Incidental Mutation 'R1763:Ifi27l2a'
ID 193218
Institutional Source Beutler Lab
Gene Symbol Ifi27l2a
Ensembl Gene ENSMUSG00000079017
Gene Name interferon, alpha-inducible protein 27 like 2A
Synonyms Ifi27, 2310061N23Rik
MMRRC Submission 039795-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1763 (G1)
Quality Score 178
Status Validated
Chromosome 12
Chromosomal Location 103408426-103409939 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 103403941 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Valine at position 127 (A127V)
Ref Sequence ENSEMBL: ENSMUSP00000082142 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055071] [ENSMUST00000066701] [ENSMUST00000076702] [ENSMUST00000076788] [ENSMUST00000079294] [ENSMUST00000085065] [ENSMUST00000140838]
AlphaFold Q8R412
Predicted Effect probably benign
Transcript: ENSMUST00000055071
SMART Domains Protein: ENSMUSP00000054698
Gene: ENSMUSG00000079017

Pfam:Ifi-6-16 10 88 4.1e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000066701
AA Change: A82V

PolyPhen 2 Score 0.162 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000068729
Gene: ENSMUSG00000064215
AA Change: A82V

transmembrane domain 21 43 N/A INTRINSIC
transmembrane domain 53 75 N/A INTRINSIC
Pfam:Ifi-6-16 85 167 2.6e-33 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000076702
SMART Domains Protein: ENSMUSP00000075994
Gene: ENSMUSG00000064215

low complexity region 43 59 N/A INTRINSIC
Pfam:Ifi-6-16 73 157 7.1e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000076788
SMART Domains Protein: ENSMUSP00000076068
Gene: ENSMUSG00000064215

Pfam:Ifi-6-16 35 117 7.2e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000079294
SMART Domains Protein: ENSMUSP00000078275
Gene: ENSMUSG00000064215

low complexity region 43 59 N/A INTRINSIC
Pfam:Ifi-6-16 122 202 8e-33 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000085065
AA Change: A127V

PolyPhen 2 Score 0.801 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000082142
Gene: ENSMUSG00000064215
AA Change: A127V

low complexity region 43 59 N/A INTRINSIC
Pfam:Ifi-6-16 132 210 1.8e-29 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000122905
Predicted Effect probably benign
Transcript: ENSMUST00000140838
SMART Domains Protein: ENSMUSP00000117403
Gene: ENSMUSG00000064215

