Incidental Mutation 'R4293:Gm16686'
Institutional Source Beutler Lab
Gene Symbol Gm16686
Ensembl Gene ENSMUSG00000085473
Gene Namepredicted gene, 16686
MMRRC Submission 041082-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.108) question?
Stock #R4293 (G1)
Quality Score225
Status Validated
Chromosomal Location88755195-88755590 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to T at 88755473 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139768 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094992] [ENSMUST00000141816] [ENSMUST00000191112]
Predicted Effect probably benign
Transcript: ENSMUST00000094992
SMART Domains Protein: ENSMUSP00000092600
Gene: ENSMUSG00000094618

signal peptide 1 21 N/A INTRINSIC
IFabd 58 170 7.8e-13 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097988
Predicted Effect noncoding transcript
Transcript: ENSMUST00000117750
Predicted Effect unknown
Transcript: ENSMUST00000141816
AA Change: W40R
SMART Domains Protein: ENSMUSP00000127029
Gene: ENSMUSG00000085473
AA Change: W40R

low complexity region 54 71 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000191112
SMART Domains Protein: ENSMUSP00000139768
Gene: ENSMUSG00000100505

signal peptide 1 21 N/A INTRINSIC
IFabd 58 170 1.65e-11 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.7%
  • 20x: 96.2%
Validation Efficiency 98% (60/61)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn3 T C 19: 4,865,440 E428G probably benign Het
Arfgef2 T C 2: 166,890,291 I1600T probably benign Het
Arid3b A T 9: 57,790,430 probably benign Het
Asgr2 C A 11: 70,098,231 T167K probably benign Het
Atf6b T A 17: 34,652,674 M428K probably benign Het
Atpaf1 A T 4: 115,788,359 M142L probably benign Het
Bivm A T 1: 44,138,633 R364S probably damaging Het
Bms1 T C 6: 118,405,347 probably null Het
Brwd1 G A 16: 96,017,604 P1343S probably damaging Het
C330027C09Rik T A 16: 49,013,249 F571Y probably benign Het
Cdca2 T C 14: 67,714,850 D24G probably benign Het
Celsr2 T C 3: 108,393,677 R2767G probably benign Het
Cyp2c55 A T 19: 39,011,791 I145F probably damaging Het
Ddx18 T C 1: 121,561,392 T309A probably benign Het
Dlg3 A T X: 100,796,682 probably benign Het
Fbf1 A G 11: 116,148,894 L713P probably damaging Het
Fhdc1 C A 3: 84,444,826 V1031F probably benign Het
Fnbp1 A G 2: 31,105,350 F24S probably damaging Het
Gmps A G 3: 63,990,619 M275V probably damaging Het
Igdcc4 A G 9: 65,124,610 probably null Het
Kcnv1 G A 15: 45,114,444 T66M probably damaging Het
Kif18a T C 2: 109,293,053 V224A probably benign Het
Lbr C T 1: 181,820,702 C398Y probably damaging Het
Lmf1 T C 17: 25,654,481 L320P probably damaging Het
Mapkapk3 T C 9: 107,258,932 probably benign Het
Mettl18 A G 1: 163,996,602 D164G probably damaging Het
Myo5a A T 9: 75,144,171 T349S probably benign Het
Olfr1378 T C 11: 50,969,426 M136T probably damaging Het
Olfr926 A G 9: 38,877,313 I46V probably damaging Het
Pcdhb5 T A 18: 37,322,681 S705T possibly damaging Het
Phf14 C T 6: 11,987,097 P559S probably damaging Het
Pik3c3 G A 18: 30,343,990 A855T probably damaging Het
Plpp4 A G 7: 129,307,632 E22G probably damaging Het
Rev1 A T 1: 38,108,419 D13E possibly damaging Het
Sec16a A G 2: 26,422,155 Y1998H probably benign Het
Slc4a5 C T 6: 83,260,529 R165C probably damaging Het
Slfn10-ps T C 11: 83,035,434 noncoding transcript Het
Slfn9 T C 11: 82,982,508 N523S probably benign Het
Spata13 T A 14: 60,709,555 M684K probably damaging Het
Srsf6 T C 2: 162,934,716 probably benign Het
Stk32c T C 7: 139,120,788 probably null Het
Tenm3 T C 8: 48,395,658 T49A probably damaging Het
Tep1 T C 14: 50,846,861 I954V probably benign Het
Tmem237 A G 1: 59,119,836 probably benign Het
Vmn2r101 A T 17: 19,612,041 R766S probably damaging Het
Vwce A G 19: 10,659,632 T693A probably benign Het
Xpr1 A G 1: 155,312,796 F366S possibly damaging Het
Zfp317 A G 9: 19,646,694 probably null Het
Other mutations in Gm16686
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02114:Gm16686 APN 4 88755502 missense probably null
R4752:Gm16686 UTSW 4 88755488 unclassified probably benign
R5478:Gm16686 UTSW 4 88755477 unclassified probably benign
R5485:Gm16686 UTSW 4 88755404 unclassified probably benign
R6518:Gm16686 UTSW 4 88755488 unclassified probably benign
R7426:Gm16686 UTSW 4 88755326 missense unknown
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-06-20