Rpgrip1l - Rpgrip1-like Gene

Also Known as RGD1311099

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 307724

Summary

Predicted to enable thromboxane A2 receptor binding activity. Predicted to be involved in negative regulation of G protein-coupled receptor signaling pathway; non-motile cilium assembly; and retinal rod cell development. Predicted to act upstream of or within several processes, including animal organ development; chordate embryonic development; and embryonic limb morphogenesis. Located in Cytoskeleton and photoreceptor connecting cilium. Human ortholog(s) of this gene implicated in several diseases, including Joubert syndrome 7; Meckel syndrome 5; anencephaly; retinitis pigmentosa 3; and vascular dementia. Orthologous to human RPGRIP1L (RPGRIP1 like). [provided by Alliance of Genome Resources, Apr 2022]

Rpgrip1l Products (1)

mRNA Protein Name
NM_001107414.1 NP_001100884.1 protein fantom

Gene Ontology

  • Cellular Component
Cellular Component GO Annotation Evidence References Source
located in axonemal microtubule IDA
IDA: Inferred from direct assay
17558407 RGD
located in ciliary basal body IDA
IDA: Inferred from direct assay
17558407 RGD
located in ciliary rootlet IDA
IDA: Inferred from direct assay
21685204 RGD
located in ciliary transition zone IDA
IDA: Inferred from direct assay
21685204 RGD
located in photoreceptor connecting cilium IDA
IDA: Inferred from direct assay
17558407 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

protein fantom

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS12156 RPGRIP1L Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Rpgrip1l NCBI NCBI:23322