Incidental Mutation 'R0830:Exosc7'
ID77497
Institutional Source Beutler Lab
Gene Symbol Exosc7
Ensembl Gene ENSMUSG00000025785
Gene Nameexosome component 7
Synonyms2610002K22Rik
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.964) question?
Stock #R0830 (G1)
Quality Score225
Status Not validated
Chromosome9
Chromosomal Location123113215-123136129 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 123119293 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Proline at position 93 (L93P)
Ref Sequence ENSEMBL: ENSMUSP00000150152 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026891] [ENSMUST00000215377]
Predicted Effect probably benign
Transcript: ENSMUST00000026891
AA Change: L71P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000026891
Gene: ENSMUSG00000025785
AA Change: L71P

DomainStartEndE-ValueType
Pfam:RNase_PH 31 166 5.8e-27 PFAM
Pfam:RNase_PH_C 196 262 1.4e-14 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159376
Predicted Effect probably benign
Transcript: ENSMUST00000215377
AA Change: L93P

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215590
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216412
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.0%
  • 20x: 90.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700056E22Rik C T 1: 184,033,427 R145H probably damaging Het
2410089E03Rik T A 15: 8,247,185 V2771E unknown Het
Adam26a C T 8: 43,568,402 V684I probably benign Het
Alk T C 17: 72,603,200 I170M probably benign Het
Apc2 T C 10: 80,315,405 Y2069H probably damaging Het
Aspm A G 1: 139,474,254 T1219A probably damaging Het
Bnip1 T C 17: 26,789,705 S94P probably benign Het
Cftr A G 6: 18,270,225 I805V probably benign Het
Col25a1 T A 3: 130,584,726 D609E probably damaging Het
Cyp2g1 A G 7: 26,814,791 K274R probably benign Het
D5Ertd579e G A 5: 36,613,757 T1098I probably damaging Het
Ddx39 T A 8: 83,719,823 C74S possibly damaging Het
E2f3 C T 13: 29,985,560 A37T probably benign Het
Emilin2 A G 17: 71,273,820 M637T probably benign Het
F2 T C 2: 91,630,200 E316G probably benign Het
Fat4 A C 3: 38,999,109 Q4084P probably benign Het
Flywch1 T C 17: 23,762,370 K160E probably benign Het
Foxi2 A G 7: 135,411,730 T230A probably benign Het
Fthl17a A G X: 85,270,073 N154S possibly damaging Het
Hykk G A 9: 54,937,317 R222Q probably damaging Het
Il18rap T A 1: 40,542,990 V357E probably damaging Het
Ing4 A G 6: 125,043,960 E15G probably damaging Het
Irak1 T C X: 74,016,583 D679G probably damaging Het
Itga1 T C 13: 115,007,032 E321G probably benign Het
Kdelc2 T G 9: 53,390,711 L32R probably damaging Het
Nudt1 T A 5: 140,335,321 probably null Het
Nupl1 A G 14: 60,243,482 F138S probably damaging Het
Olfr122 A T 17: 37,771,913 M87L probably damaging Het
Olfr448 G T 6: 42,896,598 W49L probably benign Het
Pllp T C 8: 94,679,475 Y60C probably damaging Het
Pnpla7 T C 2: 24,997,255 V37A probably damaging Het
Psme4 A G 11: 30,807,797 H310R possibly damaging Het
Rasl10b G A 11: 83,417,839 probably null Het
Sash1 C T 10: 8,729,909 V906M probably benign Het
Scn1a A T 2: 66,299,784 I1212K probably damaging Het
Stbd1 A T 5: 92,605,130 S160C probably benign Het
Tex29 T C 8: 11,854,157 V99A probably benign Het
Tg A T 15: 66,725,144 N79I probably damaging Het
Tie1 T C 4: 118,482,663 D389G probably damaging Het
Vmn1r178 A G 7: 23,894,027 T167A possibly damaging Het
Xkr4 C T 1: 3,670,745 G202S possibly damaging Het
Other mutations in Exosc7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01936:Exosc7 APN 9 123135891 splice site probably benign
R0029:Exosc7 UTSW 9 123119237 splice site probably benign
R0029:Exosc7 UTSW 9 123119237 splice site probably benign
R0268:Exosc7 UTSW 9 123118960 missense probably benign 0.08
R0319:Exosc7 UTSW 9 123130960 unclassified probably benign
R1593:Exosc7 UTSW 9 123131993 missense probably benign
R5388:Exosc7 UTSW 9 123118907 missense probably damaging 1.00
R6534:Exosc7 UTSW 9 123132012 missense probably benign 0.09
R6886:Exosc7 UTSW 9 123135958 missense probably benign 0.04
R7313:Exosc7 UTSW 9 123118948 missense probably benign 0.43
R7833:Exosc7 UTSW 9 123130919 missense probably benign
R7916:Exosc7 UTSW 9 123130919 missense probably benign
R8313:Exosc7 UTSW 9 123127877 missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- CCAAGCCATACGGGGAGAATACATC -3'
(R):5'- GCAAGCATCAGGCGATTAAAACCAG -3'

Sequencing Primer
(F):5'- GGGAGAATACATCTTTCCAGACC -3'
(R):5'- GCCTGGTGAGTAAATACCTCCTG -3'
Posted On2013-10-16