Incidental Mutation 'R7149:Nlrp1b'
ID 554011
Institutional Source Beutler Lab
Gene Symbol Nlrp1b
Ensembl Gene ENSMUSG00000070390
Gene Name NLR family, pyrin domain containing 1B
Synonyms Nalp1b
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R7149 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 71043928-71121559 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 71072482 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 454 (R454*)
Ref Sequence ENSEMBL: ENSMUSP00000104155 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094046] [ENSMUST00000108514] [ENSMUST00000108515] [ENSMUST00000108516] [ENSMUST00000136493]
AlphaFold A1Z198
Predicted Effect probably benign
Transcript: ENSMUST00000094046
SMART Domains Protein: ENSMUSP00000091588
Gene: ENSMUSG00000070390

DomainStartEndE-ValueType
Pfam:NACHT 131 300 6.7e-43 PFAM
LRR 627 654 2.24e0 SMART
LRR 656 683 8.82e0 SMART
LRR 684 711 3.49e-5 SMART
Pfam:FIIND 812 1064 8.2e-104 PFAM
Pfam:CARD 1083 1166 3.1e-22 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000108514
AA Change: R454*
SMART Domains Protein: ENSMUSP00000104154
Gene: ENSMUSG00000070390
AA Change: R454*

DomainStartEndE-ValueType
Pfam:NACHT 131 300 2.1e-40 PFAM
LRR 630 657 2.24e0 SMART
LRR 659 686 8.82e0 SMART
LRR 687 714 3.49e-5 SMART
Pfam:FIIND 814 1068 2.4e-136 PFAM
Pfam:CARD 1086 1169 3.7e-22 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000108515
AA Change: R454*
SMART Domains Protein: ENSMUSP00000104155
Gene: ENSMUSG00000070390
AA Change: R454*

DomainStartEndE-ValueType
Pfam:NACHT 131 300 6.9e-41 PFAM
LRR 630 657 2.24e0 SMART
LRR 659 686 8.82e0 SMART
LRR 687 714 3.49e-5 SMART
Pfam:FIIND 815 1067 5e-104 PFAM
Pfam:CARD 1086 1169 1e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000108516
SMART Domains Protein: ENSMUSP00000104156
Gene: ENSMUSG00000070390

DomainStartEndE-ValueType
Pfam:NACHT 131 300 2.2e-42 PFAM
LRR 627 654 2.24e0 SMART
LRR 656 683 8.82e0 SMART
LRR 684 711 3.49e-5 SMART
Pfam:FIIND 811 1065 3.9e-136 PFAM
Pfam:CARD 1083 1166 1.1e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000136493
SMART Domains Protein: ENSMUSP00000121155
Gene: ENSMUSG00000070390

DomainStartEndE-ValueType
Pfam:NACHT 131 300 8.9e-43 PFAM
PDB:4IM6|A 610 662 6e-10 PDB
Blast:LRR 627 654 3e-11 BLAST
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Ced-4 family of apoptosis proteins. Ced-family members contain a caspase recruitment domain (CARD) and are known to be key mediators of programmed cell death. The encoded protein contains a distinct N-terminal pyrin-like motif, which is possibly involved in protein-protein interactions. This protein interacts strongly with caspase 2 and weakly with caspase 9. Overexpression of this gene was demonstrated to induce apoptosis in cells. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit protection from anthrax lethal toxin-induced lung injury and pyroptosis of macrophages. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acly A C 11: 100,375,451 (GRCm39) F790V probably damaging Het
Atf4 AAGCGGGCTGAGC AAGC 15: 80,141,500 (GRCm39) probably benign Het
Brd8 C T 18: 34,737,650 (GRCm39) probably null Het
Bsn A T 9: 107,993,520 (GRCm39) L744* probably null Het
Capn9 A G 8: 125,332,448 (GRCm39) D429G probably benign Het
CK137956 A T 4: 127,864,626 (GRCm39) M1K probably null Het
Cnot6 G A 11: 49,570,970 (GRCm39) P341S probably benign Het
