Incidental Mutation 'R0504:Nlrp1b'
ID |
47374 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nlrp1b
|
Ensembl Gene |
ENSMUSG00000070390 |
Gene Name |
NLR family, pyrin domain containing 1B |
Synonyms |
Nalp1b |
MMRRC Submission |
038699-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.063)
|
Stock # |
R0504 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
71043928-71121559 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 71073241 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 201
(I201L)
|
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
Domain | Start | End | E-Value | Type |
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: I201L
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000104154 Gene: ENSMUSG00000070390 AA Change: I201L
Domain | Start | End | E-Value | Type |
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: I201L
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000104155 Gene: ENSMUSG00000070390 AA Change: I201L
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
Pfam:NACHT
|
131 |
300 |
8.9e-43 |
PFAM |
PDB:4IM6|A
|
610 |
662 |
6e-10 |
PDB |
Blast:LRR
|
627 |
654 |
3e-11 |
BLAST |
|
Meta Mutation Damage Score |
0.4909 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.6%
|
Validation Efficiency |
99% (145/147) |
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: 145 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
A |
G |
4: 103,128,057 (GRCm39) |
|
probably benign |
Het |
Adamts6 |
T |
C |
13: 104,563,438 (GRCm39) |
|
probably benign |
Het |
Adamts9 |
T |
A |
6: 92,889,626 (GRCm39) |
Y316F |
probably damaging |
Het |
Agl |
A |
T |
3: 116,580,433 (GRCm39) |
F374I |
probably damaging |
Het |
Akr1c19 |
A |
G |
13: 4,286,250 (GRCm39) |
T83A |
possibly damaging |
Het |
Ankrd36 |
T |
A |
11: 5,579,274 (GRCm39) |
S179R |
probably damaging |
Het |
Appbp2 |
A |
G |
11: 85,082,513 (GRCm39) |
S573P |
probably benign |
Het |
Arid4a |
T |
A |
12: 71,093,988 (GRCm39) |
F254I |
probably damaging |
Het |
Bin3 |
T |
C |
14: 70,361,336 (GRCm39) |
|
probably null |
Het |
Bmi1 |
T |
C |
2: 18,688,883 (GRCm39) |
|
probably null |
Het |
Bmper |
G |
T |
9: 23,317,983 (GRCm39) |
C534F |
probably damaging |
Het |
Bora |
T |
A |
14: 99,299,059 (GRCm39) |
C205* |
probably null |
Het |
Btnl2 |
A |
G |
17: 34,577,091 (GRCm39) |
E82G |
probably benign |
Het |
Ccdc8 |
A |
T |
7: 16,729,939 (GRCm39) |
D476V |
unknown |
Het |
Ccr3 |
C |
A |
9: 123,829,478 (GRCm39) |
T271K |
possibly damaging |
Het |
Cd276 |
A |
G |
9: 58,447,961 (GRCm39) |
L23P |
possibly damaging |
Het |
Cd3e |
T |
C |
9: 44,913,552 (GRCm39) |
Q61R |
probably benign |
Het |
Cep97 |
A |
G |
16: 55,726,142 (GRCm39) |
S582P |
probably benign |
Het |
Chml |
A |
T |
1: 175,514,748 (GRCm39) |
M391K |
probably damaging |
Het |
Chst1 |
A |
G |
2: 92,444,169 (GRCm39) |
N214D |
probably benign |
Het |
Chuk |
T |
C |
19: 44,070,377 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,588,750 (GRCm39) |
H1122Y |
possibly damaging |
Het |
Cpne6 |
A |
G |
14: 55,752,059 (GRCm39) |
K272R |
probably damaging |
Het |
Cpsf2 |
T |
A |
12: 101,956,262 (GRCm39) |
