Incidental Mutation 'R7237:Nlrp4b'
ID 562894
Institutional Source Beutler Lab
Gene Symbol Nlrp4b
Ensembl Gene ENSMUSG00000034087
Gene Name NLR family, pyrin domain containing 4B
Synonyms Nalp4b, Nalp-gamma
MMRRC Submission 045344-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R7237 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 10421720-10464095 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 10449143 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 449 (V449I)
Ref Sequence ENSEMBL: ENSMUSP00000043881 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047809] [ENSMUST00000117413] [ENSMUST00000132990] [ENSMUST00000211069]
AlphaFold Q8C6J9
Predicted Effect probably benign
Transcript: ENSMUST00000047809
AA Change: V449I

PolyPhen 2 Score 0.120 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000043881
Gene: ENSMUSG00000034087
AA Change: V449I

DomainStartEndE-ValueType
PYRIN 6 89 1.4e-20 SMART
Pfam:NACHT 143 312 7.9e-40 PFAM
low complexity region 520 535 N/A INTRINSIC
LRR 683 710 4.9e0 SMART
LRR 712 739 1.97e0 SMART
LRR 740 767 1.13e-4 SMART
LRR 769 796 1.93e1 SMART
LRR 797 824 1.73e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000117413
AA Change: V449I

PolyPhen 2 Score 0.120 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000113095
Gene: ENSMUSG00000034087
AA Change: V449I

DomainStartEndE-ValueType
PYRIN 6 89 1.4e-20 SMART
Pfam:NACHT 143 312 3.3e-39 PFAM
low complexity region 520 535 N/A INTRINSIC
LRR 683 710 4.9e0 SMART
LRR 712 739 1.97e0 SMART
LRR 740 767 1.13e-4 SMART
LRR 769 796 1.93e1 SMART
LRR 797 824 1.73e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000132990
AA Change: V82I

PolyPhen 2 Score 0.120 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000115831
Gene: ENSMUSG00000034087
AA Change: V82I

