Name

RPGRIP1 Gene

retinitis pigmentosa GTPase regulator interacting protein 1

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. [provided by RefSeq, Oct 2008]

RPGRIP1L Gene

RPGRIP1-like

The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

rpgrip1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term rpgrip1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

RPGRIP1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for RPGRIP1 from the Pathway Commons Protein-Protein Interactions dataset.

rpgrip1l Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term rpgrip1l in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

RPGRIP1L Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for RPGRIP1L from the Pathway Commons Protein-Protein Interactions dataset.