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IQCB1 encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. Additionally we are shipping IQ Motif Containing B1 Proteins (3) and and many more products for this protein.
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Nphp5(-/-) photoreceptor degeneration was complete at 1 mo of age but was delayed significantly in Nphp5(-/-);Nrl(-/-) (cone only) retina
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290 (show CEP290 Antibodies)) blindness: generation of an all-cone Nphp6 (show CEP290 Antibodies) hypomorph mouse that mimics the human retinal ciliopathy.
Study demonstrates the interaction between CNNM4 (show CNNM4 Antibodies) and IQCB1, which provides the first link between CNNM4 (show CNNM4 Antibodies) and IQCB1 that causes Leber congenital amaurosis and retinal dystrophy (show MERTK Antibodies) when mutated, providing important insights into the molecular pathogenic mechanisms of retinal dystrophy (show MERTK Antibodies) in Jalili syndrome.
that nephrocystin-5 is essential for photoreceptor outer segment formation
Dynamic ubiquitination and deubiquitination of NPHP5 plays a crucial role in the regulation of ciliogenesis. NPHP5 directly binds to a deubiquitinating enzyme USP9X/FAM and two E3 ubiquitin ligases BBS11/TRIM32 and MARCH7/axotrophin.
NPHP5-mutant dogs recapitulate the human phenotype of very early loss of rods, and relative retention of the central retinal cone photoreceptors that lack function.
NPHP5 and Cep290 (show CEP290 Antibodies) regulate BBSome integrity, ciliary trafficking and cargo delivery.
High-throughput mutation analysis identified a homozygous truncating mutation (c.1504C>T, p.R502*) in the NPHP5 in 5 families in Iranian children with nephronophthisis.
mutation is predicted to introduce a new open reading frame that results in the truncation of the C-terminal 235 amino acids of nephrocystin-5 and its consequent loss of function
NPHP5 mutations impair protein interaction with Cep290 (show CEP290 Antibodies) and localize to centrosomes, thereby compromising cilia formation.
in a set of consanguineous patient families with Leber congenital amaurosis study identified five putative disease-causing mutations, including four novel alleles, in six families; These five mutations are located in four genes, ALMS1 (show ALMS1 Antibodies), IQCB1, CNGA3 (show CNGA3 Antibodies), and MYO7A (show MYO7A Antibodies)
Data show that the minor allele (N) of I393N in IQCB1 and the common allele (R) of R744Q in RPGRIP1L (show RPGRIP1L Antibodies) were associated with severe disease in XlRP with RPGR (show RPGR Antibodies) mutations.
This gene encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. The encoded protein has a central coiled-coil region and two calmodulin-binding IQ domains. It is localized to the primary cilia of renal epithelial cells and connecting cilia of photoreceptor cells. The protein is thought to play a role in ciliary function. Defects in this gene result in Senior-Loken syndrome type 5. Alternative splicing results in multiple transcript variants.
IQ calmodulin-binding motif containing 1
, IQ calmodulin-binding motif-containing protein 1
, IQ motif containing B1
, nephrocystin 5
, IQ calmodulin-binding motif-containing protein 1-like
, p53 and DNA damage-regulated IQ motif protein