Incidental Mutation 'R6925:Nlrp1a'
ID |
541108 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nlrp1a
|
Ensembl Gene |
ENSMUSG00000069830 |
Gene Name |
NLR family, pyrin domain containing 1A |
Synonyms |
Nalp1 |
MMRRC Submission |
045043-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.088)
|
Stock # |
R6925 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
70983062-71035530 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 70983339 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Glutamine
at position 1209
(L1209Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000038186
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048514]
[ENSMUST00000108518]
|
AlphaFold |
Q2LKU9 |
Predicted Effect |
probably null
Transcript: ENSMUST00000048514
AA Change: L1209Q
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000038186 Gene: ENSMUSG00000069830 AA Change: L1209Q
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
11 |
N/A |
INTRINSIC |
Pfam:NACHT
|
133 |
302 |
4.6e-41 |
PFAM |
low complexity region
|
482 |
494 |
N/A |
INTRINSIC |
LRR
|
632 |
659 |
4.53e-1 |
SMART |
LRR
|
742 |
769 |
3.04e-5 |
SMART |
low complexity region
|
856 |
870 |
N/A |
INTRINSIC |
Pfam:FIIND
|
921 |
1173 |
1.6e-102 |
PFAM |
Pfam:CARD
|
1209 |
1292 |
2.3e-20 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108518
AA Change: L1091Q
PolyPhen 2
Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000104158 Gene: ENSMUSG00000069830 AA Change: L1091Q
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
11 |
N/A |
INTRINSIC |
Pfam:NACHT
|
133 |
302 |
1.1e-40 |
PFAM |
low complexity region
|
482 |
494 |
N/A |
INTRINSIC |
LRR
|
632 |
659 |
4.53e-1 |
SMART |
LRR
|
661 |
688 |
2.85e1 |
SMART |
LRR
|
689 |
716 |
3.04e-5 |
SMART |
Pfam:FIIND
|
819 |
1073 |
3e-136 |
PFAM |
Pfam:CARD
|
1091 |
1174 |
8.2e-20 |
PFAM |
|
Meta Mutation Damage Score |
0.3379 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 98.0%
|
Validation Efficiency |
100% (91/91) |
MGI Phenotype |
PHENOTYPE: Mice heterozygous for an ENU-induced allele develop a multi-organ neutrophilic inflammatory disease. Homozygotes for the same ENU-induced allele develop a similar but lethal condition and exhibit neutrophilia, lymphopenia, splenomegaly, loss of peritoneal macrophages, and premature death. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat1 |
A |
T |
9: 53,503,329 (GRCm39) |
V170E |
probably benign |
Het |
Atp2b2 |
T |
A |
6: 113,737,681 (GRCm39) |
I902F |
probably damaging |
Het |
Cacna1d |
A |
G |
14: 29,773,594 (GRCm39) |
V1697A |
probably benign |
Het |
Ccdc14 |
T |
A |
16: 34,511,119 (GRCm39) |
F31Y |
probably benign |
Het |
Ccdc17 |
T |
A |
4: 116,455,407 (GRCm39) |
V250E |
probably damaging |
Het |
Cct7 |
A |
G |
6: 85,436,164 (GRCm39) |
N25S |
probably damaging |
Het |
Cdcp3 |
A |
G |
7: 130,824,436 (GRCm39) |
Q177R |
possibly damaging |
Het |
Cep19 |
G |
C |
16: 31,922,760 (GRCm39) |
G9R |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,249,685 (GRCm39) |
|
probably null |
Het |
Chd1l |
T |
G |
3: 97,490,142 (GRCm39) |
E471A |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,855,047 (GRCm39) |
I787T |
probably damaging |
Het |
Cntnap5c |
A |
C |
17: 58,702,261 (GRCm39) |
T1194P |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,743,724 (GRCm39) |
