RP9

RP9
Identifiers
Aliases	RP9, PAP-1, PAP1, retinitis pigmentosa 9 (autosomal dominant), pre-mRNA splicing factor, RP9 pre-mRNA splicing factor
External IDs	OMIM: 607331; MGI: 2157166; HomoloGene: 10290; GeneCards: RP9; OMA:RP9 - orthologs
Gene location (Human)
Chr.	Chromosome 7 (human)
End	33,109,405 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	22,381,039 bp
RNA expression pattern
	Top expressed in
	oocyte; ; myocardium of left ventricle; ; muscle of thigh; ; secondary oocyte; ; Skeletal muscle tissue of rectus abdominis; ; apex of heart; ; gastrocnemius muscle; ; body of tongue; ; pylorus; ; sural nerve;
	Top expressed in
	lacrimal gland; ; Paneth cell; ; seminiferous tubule; ; parotid gland; ; motor neuron; ; vestibular membrane of cochlear duct; ; granulocyte; ; digastric muscle; ; yolk sac; ; migratory enteric neural crest cell;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; metal ion binding; RNA binding;
Cellular component	signal recognition particle receptor complex; nucleus; cytosol;
Biological process	cognition; RNA splicing;
	Sources:Amigo / QuickGO
Orthologs
	6100
	55934
	ENSG00000164610
	ENSMUSG00000032239
	Q8TA86
	P97762
	NM_203288
	NM_018739
	NP_976033
	NP_061209
	Wikidata
View/Edit Human	View/Edit Mouse

Retinitis pigmentosa 9 (autosomal dominant), also known as RP9 or PAP-1, is a protein which in humans is encoded by the RP9 gene.