Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930544G11Rik |
T |
C |
6: 65,930,317 (GRCm39) |
V184A |
probably benign |
Het |
Aars2 |
A |
G |
17: 45,827,497 (GRCm39) |
Y513C |
probably damaging |
Het |
Ackr2 |
G |
A |
9: 121,738,033 (GRCm39) |
C136Y |
probably damaging |
Het |
Aldh1l1 |
A |
G |
6: 90,547,782 (GRCm39) |
K414R |
probably benign |
Het |
Arl9 |
A |
G |
5: 77,155,118 (GRCm39) |
Y83C |
possibly damaging |
Het |
Atp10a |
G |
T |
7: 58,436,221 (GRCm39) |
R337L |
probably benign |
Het |
Atp6v1g3 |
A |
T |
1: 138,215,538 (GRCm39) |
Q66L |
probably damaging |
Het |
Atp7b |
A |
T |
8: 22,487,351 (GRCm39) |
N1321K |
probably damaging |
Het |
Axdnd1 |
A |
T |
1: 156,209,959 (GRCm39) |
M437K |
probably damaging |
Het |
Bap1 |
C |
A |
14: 30,976,126 (GRCm39) |
P147Q |
probably damaging |
Het |
Bicd1 |
C |
T |
6: 149,414,403 (GRCm39) |
T372I |
possibly damaging |
Het |
Brix1 |
T |
C |
15: 10,483,378 (GRCm39) |
|
probably null |
Het |
Btrc |
A |
G |
19: 45,501,967 (GRCm39) |
|
probably null |
Het |
C130050O18Rik |
A |
C |
5: 139,400,129 (GRCm39) |
I61L |
probably benign |
Het |
Cfap161 |
A |
G |
7: 83,425,258 (GRCm39) |
S278P |
probably damaging |
Het |
Cgnl1 |
T |
C |
9: 71,631,815 (GRCm39) |
D512G |
possibly damaging |
Het |
Chat |
T |
C |
14: 32,141,014 (GRCm39) |
D461G |
probably damaging |
Het |
Chl1 |
T |
A |
6: 103,668,635 (GRCm39) |
V456D |
probably benign |
Het |
Cib1 |
T |
C |
7: 79,882,120 (GRCm39) |
T20A |
possibly damaging |
Het |
Cubn |
T |
G |
2: 13,355,814 (GRCm39) |
H1806P |
probably benign |
Het |
Dapk1 |
T |
A |
13: 60,844,149 (GRCm39) |
V56E |
possibly damaging |
Het |
Dennd4a |
A |
G |
9: 64,803,756 (GRCm39) |
N1032D |
probably benign |
Het |
Dlg5 |
T |
A |
14: 24,188,723 (GRCm39) |
E1756V |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 30,996,339 (GRCm39) |
T2666A |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,009,257 (GRCm39) |
I2135N |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 73,150,528 (GRCm39) |
E745V |
probably benign |
Het |
Dock8 |
A |
T |
19: 25,158,927 (GRCm39) |
N1695I |
probably damaging |
Het |
Esf1 |
C |
T |
2: 140,006,139 (GRCm39) |
R336Q |
possibly damaging |
Het |
Fam161a |
A |
G |
11: 22,971,664 (GRCm39) |
|
probably null |
Het |
Fam89a |
T |
C |
8: 125,478,418 (GRCm39) |
E44G |
possibly damaging |
Het |
Fndc3b |
A |
T |
3: 27,510,634 (GRCm39) |
D829E |
probably benign |
Het |
Fxr1 |
C |
T |
3: 34,100,689 (GRCm39) |
T125I |
possibly damaging |
Het |
Gfer |
T |
C |
17: 24,914,836 (GRCm39) |
D69G |
probably damaging |
Het |
Gpatch2l |
T |
A |
12: 86,335,711 (GRCm39) |
S471T |
probably benign |
Het |
Grm7 |
T |
G |
6: 111,335,530 (GRCm39) |
I647S |
possibly damaging |
Het |
Gsn |
A |
G |
2: 35,188,807 (GRCm39) |
I447V |
probably benign |
Het |
H2al2c |
C |
T |
