Incidental Mutation 'R8712:Ifi206'
ID 669616
Institutional Source Beutler Lab
Gene Symbol Ifi206
Ensembl Gene ENSMUSG00000037849
Gene Name interferon activated gene 206
Synonyms Pyblhin-C, Gm4955
MMRRC Submission 068566-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.175) question?
Stock # R8712 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 173296051-173318607 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 173308074 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 641 (W641R)
Ref Sequence ENSEMBL: ENSMUSP00000134646 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000160565]
AlphaFold G3UZV2
Predicted Effect
SMART Domains Protein: ENSMUSP00000134646
Gene: ENSMUSG00000037849
AA Change: W641R

DomainStartEndE-ValueType
PYRIN 6 84 5.7e-21 SMART
low complexity region 97 108 N/A INTRINSIC
internal_repeat_1 154 349 6.25e-15 PROSPERO
internal_repeat_1 342 575 6.25e-15 PROSPERO
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (75/75)
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts1 A T 16: 85,594,896 (GRCm39) N617K probably benign Het
Adnp2 A T 18: 80,174,185 (GRCm39) C75S probably damaging Het
Agmo T C 12: 37,407,673 (GRCm39) F186L possibly damaging Het
Ahnak2 T C 12: 112,749,872 (GRCm39) Y122C Het
Ahnak2 T C 12: 112,750,709 (GRCm39) E71G Het
Aldh5a1 A G 13: 25,102,524 (GRCm39) V313A probably damaging Het
Ankib1 C A 5: 3,822,643 (GRCm39) C21F probably benign Het
Aqr A G 2: 113,949,358 (GRCm39) Y947H probably damaging Het
Atp1a2 T A 1: 172,103,547 (GRCm39) Y991F probably benign Het
Atp8b3 G A 10: 80,365,923 (GRCm39) T309M possibly damaging Het
Blzf1 T A 1: 164,125,859 (GRCm39) D259V possibly damaging Het
Cacng5 T C 11: 107,772,510 (GRCm39) I113V probably benign Het
Catsper3 T C 13: 55,953,657 (GRCm39) M269T probably benign Het
Ccdc142 A C 6: 83,079,233 (GRCm39) Y190S probably damaging Het
Ccdc159 C A 9: 21,845,051 (GRCm39) Q306K probably benign Het
Ccdc180 A T 4: 45,920,842 (GRCm39) probably null Het
Cebpz A G 17: 79,229,081 (GRCm39) F955S possibly damaging Het
Cftr C T 6: 18,274,696 (GRCm39) T938I probably damaging Het
Col28a1 T C 6: 8,013,133 (GRCm39) K973R probably benign Het
Cyp2c29 T C 19: 39,310,138 (GRCm39) probably benign Het
Ddx1 A G 12: 13,293,859 (GRCm39) probably benign Het
Duox2 A C 2: 122,119,826 (GRCm39) Y867* probably null Het
Ereg T C 5: 91,237,013 (GRCm39) Y111H possibly damaging Het
Esrrb T A 12: 86,565,724 (GRCm39) L417Q probably damaging Het
Fbxw7 G A 3: 84,859,684 (GRCm39) R2H unknown Het
Galnt6 C T 15: 100,592,501 (GRCm39) V569I probably benign Het
Gm14226 G A 2: 154,866,094 (GRCm39) C17Y unknown Het
Gpr150 T G 13: 76,204,642 (GRCm39) D101A probably damaging Het
Grm1 A T 10: 10,565,296 (GRCm39) L1004Q probably benign Het
Gtf2a1l T A 17: 89,022,351 (GRCm39) D447E probably damaging Het
Gtf2ird1 C T 5: 134,444,064 (GRCm39) V64M probably damaging Het
Ifi214 T A 1: 173,355,486 (GRCm39) E107D possibly damaging Het
Kif19a T C 11: 114,675,599 (GRCm39) V357A probably damaging Het
