Prph2 - peripherin 2 Gene

Also Known as Rds; RSRDS

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 25534

Summary

Predicted to enable protein homodimerization activity. Involved in response to low light intensity stimulus. Predicted to be located in photoreceptor outer segment. Predicted to be integral component of plasma membrane. Biomarker of retinal disease. Human ortholog(s) of this gene implicated in Leber congenital amaurosis; eye degenerative disease (multiple); and fundus albipunctatus. Orthologous to human PRPH2 (peripherin 2). [provided by Alliance of Genome Resources, Apr 2022]

Prph2 Products (1)

mRNA Protein Name
NM_013021.2 NP_037153.1 peripherin-2

Gene Ontology

  • Biological Process
Biological Process GO Annotation Evidence References Source
involved in response to low light intensity stimulus IEP
IEP: Inferred from expression pattern
8320859 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

peripherin-2

  • retinal degeneration slow protein

  • retinal degeneration, slow

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS11218 PRPH2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Prph2 NCBI NCBI:5961