Incidental Mutation 'R4387:Rpl7a-ps3'
ID 326284
Institutional Source Beutler Lab
Gene Symbol Rpl7a-ps3
Ensembl Gene ENSMUSG00000068579
Gene Name ribosomal protein L7A, pseudogene 3
Synonyms Gm5044
MMRRC Submission 041681-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4387 (G1)
Quality Score 186
Status Not validated
Chromosome 15
Chromosomal Location 36308295-36309090 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 36308429 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000087632 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090170]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000090170
SMART Domains Protein: ENSMUSP00000087632
Gene: ENSMUSG00000068579

DomainStartEndE-ValueType
low complexity region 4 32 N/A INTRINSIC
Pfam:Ribosomal_L7Ae 126 220 1.6e-25 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik T A 13: 77,464,693 (GRCm39) probably null Het
Adprm C T 11: 66,929,019 (GRCm39) R324K probably benign Het
Brd10 A G 19: 29,782,715 (GRCm39) probably benign Het
Calcr T A 6: 3,707,581 (GRCm39) N240Y probably damaging Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Cd209b A G 8: 3,975,960 (GRCm39) L67P probably damaging Het
Cp T C 3: 20,031,366 (GRCm39) V601A probably damaging Het
Cyp2a5 A G 7: 26,540,479 (GRCm39) D364G probably damaging Het
Eno4 T A 19: 58,941,640 (GRCm39) V187D probably benign Het
Fbxl7 C A 15: 26,543,345 (GRCm39) S434I probably damaging Het
Fbxw24 A T 9: 109,439,053 (GRCm39) L174Q probably damaging Het
Fryl T A 5: 73,243,903 (GRCm39) R91S possibly damaging Het
Gabrd A G 4: 155,473,389 (GRCm39) probably null Het
Gtpbp2 A G 17: 46,477,284 (GRCm39) D383G probably benign Het
Igf1r A G 7: 67,819,757 (GRCm39) I356V probably benign Het
Kcnc1 C A 7: 46,047,126 (GRCm39) R9S possibly damaging Het
Lipi T A 16: 75,370,843 (GRCm39) I125F probably damaging Het
Meig1 T C 2: 3,410,278 (GRCm39) E74G probably damaging Het
Mgat4d A T 8: 84,098,335 (GRCm39) Q366L probably damaging Het
Mrpl1 A G 5: 96,386,778 (GRCm39) N256D possibly damaging Het
Nlrp4e A G 7: 23,000,902 (GRCm39) K66E probably benign Het
Nlrp4e A G 7: 23,020,652 (GRCm39) I380V probably benign Het
Nphp3 A G 9: 103,907,219 (GRCm39) T740A possibly damaging Het
Or5an1c A G 19: 12,218,503 (GRCm39) V174A probably damaging Het
Or8k33 T C 2: 86,384,298 (GRCm39) T57A probably damaging Het
Or8k40 T A 2: 86,584,464 (GRCm39) D206V probably benign Het
Pde5a T C 3: 122,523,001 (GRCm39) I36T probably benign Het
Pign A T 1: 105,449,785 (GRCm39) L914M possibly damaging Het
Ppm1b A G 17: 85,322,847 (GRCm39) D382G probably benign Het
Psd3 T C 8: 68,453,413 (GRCm39) Y282C probably damaging Het
Ptprt A T 2: 161,769,570 (GRCm39) Y432N probably damaging Het
Rbbp6 T C 7: 122,596,534 (GRCm39) probably null Het
Recql4 A G 15: 76,590,158 (GRCm39) S659P probably benign Het
Shoc1 A T 4: 59,060,915 (GRCm39) C953S possibly damaging Het
Slit3 T C 11: 35,574,875 (GRCm39) V1063A probably benign Het
Spdye4a A G 5: 143,211,378 (GRCm39) V62A probably benign Het
Ttc6 G A 12: 57,689,836 (GRCm39) G509S probably benign Het
Ush2a C T 1: 188,175,628 (GRCm39) T1242M probably benign Het
Wwc2 T C 8: 48,284,681 (GRCm39) S1155G unknown Het
Zfp551 A T 7: 12,152,568 (GRCm39) I55N probably damaging Het
Other mutations in Rpl7a-ps3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1659:Rpl7a-ps3 UTSW 15 36,308,309 (GRCm39) exon noncoding transcript
R3623:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
R4350:Rpl7a-ps3 UTSW 15 36,308,283 (GRCm39) unclassified noncoding transcript
R4389:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
R4486:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GGCAACTTTCTTATGAAGTTCAGTG -3'
(R):5'- TAGACCCCATTGAGCTGGTG -3'

Sequencing Primer
(F):5'- TCAGTGTGTGTCCAGCAGC -3'
(R):5'- CCATTGAGCTGGTGGTTTTCCTAC -3'
Posted On 2015-07-06