Incidental Mutation 'R4910:Tlr11'
ID 379445
Institutional Source Beutler Lab
Gene Symbol Tlr11
Ensembl Gene ENSMUSG00000051969
Gene Name toll-like receptor 11
Synonyms LOC239081
MMRRC Submission 042512-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4910 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 50595371-50601120 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 50600346 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 777 (F777L)
Ref Sequence ENSEMBL: ENSMUSP00000138814 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063570] [ENSMUST00000185091]
AlphaFold Q6R5P0
Predicted Effect probably benign
Transcript: ENSMUST00000063570
AA Change: F772L

PolyPhen 2 Score 0.451 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000068906
Gene: ENSMUSG00000051969
AA Change: F772L

DomainStartEndE-ValueType
signal peptide 1 30 N/A INTRINSIC
low complexity region 105 122 N/A INTRINSIC
low complexity region 153 161 N/A INTRINSIC
LRR 311 333 3.36e1 SMART
LRR 335 361 4.44e0 SMART
LRR 362 383 2.03e1 SMART
LRR_TYP 384 407 2.57e-3 SMART
LRR_TYP 408 431 2.75e-3 SMART
low complexity region 544 556 N/A INTRINSIC
LRR 605 628 6.06e1 SMART
transmembrane domain 719 741 N/A INTRINSIC
Pfam:TIR 773 922 2.1e-9 PFAM
Pfam:TIR_2 776 894 6.6e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000185091
AA Change: F777L

PolyPhen 2 Score 0.451 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000138814
Gene: ENSMUSG00000051969
AA Change: F777L

DomainStartEndE-ValueType
transmembrane domain 16 38 N/A INTRINSIC
low complexity region 110 127 N/A INTRINSIC
low complexity region 158 166 N/A INTRINSIC
Pfam:LRR_6 221 244 5.3e-2 PFAM
LRR 316 338 3.36e1 SMART
LRR 340 366 4.44e0 SMART
LRR 367 388 2.03e1 SMART
LRR_TYP 389 412 2.57e-3 SMART
LRR_TYP 413 436 2.75e-3 SMART
low complexity region 549 561 N/A INTRINSIC
LRR 610 633 6.06e1 SMART
transmembrane domain 724 746 N/A INTRINSIC
Pfam:TIR_2 781 898 1e-12 PFAM
Pfam:TIR 781 922 1.8e-13 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.9%
  • 10x: 94.6%
  • 20x: 86.1%
Validation Efficiency 95% (144/151)
Allele List at MGI
Other mutations in this stock
Total: 123 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2fm3 T A 3: 59,776,435 (GRCm39) probably null Het
Adam3 T A 8: 25,184,321 (GRCm39) I560L probably benign Het
Agxt T C 1: 93,063,436 (GRCm39) F113L probably benign Het
Aknad1 T A 3: 108,688,568 (GRCm39) probably null Het
Alpk2 T A 18: 65,399,357 (GRCm39) K2074* probably null Het
Apob A G 12: 8,057,848 (GRCm39) Y2077C probably damaging Het
Arhgap17 A T 7: 122,907,600 (GRCm39) L254Q probably damaging Het
Arhgap26 T A 18: 39,126,690 (GRCm39) probably benign Het
Arhgef5 A G 6: 43,249,762 (GRCm39) D171G probably benign Het
Arid1b T A 17: 5,392,478 (GRCm39) S2003T probably damaging Het