M208L |
probably benign |
Het |
Coro7 |
A |
T |
16: 4,446,538 (GRCm39) |
|
probably null |
Het |
Csrnp2 |
T |
C |
15: 100,379,839 (GRCm39) |
K484R |
probably benign |
Het |
Cyp2c39 |
T |
A |
19: 39,501,639 (GRCm39) |
V64E |
probably damaging |
Het |
Ddr2 |
T |
C |
1: 169,825,701 (GRCm39) |
K300E |
probably benign |
Het |
Ddx56 |
T |
C |
11: 6,213,980 (GRCm39) |
E393G |
probably damaging |
Het |
Diaph1 |
A |
C |
18: 37,986,732 (GRCm39) |
Y1084* |
probably null |
Het |
Disp1 |
A |
T |
1: 182,868,042 (GRCm39) |
F1459L |
probably benign |
Het |
Dnajc8 |
G |
A |
4: 132,271,424 (GRCm39) |
A80T |
probably damaging |
Het |
Elfn1 |
T |
A |
5: 139,957,440 (GRCm39) |
M148K |
probably benign |
Het |
Emcn |
T |
A |
3: 137,124,763 (GRCm39) |
I154N |
probably damaging |
Het |
Enah |
T |
A |
1: 181,733,464 (GRCm39) |
|
probably null |
Het |
Enah |
C |
G |
1: 181,733,463 (GRCm39) |
|
probably null |
Het |
Ep300 |
C |
A |
15: 81,534,182 (GRCm39) |
Q2080K |
probably benign |
Het |
Epha2 |
T |
A |
4: 141,036,068 (GRCm39) |
M168K |
probably benign |
Het |
Ercc6 |
T |
A |
14: 32,284,565 (GRCm39) |
I776N |
probably damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fat4 |
G |
T |
3: 39,050,353 (GRCm39) |
|
probably null |
Het |
G3bp1 |
A |
G |
11: 55,388,786 (GRCm39) |
R333G |
possibly damaging |
Het |
Gm3604 |
A |
G |
13: 62,517,204 (GRCm39) |
F385L |
probably benign |
Het |
Gm5800 |
T |
C |
14: 51,951,157 (GRCm39) |
I147M |
possibly damaging |
Het |
Hipk1 |
A |
G |
3: 103,685,561 (GRCm39) |
F18S |
unknown |
Het |
Ighv3-8 |
A |
T |
12: 114,285,950 (GRCm39) |
C131S |
probably benign |
Het |
Il23r |
T |
G |
6: 67,400,477 (GRCm39) |
T618P |
probably damaging |
Het |
Il31ra |
G |
A |
13: 112,664,063 (GRCm39) |
T538I |
possibly damaging |
Het |
Kcns2 |
A |
G |
15: 34,840,059 (GRCm39) |
D474G |
unknown |
Het |
Klc4 |
T |
C |
17: 46,947,155 (GRCm39) |
T407A |
possibly damaging |
Het |
Klra5 |
C |
T |
6: 129,888,420 (GRCm39) |
S2N |
probably benign |
Het |
Krt10 |
T |
C |
11: 99,279,677 (GRCm39) |
Y161C |
probably damaging |
Het |
Kxd1 |
A |
T |
8: 70,975,928 (GRCm39) |
M1K |
probably null |
Het |
Lgals1 |
A |
C |
15: 78,812,240 (GRCm39) |
D27A |
possibly damaging |
Het |
Lgr5 |
T |
C |
10: 115,302,251 (GRCm39) |
S308G |
probably benign |
Het |
Lrp1 |
G |
A |
10: 127,392,857 (GRCm39) |
S2736L |
probably benign |
Het |
Lrpap1 |
G |
T |
5: 35,259,880 (GRCm39) |
H73N |
probably benign |
Het |
Mcpt1 |
C |
A |
14: 56,256,522 (GRCm39) |
T86K |
probably damaging |
Het |
Megf6 |
A |
T |
4: 154,339,044 (GRCm39) |
D527V |
probably damaging |
Het |
Mical3 |
A |
T |
6: 120,936,351 (GRCm39) |
S1392T |
probably benign |
Het |
Mmp2 |
A |
T |
8: 93,566,010 (GRCm39) |
D437V |
probably damaging |
Het |
Mob4 |
T |
A |
1: 55,191,881 (GRCm39) |
Y166* |
probably null |
Het |
Mrap2 |
G |
A |
9: 87,064,527 (GRCm39) |
M89I |
possibly damaging |
Het |
Mug1 |
G |
A |
6: 121,858,746 (GRCm39) |
A1155T |
probably damaging |
Het |
Myh2 |
G |
T |
11: 67,084,044 (GRCm39) |
A1556S |
probably benign |
Het |
Nfatc3 |
A |
G |
8: 106,845,954 (GRCm39) |
D1028G |
probably benign |
Het |
Ngef |
T |
G |
1: 87,430,985 (GRCm39) |
|
probably null |
Het |
Npr2 |
C |
T |
4: 43,647,553 (GRCm39) |
R819C |
probably damaging |
Het |
Nsd2 |
A |
T |
5: 34,036,454 (GRCm39) |