L355Q |
probably damaging |
Het |
Cyp2c29 |
T |
A |
19: 39,298,224 (GRCm39) |
D256E |
probably benign |
Het |
Daglb |
G |
A |
5: 143,479,952 (GRCm39) |
V420I |
probably benign |
Het |
Ddx42 |
G |
T |
11: 106,138,675 (GRCm39) |
G825C |
probably benign |
Het |
Dis3 |
T |
C |
14: 99,318,826 (GRCm39) |
|
probably benign |
Het |
Dkk4 |
C |
T |
8: 23,115,359 (GRCm39) |
R70C |
probably damaging |
Het |
Dock6 |
G |
T |
9: 21,713,732 (GRCm39) |
Q1933K |
probably damaging |
Het |
Dpep2 |
T |
G |
8: 106,716,620 (GRCm39) |
Q186H |
probably benign |
Het |
Dzip3 |
A |
C |
16: 48,780,006 (GRCm39) |
|
probably benign |
Het |
Egflam |
T |
A |
15: 7,252,239 (GRCm39) |
I853F |
probably damaging |
Het |
Fastkd5 |
A |
G |
2: 130,457,837 (GRCm39) |
I251T |
probably benign |
Het |
Fbn2 |
T |
A |
18: 58,172,532 (GRCm39) |
D2091V |
possibly damaging |
Het |
Fem1al |
T |
C |
11: 29,774,990 (GRCm39) |
I156V |
probably damaging |
Het |
Fer1l4 |
C |
A |
2: 155,894,115 (GRCm39) |
V63L |
probably benign |
Het |
Frem1 |
T |
A |
4: 82,830,874 (GRCm39) |
D2062V |
probably benign |
Het |
Galnt6 |
A |
C |
15: 100,594,538 (GRCm39) |
|
probably benign |
Het |
Get3 |
A |
C |
8: 85,745,236 (GRCm39) |
V277G |
probably damaging |
Het |
Gm10972 |
A |
T |
3: 94,550,440 (GRCm39) |
|
probably benign |
Het |
Gm4846 |
G |
A |
1: 166,319,114 (GRCm39) |
T208I |
probably benign |
Het |
Gorab |
A |
G |
1: 163,214,174 (GRCm39) |
L252P |
probably damaging |
Het |
Gtsf2 |
A |
G |
15: 103,352,988 (GRCm39) |
C63R |
probably damaging |
Het |
Hal |
T |
C |
10: 93,325,036 (GRCm39) |
V15A |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,752,170 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
A |
T |
11: 4,358,833 (GRCm39) |
H191Q |
possibly damaging |
Het |
Hspa2 |
A |
T |
12: 76,451,990 (GRCm39) |
D228V |
probably damaging |
Het |
Igfn1 |
A |
T |
1: 135,896,267 (GRCm39) |
M1433K |
probably benign |
Het |
Il18 |
A |
G |
9: 50,486,628 (GRCm39) |
D19G |
probably damaging |
Het |
Il1rl2 |
G |
A |
1: 40,368,216 (GRCm39) |
V129I |
probably benign |
Het |
Inpp5b |
C |
A |
4: 124,676,201 (GRCm39) |
Y352* |
probably null |
Het |
Insrr |
A |
T |
3: 87,720,463 (GRCm39) |
M1034L |
possibly damaging |
Het |
Jmjd1c |
T |
C |
10: 67,061,534 (GRCm39) |
S1296P |
probably damaging |
Het |
Kdm5b |
G |
T |
1: 134,548,761 (GRCm39) |
|
probably null |
Het |
Krba1 |
C |
T |
6: 48,393,188 (GRCm39) |
T998I |
probably benign |
Het |
L3mbtl4 |
A |
G |
17: 69,084,907 (GRCm39) |
N606S |
probably benign |
Het |
Lonrf1 |
T |
A |
8: 36,698,313 (GRCm39) |
N395I |
possibly damaging |
Het |
Lpp |
A |
G |
16: 24,790,720 (GRCm39) |
D393G |
probably damaging |
Het |
Lrrc17 |
A |
G |
5: 21,765,528 (GRCm39) |
I3M |
probably benign |
Het |
Lrrtm4 |
A |
T |
6: 79,999,029 (GRCm39) |
Q147L |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,133,422 (GRCm39) |
M1413V |
probably benign |
Het |
Mapk8ip2 |
A |
G |
15: 89,340,861 (GRCm39) |
E102G |
possibly damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,698,916 (GRCm39) |
|
probably benign |
Het |
Mfng |
A |
C |
15: 78,641,514 (GRCm39) |
H294Q |
probably benign |
Het |
Mical2 |
T |
A |
