Incidental Mutation 'R5455:Ppil6'
ID 432720
Institutional Source Beutler Lab
Gene Symbol Ppil6
Ensembl Gene ENSMUSG00000078451
Gene Name peptidylprolyl isomerase (cyclophilin)-like 6
Synonyms 2900084F20Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R5455 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 41366435-41390282 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 41374541 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 141 (T141A)
Ref Sequence ENSEMBL: ENSMUSP00000101146 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105507]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000105507
AA Change: T141A

PolyPhen 2 Score 0.147 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000101146
Gene: ENSMUSG00000078451
AA Change: T141A

DomainStartEndE-ValueType
low complexity region 20 33 N/A INTRINSIC
Pfam:Pro_isomerase 147 310 1.3e-41 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214145
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215608
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrf1 T A 17: 43,632,034 (GRCm39) probably null Het
Ascc3 T C 10: 50,725,679 (GRCm39) V2134A probably benign Het
Cct6b T G 11: 82,645,943 (GRCm39) I80L probably benign Het
Cfap20dc A T 14: 8,536,516 (GRCm38) probably null Het
Crebbp C A 16: 3,903,831 (GRCm39) V1765L probably benign Het
Cul9 C T 17: 46,821,772 (GRCm39) probably null Het
Cyp2c40 A G 19: 39,792,236 (GRCm39) I236T possibly damaging Het
Dbndd2 C A 2: 164,332,113 (GRCm39) T112K possibly damaging Het
Dmrtc2 A C 7: 24,571,916 (GRCm39) S4R probably benign Het
Dnah6 C T 6: 73,052,717 (GRCm39) V2988I probably benign Het
Dnajb12 GC G 10: 59,728,574 (GRCm39) probably null Het
Ercc3 T C 18: 32,400,262 (GRCm39) S705P possibly damaging Het
Gm10306 T G 4: 94,445,077 (GRCm39) probably benign Het
H2-Q6 T C 17: 35,643,860 (GRCm39) L3P unknown Het
Kcnn4 T C 7: 24,076,978 (GRCm39) S176P probably damaging Het
Maml2 T A 9: 13,617,039 (GRCm39) Y128* probably null Het
Map2 G A 1: 66,438,550 (GRCm39) E25K probably damaging Het
Morc2b T A 17: 33,357,584 (GRCm39) M63L probably benign Het
Mthfd1 A G 12: 76,348,062 (GRCm39) I569V probably benign Het
Myh8 G A 11: 67,192,244 (GRCm39) R1399H possibly damaging Het
Nop2 T C 6: 125,117,606 (GRCm39) I424T probably benign Het
Olfm5 T C 7: 103,803,669 (GRCm39) R265G probably damaging Het
Opalin T C 19: 41,058,392 (GRCm39) T14A probably benign Het
Or10j7 A G 1: 173,011,818 (GRCm39) F61S probably damaging Het
Or7a36 C T 10: 78,820,371 (GRCm39) S249F possibly damaging Het
Pced1b C A 15: 97,282,274 (GRCm39) S104R probably benign Het
Pdia2 T G 17: 26,416,137 (GRCm39) Q310P probably null Het
Prrc2b A G 2: 32,111,355 (GRCm39) probably null Het
Stxbp5 A G 10: 9,684,252 (GRCm39) S573P probably benign Het
Synpo2l C A 14: 20,712,360 (GRCm39) A87S probably damaging Het
Tor1b GGACG GG 2: 30,846,957 (GRCm39) probably benign Het
Vmn1r89 A T 7: 12,954,194 (GRCm39) H121L probably benign Het
Vmn2r99 T A 17: 19,614,408 (GRCm39) C709* probably null Het
Vstm4 A G 14: 32,585,835 (GRCm39) H134R possibly damaging Het
Zan C T 5: 137,452,262 (GRCm39) C1569Y unknown Het
Zdhhc13 A G 7: 48,455,323 (GRCm39) T122A possibly damaging Het
Zpbp2 G T 11: 98,448,429 (GRCm39) V249L probably benign Het
Other mutations in Ppil6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01110:Ppil6 APN 10 41,374,406 (GRCm39) missense probably benign 0.00
IGL01453:Ppil6 APN 10 41,374,473 (GRCm39) missense probably benign
IGL02964:Ppil6 APN 10 41,383,479 (GRCm39) missense probably benign 0.13
R0827:Ppil6 UTSW 10 41,370,500 (GRCm39) unclassified probably benign
R1661:Ppil6 UTSW 10 41,390,176 (GRCm39) missense probably benign 0.03
R2302:Ppil6 UTSW 10 41,377,795 (GRCm39) missense probably damaging 1.00
R2844:Ppil6 UTSW 10 41,377,689 (GRCm39) splice site probably benign
R4258:Ppil6 UTSW 10 41,383,531 (GRCm39) nonsense probably null
R5098:Ppil6 UTSW 10 41,366,616 (GRCm39) missense probably null 1.00
R5530:Ppil6 UTSW 10 41,383,494 (GRCm39) missense probably damaging 1.00
R6683:Ppil6 UTSW 10 41,374,427 (GRCm39) missense probably benign
R7288:Ppil6 UTSW 10 41,374,524 (GRCm39) missense probably benign 0.03
R7843:Ppil6 UTSW 10 41,377,862 (GRCm39) missense probably benign
R9424:Ppil6 UTSW 10 41,379,024 (GRCm39) missense probably damaging 1.00
R9590:Ppil6 UTSW 10 41,366,478 (GRCm39) start codon destroyed probably null 0.95
R9630:Ppil6 UTSW 10 41,370,550 (GRCm39) missense probably benign 0.26
Predicted Primers PCR Primer
(F):5'- TGAAACCTGGGTCTATTCCTCC -3'
(R):5'- CAGTAGCTCTCACGTAGCTG -3'

Sequencing Primer
(F):5'- AAACCTGGGTCTATTCCTCCTATGTG -3'
(R):5'- ATACAGGCCTGATGACCTGAGTTC -3'
Posted On 2016-10-06