D646V |
probably damaging |
Het |
Nsun7 |
A |
G |
5: 66,434,415 (GRCm39) |
H252R |
probably damaging |
Het |
Or2a25 |
T |
A |
6: 42,888,791 (GRCm39) |
C111* |
probably null |
Het |
Or2k2 |
A |
T |
4: 58,785,647 (GRCm39) |
I25N |
possibly damaging |
Het |
Or51a10 |
C |
T |
7: 103,698,947 (GRCm39) |
V205I |
probably benign |
Het |
Or8g32 |
A |
T |
9: 39,305,156 (GRCm39) |
Q20L |
probably benign |
Het |
Or8g32 |
G |
T |
9: 39,305,157 (GRCm39) |
Q20H |
probably benign |
Het |
Pcdhga2 |
A |
T |
18: 37,803,638 (GRCm39) |
D494V |
probably damaging |
Het |
Pcsk2 |
A |
G |
2: 143,655,667 (GRCm39) |
E617G |
probably damaging |
Het |
Pdc |
T |
C |
1: 150,208,931 (GRCm39) |
I138T |
probably damaging |
Het |
Phc2 |
T |
A |
4: 128,641,927 (GRCm39) |
S750T |
probably damaging |
Het |
Pkd2l1 |
T |
A |
19: 44,179,947 (GRCm39) |
N88Y |
possibly damaging |
Het |
Plcl1 |
C |
T |
1: 55,445,757 (GRCm39) |
R71* |
probably null |
Het |
Prag1 |
C |
A |
8: 36,571,048 (GRCm39) |
L544M |
probably damaging |
Het |
Prkg2 |
A |
G |
5: 99,114,369 (GRCm39) |
|
probably null |
Het |
Psd2 |
G |
A |
18: 36,112,764 (GRCm39) |
S153N |
probably damaging |
Het |
Rab11fip1 |
A |
T |
8: 27,643,000 (GRCm39) |
S600T |
probably damaging |
Het |
Rbms1 |
T |
G |
2: 60,592,648 (GRCm39) |
T222P |
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,904,243 (GRCm39) |
Y382* |
probably null |
Het |
Socs4 |
T |
A |
14: 47,527,195 (GRCm39) |
C43* |
probably null |
Het |
Sorl1 |
T |
A |
9: 41,944,922 (GRCm39) |
T868S |
probably damaging |
Het |
St6gal1 |
A |
G |
16: 23,174,963 (GRCm39) |
Y267C |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,076,682 (GRCm39) |
V6879A |
probably benign |
Het |
Syne2 |
C |
A |
12: 75,900,906 (GRCm39) |
H22N |
possibly damaging |
Het |
Tmeff2 |
T |
A |
1: 50,967,180 (GRCm39) |
L25Q |
probably damaging |
Het |
Tmprss11g |
G |
T |
5: 86,635,285 (GRCm39) |
D396E |
probably benign |
Het |
Tmprss11g |
T |
A |
5: 86,635,295 (GRCm39) |
H393L |
probably benign |
Het |
Vmn2r23 |
A |
G |
6: 123,681,512 (GRCm39) |
E140G |
probably damaging |
Het |
Wapl |
T |
C |
14: 34,399,320 (GRCm39) |
S130P |
probably benign |
Het |
Zeb2 |
T |
A |
2: 44,884,541 (GRCm39) |
K982M |
probably damaging |
Het |
Zfhx3 |
C |
G |
8: 109,683,453 (GRCm39) |
H3631D |
unknown |
Het |
Zfp719 |
T |
C |
7: 43,240,130 (GRCm39) |
S573P |
probably damaging |
Het |
Zfp979 |
A |
T |
4: 147,697,999 (GRCm39) |
C237S |
possibly damaging |
Het |
|
Other mutations in Nlrp1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00648:Nlrp1a
|
APN |
11 |
70,983,783 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00771:Nlrp1a
|
APN |
11 |
71,013,567 (GRCm39) |
nonsense |
probably null |
|
IGL01408:Nlrp1a
|
APN |
11 |
71,013,742 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01886:Nlrp1a
|
APN |
11 |
71,014,327 (GRCm39) |
missense |
probably benign |
|
IGL02221:Nlrp1a
|
APN |
11 |
71,013,944 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02291:Nlrp1a
|
APN |
11 |
71,013,415 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02375:Nlrp1a
|
APN |
11 |
71,004,339 (GRCm39) |
nonsense |
probably null |
|
IGL02408:Nlrp1a
|
APN |
11 |
71,013,456 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02516:Nlrp1a
|
APN |
11 |
71,005,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02583:Nlrp1a