Cracdl G A 1: 37,651,352 (GRCm39) Q1172* probably null Het
Dld T G 12: 31,385,589 (GRCm39) I251L probably benign Het
Dlg5 T C 14: 24,240,492 (GRCm39) K253R probably benign Het
Dnmt3a C T 12: 3,952,397 (GRCm39) P696L probably damaging Het
Dph1 T C 11: 75,070,001 (GRCm39) K409E probably benign Het
Dsg2 T C 18: 20,712,511 (GRCm39) S172P probably damaging Het
Gm1979 T C 5: 26,206,945 (GRCm39) N136S probably benign Het
Gm2663 A T 6: 40,974,891 (GRCm39) L60Q probably damaging Het
Hdac10 A G 15: 89,011,652 (GRCm39) F144S probably damaging Het
Ifi203 T C 1: 173,756,494 (GRCm39) T430A unknown Het
Itgb2l T C 16: 96,234,759 (GRCm39) D244G probably damaging Het
Klk1b9 A T 7: 43,628,841 (GRCm39) Y115F probably benign Het
Llcfc1 C A 6: 41,662,251 (GRCm39) A85E possibly damaging Het
Lrp1b C T 2: 40,527,872 (GRCm39) V4330M Het
Map3k13 A G 16: 21,744,187 (GRCm39) E811G probably benign Het
Myl6b A G 10: 128,333,068 (GRCm39) probably null Het
Myo15a G A 11: 60,400,836 (GRCm39) A2997T possibly damaging Het
Nalcn T C 14: 123,837,277 (GRCm39) D29G probably benign Het
Nepro T A 16: 44,550,078 (GRCm39) probably null Het
Nlrp4a T C 7: 26,149,863 (GRCm39) V490A probably benign Het
Or1e1f G A 11: 73,856,257 (GRCm39) M274I probably benign Het
Or2l13 T C 16: 19,306,260 (GRCm39) V224A probably damaging Het
Pde8b T G 13: 95,223,349 (GRCm39) M197L probably benign Het
Phldb2 T A 16: 45,571,895 (GRCm39) K1166* probably null Het
Plekhm1 A G 11: 103,285,742 (GRCm39) I231T probably damaging Het
Ppp6r2 T C 15: 89,146,599 (GRCm39) I199T probably damaging Het
Ptch1 G T 13: 63,659,550 (GRCm39) H1368N probably benign Het
Ptprj T A 2: 90,274,790 (GRCm39) T1191S possibly damaging Het
Rapgef1 T C 2: 29,610,712 (GRCm39) S748P probably damaging Het
Rigi T C 4: 40,222,079 (GRCm39) D445G possibly damaging Het
Rnmt T C 18: 68,452,222 (GRCm39) S420P probably damaging Het
Sgms2 A G 3: 131,129,908 (GRCm39) F160S possibly damaging Het
Sim1 G T 10: 50,785,636 (GRCm39) R235L probably damaging Het
Slco1a7 A G 6: 141,690,178 (GRCm39) S192P probably damaging Het
Smarcad1 T A 6: 65,029,716 (GRCm39) D101E probably benign Het
Smarcc2 G A 10: 128,318,598 (GRCm39) V627M probably damaging Het
Supt20 G A 3: 54,635,832 (GRCm39) R241H unknown Het
Tagln2 T A 1: 172,333,386 (GRCm39) I80N probably damaging Het
Tmod2 G A 9: 75,489,167 (GRCm39) T226I possibly damaging Het
Vmn2r80 A T 10: 79,030,654 (GRCm39) I827F probably benign Het
Vmn2r96 T A 17: 18,817,989 (GRCm39) M714K possibly damaging Het
Vps8 C A 16: 21,278,526 (GRCm39) D261E probably damaging Het
Yeats2 C A 16: 19,972,939 (GRCm39) A31E probably damaging Het
Zfp451 C T 1: 33,816,405 (GRCm39) R515Q probably damaging Het
Zfp553 A G 7: 126,835,605 (GRCm39) S387G possibly damaging Het
Other mutations in Nlrp1b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00161:Nlrp1b APN 11 71,072,007 (GRCm39) intron probably benign
IGL00571:Nlrp1b APN 11 71,054,799 (GRCm39) missense probably null 0.48
IGL01358:Nlrp1b APN 11 71,072,682 (GRCm39) missense possibly damaging 0.91
IGL01937:Nlrp1b APN 11 71,072,233 (GRCm39) missense probably damaging 0.98
IGL01945:Nlrp1b APN 11 71,072,233 (GRCm39) missense probably damaging 0.98
IGL02375:Nlrp1b APN 11 71,052,506 (GRCm39) missense probably damaging 1.00
IGL02552:Nlrp1b APN 11 71,063,057 (GRCm39) missense possibly damaging 0.96