Klhdc7b T A 15: 89,271,025 (GRCm39) S636T probably benign Het
Klhl25 C T 7: 75,515,420 (GRCm39) R109C probably damaging Het
Ltbp2 T C 12: 84,853,124 (GRCm39) E835G probably benign Het
Marchf1 A G 8: 66,921,000 (GRCm39) K226E probably damaging Het
Mcpt1 T C 14: 56,256,170 (GRCm39) probably benign Het
Myrf C A 19: 10,192,434 (GRCm39) R639L probably benign Het
Naip5 T C 13: 100,359,604 (GRCm39) H544R possibly damaging Het
Nccrp1 T C 7: 28,245,769 (GRCm39) I132V probably benign Het
Nprl3 C T 11: 32,187,334 (GRCm39) V333I possibly damaging Het
Or13a25 C T 7: 140,248,052 (GRCm39) S277L possibly damaging Het
Or14n1-ps1 T C 7: 86,092,923 (GRCm39) S245P probably damaging Het
Or2o1 T C 11: 49,051,297 (GRCm39) M152T probably benign Het
Or2y1 T A 11: 49,385,671 (GRCm39) S104T probably benign Het
Or4b1d A T 2: 89,969,114 (GRCm39) I123N probably damaging Het
Or4f62 A T 2: 111,986,934 (GRCm39) I213F probably damaging Het
Or52h1 T C 7: 103,829,025 (GRCm39) N197D probably damaging Het
Or56a41 C A 7: 104,741,808 (GRCm39) V73F possibly damaging Het
Or8c15 T C 9: 38,121,099 (GRCm39) V248A probably benign Het
Or8d6 T C 9: 39,853,891 (GRCm39) S112P probably damaging Het
Otx2 A G 14: 48,896,521 (GRCm39) M179T probably damaging Het
Pmfbp1 A G 8: 110,265,309 (GRCm39) probably benign Het
Ppfia3 T A 7: 45,011,129 (GRCm39) T34S probably benign Het
Prkcsh T C 9: 21,924,375 (GRCm39) Y502H probably damaging Het
Psd T C 19: 46,301,775 (GRCm39) E937G probably damaging Het
Rbbp6 T A 7: 122,600,976 (GRCm39) I1661N unknown Het
Rhobtb1 T A 10: 69,106,587 (GRCm39) M446K probably damaging Het
Sall3 T C 18: 81,017,236 (GRCm39) I231V probably benign Het
Slc12a9 C T 5: 137,325,916 (GRCm39) V270I probably damaging Het
Slc6a15 A G 10: 103,225,112 (GRCm39) K67E probably damaging Het
Slc9c1 A G 16: 45,380,646 (GRCm39) D524G probably benign Het
Smpdl3a A G 10: 57,687,526 (GRCm39) D418G probably benign Het
Sox6 T C 7: 115,196,743 (GRCm39) T296A probably benign Het
Ssu2 T C 6: 112,361,399 (GRCm39) E19G probably damaging Het
Tctn3 T C 19: 40,600,170 (GRCm39) N90S probably damaging Het
Tex24 A G 8: 27,834,652 (GRCm39) Q60R possibly damaging Het
Tlcd1 T A 11: 78,070,470 (GRCm39) *128R probably null Het
Tti1 A C 2: 157,834,930 (GRCm39) L1010R probably damaging Het
Ttn A G 2: 76,567,682 (GRCm39) L27737P probably damaging Het
Ubqln5 T A 7: 103,778,322 (GRCm39) K167N probably benign Het
Unkl A G 17: 25,450,689 (GRCm39) I492V possibly damaging Het
Vmn1r8 G A 6: 57,013,665 (GRCm39) V239I probably benign Het
Vmn2r101 T A 17: 19,811,397 (GRCm39) L494I probably benign Het
Vmn2r54 G T 7: 12,369,877 (GRCm39) T62K probably benign Het
Other mutations in Ifi206
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01509:Ifi206 APN 1 173,313,142 (GRCm39) missense probably benign 0.00
IGL02044:Ifi206 APN 1 173,308,557 (GRCm39) missense probably benign 0.41
IGL02118:Ifi206 APN 1 173,309,334 (GRCm39) missense probably benign 0.05