Armc5 T G 7: 127,839,900 (GRCm39) L406R possibly damaging Het
Arsb T C 13: 93,908,485 (GRCm39) V67A probably benign Het
Aspm A G 1: 139,419,281 (GRCm39) Y2982C probably damaging Het
Bltp1 C A 3: 37,052,348 (GRCm39) T3016K probably damaging Het
Btbd7 A G 12: 102,774,307 (GRCm39) L487P probably damaging Het
Card11 C G 5: 140,860,169 (GRCm39) D1063H probably damaging Het
Ccdc186 G A 19: 56,787,123 (GRCm39) T615M probably damaging Het
Cd101 T A 3: 100,901,205 (GRCm39) T960S probably benign Het
Cdca7l C A 12: 117,837,520 (GRCm39) S191* probably null Het
Cemip A T 7: 83,646,619 (GRCm39) I143N probably damaging Het
Cep170 C T 1: 176,609,829 (GRCm39) E161K possibly damaging Het
Cfhr4 T G 1: 139,702,301 (GRCm39) D61A probably damaging Het
Chrm2 A T 6: 36,501,168 (GRCm39) T342S probably benign Het
Cib2 A G 9: 54,457,163 (GRCm39) F34L probably benign Het
Cnot1 A T 8: 96,459,859 (GRCm39) I1836N probably benign Het
Col4a3 C A 1: 82,650,400 (GRCm39) P552Q unknown Het
Cp T A 3: 20,043,388 (GRCm39) probably benign Het
Cul3 C T 1: 80,267,806 (GRCm39) V112I probably benign Het
Dcdc5 A G 2: 106,195,895 (GRCm39) noncoding transcript Het
Disp1 A T 1: 182,917,027 (GRCm39) V133E probably damaging Het
Dlg4 A G 11: 69,921,751 (GRCm39) D30G probably damaging Het
Dop1a C T 9: 86,374,114 (GRCm39) T191I probably damaging Het
Enam T G 5: 88,650,173 (GRCm39) S561A probably benign Het
Fbxw8 G T 5: 118,263,092 (GRCm39) probably null Het
Filip1 A G 9: 79,725,214 (GRCm39) V1135A probably benign Het
Galnt6 T C 15: 100,614,059 (GRCm39) T81A probably benign Het
Ghdc T C 11: 100,657,814 (GRCm39) K472E probably benign Het
Gm10568 T G 1: 3,751,164 (GRCm39) noncoding transcript Het
Gm4953 T A 1: 158,995,929 (GRCm39) noncoding transcript Het
Gm6871 T A 7: 41,223,016 (GRCm39) H24L probably benign Het
Gpr155 G A 2: 73,197,882 (GRCm39) Q413* probably null Het
Grhl2 A G 15: 37,291,920 (GRCm39) probably null Het
Ighv1-31 G C 12: 114,793,128 (GRCm39) S36* probably null Het
Ighv8-5 A G 12: 115,031,462 (GRCm39) S26P probably damaging Het
Igkv17-134 A C 6: 67,697,910 (GRCm39) probably benign Het
Igkv5-48 A C 6: 69,703,833 (GRCm39) L24R probably damaging Het
Isg20l2 T A 3: 87,846,570 (GRCm39) V340E probably damaging Het
Lrrtm1 A G 6: 77,221,884 (GRCm39) Y447C probably damaging Het
Ltbp1 T C 17: 75,634,287 (GRCm39) S855P probably damaging Het
Mgat4e A T 1: 134,469,602 (GRCm39) N147K probably damaging Het
Mlc1 A G 15: 88,842,415 (GRCm39) L315P possibly damaging Het
Mrgpra2a A G 7: 47,076,292 (GRCm39) V322A probably benign Het
Mroh7 T C 4: 106,567,152 (GRCm39) probably null Het
Mybpc1 T A 10: 88,391,586 (GRCm39) K304* probably null Het
Nlrp14 A C 7: 106,785,790 (GRCm39) D622A possibly damaging Het
Nlrp1b T A 11: 71,108,103 (GRCm39) H466L probably benign Het
Nlrp4d T A 7: 10,112,336 (GRCm39) noncoding transcript Het