DomainStartEndE-ValueType
low complexity region 153 168 N/A INTRINSIC
LRR 316 343 4.9e0 SMART
LRR 345 372 1.97e0 SMART
LRR 373 400 1.13e-4 SMART
LRR 402 429 1.93e1 SMART
LRR 430 457 1.73e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000211069
Predicted Effect probably benign
Transcript: ENSMUST00000211258
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency 98% (83/85)
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap21 A T 2: 20,854,783 (GRCm39) C1536* probably null Het
Armc9 C A 1: 86,092,571 (GRCm39) Q169K possibly damaging Het
Aspm T A 1: 139,405,667 (GRCm39) M1518K possibly damaging Het
AU018091 A G 7: 3,209,006 (GRCm39) I360T probably benign Het
BB014433 C A 8: 15,091,765 (GRCm39) V363L probably benign Het
Bcam T C 7: 19,503,232 (GRCm39) probably null Het
Cacna1g T C 11: 94,328,705 (GRCm39) S1071G probably benign Het
Card9 A T 2: 26,246,787 (GRCm39) S354T probably benign Het
Ccdc87 A G 19: 4,889,790 (GRCm39) N94S probably benign Het
Cdc27 A G 11: 104,408,245 (GRCm39) V555A probably benign Het
Coro1a T A 7: 126,299,478 (GRCm39) D411V probably benign Het
Cybrd1 GGTCCTGCAC G 2: 70,948,553 (GRCm39) probably benign Het
Cyth1 A T 11: 118,076,321 (GRCm39) I95N probably damaging Het
Dnah7b A T 1: 46,179,126 (GRCm39) E933V probably damaging Het
Dync2h1 A T 9: 6,993,966 (GRCm39) I3968N probably benign Het
Fam184a T C 10: 53,510,489 (GRCm39) probably benign Het
Fat3 G A 9: 16,288,510 (GRCm39) L338F probably damaging Het
Fcgr3 A G 1: 170,886,870 (GRCm39) L18P probably damaging Het
Gbp5 T C 3: 142,213,461 (GRCm39) V459A probably benign Het
Gja4 A T 4: 127,205,956 (GRCm39) M269K probably benign Het
Gm4787 A G 12: 81,424,442 (GRCm39) V572A probably damaging Het
Grin2d G T 7: 45,515,600 (GRCm39) S131* probably null Het
Gys1 A G 7: 45,104,586 (GRCm39) D671G probably benign Het
Haspin T C 11: 73,027,712 (GRCm39) N459S probably benign Het
Hdac10 G T 15: 89,009,580 (GRCm39) Q451K probably benign Het
Hdac9 T C 12: 34,424,139 (GRCm39) probably null Het
Hmcn1 A G 1: 150,598,394 (GRCm39) V1636A probably damaging Het
Hpca A G 4: 129,012,407 (GRCm39) L43P probably damaging Het
Hycc2 G A 1: 58,569,107 (GRCm39) Q491* probably null Het
Insm1 C A 2: 146,064,448 (GRCm39) A88E possibly damaging Het
Itga9 A G 9: 118,465,670 (GRCm39) K175E probably benign Het
Kif13a A G 13: 46,962,632 (GRCm39) probably null Het
Kif20b T A 19: 34,928,005 (GRCm39) L1089H probably damaging Het
Lamp5 A T 2: 135,901,755 (GRCm39) H152L probably benign Het
Lrp4 T C 2: 91,303,528 (GRCm39) F76L probably benign Het
Magi3 T C 3: 103,935,227 (GRCm39) D902G probably damaging Het
Map10 C T 8: 126,397,963 (GRCm39) P452L probably benign Het
Mapk6 A G 9: 75,304,895 (GRCm39) L174P probably damaging Het
Meak7 C T 8: 120,489,054 (GRCm39) G410S probably damaging Het
Ndufa4 C T 6: 11,906,018 (GRCm39) probably null Het
Nedd4 A T 9: 72,632,346 (GRCm39) E393D probably benign Het
Nufip2 T A 11: 77,583,596 (GRCm39) N503K probably benign Het
Or10ac1 T C 6: 42,515,581 (GRCm39) D125G probably damaging Het
Or6y1 C T 1: 174,276,905 (GRCm39) R239C probably benign Het
P4ha1 A G 10: 59,184,065 (GRCm39) T176A probably benign Het
Palm3 A G 8: 84,756,117 (GRCm39) K543R probably benign Het
Parvg G A 15: 84,225,557 (GRCm39) A302T probably benign Het
Pcdh15 A G 10: 74,420,023 (GRCm39) D1227G possibly damaging Het
Pdzd8 C T 19: 59,333,571 (GRCm39) G150D probably damaging Het
