Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
RPGRIP1 encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Additionally we are shipping Retinitis Pigmentosa GTPase Regulator Interacting Protein 1 Antibodies (28) and Retinitis Pigmentosa GTPase Regulator Interacting Protein 1 Proteins (3) and many more products for this protein.
Showing 3 out of 4 products:
RPGRIP1 has an essential role in the photoreceptor connecting cilia, and photoreceptors lacking RPGRIP1 are unable to maintain the light sensing outer segments. [review]
SPATA7 (show SPATA7 ELISA Kits) plays a role in RPGRIP1-mediated protein trafficking across the connecting cilium of photoreceptor cells. Apoptotic degeneration of these cells triggered by protein mislocalization is a mechanism of disease progression in LCA3 (show SPATA7 ELISA Kits)/juvenile RP patients
Although the present patients did not show sufficient clinical findings as Leber congenital amaurosis (LCA (show CLTA ELISA Kits)), PCR findings and direct sequencing following microarray analysis confirmed that they were LCA (show CLTA ELISA Kits).
Neurodevelopmental delay is a potential feature of strictly defined LCA, documented in our series for some children with homozygous RPGRIP1 and GUCY2D mutations.
We report a novel RPGRIP1 mutation causing LCA (show CLTA ELISA Kits) in a consanguineous Emirati family. To the best of our knowledge, this alteration has not been described in the literature so far.
Recessive RPGRIP1 mutations cause a severe cone-rod Leber congenital amaurosis phenotype, often with poor or no fixation and an oculodigital sign. In the first decade of life retinal changes are clinically most evident in the periphery.
RPGRIP1 in human and in canine model involves protein network and photoreceptor cilia.
Nek4 interaction with both RPGRIP1 and the RPGRIP1L (show RPGRIP1L ELISA Kits) is involved in cilium assembly.
heterozygous non-synonymous variants of RPGRIP1 may cause or increase the susceptibility to various forms of glaucoma
Studies highlight the recent developments in understanding the mechanism of cilia-dependent photoreceptor degeneration due to mutations in RPGR (show RPGR ELISA Kits) and PGR (show PGR ELISA Kits)-interacting proteins in severe genetic diseases.
RPGRIP1 loss in photoreceptors shifts the subcellular partitioning of SDCCAG8 (show SDCCAG8 ELISA Kits) and NPHP4 (show NPHP4 ELISA Kits) to the membrane fraction associated to the endoplasmic reticulum.
RPGRIP1 is essential for rod photoreceptor outer segment morphogenesis.
RPGRIP1 and nephrocystin-4 (show NPHP4 ELISA Kits) interact strongly in vitro and in vivo, and that they colocalize in the retina
RPGR (show RPGR ELISA Kits) and RPGRIP isoforms are distributed and co-localized at restricted foci throughout the outer segments of human and bovine, but not mice rod photoreceptors.
This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness.
retinitis pigmentosa GTPase regulator interacting protein 1
, X-linked retinitis pigmentosa GTPase regulator-interacting protein 1-like
, x-linked retinitis pigmentosa GTPase regulator-interacting protein 1-like
, RPGR-interacting protein 1
, X-linked retinitis pigmentosa GTPase regulator-interacting protein 1