RPP30

10556

RPP30

Identifiers

RPP30, TSG15, ribonuclease P/MRP subunit p30

External IDs

OMIM: 606115; MGI: 1859683; GeneCards: RPP30

Gene location (Human)

Chr.	Chromosome 10 (human)^[1]

Band	10q23.31	Start	90,871,952 bp^[1]
Band	10q23.31	End	90,908,553 bp^[1]

Gene location (Mouse)

Chr.	Chromosome 19 (mouse)^[2]

Band	19\|19 C2	Start	36,061,116 bp^[2]
Band	19\|19 C2	End	36,082,177 bp^[2]

RNA expression pattern

Human

Mouse (ortholog)

Top expressed in

gonad

ventricular zone

ganglionic eminence

right testis

left testis

muscle of thigh

testicle

Achilles tendon

islet of Langerhans

gastric mucosa

Top expressed in

spermatocyte

spermatid

medial ganglionic eminence

fetal liver hematopoietic progenitor cell

morula

otic placode

primitive streak

endothelial cell of lymphatic vessel

embryo

embryo

More reference expression data


More reference expression data

Gene ontology
Molecular function	ribonuclease activity protein binding catalytic activity hydrolase activity RNA binding ribonuclease P activity
Cellular component	nucleolus nucleus nucleolar ribonuclease P complex nucleoplasm ribonuclease MRP complex multimeric ribonuclease P complex
Biological process	rRNA processing tRNA processing RNA phosphodiester bond hydrolysis, endonucleolytic tRNA 5'-leader removal RNA phosphodiester bond hydrolysis
Sources:Amigo / QuickGO

Databases

NCBI: entry; OMA: entry

Species

Human

Mouse


10556


54364


ENSG00000148688


ENSMUSG00000024800


P78346


O88796

RefSeq (mRNA)


NM_001104546 NM_006413


NM_019428

RefSeq (protein)


NP_001098016 NP_006404


NP_062301

Location (UCSC)

Chr 10: 90.87 – 90.91 Mb

Chr 19: 36.06 – 36.08 Mb

PubMed search

^[3]

^[4]

View/Edit Human

View/Edit Mouse

Ribonuclease P protein subunit p30 is an enzyme that in humans is encoded by the RPP30 gene.^[5]^[6]^[7]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000148688 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000024800 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Eder PS, Kekuda R, Stolc V, Altman S (Mar 1997). "Characterization of two scleroderma autoimmune antigens that copurify with human ribonuclease P". Proc Natl Acad Sci U S A. 94 (4): 1101–6. Bibcode:1997PNAS...94.1101E. doi:10.1073/pnas.94.4.1101. PMC 19751. PMID 9037013.
^ Stolc V, Altman S (Oct 1997). "Rpp1, an essential protein subunit of nuclear RNase P required for processing of precursor tRNA and 35S precursor rRNA in Saccharomyces cerevisiae". Genes Dev. 11 (18): 2414–25. doi:10.1101/gad.11.18.2414. PMC 316520. PMID 9308968.
^ "Entrez Gene: RPP30 ribonuclease P/MRP 30kDa subunit".

Further reading

Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Jarrous N, Eder PS, Guerrier-Takada C, et al. (1998). "Autoantigenic properties of some protein subunits of catalytically active complexes of human ribonuclease P". RNA. 4 (4): 407–17. PMC 1369627. PMID 9630247.
Jiang T, Guerrier-Takada C, Altman S (2001). "Protein-RNA interactions in the subunits of human nuclear RNase P". RNA. 7 (7): 937–41. doi:10.1017/S1355838201010299. PMC 1370153. PMID 11455963.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Welting TJ, van Venrooij WJ, Pruijn GJ (2004). "Mutual interactions between subunits of the human RNase MRP ribonucleoprotein complex". Nucleic Acids Res. 32 (7): 2138–46. doi:10.1093/nar/gkh539. PMC 407822. PMID 15096576.
Deloukas P, Earthrowl ME, Grafham DV, et al. (2004). "The DNA sequence and comparative analysis of human chromosome 10". Nature. 429 (6990): 375–81. Bibcode:2004Natur.429..375D. doi:10.1038/nature02462. PMID 15164054.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Andersen JS, Lam YW, Leung AK, et al. (2005). "Nucleolar proteome dynamics". Nature. 433 (7021): 77–83. Bibcode:2005Natur.433...77A. doi:10.1038/nature03207. PMID 15635413. S2CID 4344740.
Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
Wimplinger I, Morleo M, Rosenberger G, et al. (2006). "Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome". Am. J. Hum. Genet. 79 (5): 878–89. doi:10.1086/508474. PMC 1698567. PMID 17033964.
Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983. S2CID 7827573.

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