Nrxn3 A G 12: 89,227,130 (GRCm39) E628G possibly damaging Het
Nup133 T C 8: 124,653,870 (GRCm39) R530G possibly damaging Het
Nup98 A G 7: 101,845,007 (GRCm39) S21P unknown Het
Or2h2b-ps1 T C 17: 37,480,934 (GRCm39) I202V probably benign Het
Or2l13b T C 16: 19,348,768 (GRCm39) T301A probably benign Het
Or4f14b A T 2: 111,775,423 (GRCm39) I126K possibly damaging Het
Or52e8 G A 7: 104,624,686 (GRCm39) P169S possibly damaging Het
Or5k1 T A 16: 58,617,805 (GRCm39) T135S probably benign Het
Or6c66 T C 10: 129,461,676 (GRCm39) T85A probably damaging Het
Or8c11 T A 9: 38,290,038 (GRCm39) V287E probably null Het
Otog A T 7: 45,913,486 (GRCm39) Y773F probably damaging Het
Otog A T 7: 45,947,958 (GRCm39) I2320F probably damaging Het
Otogl T C 10: 107,715,378 (GRCm39) S433G probably benign Het
Pcdhb17 A T 18: 37,618,212 (GRCm39) M1L possibly damaging Het
Pde7b T A 10: 20,600,480 (GRCm39) probably benign Het
Pgm1 T C 4: 99,820,724 (GRCm39) V207A probably damaging Het
Pkd1 T A 17: 24,791,661 (GRCm39) V1116E probably damaging Het
Pkd1l1 T A 11: 8,879,360 (GRCm39) Y497F possibly damaging Het
Pomgnt2 T C 9: 121,812,013 (GRCm39) N256S probably benign Het
Pot1a A T 6: 25,746,020 (GRCm39) probably benign Het
Prdm9 T C 17: 15,764,585 (GRCm39) T732A probably benign Het
Prg4 T A 1: 150,331,574 (GRCm39) probably benign Het
Ptpro T C 6: 137,345,336 (GRCm39) V114A probably damaging Het
Pyurf A G 6: 57,668,933 (GRCm39) S20P unknown Het
Rasgrf1 A G 9: 89,858,805 (GRCm39) T488A probably benign Het
Rassf8 A T 6: 145,761,006 (GRCm39) K111* probably null Het
Reps1 A T 10: 17,983,436 (GRCm39) E426D probably damaging Het
Robo2 T C 16: 73,730,666 (GRCm39) K982R probably damaging Het
Rps23 T C 13: 91,071,871 (GRCm39) probably null Het
Scamp4 T A 10: 80,445,505 (GRCm39) V56E probably damaging Het
Serpina1c C T 12: 103,861,291 (GRCm39) V408I probably benign Het
Sigirr A G 7: 140,673,701 (GRCm39) W49R probably damaging Het
Slc17a6 A T 7: 51,308,489 (GRCm39) H271L possibly damaging Het
Slc7a5 G T 8: 122,611,861 (GRCm39) T389K probably damaging Het
Slf1 T A 13: 77,191,999 (GRCm39) H945L probably benign Het
Slit3 T C 11: 35,523,549 (GRCm39) S662P probably damaging Het
Snta1 C A 2: 154,218,938 (GRCm39) E466* probably null Het
Sowaha A G 11: 53,369,272 (GRCm39) L488P probably damaging Het
Spata17 C A 1: 186,926,208 (GRCm39) V41F probably damaging Het
Spta1 T A 1: 174,045,429 (GRCm39) probably null Het
Srrm2 T A 17: 24,034,362 (GRCm39) probably benign Het
Stard13 T C 5: 150,985,992 (GRCm39) N388S probably benign Het
Stmn3 T C 2: 180,950,630 (GRCm39) K59E probably damaging Het
Sval1 A G 6: 41,932,378 (GRCm39) N76S probably benign Het
Svep1 T C 4: 58,096,276 (GRCm39) H1448R possibly damaging Het
Sycp2 A T 2: 178,000,017 (GRCm39) D986E probably benign Het
