Incidental Mutation 'R5729:Irf2bp1'
ID 452657
Institutional Source Beutler Lab
Gene Symbol Irf2bp1
Ensembl Gene ENSMUSG00000044030
Gene Name interferon regulatory factor 2 binding protein 1
Synonyms 6330414O09Rik
MMRRC Submission 043346-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.658) question?
Stock # R5729 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 18737983-18740688 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 18739172 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 271 (E271*)
Ref Sequence ENSEMBL: ENSMUSP00000061234 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053713] [ENSMUST00000059331] [ENSMUST00000131087]
AlphaFold Q8R3Y8
Predicted Effect probably null
Transcript: ENSMUST00000053713
AA Change: E271*
SMART Domains Protein: ENSMUSP00000061234
Gene: ENSMUSG00000044030
AA Change: E271*

DomainStartEndE-ValueType
Pfam:IRF-2BP1_2 8 59 9.5e-37 PFAM
low complexity region 82 105 N/A INTRINSIC
low complexity region 114 128 N/A INTRINSIC
low complexity region 139 156 N/A INTRINSIC
low complexity region 165 179 N/A INTRINSIC
low complexity region 441 458 N/A INTRINSIC
low complexity region 481 500 N/A INTRINSIC
Pfam:zf-C3HC4 503 549 1.9e-6 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000059331
SMART Domains Protein: ENSMUSP00000058718
Gene: ENSMUSG00000048481

DomainStartEndE-ValueType
low complexity region 2 17 N/A INTRINSIC
SANT 20 90 4.06e-5 SMART
low complexity region 125 157 N/A INTRINSIC
low complexity region 212 250 N/A INTRINSIC
low complexity region 278 322 N/A INTRINSIC
low complexity region 323 347 N/A INTRINSIC
low complexity region 358 374 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124897
Predicted Effect probably benign
Transcript: ENSMUST00000131087
SMART Domains Protein: ENSMUSP00000117357
Gene: ENSMUSG00000048481

