Incidental Mutation 'R5860:Oas1e'
ID 453835
Institutional Source Beutler Lab
Gene Symbol Oas1e
Ensembl Gene ENSMUSG00000066867
Gene Name 2'-5' oligoadenylate synthetase 1E
Synonyms 2'-5' oligoadenylate synthetase-like 7
MMRRC Submission 044072-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R5860 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 120924377-120933595 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 120930015 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 168 (S168T)
Ref Sequence ENSEMBL: ENSMUSP00000144529 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100785] [ENSMUST00000200786] [ENSMUST00000201172]
AlphaFold A0A0J9YV76
Predicted Effect probably benign
Transcript: ENSMUST00000100785
AA Change: S168T

PolyPhen 2 Score 0.043 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000098348
Gene: ENSMUSG00000066867
AA Change: S168T

DomainStartEndE-ValueType
Pfam:OAS1_C 168 353 4.3e-74 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000200786
AA Change: N71K
SMART Domains Protein: ENSMUSP00000144442
Gene: ENSMUSG00000066867
AA Change: N71K

DomainStartEndE-ValueType
PDB:1PX5|B 4 60 4e-14 PDB
low complexity region 82 100 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201006
Predicted Effect probably benign
Transcript: ENSMUST00000201172
AA Change: S168T

PolyPhen 2 Score 0.129 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000144529
Gene: ENSMUSG00000066867
AA Change: S168T