|
APN |
11 |
71,014,227 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02622:Nlrp1a
|
APN |
11 |
71,013,826 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02642:Nlrp1a
|
APN |
11 |
71,014,358 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02823:Nlrp1a
|
APN |
11 |
70,983,249 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02859:Nlrp1a
|
APN |
11 |
70,996,912 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02997:Nlrp1a
|
APN |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03342:Nlrp1a
|
APN |
11 |
71,013,617 (GRCm39) |
missense |
probably benign |
0.19 |
Ants
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
dreary
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
picnic
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
seedless
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
watermelon
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R0022:Nlrp1a
|
UTSW |
11 |
71,014,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R0345:Nlrp1a
|
UTSW |
11 |
71,014,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0364:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0566:Nlrp1a
|
UTSW |
11 |
71,013,768 (GRCm39) |
missense |
probably benign |
0.00 |
R1177:Nlrp1a
|
UTSW |
11 |
70,998,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Nlrp1a
|
UTSW |
11 |
71,004,292 (GRCm39) |
critical splice donor site |
probably null |
|
R1263:Nlrp1a
|
UTSW |
11 |
70,987,948 (GRCm39) |
missense |
probably benign |
0.01 |
R1681:Nlrp1a
|
UTSW |
11 |
71,033,184 (GRCm39) |
missense |
unknown |
|
R1743:Nlrp1a
|
UTSW |
11 |
71,015,032 (GRCm39) |
missense |
probably benign |
0.04 |
R1826:Nlrp1a
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1826:Nlrp1a
|
UTSW |
11 |
70,998,806 (GRCm39) |
intron |
probably benign |
|
R1981:Nlrp1a
|
UTSW |
11 |
70,989,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Nlrp1a
|
UTSW |
11 |
71,015,046 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2116:Nlrp1a
|
UTSW |
11 |
71,005,326 (GRCm39) |
nonsense |
probably null |
|
R2134:Nlrp1a
|
UTSW |
11 |
71,015,014 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Nlrp1a
|
UTSW |
11 |
71,013,733 (GRCm39) |
nonsense |
probably null |
|
R2301:Nlrp1a
|
UTSW |
11 |
70,996,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3029:Nlrp1a
|
UTSW |
11 |
71,014,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Nlrp1a
|
UTSW |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Nlrp1a
|
UTSW |
11 |
71,013,529 (GRCm39) |
missense |
probably benign |
0.08 |
R3898:Nlrp1a
|
UTSW |
11 |
71,013,700 (GRCm39) |
missense |
probably benign |
0.00 |
R4254:Nlrp1a
|
UTSW |
11 |
71,013,854 (GRCm39) |
nonsense |
probably null |
|
R4397:Nlrp1a
|
UTSW |
11 |
70,988,030 (GRCm39) |
missense |
probably benign |
0.00 |
R4647:Nlrp1a
|
UTSW |
11 |
70,987,952 (GRCm39) |
splice site |
probably null |
|
R4740:Nlrp1a
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4965:Nlrp1a
|
UTSW |
11 |
70,983,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5009:Nlrp1a
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R5103:Nlrp1a
|
UTSW |
11 |
70,990,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R5355:Nlrp1a
|
UTSW |
11 |
71,015,077 (GRCm39) |
missense |
probably benign |
0.00 |
R5577:Nlrp1a
|
UTSW |