low complexity region 43 59 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148824
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153670
Meta Mutation Damage Score 0.1153 question?
Coding Region Coverage
  • 1x: 97.4%
  • 3x: 96.8%
  • 10x: 95.1%
  • 20x: 92.0%
Validation Efficiency 98% (85/87)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal susceptibility to infection with H1N1 or H7N7 influenza A virus, although sloughing of dead cells into bronchiolar lumen persists somewhat longer after infection than in infected controls. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm4 A G 4: 144,396,529 (GRCm39) V401A probably benign Het
Abca4 G A 3: 121,904,330 (GRCm39) V794M probably benign Het
Abca4 A T 3: 121,957,479 (GRCm39) T772S probably damaging Het
Acox3 G A 5: 35,765,683 (GRCm39) probably null Het
Adamts17 A G 7: 66,797,463 (GRCm39) N1060S probably damaging Het
Akap8l C T 17: 32,551,457 (GRCm39) R511H probably damaging Het
Als2 T C 1: 59,214,150 (GRCm39) Y1346C probably benign Het
Apol10b A T 15: 77,469,215 (GRCm39) F321I probably benign Het
Atp5pb A G 3: 105,858,905 (GRCm39) probably null Het
Bloc1s5 A G 13: 38,803,060 (GRCm39) probably benign Het
Btbd9 T C 17: 30,553,271 (GRCm39) N397S possibly damaging Het
Cacna1d A G 14: 29,821,153 (GRCm39) V1121A probably benign Het
Cad G A 5: 31,218,295 (GRCm39) V460I probably damaging Het
Caprin2 A T 6: 148,744,619 (GRCm39) D935E probably damaging Het
Ccdc150 A T 1: 54,393,795 (GRCm39) K686N probably benign Het
Ccnt2 T C 1: 127,727,143 (GRCm39) F186L possibly damaging Het
Cd5l G A 3: 87,275,187 (GRCm39) probably null Het
Chrna7 A G 7: 62,749,000 (GRCm39) V494A probably benign Het
Clec2i T G 6: 128,872,388 (GRCm39) Y198* probably null Het
Col22a1 A G 15: 71,879,025 (GRCm39) V44A probably damaging Het
Cspg4 T A 9: 56,794,263 (GRCm39) I666N probably damaging Het
Cyp3a16 A T 5: 145,401,841 (GRCm39) probably null Het
Dlk1 G T 12: 109,424,045 (GRCm39) C102F probably damaging Het
Dscc1 CTGAATGAAT CTGAAT 15: 54,943,572 (GRCm39) probably benign Het
Dscc1 T A 15: 54,947,535 (GRCm39) H215L probably damaging Het
Dus1l C G 11: 120,686,497 (GRCm39) G15R probably benign Het
Eps8l1 G T 7: 4,474,822 (GRCm39) V268L probably benign Het
F2 A C 2: 91,465,251 (GRCm39) C104W probably damaging Het
F5 C A 1: 164,020,104 (GRCm39) Q860K probably benign Het
Fmn2 T C 1: 174,329,832 (GRCm39) L74P unknown Het
Frmd6 G A 12: 70,940,396 (GRCm39) R347Q possibly damaging Het
Gabbr1 T G 17: 37,365,659 (GRCm39) S158A probably damaging Het
Galc T C 12: 98,200,525 (GRCm39) N295S probably damaging Het
Gm6408 A T 5: 146,419,132 (GRCm39) N49I probably damaging Het
Grm1 T A 10: 10,955,610 (GRCm39) T225S possibly damaging Het
Grm8 C T 6: 27,285,866 (GRCm39) V849I possibly damaging Het
Hmcn2 A G 2: 31,204,602 (GRCm39) D59G probably damaging Het
Iars1 G A 13: 49,876,553 (GRCm39) probably null Het
Ikbip A G 10: 90,932,343 (GRCm39) N329S probably damaging Het
Ikbke T C 1: 131,193,614 (GRCm39) T479A probably benign Het
Krt12 T A 11: 99,306,886 (GRCm39) N472I probably damaging Het
Lmnb2 A T 10: 80,743,025 (GRCm39) L193Q probably damaging Het
Lrriq4 T C 3: 30,704,401 (GRCm39) V128A probably benign Het
Map4k4 C A 1: 40,039,917 (GRCm39) probably benign Het
Mtmr7 T C 8: 41,004,852 (GRCm39) T575A probably benign Het
Myh13 G A 11: 67,225,402 (GRCm39) A256T probably benign Het
Napepld A G 5: 21,888,408 (GRCm39) Y14H probably benign Het
Npr1 T C 3: 90,366,644 (GRCm39) T552A probably damaging Het
Nudt15 A G 14: 73,759,087 (GRCm39) F127S probably benign Het
Nwd2 T A 5: 63,965,614 (GRCm39) S1733T probably benign Het
Or11a4 T C 17: 37,536,321 (GRCm39) F102L probably benign Het
Or4c102 A G 2: 88,422,780 (GRCm39) I211V probably benign Het
Or4c10b G A 2: 89,711,473 (GRCm39) G101E probably damaging Het
Or6z1 T G 7: 6,504,440 (GRCm39) I262L probably benign Het
Or8b44 A G 9: 38,410,334 (GRCm39) Y123C probably damaging Het
Paqr7 A T 4: 134,234,409 (GRCm39) I89F probably benign Het
Pidd1 C A 7: 141,019,543 (GRCm39) V706L probably benign Het
Polr3c A T 3: 96,620,911 (GRCm39) I469N probably damaging Het
Ppip5k1 A G 2: 121,179,028 (GRCm39) Y233H probably damaging Het
Psmc3 A G 2: 90,886,340 (GRCm39) T166A possibly damaging Het
Ptchd3 A T 11: 121,733,368 (GRCm39) I753L probably benign Het
Rad21 T C 15: 51,841,566 (GRCm39) K50R probably damaging Het
Rad54b A G 4: 11,604,989 (GRCm39) E479G possibly damaging Het
Rfwd3 C T 8: 112,014,874 (GRCm39) R326Q probably damaging Het
Rgs20 C T 1: 4,980,863 (GRCm39) R154Q probably damaging Het
Sbf1 T C 15: 89,178,628 (GRCm39) D1449G probably damaging Het
Sema4g C T 19: 44,990,044 (GRCm39) R708* probably null Het
Septin9 T C 11: 117,181,254 (GRCm39) I18T probably benign Het
Serpinb6b A G 13: 33,162,041 (GRCm39) E280G probably damaging Het
Slamf6 T C 1: 171,770,154 (GRCm39) probably benign Het
Slc6a21 G A 7: 44,937,158 (GRCm39) W554* probably null Het
Slco1a4 A C 6: 141,758,457 (GRCm39) I518R probably benign Het
Stab1 T A 14: 30,890,373 (GRCm39) Q26L probably benign Het
Stox1 A G 10: 62,503,744 (GRCm39) F104L probably damaging Het
Suco T C 1: 161,662,518 (GRCm39) K638E possibly damaging Het
Synpo T C 18: 60,735,856 (GRCm39) K458E probably damaging Het
Szt2 A T 4: 118,229,565 (GRCm39) W2820R unknown Het
Tmtc1 C A 6: 148,196,116 (GRCm39) G499W probably damaging Het
Tonsl A C 15: 76,522,266 (GRCm39) S242R probably damaging Het
Trpc4 G T 3: 54,102,243 (GRCm39) S47I possibly damaging Het
Zfp106 G A 2: 120,350,909 (GRCm39) R1581C probably benign Het
Zfp27 A G 7: 29,594,801 (GRCm39) L388P possibly damaging Het
Other mutations in Ifi27l2a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01114:Ifi27l2a APN 12 103,403,792 (GRCm39) unclassified probably benign
IGL01872:Ifi27l2a APN 12 103,401,719 (GRCm39) missense probably damaging 0.99
IGL03061:Ifi27l2a APN 12 103,401,803 (GRCm39) missense possibly damaging 0.85
IGL03402:Ifi27l2a APN 12 103,405,772 (GRCm39) missense probably damaging 1.00
R0924:Ifi27l2a UTSW 12 103,408,639 (GRCm39) missense probably damaging 0.99
R1428:Ifi27l2a UTSW 12 103,409,093 (GRCm39) unclassified probably benign
R1712:Ifi27l2a UTSW 12 103,406,202 (GRCm39) splice site probably null
R6883:Ifi27l2a UTSW 12 103,409,756 (GRCm39) unclassified probably benign
R8325:Ifi27l2a UTSW 12 103,409,144 (GRCm39) missense unknown
R8868:Ifi27l2a UTSW 12 103,402,899 (GRCm39) missense possibly damaging 0.93
R9149:Ifi27l2a UTSW 12 103,405,678 (GRCm39) missense possibly damaging 0.92
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2014-05-23