DomainStartEndE-ValueType
low complexity region 2 17 N/A INTRINSIC
SANT 20 90 4.06e-5 SMART
low complexity region 125 157 N/A INTRINSIC
low complexity region 212 250 N/A INTRINSIC
low complexity region 278 322 N/A INTRINSIC
low complexity region 323 347 N/A INTRINSIC
low complexity region 358 374 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206304
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206381
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 95.2%
Validation Efficiency 97% (62/64)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adss2 A T 1: 177,623,824 (GRCm39) V46E possibly damaging Het
Aldoart2 T C 12: 55,612,690 (GRCm39) V205A probably benign Het
Atp1a2 A G 1: 172,120,938 (GRCm39) S45P probably damaging Het
Atp4a A G 7: 30,411,851 (GRCm39) K29E possibly damaging Het
AU040320 T A 4: 126,724,208 (GRCm39) D428E probably damaging Het
Bend7 T C 2: 4,768,085 (GRCm39) L347P probably damaging Het
Cacna2d1 T A 5: 16,140,037 (GRCm39) L9* probably null Het
Ccdc103 A T 11: 102,773,904 (GRCm39) I50F probably damaging Het
Cdc5l T C 17: 45,737,495 (GRCm39) I88V probably benign Het
Cracr2a T C 6: 127,584,199 (GRCm39) V86A possibly damaging Het
Cybb C G X: 9,316,989 (GRCm39) D246H probably benign Het
Dgkd C T 1: 87,864,054 (GRCm39) Q90* probably null Het
Dnajc21 A T 15: 10,449,682 (GRCm39) D446E probably benign Het
Fam13a T G 6: 58,916,292 (GRCm39) R648S probably damaging Het
Gabrg2 A G 11: 41,858,450 (GRCm39) V226A probably damaging Het
Gm5499 A T 17: 87,385,944 (GRCm39) noncoding transcript Het
Gprc5c G T 11: 114,755,093 (GRCm39) V257L possibly damaging Het
Krt86 T G 15: 101,374,429 (GRCm39) V274G probably benign Het
Lats2 A T 14: 57,960,192 (GRCm39) C151S probably benign Het
Mapk3 A T 7: 126,363,979 (GRCm39) T254S probably benign Het
Mat2b A T 11: 40,573,373 (GRCm39) M202K probably damaging Het
Mos A G 4: 3,870,971 (GRCm39) Y282H probably benign Het
Myo3b A G 2: 69,936,083 (GRCm39) K108R probably damaging Het
Naa16 A G 14: 79,593,220 (GRCm39) Y417H probably damaging Het
Oat A T 7: 132,159,984 (GRCm39) I412N probably damaging Het
Or4d11 A T 19: 12,013,272 (GRCm39) I278N probably damaging Het
Pcdh1 A T 18: 38,335,999 (GRCm39) V73D probably damaging Het
Pigv A T 4: 133,392,134 (GRCm39) Y345* probably null Het
Pitpnc1 G T 11: 107,228,264 (GRCm39) F34L probably benign Het
Plxnd1 A G 6: 115,942,838 (GRCm39) L1282P probably damaging Het
Ppp1r3a T C 6: 14,719,762 (GRCm39) D384G probably benign Het
Ppp2ca G A 11: 52,008,856 (GRCm39) E119K probably damaging Het
Psg29 A T 7: 16,944,459 (GRCm39) N323I probably damaging Het
Rasa4 T C 5: 136,122,016 (GRCm39) V108A probably benign Het
Rbm14 A G 19: 4,852,577 (GRCm39) probably benign Het
Rfc1 A T 5: 65,434,795 (GRCm39) V657E probably damaging Het
Rhcg A T 7: 79,250,371 (GRCm39) N237K probably damaging Het
Rpgrip1 A G 14: 52,397,617 (GRCm39) Q1302R probably benign Het
Rragc A G 4: 123,818,645 (GRCm39) M287V possibly damaging Het
Scn7a A G 2: 66,572,301 (GRCm39) probably null Het
Sema6a C T 18: 47,414,410 (GRCm39) C506Y probably damaging Het
Senp1 G T 15: 97,964,412 (GRCm39) H267Q possibly damaging Het
Skor2 A G 18: 76,946,578 (GRCm39) E100G unknown Het
Slc38a11 A T 2: 65,147,365 (GRCm39) C371S probably benign Het
Snai3 G A 8: 123,181,629 (GRCm39) A276V probably benign Het
Sp110 C G 1: 85,516,839 (GRCm39) E219D probably damaging Het
Spag6 C T 2: 18,720,525 (GRCm39) T99I probably benign Het
Spop A G 11: 95,376,675 (GRCm39) I243V possibly damaging Het
Sra1 A T 18: 36,800,496 (GRCm39) probably benign Het
Stag3 T A 5: 138,288,485 (GRCm39) S140T possibly damaging Het
Stx16 G A 2: 173,935,292 (GRCm39) G156R probably damaging Het
Tbc1d2b G C 9: 90,089,925 (GRCm39) A868G probably benign Het
Tead2 A G 7: 44,870,166 (GRCm39) probably benign Het
Tmem53 C A 4: 117,125,669 (GRCm39) H261N probably damaging Het
Ube4a A T 9: 44,844,627 (GRCm39) S932T probably damaging Het
Usp9y A T Y: 1,381,339 (GRCm39) D827E probably damaging Het
Vmn2r53 T C 7: 12,334,733 (GRCm39) E309G probably damaging Het
Wrn T C 8: 33,758,806 (GRCm39) S1026G probably benign Het
Zfp646 G A 7: 127,484,626 (GRCm39) A1760T probably damaging Het
Other mutations in Irf2bp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01376:Irf2bp1 APN 7 18,739,952 (GRCm39) missense possibly damaging 0.86
IGL01983:Irf2bp1 APN 7 18,739,220 (GRCm39) missense possibly damaging 0.70
R0063:Irf2bp1 UTSW 7 18,739,772 (GRCm39) missense possibly damaging 0.91
R0255:Irf2bp1 UTSW 7 18,738,927 (GRCm39) missense possibly damaging 0.91
R0849:Irf2bp1 UTSW 7 18,738,659 (GRCm39) missense possibly damaging 0.73
R2250:Irf2bp1 UTSW 7 18,739,724 (GRCm39) missense probably benign 0.12
R3972:Irf2bp1 UTSW 7 18,739,369 (GRCm39) missense possibly damaging 0.70
R4703:Irf2bp1 UTSW 7 18,739,496 (GRCm39) missense possibly damaging 0.91
R5290:Irf2bp1 UTSW 7 18,738,923 (GRCm39) missense possibly damaging 0.85
R5902:Irf2bp1 UTSW 7 18,738,372 (GRCm39) missense probably benign 0.07
R6874:Irf2bp1 UTSW 7 18,739,142 (GRCm39) missense possibly damaging 0.70
R8260:Irf2bp1 UTSW 7 18,740,079 (GRCm39) missense possibly damaging 0.85
R9291:Irf2bp1 UTSW 7 18,738,458 (GRCm39) missense probably damaging 1.00
R9295:Irf2bp1 UTSW 7 18,739,740 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AGAGGAATGCGGACTGCTTG -3'
(R):5'- TCCGTAAGCAGCTCTCCTAAC -3'

Sequencing Primer
(F):5'- TGCTTGGCAGAACTGAACG -3'
(R):5'- TAAGCAGCTCTCCTAACTGGCG -3'
Posted On 2017-01-03