Incidental Mutation 'R4241:Peli3'
Institutional Source Beutler Lab
Gene Symbol Peli3
Ensembl Gene ENSMUSG00000024901
Gene Namepellino 3
MMRRC Submission 041058-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.100) question?
Stock #R4241 (G1)
Quality Score225
Status Validated
Chromosomal Location4930651-4943127 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 4932398 bp
Amino Acid Change Histidine to Arginine at position 413 (H413R)
Ref Sequence ENSEMBL: ENSMUSP00000025834 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025834] [ENSMUST00000025851] [ENSMUST00000120475] [ENSMUST00000133254]
Predicted Effect probably damaging
Transcript: ENSMUST00000025834
AA Change: H413R

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000025834
Gene: ENSMUSG00000024901
AA Change: H413R

Pfam:Pellino 35 445 3.8e-211 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000025851
SMART Domains Protein: ENSMUSP00000025851
Gene: ENSMUSG00000063904

Pfam:Peptidase_M49 143 704 1.3e-236 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000120475
AA Change: H379R

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000113193
Gene: ENSMUSG00000024901
AA Change: H379R

Pfam:Pellino 30 95 1.8e-24 PFAM
Pfam:Pellino 92 411 5.3e-175 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000133254
SMART Domains Protein: ENSMUSP00000118173
Gene: ENSMUSG00000024901

Pfam:Pellino 30 155 3.5e-58 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133504
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139436
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146289
Meta Mutation Damage Score 0.8042 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 95.9%
Validation Efficiency 98% (49/50)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a scaffold protein and an intermediate signaling protein in the innate immune response pathway. The encoded protein helps transmit the immune response signal from Toll-like receptors to IRAK1/TRAF6 complexes. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]
PHENOTYPE: Mice homozygous for a null mutation display decreased susceptibility to viral infection. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik A G 7: 28,154,335 S1575G probably damaging Het
Agl A T 3: 116,754,848 probably benign Het
Ap5b1 C T 19: 5,568,797 L82F possibly damaging Het
Arfgef3 A G 10: 18,625,164 S1113P probably damaging Het
Atoh1 A C 6: 64,729,774 N151T probably damaging Het
Bcas3 T A 11: 85,470,826 S25R probably damaging Het
Blcap T A 2: 157,560,423 probably benign Het
Btbd6 C T 12: 112,976,796 A13V probably benign Het
Ccdc83 A C 7: 90,247,138 N74K probably damaging Het
Cdh9 A G 15: 16,849,079 probably null Het
Chd1 C T 17: 15,770,027 R1614* probably null Het
Col16a1 G T 4: 130,099,050 Q1567H probably damaging Het
Coq6 A T 12: 84,373,789 probably benign Het
Cpd T C 11: 76,846,785 D61G probably benign Het
Csnk1e A G 15: 79,424,895 F277S probably damaging Het
Cyp2d41-ps T A 15: 82,779,586 noncoding transcript Het
Dbt T C 3: 116,533,296 I98T probably damaging Het
Eif3e G A 15: 43,262,690 T287I probably damaging Het
Gm7135 A G 1: 97,353,953 noncoding transcript Het
Gpr176 A T 2: 118,279,610 S389R probably benign Het
Hax1 A G 3: 89,995,690 S257P probably damaging Het
Herc1 CTGAGGACTCTTTG CTG 9: 66,448,348 probably null Het
Ighv1-53 C T 12: 115,158,822 C5Y probably benign Het
Klhl13 T A X: 23,315,175 D2V probably damaging Het
Kynu A T 2: 43,681,410 H446L probably benign Het
Lingo1 A G 9: 56,620,102 F401S probably damaging Het
Lmbrd1 C T 1: 24,692,968 Q89* probably null Het
Mov10 T A 3: 104,797,276 Q773L probably benign Het
Olfr1356 T A 10: 78,847,905 R3S probably benign Het
Olfr596 G T 7: 103,310,661 *313Y probably null Het
Pde6c G A 19: 38,162,845 G608S probably damaging Het
Pkdrej C T 15: 85,818,144 R1197Q probably damaging Het
Rcan2 T A 17: 43,953,479 V10D probably benign Het
Slc10a5 A G 3: 10,335,460 S47P probably damaging Het
Sprr3 A G 3: 92,456,907 V210A possibly damaging Het
Tcerg1l G T 7: 138,397,632 Q8K unknown Het
Ubfd1 T C 7: 122,071,754 V265A possibly damaging Het
Ubr1 T C 2: 120,934,386 D529G possibly damaging Het
Vmn1r180 A T 7: 23,952,873 I154F probably damaging Het
Vmn1r237 A G 17: 21,314,663 H216R possibly damaging Het
Whrn C T 4: 63,432,973 probably benign Het
Zfr T G 15: 12,149,659 D388E probably damaging Het
Zic5 T C 14: 122,464,663 I219V probably benign Het
Zmat5 A G 11: 4,728,614 N53D probably benign Het
Other mutations in Peli3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01555:Peli3 APN 19 4935058 missense probably damaging 0.99
IGL01608:Peli3 APN 19 4932827 missense probably damaging 0.99
IGL03164:Peli3 APN 19 4936116 critical splice donor site probably null
R0540:Peli3 UTSW 19 4941911 start codon destroyed probably null 0.88
R0633:Peli3 UTSW 19 4941782 missense probably damaging 1.00
R4578:Peli3 UTSW 19 4934458 missense probably benign 0.00
R4817:Peli3 UTSW 19 4932566 missense probably damaging 1.00
R7360:Peli3 UTSW 19 4935075 missense possibly damaging 0.95
R7718:Peli3 UTSW 19 4934556 critical splice acceptor site probably null
R8553:Peli3 UTSW 19 4934932 missense probably damaging 0.99
R8684:Peli3 UTSW 19 4934994 missense probably damaging 1.00
Z1176:Peli3 UTSW 19 4934967 missense probably benign 0.01
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-06-12