|Institutional Source||Beutler Lab|
|Gene Name||polyribonucleotide nucleotidyltransferase 1|
|Synonyms||PNPase, polynucleotide phosphorylase, 1200003F12Rik|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||PIT4651001 (G1)|
|Chromosomal Location||29130744-29161828 bp(+) (GRCm38)|
|Type of Mutation||critical splice donor site (2 bp from exon)|
|DNA Base Change (assembly)||T to C at 29156945 bp|
|Amino Acid Change|
|Ref Sequence||ENSEMBL: ENSMUSP00000020756 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000020756]|
|PDB Structure||Solution structure of the alpha-helical domain from mouse hypothetical PNPase [SOLUTION NMR]|
|Predicted Effect||probably null
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the evolutionary conserved polynucleotide phosphorylase family comprised of phosphate dependent 3'-to-5' exoribonucleases implicated in RNA processing and degradation. This enzyme is predominantly localized in the mitochondrial intermembrane space and is involved in import of RNA to mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70. Related pseudogenes are found on chromosomes 3 and 7. [provided by RefSeq, Dec 2012]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic lethality and impaired mitochondrial RNA import. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Pnpt1||
(F):5'- CAATTGTTTTGAGGCCCCTC -3'
(R):5'- GTCTTTTAAAAGTGAGCCCATTGC -3'
(F):5'- AGTCACCTTTGGCAATGAGATTG -3'
(R):5'- GCCCATTGCTTACTTGTAATTACCTG -3'