protein levels ( 28240269) Mean corpuscular hemoglobin ( 27863252) Mean corpuscular volume ( 27863252) Menarche (age at onset) ( 27182965 21102462)
Interacting Genes		16 interacting genes: ADAM15 ARHGAP32 BCAR1 FBXO7 FLNA FLNB FLNC INVS KHDRBS1 NPHP3 NPHP4 PAK2 PTK2B TNK2 TUBB UBQLN4	2 interacting genes: ATXN1 NPHP1
Entrez ID		4867	27031
HPRD ID		09524	06417
Ensembl ID		ENSG00000144061	ENSG00000113971
Uniprot IDs		B4DQY0 C9JNM7 O15259	Q7Z494
PDB IDs		1S1N 6O1Q	5L7K
Enriched GO Terms of Interacting Partners?
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