Incidental Mutation 'R5095:Oas1e'
ID395814
Institutional Source Beutler Lab
Gene Symbol Oas1e
Ensembl Gene ENSMUSG00000066867
Gene Name2'-5' oligoadenylate synthetase 1E
Synonyms2'-5' oligoadenylate synthetase-like 7
MMRRC Submission 042684-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.057) question?
Stock #R5095 (G1)
Quality Score225
Status Validated
Chromosome5
Chromosomal Location120786226-120795530 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 120794264 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Stop codon at position 105 (K105*)
Ref Sequence ENSEMBL: ENSMUSP00000144529 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100785] [ENSMUST00000200786] [ENSMUST00000201172]
Predicted Effect probably null
Transcript: ENSMUST00000100785
AA Change: K105*
SMART Domains Protein: ENSMUSP00000098348
Gene: ENSMUSG00000066867
AA Change: K105*

DomainStartEndE-ValueType
Pfam:OAS1_C 168 353 4.3e-74 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000200786
SMART Domains Protein: ENSMUSP00000144442
Gene: ENSMUSG00000066867

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 null
Transcript: ENSMUST00000201172
AA Change: K105*
SMART Domains Protein: ENSMUSP00000144529
Gene: ENSMUSG00000066867
AA Change: K105*

DomainStartEndE-ValueType
Pfam:OAS1_C 168 353 2.7e-71 PFAM
Meta Mutation Damage Score 0.6348 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 98% (59/60)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700021A07Rik G C 10: 21,425,593 noncoding transcript Het
4932415D10Rik G T 10: 82,283,667 A4503E probably damaging Het
Adgrv1 C T 13: 81,095,487 V6265I probably benign Het
Agbl1 G A 7: 76,720,133 G660D probably damaging Het
Arap2 A G 5: 62,654,049 Y1140H probably damaging Het
Atp6v1c1 T C 15: 38,679,413 probably null Het
C1rb A T 6: 124,580,313 R470W possibly damaging Het
Caskin2 T C 11: 115,800,738 T1074A probably benign Het
Cdh19 T A 1: 110,954,661 T34S probably benign Het
Csnk1a1 T A 18: 61,575,476 Y175N probably damaging Het
F2 CAGAAAG CAG 2: 91,634,957 probably benign Het
Flt4 T A 11: 49,627,159 V342D possibly damaging Het
Frmd5 A T 2: 121,548,921 C394S possibly damaging Het
Gm5414 T G 15: 101,624,038 N550T probably benign Het
Hcn3 C A 3: 89,149,923 R456L probably damaging Het
Htt T C 5: 34,824,395 V893A possibly damaging Het
Ift46 A G 9: 44,786,849 D203G probably damaging Het
Itga10 G T 3: 96,648,164 V145L probably benign Het
Kcnh6 A G 11: 106,017,254 D232G possibly damaging Het
Mbtd1 T C 11: 93,929,671 S431P probably damaging Het
Mmp27 T A 9: 7,572,158 W120R probably damaging Het
Mmp27 A T 9: 7,579,000 D418V probably damaging Het
Myo5a A G 9: 75,152,020 D510G probably damaging Het
Myo5a A T 9: 75,184,389 K1179* probably null Het
Neto1 T C 18: 86,398,281 S38P probably benign Het
Nos3 A G 5: 24,368,918 probably benign Het
Nuggc C T 14: 65,635,090 R512* probably null Het
Olfr135 A C 17: 38,208,317 E24A possibly damaging Het
Olfr512 T C 7: 108,713,812 F141S probably damaging Het
Omd T A 13: 49,589,698 S75T possibly damaging Het
Pbrm1 A G 14: 31,032,530 N190S probably benign Het
Picalm T C 7: 90,170,633 F85L probably damaging Het
Polg A G 7: 79,460,300 V360A possibly damaging Het
Prex1 T C 2: 166,581,921 D1017G probably damaging Het
Prss56 G C 1: 87,188,111 R569P probably damaging Het
Rab6b G A 9: 103,140,384 G25R probably damaging Het
Rdh10 A G 1: 16,131,385 T332A probably benign Het
Rheb A T 5: 24,807,641 M115K probably benign Het
Rnf149 A T 1: 39,555,656 D321E probably benign Het
Rps28 C T 17: 33,823,203 probably null Het
Slc6a20b A G 9: 123,595,054 V616A probably benign Het
Smarcc2 A G 10: 128,469,300 K300R probably damaging Het
Sparcl1 C T 5: 104,085,763 M573I probably damaging Het
Srp68 C T 11: 116,248,747 V459M probably damaging Het
Stxbp4 C T 11: 90,548,975 V346I probably benign Het
Syne2 A G 12: 75,952,826 D2331G probably damaging Het
Ttn A T 2: 76,734,192 Y28534N probably damaging Het
Usp44 A T 10: 93,846,845 I386F possibly damaging Het
Vmn2r15 T C 5: 109,288,451 probably null Het
Vmn2r72 T A 7: 85,737,853 L834F probably damaging Het
Vps13b T A 15: 35,923,202 I3741K probably damaging Het
Zdbf2 A G 1: 63,309,073 T2204A possibly damaging Het
Zfp607b T A 7: 27,693,636 probably benign Het
Other mutations in Oas1e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00583:Oas1e APN 5 120794272 missense probably damaging 1.00
IGL02072:Oas1e APN 5 120791781 critical splice donor site probably null
IGL02652:Oas1e APN 5 120795405 missense probably damaging 0.99
R0049:Oas1e UTSW 5 120795330 missense probably benign 0.01
R0242:Oas1e UTSW 5 120791774 splice site probably benign
R0325:Oas1e UTSW 5 120795395 missense probably damaging 1.00
R1528:Oas1e UTSW 5 120787989 missense probably damaging 1.00
R3438:Oas1e UTSW 5 120795410 missense probably damaging 1.00
R3790:Oas1e UTSW 5 120795410 missense probably damaging 1.00
R3963:Oas1e UTSW 5 120794140 missense probably damaging 1.00
R4811:Oas1e UTSW 5 120795383 missense probably damaging 0.98
R5327:Oas1e UTSW 5 120791941 missense probably damaging 1.00
R5860:Oas1e UTSW 5 120791950 missense probably benign 0.13
R5909:Oas1e UTSW 5 120788907 missense probably damaging 0.98
R6503:Oas1e UTSW 5 120787977 missense probably benign 0.39
R7167:Oas1e UTSW 5 120795422 missense probably benign 0.35
Predicted Primers PCR Primer
(F):5'- GAACTCTGCTGCTCTCTGAC -3'
(R):5'- CTCTTGGTGATGGACTCCTAC -3'

Sequencing Primer
(F):5'- TGACTTACACAGAGCATCATAGGCTG -3'
(R):5'- GGTGATGGACTCCTACTCTGTTC -3'
Posted On2016-06-21