IGL02476:Ifi206 APN 1 173,309,132 (GRCm39) missense probably benign 0.02
IGL02824:Ifi206 APN 1 173,309,438 (GRCm39) missense possibly damaging 0.95
IGL03375:Ifi206 APN 1 173,308,344 (GRCm39) missense probably benign 0.06
PIT4142001:Ifi206 UTSW 1 173,308,730 (GRCm39) missense probably benign 0.02
R0069:Ifi206 UTSW 1 173,314,413 (GRCm39) missense probably damaging 1.00
R0741:Ifi206 UTSW 1 173,301,315 (GRCm39) missense probably benign 0.41
R1572:Ifi206 UTSW 1 173,314,419 (GRCm39) missense probably benign 0.10
R1742:Ifi206 UTSW 1 173,309,537 (GRCm39) missense probably benign 0.06
R4109:Ifi206 UTSW 1 173,308,554 (GRCm39) missense probably benign 0.00
R4707:Ifi206 UTSW 1 173,308,432 (GRCm39) missense probably benign 0.00
R4783:Ifi206 UTSW 1 173,308,432 (GRCm39) missense probably benign 0.00
R4785:Ifi206 UTSW 1 173,308,432 (GRCm39) missense probably benign 0.00
R4805:Ifi206 UTSW 1 173,308,952 (GRCm39) missense possibly damaging 0.55
R4918:Ifi206 UTSW 1 173,309,610 (GRCm39) missense possibly damaging 0.73
R5043:Ifi206 UTSW 1 173,314,284 (GRCm39) missense probably damaging 1.00
R5080:Ifi206 UTSW 1 173,301,414 (GRCm39) missense possibly damaging 0.61
R5419:Ifi206 UTSW 1 173,308,797 (GRCm39) missense probably benign 0.05
R5420:Ifi206 UTSW 1 173,308,599 (GRCm39) missense possibly damaging 0.84
R5777:Ifi206 UTSW 1 173,308,928 (GRCm39) missense possibly damaging 0.55
R5988:Ifi206 UTSW 1 173,308,906 (GRCm39) missense possibly damaging 0.90
R6772:Ifi206 UTSW 1 173,308,773 (GRCm39) missense unknown
R6782:Ifi206 UTSW 1 173,308,923 (GRCm39) missense unknown
R6806:Ifi206 UTSW 1 173,309,137 (GRCm39) missense probably benign 0.06
R7042:Ifi206 UTSW 1 173,308,808 (GRCm39) missense
R7091:Ifi206 UTSW 1 173,301,441 (GRCm39) missense unknown
R7292:Ifi206 UTSW 1 173,301,428 (GRCm39) missense unknown
R7429:Ifi206 UTSW 1 173,308,157 (GRCm39) missense
R7499:Ifi206 UTSW 1 173,309,607 (GRCm39) missense
R7772:Ifi206 UTSW 1 173,308,640 (GRCm39) missense
R7853:Ifi206 UTSW 1 173,299,100 (GRCm39) nonsense probably null
R7971:Ifi206 UTSW 1 173,298,976 (GRCm39) missense unknown
R8079:Ifi206 UTSW 1 173,308,724 (GRCm39) missense
R8205:Ifi206 UTSW 1 173,309,450 (GRCm39) missense
R8289:Ifi206 UTSW 1 173,308,032 (GRCm39) missense
R8390:Ifi206 UTSW 1 173,308,511 (GRCm39) missense
R8500:Ifi206 UTSW 1 173,314,311 (GRCm39) missense
R8753:Ifi206 UTSW 1 173,301,223 (GRCm39) missense unknown
R8875:Ifi206 UTSW 1 173,301,353 (GRCm39) missense unknown
R9128:Ifi206 UTSW 1 173,299,022 (GRCm39) missense unknown
R9369:Ifi206 UTSW 1 173,301,489 (GRCm39) missense unknown
R9569:Ifi206 UTSW 1 173,314,209 (GRCm39) missense
R9676:Ifi206 UTSW 1 173,308,718 (GRCm39) missense
R9695:Ifi206 UTSW 1 173,301,249 (GRCm39) missense unknown
R9776:Ifi206 UTSW 1 173,308,075 (GRCm39) missense
X0052:Ifi206 UTSW 1 173,309,535 (GRCm39) missense possibly damaging 0.89
Z1088:Ifi206 UTSW 1 173,301,577 (GRCm39) missense probably damaging 1.00
Z1176:Ifi206 UTSW 1 173,309,614 (GRCm39) missense
Predicted Primers
Posted On 2021-04-30