7: 111,870,524 (GRCm39) |
N4K |
probably benign |
Het |
Mov10l1 |
T |
A |
15: 88,883,042 (GRCm39) |
V384E |
probably damaging |
Het |
Myo18b |
A |
G |
5: 113,021,442 (GRCm39) |
|
probably benign |
Het |
Nos2 |
C |
T |
11: 78,830,903 (GRCm39) |
P249L |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,794,065 (GRCm39) |
T681A |
probably damaging |
Het |
Nr1i3 |
C |
T |
1: 171,044,805 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 58,899,333 (GRCm39) |
|
probably null |
Het |
Onecut2 |
A |
T |
18: 64,473,820 (GRCm39) |
I124F |
possibly damaging |
Het |
Or10a49 |
C |
T |
7: 108,468,057 (GRCm39) |
M101I |
possibly damaging |
Het |
Or2a14 |
A |
T |
6: 43,130,395 (GRCm39) |
H52L |
probably benign |
Het |
Or2ag1 |
T |
A |
7: 106,313,908 (GRCm39) |
|
probably benign |
Het |
Or2f2 |
C |
T |
6: 42,767,530 (GRCm39) |
R186* |
probably null |
Het |
Or2t47 |
C |
A |
11: 58,442,462 (GRCm39) |
C201F |
probably damaging |
Het |
Or4a75 |
A |
T |
2: 89,448,438 (GRCm39) |
Y33N |
probably damaging |
Het |
Or4c123 |
C |
T |
2: 89,127,083 (GRCm39) |
C177Y |
probably damaging |
Het |
Or52u1 |
C |
T |
7: 104,237,682 (GRCm39) |
R224* |
probably null |
Het |
Or5m12 |
T |
A |
2: 85,735,030 (GRCm39) |
M123L |
possibly damaging |
Het |
Or8b35 |
A |
G |
9: 37,904,438 (GRCm39) |
T217A |
probably benign |
Het |
Otol1 |
G |
A |
3: 69,934,937 (GRCm39) |
G310R |
probably damaging |
Het |
Oxct2b |
T |
A |
4: 123,010,633 (GRCm39) |
S184R |
possibly damaging |
Het |
Oxct2b |
ACTG |
A |
4: 123,010,705 (GRCm39) |
|
probably benign |
Het |
P2rx6 |
A |
G |
16: 17,385,291 (GRCm39) |
|
probably benign |
Het |
Pde4a |
A |
G |
9: 21,115,699 (GRCm39) |
N411S |
probably damaging |
Het |
Phkb |
A |
T |
8: 86,783,153 (GRCm39) |
D983V |
probably benign |
Het |
Piezo2 |
G |
A |
18: 63,157,522 (GRCm39) |
T2396I |
probably damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,275,929 (GRCm39) |
D717V |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,766,465 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
A |
G |
10: 3,887,853 (GRCm39) |
I261V |
probably damaging |
Het |
Ppfia4 |
T |
C |
1: 134,251,851 (GRCm39) |
H441R |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,392,768 (GRCm39) |
|
probably benign |
Het |
Ptn |
T |
A |
6: 36,718,388 (GRCm39) |
|
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,649,362 (GRCm39) |
Y255C |
possibly damaging |
Het |
Ptpn4 |
A |
G |
1: 119,693,645 (GRCm39) |
Y126H |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,016,435 (GRCm39) |
N505D |
probably damaging |
Het |
Ptprs |
T |
A |
17: 56,761,220 (GRCm39) |
I116F |
possibly damaging |
Het |
Rab1a |
T |
G |
11: 20,173,169 (GRCm39) |
V90G |
probably damaging |
Het |
Rcor1 |
T |
C |
12: 111,068,102 (GRCm39) |
V267A |
probably benign |
Het |
Reep4 |
A |
G |
14: 70,784,678 (GRCm39) |
|
probably null |
Het |
Rere |
T |
A |
4: 150,699,779 (GRCm39) |
|
probably benign |
Het |
Rin3 |
T |
A |
12: 102,353,823 (GRCm39) |
Y743* |
probably null |
Het |
Rprm |
A |
G |
2: 53,975,067 (GRCm39) |
S84P |
probably damaging |
Het |
Sdhaf2 |
C |
T |
19: 10,494,383 (GRCm39) |
E109K |
probably damaging |
Het |
Sec31b |
