Gene Symbol | Pnpt1 |
Entrez Gene ID | 360992 |
Full Name | polyribonucleotide nucleotidyltransferase 1 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
ORF » Species Summary » Rattus norvegicus » Pnpt1 cDNA ORF clone
Gene Symbol | Pnpt1 |
Entrez Gene ID | 360992 |
Full Name | polyribonucleotide nucleotidyltransferase 1 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
mRNA | Protein | Name |
---|---|---|
NM_001142371.1 | NP_001135843.1 | polyribonucleotide nucleotidyltransferase 1, mitochondrial |
Canis lupus familiaris (dog) | PNPT1 | XP_538497.3 |
Bos taurus (cattle) | PNPT1 | NP_001179126.1 |
Drosophila melanogaster (fruit fly) | CG11337 | NP_001097990.2 |
Anopheles gambiae (African malaria mosquito) | AgaP_AGAP010791 | XP_318517.3 |
Homo sapiens (human) | PNPT1 | NP_149100.2 |
PNPT1 | XP_001112421.1 | |
Danio rerio (zebrafish) | pnpt1 | NP_001238761.1 |
Gallus gallus (chicken) | PNPT1 | XP_419282.4 |
Caenorhabditis elegans (roundworm) | BE0003N10.1 | NP_497324.3 |
Xenopus tropicalis (tropical clawed frog) | pnpt1 | NP_001017033.1 |
Pan troglodytes (chimpanzee) | PNPT1 | XP_515490.2 |
Mus musculus (house mouse) | Pnpt1 | NP_082145.1 |
Rattus norvegicus (Norway rat) | Pnpt1 | NP_001135843.1 |
Arabidopsis thaliana (thale cress) | AT5G14580 | NP_196962.1 |
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, N?rnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, N?rnberg P, Hofmann K, Richardson GP, Hammerschmidt M, Moser T, Wollnik B, Koehler CM, Teitell MA, Barakat A, Kubisch C
American journal of human genetics91(5)919-27(2012 Nov)
The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.
Baltz AG, Munschauer M, Schwanh?usser B, Vasile A, Murakawa Y, Schueler M, Youngs N, Penfold-Brown D, Drew K, Milek M, Wyler E, Bonneau R, Selbach M, Dieterich C, Landthaler M
Molecular cell46(5)674-90(2012 Jun)
PNPASE regulates RNA import into mitochondria.
Wang G, Chen HW, Oktay Y, Zhang J, Allen EL, Smith GM, Fan KC, Hong JS, French SW, McCaffery JM, Lightowlers RN, Morse HC 3rd, Koehler CM, Teitell MA
Cell142(3)456-67(2010 Aug)
Human polynucleotide phosphorylase selectively and preferentially degrades microRNA-221 in human melanoma cells.
Das SK, Sokhi UK, Bhutia SK, Azab B, Su ZZ, Sarkar D, Fisher PB
Proceedings of the National Academy of Sciences of the United States of America107(26)11948-53(2010 Jun)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
The following Pnpt1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Pnpt1 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
CloneID | ORa04321 | |
Clone ID Related Accession (Same CDS sequence) | NM_001142371.1 | |
Accession Version | NM_001142371.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 2355bp) Protein sequence SNP |
|
Vector | pcDNA3.1-C-(k)DYK or customized vector | User Manual |
Clone information | Clone Map | MSDS |
Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
ORF Insert Method | CloneEZ™ Seamless cloning technology | |
Insert Structure | linear | |
Update Date | 2019-10-09 | |
Organism | Rattus norvegicus(Norway rat) | |
Product | polyribonucleotide nucleotidyltransferase 1, mitochondrial | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from AABR07016754.1. On Nov 29, 2008 this sequence version replaced XM_341266.3. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## RNAseq introns :: single sample supports all introns SAMD00052296, SAMD00052297 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## gene product(s) localized to mito. :: inferred from homology ##RefSeq-Attributes-END## |
1 | ATGGCGGCTT GCAGGCCGTG CTGCTTGTGC CTGTGTCTCC GACCGCTGAG CTGCGGTCCC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001135843.1 |
CDS | 11..2365 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001142371.1 |
1 | ATGGCGGCTT GCAGGCCGTG CTGCTTGTGC CTGTGTCTCC GACCGCTGAG CTGCGGTCCC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss. |
The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts. |
PNPASE regulates RNA import into mitochondria. |
Human polynucleotide phosphorylase selectively and preferentially degrades microRNA-221 in human melanoma cells. |