Incidental Mutation 'R4517:Ifit1bl2'
ID 332972
Institutional Source Beutler Lab
Gene Symbol Ifit1bl2
Ensembl Gene ENSMUSG00000067297
Gene Name interferon induced protein with tetratricopeptide repeats 1B like 2
Synonyms 2010002M12Rik
MMRRC Submission 041761-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4517 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 34594449-34618143 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) C to T at 34607164 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000108082 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087357] [ENSMUST00000112463]
AlphaFold Q3U687
Predicted Effect probably benign
Transcript: ENSMUST00000087357
SMART Domains Protein: ENSMUSP00000093816
Gene: ENSMUSG00000067297

DomainStartEndE-ValueType
TPR 60 93 2.92e1 SMART
TPR 100 133 6.24e1 SMART
TPR 144 179 4.32e1 SMART
low complexity region 217 230 N/A INTRINSIC
TPR 249 282 2.24e1 SMART
TPR 334 367 4.55e1 SMART
low complexity region 411 421 N/A INTRINSIC
TPR 429 462 1.45e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000112463
SMART Domains Protein: ENSMUSP00000108082
Gene: ENSMUSG00000067297

DomainStartEndE-ValueType
TPR 60 93 2.92e1 SMART
TPR 100 133 6.24e1 SMART
TPR 144 179 4.32e1 SMART
low complexity region 217 230 N/A INTRINSIC
TPR 249 282 2.24e1 SMART
TPR 334 367 4.55e1 SMART
low complexity region 411 421 N/A INTRINSIC
TPR 429 462 1.45e-1 SMART
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 95% (39/41)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ank A G 15: 27,562,835 (GRCm39) H181R possibly damaging Het
B4galnt4 A G 7: 140,647,635 (GRCm39) K408E probably damaging Het
Cd209a T A 8: 3,795,525 (GRCm39) D123V probably damaging Het
Cyp4f37 A G 17: 32,850,566 (GRCm39) I340V probably benign Het
Echs1 A G 7: 139,692,409 (GRCm39) S113P possibly damaging Het
Fap T C 2: 62,361,059 (GRCm39) I391V probably benign Het
Glb1l C T 1: 75,185,347 (GRCm39) C121Y probably damaging Het
Glod4 T A 11: 76,134,397 (GRCm39) D25V probably damaging Het
Gpc5 T A 14: 115,789,651 (GRCm39) N508K possibly damaging Het
H2-M10.3 C T 17: 36,678,722 (GRCm39) probably null Het
Ibsp C A 5: 104,453,863 (GRCm39) S67* probably null Het
Iqgap2 A G 13: 95,800,569 (GRCm39) probably null Het
Kcnma1 A G 14: 23,387,097 (GRCm39) S982P probably damaging Het
Kif5b T C 18: 6,213,272 (GRCm39) S707G probably benign Het
Lrrk2 A G 15: 91,589,323 (GRCm39) I437V probably benign Het
Mapkbp1 T C 2: 119,855,545 (GRCm39) probably benign Het
Mcu T C 10: 59,303,456 (GRCm39) Y127C probably damaging Het
Mlst8 T C 17: 24,695,031 (GRCm39) Y284C probably damaging Het
Nr2f2 T G 7: 70,007,870 (GRCm39) N204T probably benign Het
Or13a26 A G 7: 140,285,004 (GRCm39) Y280C probably damaging Het
Or7a42 T A 10: 78,791,877 (GRCm39) Y279* probably null Het
Pabir3 G A X: 52,382,376 (GRCm39) R94H possibly damaging Het
Pcf11 T C 7: 92,295,696 (GRCm39) Y1451C probably damaging Het
Plekhn1 T C 4: 156,309,988 (GRCm39) S109G probably damaging Het
Rttn T C 18: 89,047,097 (GRCm39) S920P probably damaging Het
Rufy4 T C 1: 74,186,822 (GRCm39) C537R probably damaging Het
Tas2r135 A T 6: 42,383,013 (GRCm39) H184L probably benign Het
Tmem38a C T 8: 73,326,005 (GRCm39) P20S possibly damaging Het
Ubqlnl C T 7: 103,798,925 (GRCm39) V191M probably benign Het
Vmn2r102 A G 17: 19,901,475 (GRCm39) Y534C probably damaging Het
Wdr62 A G 7: 29,969,683 (GRCm39) V259A probably damaging Het
Whrn A G 4: 63,379,517 (GRCm39) probably null Het
Other mutations in Ifit1bl2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00321:Ifit1bl2 APN 19 34,597,319 (GRCm39) missense probably benign 0.22
IGL00706:Ifit1bl2 APN 19 34,596,282 (GRCm39) missense probably benign 0.09
IGL01322:Ifit1bl2 APN 19 34,596,404 (GRCm39) missense probably benign 0.10
IGL01362:Ifit1bl2 APN 19 34,596,884 (GRCm39) missense probably benign 0.04
IGL03061:Ifit1bl2 APN 19 34,597,124 (GRCm39) missense probably benign 0.41
R0039:Ifit1bl2 UTSW 19 34,596,846 (GRCm39) nonsense probably null
R1079:Ifit1bl2 UTSW 19 34,596,885 (GRCm39) missense probably benign 0.00
R1438:Ifit1bl2 UTSW 19 34,596,569 (GRCm39) missense possibly damaging 0.70
R2050:Ifit1bl2 UTSW 19 34,596,870 (GRCm39) missense possibly damaging 0.75
R2104:Ifit1bl2 UTSW 19 34,596,920 (GRCm39) missense probably benign 0.01
R2228:Ifit1bl2 UTSW 19 34,596,630 (GRCm39) missense possibly damaging 0.70
R2229:Ifit1bl2 UTSW 19 34,596,630 (GRCm39) missense possibly damaging 0.70
R4468:Ifit1bl2 UTSW 19 34,596,468 (GRCm39) nonsense probably null
R5723:Ifit1bl2 UTSW 19 34,597,458 (GRCm39) missense probably benign 0.07
R5935:Ifit1bl2 UTSW 19 34,597,128 (GRCm39) missense probably benign 0.04
R6024:Ifit1bl2 UTSW 19 34,597,438 (GRCm39) missense probably benign 0.00
R6083:Ifit1bl2 UTSW 19 34,597,217 (GRCm39) missense possibly damaging 0.80
R6085:Ifit1bl2 UTSW 19 34,597,217 (GRCm39) missense possibly damaging 0.80
R6280:Ifit1bl2 UTSW 19 34,597,534 (GRCm39) missense possibly damaging 0.70
R6368:Ifit1bl2 UTSW 19 34,596,525 (GRCm39) missense probably benign 0.00
R6905:Ifit1bl2 UTSW 19 34,596,990 (GRCm39) missense possibly damaging 0.90
R7048:Ifit1bl2 UTSW 19 34,596,551 (GRCm39) missense probably benign 0.04
R7355:Ifit1bl2 UTSW 19 34,597,061 (GRCm39) missense probably damaging 1.00
R7447:Ifit1bl2 UTSW 19 34,596,974 (GRCm39) missense probably damaging 1.00
R7661:Ifit1bl2 UTSW 19 34,596,428 (GRCm39) missense probably damaging 0.99
R9500:Ifit1bl2 UTSW 19 34,596,508 (GRCm39) nonsense probably null
Predicted Primers
Posted On 2015-08-18