G |
T |
19: 44,523,225 (GRCm39) |
Q24K |
probably damaging |
Het |
Sema5a |
T |
C |
15: 32,574,949 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2a |
T |
C |
19: 47,256,186 (GRCm39) |
Y844C |
probably damaging |
Het |
Shmt2 |
A |
C |
10: 127,355,941 (GRCm39) |
N134K |
probably damaging |
Het |
Slc9a8 |
C |
T |
2: 167,266,125 (GRCm39) |
A34V |
probably benign |
Het |
Spidr |
A |
C |
16: 15,957,936 (GRCm39) |
S64A |
possibly damaging |
Het |
Stk10 |
A |
G |
11: 32,567,882 (GRCm39) |
T895A |
probably benign |
Het |
Syne2 |
A |
T |
12: 76,080,365 (GRCm39) |
|
probably benign |
Het |
Szt2 |
T |
C |
4: 118,230,149 (GRCm39) |
|
probably null |
Het |
Tecpr1 |
A |
T |
5: 144,150,899 (GRCm39) |
V303D |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,350,776 (GRCm39) |
Y1048H |
probably damaging |
Het |
Tfb2m |
A |
G |
1: 179,373,396 (GRCm39) |
C101R |
probably damaging |
Het |
Tg |
T |
C |
15: 66,554,253 (GRCm39) |
V556A |
probably damaging |
Het |
Thbs4 |
A |
C |
13: 92,903,692 (GRCm39) |
I441M |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,379,593 (GRCm39) |
Y944N |
probably damaging |
Het |
Tm9sf3 |
C |
A |
19: 41,236,331 (GRCm39) |
|
probably benign |
Het |
Tmem145 |
T |
C |
7: 25,010,787 (GRCm39) |
F359S |
probably damaging |
Het |
Ttc21b |
C |
T |
2: 66,053,142 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,579,880 (GRCm39) |
V23671A |
probably damaging |
Het |
Txnl4b |
T |
C |
8: 110,298,103 (GRCm39) |
I78T |
probably benign |
Het |
Ubr4 |
C |
A |
4: 139,133,889 (GRCm39) |
L762I |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,208,149 (GRCm39) |
|
probably null |
Het |
Ugt1a8 |
C |
T |
1: 88,016,079 (GRCm39) |
P164L |
probably damaging |
Het |
Unc13b |
T |
C |
4: 43,263,559 (GRCm39) |
S1594P |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,278,639 (GRCm39) |
F912I |
probably benign |
Het |
Vat1l |
T |
C |
8: 114,963,319 (GRCm39) |
|
probably benign |
Het |
Vmn1r50 |
T |
A |
6: 90,084,863 (GRCm39) |
S203T |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,296,784 (GRCm39) |
L667Q |
probably damaging |
Het |
Vmn2r66 |
T |
G |
7: 84,656,023 (GRCm39) |
Q331P |
probably damaging |
Het |
Wdsub1 |
A |
T |
2: 59,708,669 (GRCm39) |
V68D |
possibly damaging |
Het |
Wnk2 |
C |
G |
13: 49,238,870 (GRCm39) |
A564P |
possibly damaging |
Het |
Wnk2 |
T |
A |
13: 49,238,872 (GRCm39) |
K563M |
probably damaging |
Het |
Zan |
T |
A |
5: 137,468,580 (GRCm39) |
H297L |
probably damaging |
Het |
Zfp426 |
A |
T |
9: 20,381,327 (GRCm39) |
H539Q |
probably damaging |
Het |
Zfp488 |
T |
A |
14: 33,692,497 (GRCm39) |
N222I |
probably damaging |
Het |
Zfp536 |
T |
A |
7: 37,268,243 (GRCm39) |
H391L |
probably damaging |
Het |
Zp1 |
T |
A |
19: 10,893,571 (GRCm39) |
N31I |
probably damaging |
Het |
|
Other mutations in Nlrp1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |
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 |
|
|
Predicted Primers |
PCR Primer
(F):5'- ACCTGACATGACTGTGGCAAAGAAG -3'
(R):5'- GCTGGGATTGGGAAGTCAACACTG -3'
Sequencing Primer
(F):5'- GTGCGAGTTGTGAGCAAG -3'
(R):5'- GGCCAGGCAGGTGAAGAG -3'
|
Posted On |
2013-06-12 |