Incidental Mutation 'IGL02644:Tlr13'
ID 301871
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tlr13
Ensembl Gene ENSMUSG00000033777
Gene Name toll-like receptor 13
Synonyms LOC279572
Accession Numbers
Essential gene? Not available question?
Stock # IGL02644
Quality Score
Status
Chromosome X
Chromosomal Location 105186881-105204099 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 105200503 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 80 (D80G)
Ref Sequence ENSEMBL: ENSMUSP00000043101 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040065]
AlphaFold Q6R5N8
Predicted Effect probably benign
Transcript: ENSMUST00000040065
AA Change: D80G

PolyPhen 2 Score 0.117 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000043101
Gene: ENSMUSG00000033777
AA Change: D80G

DomainStartEndE-ValueType
LRR 106 125 5.12e1 SMART
LRR_TYP 126 149 8.81e-2 SMART
LRR 150 172 1.45e1 SMART
LRR_TYP 173 196 5.67e-5 SMART
LRR 197 219 1.49e1 SMART
LRR 223 245 3.76e1 SMART
LRR 246 269 1.33e1 SMART
LRR 395 418 4.7e0 SMART
LRR_TYP 419 442 8.47e-4 SMART
LRR 443 466 1.16e-1 SMART
LRR 467 490 6.06e1 SMART
LRR_TYP 491 514 2.09e-3 SMART
LRR_TYP 515 538 3.39e-3 SMART
LRR_TYP 539 562 6.23e-2 SMART
LRR 563 586 1.97e2 SMART
LRR 592 617 3.36e2 SMART
LRR_TYP 670 693 3.58e-2 SMART
LRR 694 717 8.26e1 SMART
TIR 833 978 1.8e-29 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Macrophages isolated from mice carrying an ENU-induced mutation respond normally to known TLR ligands and can contain various viral infections; however, mice carrying this allele have not been tested for immune responses in vivo. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl4 A T 3: 151,198,007 (GRCm39) Y89F probably benign Het
Agl A G 3: 116,580,246 (GRCm39) Y406H probably damaging Het
Ankhd1 G A 18: 36,711,828 (GRCm39) probably null Het
Ankmy1 T C 1: 92,812,776 (GRCm39) D511G probably benign Het
Arid2 T C 15: 96,266,589 (GRCm39) Y546H probably damaging Het
Asap1 G T 15: 63,982,911 (GRCm39) P806T probably damaging Het
Aspa T A 11: 73,212,992 (GRCm39) T117S probably damaging Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Bspry A T 4: 62,414,565 (GRCm39) H386L probably damaging Het
C1qc T C 4: 136,617,629 (GRCm39) T156A possibly damaging Het
Cfhr4 A G 1: 139,708,905 (GRCm39) M1T probably null Het
Copz2 A T 11: 96,744,257 (GRCm39) probably benign Het
Cybb A G X: 9,333,395 (GRCm39) V23A probably benign Het
D630003M21Rik T A 2: 158,058,730 (GRCm39) D390V possibly damaging Het
Dennd10 T A 19: 60,810,741 (GRCm39) S43T possibly damaging Het
Dpy19l2 G T 9: 24,569,888 (GRCm39) P355Q probably damaging Het
Gcn1 A T 5: 115,713,250 (GRCm39) Q71L probably benign Het
Gpd1l T C 9: 114,732,725 (GRCm39) probably null Het
Hydin A G 8: 111,265,100 (GRCm39) D2761G probably damaging Het
Ifi202b T A 1: 173,799,280 (GRCm39) H256L probably benign Het
Igkv8-24 T C 6: 70,193,872 (GRCm39) Y112C probably damaging Het
Lama3 G A 18: 12,658,910 (GRCm39) R2022Q probably benign Het
Mroh4 T A 15: 74,482,224 (GRCm39) R675S possibly damaging Het
Mtf1 T G 4: 124,714,028 (GRCm39) C146G probably damaging Het
Nubpl A G 12: 52,317,841 (GRCm39) D178G probably damaging Het
Or7e165 A C 9: 19,695,010 (GRCm39) I194L probably benign Het
Pam16 A G 16: 4,434,697 (GRCm39) S91P probably damaging Het
Pcdhac2 A G 18: 37,278,232 (GRCm39) E404G probably benign Het
Pde7a C A 3: 19,311,031 (GRCm39) probably benign Het
Perm1 G T 4: 156,303,043 (GRCm39) G529V probably damaging Het
Pik3c2a T C 7: 115,972,049 (GRCm39) T794A probably benign Het
Ppfibp1 A G 6: 146,923,938 (GRCm39) Y722C probably damaging Het
Ppm1m A T 9: 106,074,082 (GRCm39) I241N probably damaging Het
Psd T C 19: 46,311,834 (GRCm39) Y282C probably damaging Het
Rpl27 T A 11: 101,336,317 (GRCm39) probably benign Het
Scaf1 A G 7: 44,655,357 (GRCm39) probably benign Het
Sec14l2 A T 11: 4,053,380 (GRCm39) probably benign Het
Smchd1 T A 17: 71,667,016 (GRCm39) probably benign Het
Sptb A T 12: 76,652,391 (GRCm39) D1615E probably damaging Het
Stt3a A C 9: 36,663,649 (GRCm39) C198G possibly damaging Het
Tas2r144 T C 6: 42,192,787 (GRCm39) S176P possibly damaging Het
Tmco4 A G 4: 138,737,920 (GRCm39) probably benign Het
Tnpo2 T A 8: 85,771,109 (GRCm39) C132S possibly damaging Het
Tubgcp3 T C 8: 12,698,733 (GRCm39) D406G probably damaging Het
Vmn2r125 G A 4: 156,703,294 (GRCm39) R224Q probably benign Het
Zfp524 C A 7: 5,020,479 (GRCm39) D2E probably damaging Het
Other mutations in Tlr13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02044:Tlr13 APN X 105,200,703 (GRCm39) missense probably damaging 1.00
IGL02809:Tlr13 APN X 105,200,297 (GRCm39) splice site probably benign
Tlr13rev1 UTSW X 105,200,983 (GRCm39) missense probably benign
X0024:Tlr13 UTSW X 105,200,334 (GRCm39) missense probably benign
X0028:Tlr13 UTSW X 105,200,928 (GRCm39) missense probably benign 0.04
X0067:Tlr13 UTSW X 105,200,839 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16