DomainStartEndE-ValueType
Pfam:OAS1_C 168 353 2.7e-71 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 97.1%
  • 20x: 90.8%
Validation Efficiency 97% (75/77)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930568A12Rik A G 1: 34,524,661 (GRCm39) noncoding transcript Het
A2ml1 T C 6: 128,518,024 (GRCm39) T1421A probably benign Het
Actr8 T A 14: 29,708,242 (GRCm39) Y150* probably null Het
Adamts1 A G 16: 85,595,432 (GRCm39) C249R probably damaging Het
Adgre1 T A 17: 57,752,034 (GRCm39) I594N probably damaging Het
Atf6 A T 1: 170,669,344 (GRCm39) L119H probably damaging Het
Atf6 G A 1: 170,669,345 (GRCm39) L119F possibly damaging Het
B3gat2 G A 1: 23,854,400 (GRCm39) W33* probably null Het
Bach2 A G 4: 32,580,268 (GRCm39) D831G probably damaging Het
Ccnk A T 12: 108,153,466 (GRCm39) I76F probably damaging Het
Cdyl A C 13: 36,042,066 (GRCm39) K368T possibly damaging Het
Chi3l1 A G 1: 134,112,909 (GRCm39) T114A probably benign Het
Cnppd1 A G 1: 75,113,131 (GRCm39) V379A probably benign Het
Col11a2 C A 17: 34,283,159 (GRCm39) probably benign Het
Creb3l1 T C 2: 91,854,399 (GRCm39) S18G probably benign Het
Crybg3 A C 16: 59,385,632 (GRCm39) D197E probably damaging Het
Cryga T C 1: 65,142,527 (GRCm39) probably benign Het
Cthrc1 T C 15: 38,950,080 (GRCm39) C146R probably damaging Het
Cyp2c39 A T 19: 39,525,270 (GRCm39) D191V probably damaging Het
Dchs1 C T 7: 105,421,242 (GRCm39) A393T probably damaging Het
Dhx30 G A 9: 109,913,645 (GRCm39) T1126I probably damaging Het
Dock2 C T 11: 34,206,562 (GRCm39) G1345R probably damaging Het
Dsc1 T C 18: 20,228,081 (GRCm39) E425G probably damaging Het
Dynlt2b A G 16: 32,247,614 (GRCm39) Y143C probably damaging Het
Exosc8 C T 3: 54,642,463 (GRCm39) probably benign Het
Fat1 C T 8: 45,504,166 (GRCm39) A4553V probably benign Het
Flnb T A 14: 7,931,135 (GRCm38) L2119Q probably damaging Het
Fnbp4 T A 2: 90,587,826 (GRCm39) D401E probably benign Het
Glyctk T C 9: 106,032,906 (GRCm39) E369G possibly damaging Het
Gm14149 C A 2: 151,066,225 (GRCm39) noncoding transcript Het
Golga4 T C 9: 118,387,174 (GRCm39) L1432P probably damaging Het
Gtpbp4 A T 13: 9,023,196 (GRCm39) S623T probably benign Het
Insc A C 7: 114,390,383 (GRCm39) S85R probably damaging Het
Lgr4 G A 2: 109,821,496 (GRCm39) R126H probably damaging Het
M1ap T A 6: 82,980,795 (GRCm39) L227Q probably damaging Het
Marchf7 T C 2: 60,067,187 (GRCm39) I569T probably damaging Het
Mbd1 C A 18: 74,409,768 (GRCm39) C339* probably null Het
Moxd2 T A 6: 40,857,341 (GRCm39) Y473F probably damaging Het
Mrgpra6 T C 7: 46,839,099 (GRCm39) H2R probably benign Het
Mtus1 T G 8: 41,529,303 (GRCm39) L742F probably damaging Het
Nek11 A G 9: 105,270,160 (GRCm39) Y21H probably benign Het
Notch4 G T 17: 34,801,392 (GRCm39) C1080F probably damaging Het
Nsd3 C A 8: 26,156,107 (GRCm39) P558Q probably damaging Het
Ogfr T C 2: 180,234,285 (GRCm39) S119P probably damaging Het
Or2y15 A G 11: 49,350,563 (GRCm39) D19G probably damaging Het
Or8g20 T A 9: 39,395,767 (GRCm39) M261L probably benign Het
Pde4dip A G 3: 97,631,504 (GRCm39) I1135T possibly damaging Het
Prex1 G A 2: 166,486,604 (GRCm39) probably benign Het
Ptprf T C 4: 118,068,486 (GRCm39) probably benign Het
Rapsn T C 2: 90,875,859 (GRCm39) V359A probably damaging Het
Ric1 A G 19: 29,577,245 (GRCm39) S1050G possibly damaging Het
Rnft2 A G 5: 118,366,868 (GRCm39) I290T possibly damaging Het
Senp7 C A 16: 55,975,722 (GRCm39) A476E possibly damaging Het
Serpinh1 G A 7: 98,995,571 (GRCm39) S337L probably damaging Het
Slc5a12 C A 2: 110,427,969 (GRCm39) A8D probably benign Het
Smg5 T A 3: 88,250,214 (GRCm39) C109S probably damaging Het
Speer4b T C 5: 27,705,226 (GRCm39) H49R possibly damaging Het
Tas2r109 T C 6: 132,957,664 (GRCm39) I89V probably benign Het
Tet1 A G 10: 62,648,399 (GRCm39) probably null Het
Tmed6 G T 8: 107,790,786 (GRCm39) T87K probably damaging Het
Tpgs1 G A 10: 79,505,545 (GRCm39) G101D probably damaging Het
Trim13 T G 14: 61,842,188 (GRCm39) S68R probably damaging Het
Vwf A G 6: 125,620,053 (GRCm39) N1577S Het
Vwf G T 6: 125,656,228 (GRCm39) probably benign Het
Xpr1 T C 1: 155,207,868 (GRCm39) probably benign Het
Ylpm1 C T 12: 85,087,660 (GRCm39) P1148L probably damaging Het
Zftraf1 A T 15: 76,532,391 (GRCm39) I239N probably damaging Het
Zftraf1 T C 15: 76,540,615 (GRCm39) Y101C probably damaging Het
Zscan29 G T 2: 120,994,518 (GRCm39) T489N probably damaging Het
Other mutations in Oas1e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00583:Oas1e APN 5 120,932,337 (GRCm39) missense probably damaging 1.00
IGL02072:Oas1e APN 5 120,929,846 (GRCm39) critical splice donor site probably null
IGL02652:Oas1e APN 5 120,933,470 (GRCm39) missense probably damaging 0.99
R0049:Oas1e UTSW 5 120,933,395 (GRCm39) missense probably benign 0.01
R0242:Oas1e UTSW 5 120,929,839 (GRCm39) splice site probably benign
R0325:Oas1e UTSW 5 120,933,460 (GRCm39) missense probably damaging 1.00
R1528:Oas1e UTSW 5 120,926,054 (GRCm39) missense probably damaging 1.00
R3438:Oas1e UTSW 5 120,933,475 (GRCm39) missense probably damaging 1.00
R3790:Oas1e UTSW 5 120,933,475 (GRCm39) missense probably damaging 1.00
R3963:Oas1e UTSW 5 120,932,205 (GRCm39) missense probably damaging 1.00
R4811:Oas1e UTSW 5 120,933,448 (GRCm39) missense probably damaging 0.98
R5095:Oas1e UTSW 5 120,932,329 (GRCm39) nonsense probably null
R5327:Oas1e UTSW 5 120,930,006 (GRCm39) missense probably damaging 1.00
R5909:Oas1e UTSW 5 120,926,972 (GRCm39) missense probably damaging 0.98
R6503:Oas1e UTSW 5 120,926,042 (GRCm39) missense probably benign 0.39
R7167:Oas1e UTSW 5 120,933,487 (GRCm39) missense probably benign 0.35
R7515:Oas1e UTSW 5 120,929,951 (GRCm39) missense probably damaging 1.00
R7563:Oas1e UTSW 5 120,927,021 (GRCm39) missense probably benign 0.00
R8114:Oas1e UTSW 5 120,924,708 (GRCm39) missense unknown
R8133:Oas1e UTSW 5 120,926,060 (GRCm39) missense probably benign 0.00
R8351:Oas1e UTSW 5 120,925,008 (GRCm39) splice site probably null
R8710:Oas1e UTSW 5 120,930,027 (GRCm39) nonsense probably null
R9667:Oas1e UTSW 5 120,932,347 (GRCm39) missense probably benign 0.28
RF020:Oas1e UTSW 5 120,932,383 (GRCm39) missense possibly damaging 0.58
Predicted Primers PCR Primer
(F):5'- ACATAGGGTCCACAGGATCTGG -3'
(R):5'- CATGTATGCAGTCCAGAGGTGG -3'

Sequencing Primer
(F):5'- GTCGGATGCCTTACCAGTTGATAC -3'
(R):5'- TCCAGAGGTGGGCTCATGTC -3'
Posted On 2017-02-10