IGL02552:Nlrp1b APN 11 71,072,878 (GRCm39) missense possibly damaging 0.57
IGL02588:Nlrp1b APN 11 71,073,105 (GRCm39) nonsense probably null
IGL02833:Nlrp1b APN 11 71,051,998 (GRCm39) missense probably benign
IGL02955:Nlrp1b APN 11 71,060,637 (GRCm39) missense possibly damaging 0.73
IGL03002:Nlrp1b APN 11 71,059,685 (GRCm39) missense probably benign 0.00
IGL03033:Nlrp1b APN 11 71,052,665 (GRCm39) missense probably benign 0.22
IGL03122:Nlrp1b APN 11 71,072,659 (GRCm39) missense probably benign 0.00
IGL03131:Nlrp1b APN 11 71,052,741 (GRCm39) missense possibly damaging 0.82
androcles UTSW 11 71,062,901 (GRCm39) nonsense probably null
Fangled UTSW 11 71,062,997 (GRCm39) missense possibly damaging 0.94
glitz UTSW 11 71,072,376 (GRCm39) missense possibly damaging 0.89
honeydew UTSW 11 71,108,710 (GRCm39) missense possibly damaging 0.93
Mush UTSW 11 71,046,905 (GRCm39) missense probably damaging 1.00
Thorn UTSW 11 71,047,126 (GRCm39) splice site probably benign
R0001:Nlrp1b UTSW 11 71,052,585 (GRCm39) missense probably damaging 1.00
R0022:Nlrp1b UTSW 11 71,052,755 (GRCm39) missense possibly damaging 0.61
R0022:Nlrp1b UTSW 11 71,052,755 (GRCm39) missense possibly damaging 0.61
R0038:Nlrp1b UTSW 11 71,062,997 (GRCm39) missense possibly damaging 0.94
R0038:Nlrp1b UTSW 11 71,062,997 (GRCm39) missense possibly damaging 0.94
R0164:Nlrp1b UTSW 11 71,054,925 (GRCm39) missense probably damaging 1.00
R0164:Nlrp1b UTSW 11 71,054,925 (GRCm39) missense probably damaging 1.00
R0271:Nlrp1b UTSW 11 71,052,591 (GRCm39) missense possibly damaging 0.51
R0464:Nlrp1b UTSW 11 71,109,070 (GRCm39) missense probably damaging 1.00
R0504:Nlrp1b UTSW 11 71,073,241 (GRCm39) missense probably damaging 0.99
R0605:Nlrp1b UTSW 11 71,047,005 (GRCm39) missense possibly damaging 0.88
R0863:Nlrp1b UTSW 11 71,072,173 (GRCm39) missense probably benign 0.00
R1075:Nlrp1b UTSW 11 71,072,512 (GRCm39) missense probably benign 0.35
R1221:Nlrp1b UTSW 11 71,072,290 (GRCm39) missense probably benign 0.07
R1501:Nlrp1b UTSW 11 71,046,885 (GRCm39) missense probably damaging 1.00
R1654:Nlrp1b UTSW 11 71,072,124 (GRCm39) missense probably damaging 0.99
R1671:Nlrp1b UTSW 11 71,092,085 (GRCm39) missense probably benign 0.45
R1676:Nlrp1b UTSW 11 71,073,637 (GRCm39) missense probably benign 0.13
R1694:Nlrp1b UTSW 11 71,107,681 (GRCm39) critical splice donor site probably null
R1709:Nlrp1b UTSW 11 71,092,099 (GRCm39) missense probably benign 0.11
R1770:Nlrp1b UTSW 11 71,050,979 (GRCm39) missense probably benign 0.22
R1775:Nlrp1b UTSW 11 71,052,647 (GRCm39) missense probably damaging 1.00
R1851:Nlrp1b UTSW 11 71,073,442 (GRCm39) missense possibly damaging 0.96
R1932:Nlrp1b UTSW 11 71,072,964 (GRCm39) missense probably damaging 0.96
R2063:Nlrp1b UTSW 11 71,051,912 (GRCm39) missense probably benign 0.09
R2189:Nlrp1b UTSW 11 71,060,621 (GRCm39) missense probably damaging 1.00
R2223:Nlrp1b UTSW 11 71,046,815 (GRCm39) splice site probably benign
R2284:Nlrp1b UTSW 11 71,047,110 (GRCm39) missense probably benign 0.00
R2434:Nlrp1b UTSW 11 71,047,552 (GRCm39) splice site probably null
R3079:Nlrp1b UTSW 11 71,108,794 (GRCm39) missense probably benign 0.27
R3775:Nlrp1b UTSW 11 71,047,126 (GRCm39) splice site probably benign
R3980:Nlrp1b UTSW 11 71,072,437 (GRCm39) missense possibly damaging 0.56
R4016:Nlrp1b UTSW 11 71,063,911 (GRCm39) missense probably damaging 1.00