Pitpnm2 A G 5: 124,263,360 (GRCm39) probably null Het
Pld5 T C 1: 176,102,301 (GRCm39) Q47R possibly damaging Het
Ppp2r5d T C 17: 46,997,206 (GRCm39) S329G possibly damaging Het
Prss56 T C 1: 87,112,637 (GRCm39) V144A probably damaging Het
Psg28 A T 7: 18,161,769 (GRCm39) Y245N possibly damaging Het
Ptpn3 C T 4: 57,239,625 (GRCm39) V302I probably damaging Het
Ptprn2 A G 12: 117,125,347 (GRCm39) H627R probably benign Het
Rasgrp2 A T 19: 6,454,838 (GRCm39) H226L possibly damaging Het
Rbm20 C T 19: 53,839,930 (GRCm39) T973M probably benign Het
Rigi T A 4: 40,205,938 (GRCm39) I885F probably benign Het
Riok2 T A 17: 17,598,045 (GRCm39) L44Q probably damaging Het
Rusc1 G T 3: 88,998,805 (GRCm39) Q326K possibly damaging Het
Rxylt1 A T 10: 121,917,523 (GRCm39) L330* probably null Het
Sart3 A T 5: 113,892,307 (GRCm39) H397Q possibly damaging Het
Sec31b T A 19: 44,506,147 (GRCm39) T920S probably damaging Het
Serpinb13 A G 1: 106,926,679 (GRCm39) E225G probably damaging Het
Slc25a47 T C 12: 108,821,386 (GRCm39) L165P probably damaging Het
Slc2a10 G A 2: 165,357,197 (GRCm39) V286I probably benign Het
Slc39a13 G T 2: 90,895,979 (GRCm39) T174N probably benign Het
Slc7a13 T A 4: 19,839,364 (GRCm39) N322K probably benign Het
Stk38 T C 17: 29,193,620 (GRCm39) T326A possibly damaging Het
Sult1a1 T C 7: 126,272,622 (GRCm39) M244V probably benign Het
Tas2r144 C T 6: 42,192,800 (GRCm39) T180I probably damaging Het
Tbc1d12 T A 19: 38,887,346 (GRCm39) M366K probably benign Het
Terb1 T C 8: 105,221,959 (GRCm39) I147V possibly damaging Het
Tnik T C 3: 28,692,568 (GRCm39) Y820H probably damaging Het
Tnxb C A 17: 34,901,170 (GRCm39) L995I possibly damaging Het
Trim34b A G 7: 103,978,794 (GRCm39) T14A possibly damaging Het
Urb1 T C 16: 90,588,054 (GRCm39) E418G probably damaging Het
Vmn1r12 T A 6: 57,136,550 (GRCm39) C216S possibly damaging Het
Vmn2r90 T A 17: 17,924,249 (GRCm39) V16E possibly damaging Het
Vps11 A T 9: 44,265,803 (GRCm39) V492D probably damaging Het
Wdr62 A C 7: 29,969,869 (GRCm39) probably null Het
Zc3h14 T A 12: 98,746,408 (GRCm39) M539K probably benign Het
Zfp871 A T 17: 32,994,289 (GRCm39) H295Q probably damaging Het
Other mutations in Nlrp4b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00971:Nlrp4b APN 7 10,448,882 (GRCm39) missense possibly damaging 0.68
IGL01456:Nlrp4b APN 7 10,448,150 (GRCm39) missense probably benign 0.26
IGL01537:Nlrp4b APN 7 10,448,918 (GRCm39) missense probably damaging 1.00
IGL02539:Nlrp4b APN 7 10,448,355 (GRCm39) missense probably damaging 0.96
IGL02730:Nlrp4b APN 7 10,448,685 (GRCm39) missense probably damaging 1.00
IGL02871:Nlrp4b APN 7 10,449,192 (GRCm39) missense probably benign 0.26
IGL03008:Nlrp4b APN 7 10,448,516 (GRCm39) missense probably benign 0.00
IGL03109:Nlrp4b APN 7 10,448,873 (GRCm39) missense probably damaging 1.00
IGL03251:Nlrp4b APN 7 10,448,427 (GRCm39) missense probably benign 0.01
IGL03354:Nlrp4b APN 7 10,448,465 (GRCm39) missense probably damaging 0.99
R0052:Nlrp4b UTSW 7 10,459,889 (GRCm39) nonsense probably null
R0348:Nlrp4b UTSW 7 10,449,108 (GRCm39) missense possibly damaging 0.60
R0564:Nlrp4b UTSW 7 10,448,585 (GRCm39) missense probably benign 0.15
R0573:Nlrp4b UTSW 7 10,448,142 (GRCm39) missense probably benign 0.01
R0581:Nlrp4b UTSW 7 10,448,457 (GRCm39) missense probably damaging 1.00
R1201:Nlrp4b UTSW 7 10,449,363 (GRCm39) missense possibly damaging 0.64
