Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apob |
T |
C |
12: 8,060,379 (GRCm39) |
S2921P |
probably damaging |
Het |
Asxl3 |
G |
A |
18: 22,650,362 (GRCm39) |
A784T |
probably benign |
Het |
Atm |
T |
C |
9: 53,370,153 (GRCm39) |
I2320V |
probably benign |
Het |
Ccdc152 |
T |
A |
15: 3,310,195 (GRCm39) |
I227F |
probably damaging |
Het |
Cd109 |
T |
C |
9: 78,587,357 (GRCm39) |
V675A |
probably benign |
Het |
Col3a1 |
T |
C |
1: 45,386,892 (GRCm39) |
Y235H |
probably damaging |
Het |
Dnmbp |
T |
C |
19: 43,889,652 (GRCm39) |
D705G |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Ermn |
T |
C |
2: 57,938,046 (GRCm39) |
D189G |
possibly damaging |
Het |
Evx2 |
C |
A |
2: 74,486,499 (GRCm39) |
A297S |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,477,410 (GRCm39) |
F2152S |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,990,642 (GRCm39) |
V1018A |
unknown |
Het |
Hyou1 |
T |
C |
9: 44,292,431 (GRCm39) |
|
probably null |
Het |
Kcnma1 |
G |
A |
14: 24,052,882 (GRCm39) |
Q187* |
probably null |
Het |
Macf1 |
C |
T |
4: 123,304,555 (GRCm39) |
|
probably benign |
Het |
Mcam |
T |
A |
9: 44,048,217 (GRCm39) |
D124E |
probably benign |
Het |
Mical3 |
T |
C |
6: 120,986,761 (GRCm39) |
|
probably benign |
Het |
Mlxipl |
A |
T |
5: 135,166,094 (GRCm39) |
|
probably null |
Het |
Myt1 |
A |
G |
2: 181,453,005 (GRCm39) |
M1V |
probably null |
Het |
Nlrc3 |
C |
T |
16: 3,782,945 (GRCm39) |
V155I |
probably damaging |
Het |
Omd |
A |
G |
13: 49,743,349 (GRCm39) |
D133G |
probably damaging |
Het |
Or5h19 |
T |
C |
16: 58,856,225 (GRCm39) |
R292G |
probably damaging |
Het |
Or9r7 |
T |
A |
10: 129,962,024 (GRCm39) |
K301* |
probably null |
Het |
Pappa |
G |
A |
4: 65,123,161 (GRCm39) |
C832Y |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,736,515 (GRCm39) |
V174E |
possibly damaging |
Het |
Pfkl |
C |
T |
10: 77,832,200 (GRCm39) |
G297D |
probably damaging |
Het |
Polr3a |
A |
G |
14: 24,511,910 (GRCm39) |
L882P |
probably damaging |
Het |
Ptchd4 |
A |
G |
17: 42,627,931 (GRCm39) |
T131A |
probably benign |
Het |
Rad50 |
T |
C |
11: 53,589,745 (GRCm39) |
N152S |
probably damaging |
Het |
Ruvbl1 |
T |
A |
6: 88,456,187 (GRCm39) |
M147K |
probably benign |
Het |
Septin4 |
T |
A |
11: 87,479,856 (GRCm39) |
I277N |
probably damaging |
Het |
Serpini1 |
T |
C |
3: 75,545,255 (GRCm39) |
V337A |
probably damaging |
Het |
Tmem131 |
A |
G |
1: 36,835,261 (GRCm39) |
V1620A |
possibly damaging |
Het |
Tpr |
A |
G |
1: 150,282,259 (GRCm39) |
E248G |
possibly damaging |
Het |
Ugt2b36 |
C |
A |
5: 87,239,990 (GRCm39) |
V132F |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,621,035 (GRCm39) |
E212G |
probably damaging |
Het |
Zc2hc1c |
A |
T |
12: 85,337,258 (GRCm39) |
Q305L |
possibly damaging |
Het |
|
Other mutations in Nlrp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00485:Nlrp2
|
APN |
7 |
5,340,547 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00545:Nlrp2
|
APN |
7 |
5,331,251 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01311:Nlrp2
|
APN |
7 |
5,322,238 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01345:Nlrp2
|
APN |
7 |
5,320,491 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01583:Nlrp2
|
APN |
7 |
5,340,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01659:Nlrp2
|
APN |
7 |