R4085:Nlrp1b UTSW 11 71,052,588 (GRCm39) missense probably damaging 0.98
R4542:Nlrp1b UTSW 11 71,119,151 (GRCm39) missense probably damaging 1.00
R4623:Nlrp1b UTSW 11 71,052,669 (GRCm39) missense probably benign 0.00
R4726:Nlrp1b UTSW 11 71,072,232 (GRCm39) missense probably benign 0.10
R4764:Nlrp1b UTSW 11 71,073,489 (GRCm39) missense probably damaging 1.00
R4885:Nlrp1b UTSW 11 71,108,710 (GRCm39) missense possibly damaging 0.93
R4910:Nlrp1b UTSW 11 71,108,103 (GRCm39) missense probably benign 0.09
R4997:Nlrp1b UTSW 11 71,109,160 (GRCm39) missense probably damaging 1.00
R5046:Nlrp1b UTSW 11 71,050,898 (GRCm39) missense possibly damaging 0.95
R5126:Nlrp1b UTSW 11 71,072,359 (GRCm39) missense possibly damaging 0.67
R5369:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
R5388:Nlrp1b UTSW 11 71,062,967 (GRCm39) missense probably damaging 1.00
R5445:Nlrp1b UTSW 11 71,108,701 (GRCm39) missense probably benign 0.21
R5546:Nlrp1b UTSW 11 71,108,102 (GRCm39) missense probably benign 0.04
R5567:Nlrp1b UTSW 11 71,072,229 (GRCm39) missense probably benign
R5826:Nlrp1b UTSW 11 71,072,022 (GRCm39) missense probably benign 0.17
R5955:Nlrp1b UTSW 11 71,108,691 (GRCm39) missense probably damaging 1.00
R5995:Nlrp1b UTSW 11 71,072,572 (GRCm39) missense probably damaging 1.00
R6059:Nlrp1b UTSW 11 71,107,836 (GRCm39) missense possibly damaging 0.53
R6170:Nlrp1b UTSW 11 71,046,905 (GRCm39) missense probably damaging 1.00
R6191:Nlrp1b UTSW 11 71,109,283 (GRCm39) nonsense probably null
R6250:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign 0.11
R6312:Nlrp1b UTSW 11 71,119,223 (GRCm39) missense probably benign 0.38
R6352:Nlrp1b UTSW 11 71,072,527 (GRCm39) missense probably damaging 0.99
R6807:Nlrp1b UTSW 11 71,108,530 (GRCm39) missense probably damaging 1.00
R6854:Nlrp1b UTSW 11 71,119,259 (GRCm39) missense possibly damaging 0.93
R6908:Nlrp1b UTSW 11 71,108,122 (GRCm39) missense probably benign
R6938:Nlrp1b UTSW 11 71,109,042 (GRCm39) missense probably damaging 1.00
R7098:Nlrp1b UTSW 11 71,109,100 (GRCm39) missense possibly damaging 0.89
R7142:Nlrp1b UTSW 11 71,062,901 (GRCm39) nonsense probably null
R7349:Nlrp1b UTSW 11 71,072,943 (GRCm39) missense probably benign 0.36
R7354:Nlrp1b UTSW 11 71,072,376 (GRCm39) missense possibly damaging 0.89
R7750:Nlrp1b UTSW 11 71,059,665 (GRCm39) missense probably benign 0.11
R7913:Nlrp1b UTSW 11 71,108,537 (GRCm39) missense possibly damaging 0.93
R8031:Nlrp1b UTSW 11 71,107,747 (GRCm39) missense probably benign 0.15
R8087:Nlrp1b UTSW 11 71,062,897 (GRCm39) missense probably benign 0.04
R8164:Nlrp1b UTSW 11 71,119,243 (GRCm39) missense possibly damaging 0.78
R8378:Nlrp1b UTSW 11 71,052,545 (GRCm39) missense possibly damaging 0.95
R8405:Nlrp1b UTSW 11 71,073,356 (GRCm39) missense possibly damaging 0.66
R8441:Nlrp1b UTSW 11 71,073,204 (GRCm39) missense probably damaging 1.00
R8792:Nlrp1b UTSW 11 71,050,919 (GRCm39) missense probably benign 0.02
R8898:Nlrp1b UTSW 11 71,073,288 (GRCm39) missense probably damaging 1.00
R8953:Nlrp1b UTSW 11 71,052,632 (GRCm39) missense probably damaging 0.96
R8963:Nlrp1b UTSW 11 71,108,658 (GRCm39) missense probably damaging 1.00
R9145:Nlrp1b UTSW 11 71,109,193 (GRCm39) missense probably benign
R9184:Nlrp1b UTSW 11 71,072,067 (GRCm39) missense probably damaging 1.00
R9286:Nlrp1b UTSW 11 71,060,573 (GRCm39) missense probably benign
R9322:Nlrp1b UTSW 11 71,108,118 (GRCm39) missense probably benign 0.12