Sytl5 C T X: 9,781,841 (GRCm39) P181L possibly damaging Het
Tbkbp1 G A 11: 97,029,956 (GRCm39) S400L probably benign Het
Tesc G T 5: 118,194,531 (GRCm39) probably benign Het
Tjp1 C T 7: 64,993,475 (GRCm39) G33R probably damaging Het
Tmem156 A G 5: 65,248,805 (GRCm39) probably benign Het
Top3a A G 11: 60,643,204 (GRCm39) probably benign Het
Tpcn1 A G 5: 120,694,584 (GRCm39) W162R probably damaging Het
Tpd52l2 A T 2: 181,157,005 (GRCm39) probably benign Het
Trim80 G A 11: 115,337,281 (GRCm39) G381D probably damaging Het
Ugt1a10 C T 1: 88,142,845 (GRCm39) P113L probably damaging Het
Vmn2r117 TC T 17: 23,698,487 (GRCm39) probably null Het
Vmn2r56 T A 7: 12,449,462 (GRCm39) I259F possibly damaging Het
Vmn2r59 T C 7: 41,693,077 (GRCm39) T508A probably benign Het
Wdr73 A G 7: 80,541,456 (GRCm39) V362A probably damaging Het
Zdhhc21 G T 4: 82,738,568 (GRCm39) T207K possibly damaging Het
Zfp120 T A 2: 149,959,872 (GRCm39) Q150L probably damaging Het
Zfp212 C A 6: 47,908,433 (GRCm39) Q471K possibly damaging Het
Zfp804b C T 5: 6,820,540 (GRCm39) G841D possibly damaging Het
Znfx1 A T 2: 166,878,724 (GRCm39) M1884K probably damaging Het
Znfx1 G T 2: 166,879,402 (GRCm39) A1658D probably benign Het
Other mutations in Tlr11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00590:Tlr11 APN 14 50,598,373 (GRCm39) missense probably benign
IGL02090:Tlr11 APN 14 50,600,489 (GRCm39) missense probably damaging 0.99
IGL02286:Tlr11 APN 14 50,598,328 (GRCm39) missense possibly damaging 0.91
IGL02671:Tlr11 APN 14 50,598,149 (GRCm39) missense probably damaging 1.00
IGL03064:Tlr11 APN 14 50,598,557 (GRCm39) missense probably damaging 1.00
IGL03068:Tlr11 APN 14 50,598,941 (GRCm39) missense probably benign
R0099:Tlr11 UTSW 14 50,598,275 (GRCm39) missense probably benign 0.14
R0727:Tlr11 UTSW 14 50,598,926 (GRCm39) missense possibly damaging 0.67
R0944:Tlr11 UTSW 14 50,599,793 (GRCm39) missense probably benign 0.12
R1490:Tlr11 UTSW 14 50,600,633 (GRCm39) missense probably benign 0.00
R1726:Tlr11 UTSW 14 50,598,998 (GRCm39) missense probably benign 0.00
R1803:Tlr11 UTSW 14 50,598,104 (GRCm39) missense probably benign 0.00
R1908:Tlr11 UTSW 14 50,598,664 (GRCm39) missense probably benign 0.00
R1971:Tlr11 UTSW 14 50,598,691 (GRCm39) missense probably benign
R1981:Tlr11 UTSW 14 50,599,445 (GRCm39) missense possibly damaging 0.95
R2023:Tlr11 UTSW 14 50,600,026 (GRCm39) missense probably damaging 0.96
R2079:Tlr11 UTSW 14 50,598,437 (GRCm39) missense probably damaging 0.99
R2155:Tlr11 UTSW 14 50,598,139 (GRCm39) missense probably benign 0.01
R2251:Tlr11 UTSW 14 50,598,249 (GRCm39) missense probably benign 0.02
R3017:Tlr11 UTSW 14 50,600,178 (GRCm39) nonsense probably null
R3760:Tlr11 UTSW 14 50,599,700 (GRCm39) missense probably damaging 1.00
R3876:Tlr11 UTSW 14 50,600,611 (GRCm39) missense probably benign