R1541:Nlrp4b UTSW 7 10,458,979 (GRCm39) missense possibly damaging 0.91
R1771:Nlrp4b UTSW 7 10,452,520 (GRCm39) missense probably damaging 0.96
R1781:Nlrp4b UTSW 7 10,449,266 (GRCm39) missense probably benign 0.13
R1833:Nlrp4b UTSW 7 10,459,863 (GRCm39) missense probably benign 0.00
R2405:Nlrp4b UTSW 7 10,448,655 (GRCm39) missense probably benign 0.08
R2871:Nlrp4b UTSW 7 10,444,170 (GRCm39) nonsense probably null
R2871:Nlrp4b UTSW 7 10,444,170 (GRCm39) nonsense probably null
R2873:Nlrp4b UTSW 7 10,444,170 (GRCm39) nonsense probably null
R2904:Nlrp4b UTSW 7 10,448,294 (GRCm39) missense probably damaging 1.00
R3410:Nlrp4b UTSW 7 10,449,456 (GRCm39) missense probably damaging 1.00
R3714:Nlrp4b UTSW 7 10,448,808 (GRCm39) missense probably benign 0.04
R3982:Nlrp4b UTSW 7 10,448,358 (GRCm39) missense possibly damaging 0.95
R4668:Nlrp4b UTSW 7 10,448,660 (GRCm39) missense possibly damaging 0.66
R4690:Nlrp4b UTSW 7 10,453,130 (GRCm39) missense probably benign 0.00
R4857:Nlrp4b UTSW 7 10,449,225 (GRCm39) missense probably benign 0.05
R5247:Nlrp4b UTSW 7 10,448,145 (GRCm39) missense probably benign 0.21
R5381:Nlrp4b UTSW 7 10,449,172 (GRCm39) nonsense probably null
R5529:Nlrp4b UTSW 7 10,448,873 (GRCm39) missense possibly damaging 0.91
R5589:Nlrp4b UTSW 7 10,449,512 (GRCm39) missense probably benign 0.34
R5770:Nlrp4b UTSW 7 10,449,414 (GRCm39) missense probably benign 0.00
R5990:Nlrp4b UTSW 7 10,448,418 (GRCm39) missense possibly damaging 0.61
R6049:Nlrp4b UTSW 7 10,448,640 (GRCm39) nonsense probably null
R6329:Nlrp4b UTSW 7 10,458,847 (GRCm39) missense probably benign 0.16
R6377:Nlrp4b UTSW 7 10,449,339 (GRCm39) missense probably benign 0.00
R7107:Nlrp4b UTSW 7 10,449,144 (GRCm39) missense probably damaging 0.96
R7209:Nlrp4b UTSW 7 10,444,297 (GRCm39) missense probably benign 0.01
R7537:Nlrp4b UTSW 7 10,448,816 (GRCm39) missense probably benign 0.05
R7793:Nlrp4b UTSW 7 10,459,001 (GRCm39) missense probably benign 0.00
R8138:Nlrp4b UTSW 7 10,449,458 (GRCm39) missense probably benign 0.01
R8190:Nlrp4b UTSW 7 10,448,319 (GRCm39) missense probably damaging 0.96
R8326:Nlrp4b UTSW 7 10,452,471 (GRCm39) missense probably benign 0.05
R8353:Nlrp4b UTSW 7 10,449,528 (GRCm39) missense probably damaging 0.99
R8417:Nlrp4b UTSW 7 10,459,880 (GRCm39) nonsense probably null
R8453:Nlrp4b UTSW 7 10,449,528 (GRCm39) missense probably damaging 0.99
R8998:Nlrp4b UTSW 7 10,449,629 (GRCm39) missense probably null 0.00
R9002:Nlrp4b UTSW 7 10,448,886 (GRCm39) missense probably damaging 1.00
R9072:Nlrp4b UTSW 7 10,459,870 (GRCm39) missense probably benign 0.02
R9073:Nlrp4b UTSW 7 10,459,870 (GRCm39) missense probably benign 0.02
R9258:Nlrp4b UTSW 7 10,444,087 (GRCm39) missense probably damaging 1.00
R9373:Nlrp4b UTSW 7 10,449,126 (GRCm39) missense probably benign 0.01
R9525:Nlrp4b UTSW 7 10,448,748 (GRCm39) missense probably damaging 0.99
R9604:Nlrp4b UTSW 7 10,444,295 (GRCm39) missense probably benign 0.00
R9670:Nlrp4b UTSW 7 10,448,651 (GRCm39) missense probably benign 0.11
R9679:Nlrp4b UTSW 7 10,449,184 (GRCm39) missense probably benign 0.00
X0063:Nlrp4b UTSW 7 10,463,514 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- CGAAGACCTGCTGGATAACTTG -3'
(R):5'- TCCAATAGGAGTTCCAGCCAC -3'

Sequencing Primer
(F):5'- AGACCTGCTGGATAACTTGTGTTTTC -3'
(R):5'- AAAAATGCCTCCAGCTTTTCTTG -3'
Posted On 2019-06-26