R9453:Nlrp1b UTSW 11 71,072,913 (GRCm39) missense probably damaging 0.98
R9533:Nlrp1b UTSW 11 71,109,095 (GRCm39) missense probably benign 0.12
R9659:Nlrp1b UTSW 11 71,073,132 (GRCm39) missense possibly damaging 0.77
Z1176:Nlrp1b UTSW 11 71,073,096 (GRCm39) missense probably damaging 1.00
Z1177:Nlrp1b UTSW 11 71,108,050 (GRCm39) missense probably benign 0.03
Z1177:Nlrp1b UTSW 11 71,072,125 (GRCm39) nonsense probably null
Z1186:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1186:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1186:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,073,135 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1186:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1186:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1186:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1187:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1187:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1187:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1187:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1187:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1188:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1188:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,135 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1188:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1188:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1189:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1189:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1189:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,073,135 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1189:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1189:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1189:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1190:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1190:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1190:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,135 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1190:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1191:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1191:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,073,135 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,072,539 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1191:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1191:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1191:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1192:Nlrp1b UTSW 11 71,073,396 (GRCm39) missense probably benign 0.02
Z1192:Nlrp1b UTSW 11 71,073,378 (GRCm39) missense probably benign
Z1192:Nlrp1b UTSW 11 71,073,370 (GRCm39) missense probably benign 0.00
Z1192:Nlrp1b UTSW 11 71,073,280 (GRCm39) missense probably benign 0.00
Z1192:Nlrp1b UTSW 11 71,073,266 (GRCm39) missense probably benign
Z1192:Nlrp1b UTSW 11 71,073,148 (GRCm39) missense probably benign
Z1192:Nlrp1b UTSW 11 71,072,625 (GRCm39) missense probably benign
Z1192:Nlrp1b UTSW 11 71,072,534 (GRCm39) missense probably benign 0.02
Z1192:Nlrp1b UTSW 11 71,073,503 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AAACCCAGGCAAGGTGGTTG -3'
(R):5'- TTCAGTGAAAGCGACCTCTG -3'

Sequencing Primer
(F):5'- CAGGCAAGGTGGTTGATGGG -3'
(R):5'- TCAGTGAAAGCGACCTCTGTAAGC -3'
Posted On 2019-05-15