Incidental Mutation 'IGL02375:Nlrp1b'
ID 291053
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 # IGL02375
Quality Score
Status
Chromosome 11
Chromosomal Location 71043928-71121559 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 71052506 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 971 (I971T)
Ref Sequence ENSEMBL: ENSMUSP00000104156 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094046] [ENSMUST00000108514] [ENSMUST00000108515] [ENSMUST00000108516] [ENSMUST00000136493]
AlphaFold A1Z198
Predicted Effect probably damaging
Transcript: ENSMUST00000094046
AA Change: I971T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000091588
Gene: ENSMUSG00000070390
AA Change: I971T

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 damaging
Transcript: ENSMUST00000108514
AA Change: I974T

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000104154
Gene: ENSMUSG00000070390
AA Change: I974T

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 damaging
Transcript: ENSMUST00000108515
AA Change: I974T

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000104155
Gene: ENSMUSG00000070390
AA Change: I974T

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 damaging
Transcript: ENSMUST00000108516
AA Change: I971T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000104156
Gene: ENSMUSG00000070390
AA Change: I971T

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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034J05Rik T A 6: 146,854,813 (GRCm39) K76N possibly damaging Het
Agxt A G 1: 93,063,425 (GRCm39) E109G probably damaging Het
Alcam T C 16: 52,109,299 (GRCm39) T325A probably benign Het
Apol7c T C 15: 77,413,049 (GRCm39) E67G probably damaging Het
Bco1 C A 8: 117,840,178 (GRCm39) S232Y probably benign Het
Cacna1c A T 6: 118,652,884 (GRCm39) V763D probably damaging Het
Ccdc15 T C 9: 37,215,628 (GRCm39) D618G probably damaging Het
Cimip1 A G 2: 173,364,496 (GRCm39) M14V probably benign Het
Col6a5 T C 9: 105,783,312 (GRCm39) N1603S unknown Het
Cyp4v3 A G 8: 45,761,411 (GRCm39) probably null Het
Eml5 A T 12: 98,810,346 (GRCm39) V870E probably damaging Het
Epn2 A G 11: 61,410,497 (GRCm39) V512A probably damaging Het
Farp2 A G 1: 93,504,185 (GRCm39) R321G probably damaging Het
Garin3 G T 11: 46,297,379 (GRCm39) V228L probably damaging Het
Gprasp1 T C X: 134,701,552 (GRCm39) S582P probably damaging Het
Grhl2 T C 15: 37,291,821 (GRCm39) V303A probably damaging Het
Grik1 A T 16: 87,743,444 (GRCm39) F594L probably damaging Het
Hivep1 A G 13: 42,309,925 (GRCm39) K722E probably benign Het
Htr5b G A 1: 121,455,564 (GRCm39) R119C probably damaging Het
Ifit2 T C 19: 34,551,737 (GRCm39) S426P probably benign Het
Kif13a T C 13: 46,978,698 (GRCm39) Y234C probably damaging Het
Mios T A 6: 8,222,598 (GRCm39) F511I probably benign Het
Mtfmt T C 9: 65,346,849 (GRCm39) W148R probably damaging Het
Myo1c C A 11: 75,552,400 (GRCm39) T391N probably benign Het
Nlrp1a A T 11: 71,004,339 (GRCm39) L710* probably null Het
Nup43 A G 10: 7,549,358 (GRCm39) D171G probably damaging Het
Or5b12b A G 19: 12,861,305 (GRCm39) E20G probably benign Het
P2rx7 T C 5: 122,811,719 (GRCm39) probably benign Het
Pgap6 T A 17: 26,338,473 (GRCm39) Y512N probably benign Het
Poli C T 18: 70,656,363 (GRCm39) G155R probably damaging Het
Rad9b T C 5: 122,471,405 (GRCm39) S220G possibly damaging Het
Rgn C T X: 20,416,700 (GRCm39) S28L probably damaging Het
Tcp11l2 G A 10: 84,440,932 (GRCm39) probably null Het
Tenm4 G A 7: 96,353,344 (GRCm39) V379I possibly damaging Het
Thsd7a A T 6: 12,343,264 (GRCm39) C1118S probably damaging Het
Trpm7 A G 2: 126,667,664 (GRCm39) Y776H probably damaging Het
Trpv4 T C 5: 114,774,418 (GRCm39) N222S probably benign Het
Tut1 C T 19: 8,941,403 (GRCm39) R397C probably damaging Het
Vmn1r72 T A 7: 11,403,672 (GRCm39) T259S probably benign Het
Wdr17 A G 8: 55,149,423 (GRCm39) S2P 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
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
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 2015-04-16