Incidental Mutation 'R5231:Rpl15-ps6'
ID 398564
Institutional Source Beutler Lab
Gene Symbol Rpl15-ps6
Ensembl Gene ENSMUSG00000057262
Gene Name ribosomal protein L15, pseudogene 6
Synonyms Gm10020
MMRRC Submission 042803-MU
Accession Numbers
Essential gene? Not available question?
Stock # R5231 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 52341013-52341624 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 52341440 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130678 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081993]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000081993
SMART Domains Protein: ENSMUSP00000130678
Gene: ENSMUSG00000057262

DomainStartEndE-ValueType
Pfam:Ribosomal_L15e 2 193 4e-101 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adat3 T C 10: 80,442,260 (GRCm39) S33P possibly damaging Het
Bche G A 3: 73,608,194 (GRCm39) P411S probably benign Het
Chil3 A G 3: 106,063,045 (GRCm39) S182P probably damaging Het
Col6a4 T C 9: 105,902,730 (GRCm39) E1653G probably damaging Het
Csk G T 9: 57,537,661 (GRCm39) H84Q probably damaging Het
Csmd2 A G 4: 128,439,842 (GRCm39) T3099A probably benign Het
Deup1 G T 9: 15,486,495 (GRCm39) A395E probably damaging Het
Frem2 T C 3: 53,429,716 (GRCm39) Y2778C probably damaging Het
Igfn1 T C 1: 135,894,474 (GRCm39) T2031A probably benign Het
Ighv1-53 C A 12: 115,122,225 (GRCm39) S50I probably benign Het
Ighv1-62-3 A T 12: 115,424,671 (GRCm39) M100K possibly damaging Het
Igkv2-109 T A 6: 68,279,429 (GRCm39) F3I probably benign Het
Isl1 T C 13: 116,438,193 (GRCm39) D296G probably benign Het
Klk1b16 T A 7: 43,786,771 (GRCm39) L10Q probably damaging Het
Kmt2c A T 5: 25,520,471 (GRCm39) S1880T possibly damaging Het
Lhcgr T A 17: 89,063,039 (GRCm39) N211I probably damaging Het
Ltb C T 17: 35,414,802 (GRCm39) L201F probably damaging Het
Mfsd2a A G 4: 122,853,094 (GRCm39) F64S possibly damaging Het
Mmp10 T C 9: 7,502,501 (GRCm39) probably null Het
Mycbp2 A C 14: 103,583,650 (GRCm39) probably null Het
Or1e34 C A 11: 73,778,781 (GRCm39) C139F probably damaging Het
Or52e2 A T 7: 102,804,175 (GRCm39) F260I probably damaging Het
Or5k17 T C 16: 58,746,077 (GRCm39) I286V possibly damaging Het
Or9i14 A T 19: 13,792,711 (GRCm39) I81N probably damaging Het
Peg10 C T 6: 4,756,939 (GRCm39) probably benign Het
Plscr1 C A 9: 92,148,784 (GRCm39) P208H probably damaging Het
Rhot1 T C 11: 80,118,160 (GRCm39) probably null Het
Smarcc2 T C 10: 128,297,221 (GRCm39) Y38H probably damaging Het
Spata31e2 T A 1: 26,723,032 (GRCm39) H716L possibly damaging Het
Stat2 T C 10: 128,117,111 (GRCm39) probably null Het
Trip11 T C 12: 101,851,860 (GRCm39) K735E probably damaging Het
Ttll1 T A 15: 83,373,667 (GRCm39) probably null Het
Vmn2r37 C A 7: 9,209,594 (GRCm39) L639F possibly damaging Het
Vmn2r60 A T 7: 41,786,448 (GRCm39) Q417L possibly damaging Het
Vps8 A T 16: 21,395,475 (GRCm39) D1255V probably damaging Het
Zfp354b A C 11: 50,813,917 (GRCm39) I336S probably benign Het
Zfp747l1 T C 7: 126,984,586 (GRCm39) Y172C probably damaging Het
Other mutations in Rpl15-ps6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02367:Rpl15-ps6 APN 15 52,341,368 (GRCm39) exon noncoding transcript
R5080:Rpl15-ps6 UTSW 15 52,341,446 (GRCm39) exon noncoding transcript
R5569:Rpl15-ps6 UTSW 15 52,341,624 (GRCm39) exon noncoding transcript
R6516:Rpl15-ps6 UTSW 15 52,341,200 (GRCm39) exon noncoding transcript
R6640:Rpl15-ps6 UTSW 15 52,341,016 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- ATTCAGGACTCTCAAAGCCC -3'
(R):5'- GAGTTTCTGCCTTGCACGAG -3'

Sequencing Primer
(F):5'- GACTCTCAAAGCCCCACAATGG -3'
(R):5'- TGGGTGCATACAAGTACATCC -3'
Posted On 2016-07-06