11 |
70,990,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Nlrp1a
|
UTSW |
11 |
70,990,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Nlrp1a
|
UTSW |
11 |
70,989,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Nlrp1a
|
UTSW |
11 |
71,013,846 (GRCm39) |
missense |
probably benign |
0.00 |
R6220:Nlrp1a
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
R6564:Nlrp1a
|
UTSW |
11 |
71,014,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:Nlrp1a
|
UTSW |
11 |
70,996,899 (GRCm39) |
missense |
probably benign |
0.00 |
R7013:Nlrp1a
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
R7155:Nlrp1a
|
UTSW |
11 |
71,014,905 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7214:Nlrp1a
|
UTSW |
11 |
71,014,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Nlrp1a
|
UTSW |
11 |
71,015,068 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Nlrp1a
|
UTSW |
11 |
71,014,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Nlrp1a
|
UTSW |
11 |
70,987,919 (GRCm39) |
nonsense |
probably null |
|
R7409:Nlrp1a
|
UTSW |
11 |
71,013,634 (GRCm39) |
missense |
probably benign |
0.03 |
R7410:Nlrp1a
|
UTSW |
11 |
71,014,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7440:Nlrp1a
|
UTSW |
11 |
70,983,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R7447:Nlrp1a
|
UTSW |
11 |
70,983,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Nlrp1a
|
UTSW |
11 |
70,998,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7569:Nlrp1a
|
UTSW |
11 |
70,999,869 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Nlrp1a
|
UTSW |
11 |
70,989,740 (GRCm39) |
missense |
probably damaging |
0.96 |
R7634:Nlrp1a
|
UTSW |
11 |
70,990,354 (GRCm39) |
missense |
probably benign |
0.19 |
R7734:Nlrp1a
|
UTSW |
11 |
70,998,826 (GRCm39) |
missense |
unknown |
|
R7747:Nlrp1a
|
UTSW |
11 |
71,014,234 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8471:Nlrp1a
|
UTSW |
11 |
71,013,885 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8482:Nlrp1a
|
UTSW |
11 |
70,999,901 (GRCm39) |
splice site |
probably null |
|
R9008:Nlrp1a
|
UTSW |
11 |
71,014,735 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9028:Nlrp1a
|
UTSW |
11 |
71,013,819 (GRCm39) |
missense |
probably benign |
0.27 |
R9441:Nlrp1a
|
UTSW |
11 |
71,013,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Nlrp1a
|
UTSW |
11 |
70,998,488 (GRCm39) |
missense |
probably benign |
0.05 |
R9701:Nlrp1a
|
UTSW |
11 |
70,987,946 (GRCm39) |
missense |
probably benign |
0.08 |
X0026:Nlrp1a
|
UTSW |
11 |
71,033,142 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Nlrp1a
|
UTSW |
11 |
71,013,995 (GRCm39) |
missense |
probably benign |
0.27 |
Z1186:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1186:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1187:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1188:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1189:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1190:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1191:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1192:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- TCCATGACCAGGTGAGGATG -3'
(R):5'- GGTAAAGATATTTTCCCAATGGCC -3'
Sequencing Primer
(F):5'- GTAGAATTGGTCTTTGCAATCCCAGC -3'
(R):5'- GACACCAAAGGAGCATTC -3'
|
Posted On |
2018-11-28 |