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Nephronophthisis 1 (Juvenile) Proteins (NPHP1)

NPHP1 encodes a protein with src homology domain 3 (SH3) patterns. Additionally we are shipping NPHP1 Antibodies (36) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
NPHP1 4867 O15259
Rat NPHP1 NPHP1 296136  
NPHP1 53885 Q9QY53
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Top NPHP1 Proteins at

Showing 5 out of 6 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific pu... 1 mg Log in to see 39 to 44 Days
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific pu... 1 mg Log in to see 39 to 44 Days
HOST_Escherichia coli (E. coli) Human GST tag 50 μg Log in to see 21 to 26 Days
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
HOST_Escherichia coli (E. coli) Human Un-conjugated   50 μg Log in to see 16 to 21 Days

NPHP1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
Mouse (Murine)

More Proteins for Nephronophthisis 1 (Juvenile) (NPHP1) Interaction Partners

Human Nephronophthisis 1 (Juvenile) (NPHP1) interaction partners

  1. dynamic genomic rearrangements occurred historically within the NPHP1 locus and generated SV haplotypes observed in the human population today, which may confer differential susceptibility to genomic instability and the NPHP1 deletion

  2. We report the unexpectedly common retinal involvement of NPHP type 1 with an additional MALL (show Mall Proteins) deletion in a Korean cohort.

  3. A homozygous deletion was identified in the NPHP1 gene spanning at least from exon 5 to exon 20 in two families in Iranian children with nephronophthisis.

  4. These results suggest that NPHP1 mutations are probably rare primary causes of Bardet-Biedl syndrome that contribute to the mutational burden of the disorder.

  5. NPHP1 genetic testing is important to diagnose patients with nephronophthisis, familial juvenile disease.

  6. Congenital ocular motor apraxia and Joubert syndrome found to have a compound heterozygous mutation in the NPHP1 gene that is responsible for juvenile nephronophthisis type 1.

  7. Prevalence and incidence estimation of large NPHP1 homozygous deletion in Tunisian patients with clinical pictures of tubulo-interstitiel kidney disorder and chronic renal failure.

  8. Report NPHP1 mutations in nephronophthisis and associated ciliopathies and Joubert syndrome-related disorders.

  9. Plk1 colocalizes with nephrocystin-1 and induces it's phosphorylation in the transition zone of primary cilia in epithelial cells.

  10. NPHP1 deletion analysis should always be considered in patients with apparently dominant nephronophthisis.

Mouse (Murine) Nephronophthisis 1 (Juvenile) (NPHP1) interaction partners

  1. PC-1 (show PCSK1 Proteins) polyproline motif interacts with the SH3 domain of NPHP1.

  2. casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to cilia

  3. homozygous Nphp1 mutant mice were viable without renal manifestations of nephronophthisis, but males were infertile with oligoteratozoospermia

  4. Nphp1 affect the sorting mechanism and transportation efficiency of the traffic machinery between inner and outer segments of photoreceptors.

  5. Nphp1 is most abundantly expressed in tissues rich in highly ciliated cells, such as olfactory sensory neurons, and is predicted to be important to cilia.

NPHP1 Protein Profile

Protein Summary

This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with NPHP1

  • nephronophthisis 1 (juvenile) (NPHP1)
  • nephronophthisis 1 (juvenile) (LOC100221020)
  • nephronophthisis 1 (juvenile) (LOC100227206)
  • nephronophthisis 1 (nphp1)
  • nephronophthisis 1 (juvenile) (Nphp1)
  • nephronophthisis 1 (juvenile) (nphp1)
  • nephronophthisis 1 (juvenile) homolog (human) (Nphp1)
  • im:7162391 protein
  • JBTS4 protein
  • nephrocystin-1 protein
  • NPH1 protein
  • NPHP1 protein
  • SLSN1 protein
  • wu:fi59g07 protein
  • zgc:152930 protein

Protein level used designations for NPHP1

nephronophthisis 1 (juvenile) , nephrocystin , nephrocystin-1-like , nephrocystin-1 , juvenile nephronophthisis 1 protein , nephrocystin 1 , nephronophthisis 1 (juvenile) homolog , nephrocystin1

459483 Pan troglodytes
696218 Macaca mulatta
100033209 Monodelphis domestica
100051808 Equus caballus
100221020 Taeniopygia guttata
100227206 Taeniopygia guttata
100437705 Pongo abelii
100523176 Sus scrofa
100595925 Nomascus leucogenys
100002391 Danio rerio
4867 Homo sapiens
296136 Rattus norvegicus
432293 Xenopus laevis
421223 Gallus gallus
403780 Canis lupus familiaris
505421 Bos taurus
53885 Mus musculus
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