5,331,034 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02240:Nlrp2
|
APN |
7 |
5,330,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02353:Nlrp2
|
APN |
7 |
5,340,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02360:Nlrp2
|
APN |
7 |
5,340,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:Nlrp2
|
APN |
7 |
5,331,809 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02441:Nlrp2
|
APN |
7 |
5,338,566 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02588:Nlrp2
|
APN |
7 |
5,330,551 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Nlrp2
|
APN |
7 |
5,331,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02968:Nlrp2
|
APN |
7 |
5,304,024 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03342:Nlrp2
|
APN |
7 |
5,320,482 (GRCm39) |
missense |
probably damaging |
1.00 |
BB006:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Nlrp2
|
UTSW |
7 |
5,325,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Nlrp2
|
UTSW |
7 |
5,325,333 (GRCm39) |
unclassified |
probably benign |
|
R0079:Nlrp2
|
UTSW |
7 |
5,330,729 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0130:Nlrp2
|
UTSW |
7 |
5,325,417 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0157:Nlrp2
|
UTSW |
7 |
5,311,769 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0201:Nlrp2
|
UTSW |
7 |
5,331,328 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Nlrp2
|
UTSW |
7 |
5,331,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0288:Nlrp2
|
UTSW |
7 |
5,331,544 (GRCm39) |
missense |
probably benign |
0.19 |
R0332:Nlrp2
|
UTSW |
7 |
5,320,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Nlrp2
|
UTSW |
7 |
5,322,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Nlrp2
|
UTSW |
7 |
5,331,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Nlrp2
|
UTSW |
7 |
5,330,490 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1392:Nlrp2
|
UTSW |
7 |
5,332,014 (GRCm39) |
splice site |
probably benign |
|
R1470:Nlrp2
|
UTSW |
7 |
5,303,950 (GRCm39) |
missense |
probably benign |
0.18 |
R1470:Nlrp2
|
UTSW |
7 |
5,303,950 (GRCm39) |
missense |
probably benign |
0.18 |
R1563:Nlrp2
|
UTSW |
7 |
5,311,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Nlrp2
|
UTSW |
7 |
5,330,715 (GRCm39) |
nonsense |
probably null |
|
R1942:Nlrp2
|
UTSW |
7 |
5,325,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Nlrp2
|
UTSW |
7 |
5,330,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Nlrp2
|
UTSW |
7 |
5,330,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1961:Nlrp2
|
UTSW |
7 |
5,330,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Nlrp2
|
UTSW |
7 |
5,328,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Nlrp2
|
UTSW |
7 |
5,328,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2190:Nlrp2
|
UTSW |
7 |
5,322,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2243:Nlrp2
|
UTSW |
7 |
5,338,597 (GRCm39) |
missense |
probably benign |
0.03 |
R2277:Nlrp2
|
UTSW |
7 |
5,331,128 (GRCm39) |
missense |
probably benign |
|
R2334:Nlrp2
|
UTSW |
7 |
5,340,534 (GRCm39) |
missense |
probably benign |
0.39 |
R3030:Nlrp2
|
UTSW |
7 |
5,330,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Nlrp2
|
UTSW |
7 |
5,322,286 (GRCm39) |
missense |
probably benign |
0.01 |
R3941:Nlrp2
|
UTSW |
7 |
5,330,551 (GRCm39) |
nonsense |
probably null |
|
R4021:Nlrp2
|
UTSW |
7 |