R3936:Tlr11 UTSW 14 50,600,192 (GRCm39) missense possibly damaging 0.78
R4002:Tlr11 UTSW 14 50,599,984 (GRCm39) missense probably benign
R4024:Tlr11 UTSW 14 50,600,303 (GRCm39) missense probably benign 0.02
R4118:Tlr11 UTSW 14 50,600,684 (GRCm39) missense probably damaging 1.00
R4222:Tlr11 UTSW 14 50,599,306 (GRCm39) missense probably damaging 0.99
R4365:Tlr11 UTSW 14 50,598,926 (GRCm39) missense probably damaging 0.98
R4678:Tlr11 UTSW 14 50,598,439 (GRCm39) missense possibly damaging 0.85
R4779:Tlr11 UTSW 14 50,598,707 (GRCm39) missense possibly damaging 0.76
R4921:Tlr11 UTSW 14 50,600,342 (GRCm39) missense possibly damaging 0.48
R5114:Tlr11 UTSW 14 50,600,578 (GRCm39) missense possibly damaging 0.81
R5126:Tlr11 UTSW 14 50,598,287 (GRCm39) missense probably damaging 1.00
R5349:Tlr11 UTSW 14 50,598,337 (GRCm39) missense probably benign 0.45
R5606:Tlr11 UTSW 14 50,599,717 (GRCm39) missense probably benign 0.08
R5650:Tlr11 UTSW 14 50,598,658 (GRCm39) missense probably benign 0.03
R5958:Tlr11 UTSW 14 50,598,234 (GRCm39) missense probably damaging 0.99
R5966:Tlr11 UTSW 14 50,599,712 (GRCm39) missense probably benign 0.02
R6480:Tlr11 UTSW 14 50,600,512 (GRCm39) missense possibly damaging 0.62
R6484:Tlr11 UTSW 14 50,600,135 (GRCm39) missense probably damaging 0.99
R6679:Tlr11 UTSW 14 50,600,311 (GRCm39) missense probably benign 0.00
R6717:Tlr11 UTSW 14 50,599,561 (GRCm39) missense probably benign
R7085:Tlr11 UTSW 14 50,600,113 (GRCm39) missense probably damaging 0.99
R7241:Tlr11 UTSW 14 50,599,598 (GRCm39) missense possibly damaging 0.95
R7440:Tlr11 UTSW 14 50,598,801 (GRCm39) missense probably benign 0.00
R7482:Tlr11 UTSW 14 50,600,456 (GRCm39) missense probably damaging 0.99
R7582:Tlr11 UTSW 14 50,599,186 (GRCm39) nonsense probably null
R7790:Tlr11 UTSW 14 50,599,382 (GRCm39) missense probably benign
R7818:Tlr11 UTSW 14 50,599,285 (GRCm39) missense probably damaging 1.00
R7827:Tlr11 UTSW 14 50,598,611 (GRCm39) missense probably benign 0.00
R8144:Tlr11 UTSW 14 50,599,945 (GRCm39) missense probably damaging 0.99
R8847:Tlr11 UTSW 14 50,600,182 (GRCm39) missense possibly damaging 0.85
R9027:Tlr11 UTSW 14 50,598,749 (GRCm39) missense probably damaging 1.00
R9035:Tlr11 UTSW 14 50,598,434 (GRCm39) missense probably benign 0.00
R9393:Tlr11 UTSW 14 50,599,547 (GRCm39) missense probably benign 0.03
RF002:Tlr11 UTSW 14 50,598,682 (GRCm39) missense possibly damaging 0.63
Z1088:Tlr11 UTSW 14 50,599,795 (GRCm39) missense possibly damaging 0.48
Z1176:Tlr11 UTSW 14 50,599,793 (GRCm39) missense probably benign 0.40
Z1176:Tlr11 UTSW 14 50,598,119 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCCACACGGTACTGAGTTTTGG -3'
(R):5'- TGCACCAGGGACTTGCTAAG -3'

Sequencing Primer
(F):5'- TTTGGGGCTTTCTCACCAG -3'
(R):5'- GACTTGCTAAGGCCTGTCCTG -3'
Posted On 2016-04-15