Prr13 proline rich 13 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Prr13provided by RGD
Official Full Name: proline rich 13provided by RGD
Primary source: RGD:1307129
See related: EnsemblRapid:ENSRNOG00000042094 AllianceGenome:RGD:1307129
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: RGD1307129
Summary: Predicted to be located in cytosol. Predicted to be active in nucleoplasm. Orthologous to human PRR13 (proline rich 13). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Thymus (RPKM 181.8), Spleen (RPKM 174.5) and 9 other tissues See more
Orthologs: human mouse all
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Genomic context

Location:: 7q36

Exon count:: 4

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	7	NC_086025.1 (135471040..135474344)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	7	NC_051342.1 (133592511..133595817)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	7	NC_005106.4 (144064931..144068235)

Chromosome 7 - NC_086025.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

RH129196 (e-PCR)
- UniSTS:212504

RH128296 (e-PCR)
- UniSTS:211604

d7rat114 (e-PCR)
- UniSTS:122308

Gene Ontology Provided by RGD

Component	Evidence Code	Pubs
located_in cytosol	ISO Inferred from Sequence Orthology more info
is_active_in nucleoplasm	IBA Inferred from Biological aspect of Ancestor more info
located_in nucleoplasm	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: proline-rich protein 13

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.