Incidental Mutation 'IGL03002:Nlrp1b'
ID 407388
Institutional Source Australian Phenomics Network (link to record)
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 # IGL03002
Quality Score
Status
Chromosome 11
Chromosomal Location 71043928-71121559 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 71059685 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 759 (E759G)
Ref Sequence ENSEMBL: ENSMUSP00000104156 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094046] [ENSMUST00000108514] [ENSMUST00000108515] [ENSMUST00000108516] [ENSMUST00000136493]
AlphaFold A1Z198
Predicted Effect probably benign
Transcript: ENSMUST00000094046
AA Change: E759G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000091588
Gene: ENSMUSG00000070390
AA Change: E759G

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 benign
Transcript: ENSMUST00000108514
AA Change: E762G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000104154
Gene: ENSMUSG00000070390
AA Change: E762G

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 benign
Transcript: ENSMUST00000108515
AA Change: E762G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000104155
Gene: ENSMUSG00000070390
AA Change: E762G

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
AA Change: E759G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000104156
Gene: ENSMUSG00000070390
AA Change: E759G

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
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acadl T C 1: 66,876,128 (GRCm39) I398V probably benign Het
Adcy4 A T 14: 56,011,013 (GRCm39) C635S probably benign Het
Aoc1l3 A G 6: 48,964,052 (GRCm39) H20R probably benign Het
Asic4 C A 1: 75,427,967 (GRCm39) D164E possibly damaging Het
C8g T A 2: 25,388,823 (GRCm39) *203L probably null Het
Cad T C 5: 31,212,330 (GRCm39) V11A probably benign Het
Cckar T C 5: 53,860,247 (GRCm39) N194S probably damaging Het
Cdc123 T C 2: 5,803,166 (GRCm39) probably benign Het
Chrm5 T C 2: 112,310,706 (GRCm39) T137A probably damaging Het
Cyp1a1 A G 9: 57,609,724 (GRCm39) probably benign Het
Dapk3 G T 10: 81,026,437 (GRCm39) E187* probably null Het
Dmtf1 T C 5: 9,190,474 (GRCm39) E80G probably damaging Het
Dusp19 T A 2: 80,461,279 (GRCm39) N189K probably damaging Het
Gfral A G 9: 76,104,520 (GRCm39) V164A possibly damaging Het
Hk1 A T 10: 62,107,578 (GRCm39) V799E probably damaging Het
Iars2 C T 1: 185,055,013 (GRCm39) probably null Het
Jcad T A 18: 4,675,153 (GRCm39) Y972N probably benign Het
Lrp1 A T 10: 127,425,505 (GRCm39) D708E probably damaging Het
Mbtd1 T A 11: 93,815,316 (GRCm39) H301Q probably benign Het
Med12 A G X: 100,339,461 (GRCm39) T2004A probably benign Het
Mib1 T C 18: 10,798,356 (GRCm39) I739T possibly damaging Het
Mthfsd C T 8: 121,835,018 (GRCm39) probably benign Het
Mybpc3 T G 2: 90,954,234 (GRCm39) F369C probably damaging Het
Nfatc2 C T 2: 168,376,904 (GRCm39) V329M probably damaging Het
Ngef A T 1: 87,437,114 (GRCm39) probably null Het
Or10aa3 C A 1: 173,878,191 (GRCm39) T84N probably benign Het
Prdm4 T C 10: 85,729,016 (GRCm39) E790G probably benign Het
Psmd12 A G 11: 107,376,607 (GRCm39) D81G probably benign Het
Rnf144b A G 13: 47,396,359 (GRCm39) H232R probably damaging Het
Sec63 C T 10: 42,686,905 (GRCm39) T475M possibly damaging Het
Slc16a4 A T 3: 107,208,102 (GRCm39) N204I probably benign Het
Socs1 T C 16: 10,602,404 (GRCm39) N111S probably damaging Het
Srpra A G 9: 35,126,017 (GRCm39) N432D probably damaging Het
Srrm2 A G 17: 24,034,708 (GRCm39) probably benign Het
Tgoln1 A G 6: 72,593,055 (GRCm39) S142P possibly damaging Het
Trbv13-1 A G 6: 41,093,169 (GRCm39) N34S probably benign Het
Vmn2r26 T C 6: 124,016,754 (GRCm39) V406A possibly damaging Het
Vsig1 G T X: 139,827,088 (GRCm39) G79V probably 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
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
R7149:Nlrp1b UTSW 11 71,072,482 (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
Posted On 2016-08-02