5,328,011 (GRCm39) |
missense |
probably benign |
0.40 |
R4518:Nlrp2
|
UTSW |
7 |
5,328,055 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4666:Nlrp2
|
UTSW |
7 |
5,322,188 (GRCm39) |
missense |
probably benign |
0.18 |
R4767:Nlrp2
|
UTSW |
7 |
5,331,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Nlrp2
|
UTSW |
7 |
5,331,950 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4873:Nlrp2
|
UTSW |
7 |
5,301,858 (GRCm39) |
missense |
probably benign |
0.09 |
R4875:Nlrp2
|
UTSW |
7 |
5,301,858 (GRCm39) |
missense |
probably benign |
0.09 |
R5020:Nlrp2
|
UTSW |
7 |
5,331,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5293:Nlrp2
|
UTSW |
7 |
5,330,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Nlrp2
|
UTSW |
7 |
5,328,007 (GRCm39) |
missense |
probably benign |
0.00 |
R5336:Nlrp2
|
UTSW |
7 |
5,331,118 (GRCm39) |
missense |
probably benign |
|
R5390:Nlrp2
|
UTSW |
7 |
5,303,908 (GRCm39) |
missense |
probably benign |
0.00 |
R5864:Nlrp2
|
UTSW |
7 |
5,325,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5913:Nlrp2
|
UTSW |
7 |
5,327,902 (GRCm39) |
splice site |
probably null |
|
R6173:Nlrp2
|
UTSW |
7 |
5,340,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R6274:Nlrp2
|
UTSW |
7 |
5,320,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Nlrp2
|
UTSW |
7 |
5,340,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6343:Nlrp2
|
UTSW |
7 |
5,303,925 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6814:Nlrp2
|
UTSW |
7 |
5,311,709 (GRCm39) |
missense |
probably benign |
0.01 |
R6872:Nlrp2
|
UTSW |
7 |
5,311,709 (GRCm39) |
missense |
probably benign |
0.01 |
R7023:Nlrp2
|
UTSW |
7 |
5,331,228 (GRCm39) |
nonsense |
probably null |
|
R7028:Nlrp2
|
UTSW |
7 |
5,331,571 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7109:Nlrp2
|
UTSW |
7 |
5,331,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Nlrp2
|
UTSW |
7 |
5,320,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Nlrp2
|
UTSW |
7 |
5,311,644 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7339:Nlrp2
|
UTSW |
7 |
5,330,627 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7573:Nlrp2
|
UTSW |
7 |
5,320,468 (GRCm39) |
critical splice donor site |
probably null |
|
R7657:Nlrp2
|
UTSW |
7 |
5,322,167 (GRCm39) |
missense |
probably benign |
0.01 |
R7929:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Nlrp2
|
UTSW |
7 |
5,331,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Nlrp2
|
UTSW |
7 |
5,330,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Nlrp2
|
UTSW |
7 |
5,320,494 (GRCm39) |
missense |
probably benign |
0.40 |
R8785:Nlrp2
|
UTSW |
7 |
5,330,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Nlrp2
|
UTSW |
7 |
5,330,887 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8982:Nlrp2
|
UTSW |
7 |
5,327,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Nlrp2
|
UTSW |
7 |
5,325,457 (GRCm39) |
missense |
probably null |
0.00 |
R9038:Nlrp2
|
UTSW |
7 |
5,330,478 (GRCm39) |
missense |
probably benign |
0.14 |
R9149:Nlrp2
|
UTSW |
7 |
5,330,572 (GRCm39) |
missense |
probably benign |
0.01 |
R9229:Nlrp2
|
UTSW |
7 |
5,304,052 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9584:Nlrp2
|
UTSW |
7 |
5,322,215 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Nlrp2
|
UTSW |
7 |
5,330,641 (GRCm39) |
missense |
probably benign |
0.03 |
|