Y: 2,599,234 (GRCm39) |
L46F |
possibly damaging |
Het |
Hao2 |
A |
C |
3: 98,784,598 (GRCm39) |
|
probably null |
Het |
Ifitm10 |
T |
C |
7: 141,882,305 (GRCm39) |
E155G |
probably benign |
Het |
Igkv8-16 |
C |
A |
6: 70,363,794 (GRCm39) |
W76L |
probably benign |
Het |
Igsf21 |
A |
T |
4: 139,834,648 (GRCm39) |
F75I |
possibly damaging |
Het |
Ints14 |
T |
A |
9: 64,871,701 (GRCm39) |
M13K |
probably damaging |
Het |
Ipmk |
A |
T |
10: 71,199,298 (GRCm39) |
D53V |
possibly damaging |
Het |
Iqcn |
A |
T |
8: 71,169,597 (GRCm39) |
E1229V |
probably benign |
Het |
Itga8 |
A |
G |
2: 12,234,906 (GRCm39) |
F451L |
possibly damaging |
Het |
Jup |
A |
G |
11: 100,272,560 (GRCm39) |
F284S |
probably damaging |
Het |
Kctd5 |
T |
C |
17: 24,292,209 (GRCm39) |
D65G |
probably benign |
Het |
Klrc1 |
A |
T |
6: 129,654,184 (GRCm39) |
S148T |
probably benign |
Het |
Kmt5b |
A |
G |
19: 3,864,147 (GRCm39) |
K404E |
probably damaging |
Het |
Krt9 |
A |
C |
11: 100,081,617 (GRCm39) |
M304R |
probably damaging |
Het |
Krtap5-1 |
A |
T |
7: 141,850,299 (GRCm39) |
S143T |
unknown |
Het |
Kyat3 |
A |
G |
3: 142,426,162 (GRCm39) |
N68D |
probably damaging |
Het |
Kynu |
A |
G |
2: 43,571,365 (GRCm39) |
D427G |
probably damaging |
Het |
Leo1 |
A |
G |
9: 75,353,278 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
A |
G |
18: 77,501,892 (GRCm39) |
D1737G |
probably damaging |
Het |
Lpo |
C |
A |
11: 87,700,077 (GRCm39) |
L521F |
possibly damaging |
Het |
Lrrk1 |
A |
G |
7: 65,920,573 (GRCm39) |
S1477P |
probably damaging |
Het |
Lrrtm1 |
C |
A |
6: 77,220,584 (GRCm39) |
L14M |
probably damaging |
Het |
Ly75 |
G |
A |
2: 60,154,196 (GRCm39) |
R1084* |
probably null |
Het |
Mcf2l |
A |
G |
8: 13,060,456 (GRCm39) |
D764G |
probably benign |
Het |
Mmut |
A |
T |
17: 41,249,564 (GRCm39) |
M180L |
probably benign |
Het |
Mrgprd |
A |
T |
7: 144,876,086 (GRCm39) |
D319V |
probably benign |
Het |
Myom3 |
T |
C |
4: 135,522,490 (GRCm39) |
L897P |
possibly damaging |
Het |
Ncapd2 |
A |
T |
6: 125,161,291 (GRCm39) |
M247K |
possibly damaging |
Het |
Npy6r |
A |
G |
18: 44,408,999 (GRCm39) |
N140S |
probably damaging |
Het |
Nsmce4a |
T |
C |
7: 130,141,602 (GRCm39) |
K196E |
probably benign |
Het |
Nup88 |
T |
C |
11: 70,836,080 (GRCm39) |
K532R |
probably benign |
Het |
Or6k4 |
T |
A |
1: 173,964,680 (GRCm39) |
Y123* |
probably null |
Het |
Or8d6 |
T |
A |
9: 39,853,805 (GRCm39) |
V83E |
probably benign |
Het |
Or8g29-ps1 |
A |
T |
9: 39,200,589 (GRCm39) |
I199N |
unknown |
Het |
Pbxip1 |
A |
T |
3: 89,354,735 (GRCm39) |
D418V |
possibly damaging |
Het |
Pde2a |
C |
A |
7: 101,159,151 (GRCm39) |
R761S |
possibly damaging |
Het |
Phf10 |
A |
T |
17: 15,166,575 (GRCm39) |
C432S |
probably damaging |
Het |
Pitpnm2 |
T |
C |
5: 124,259,522 (GRCm39) |
D1271G |
probably damaging |
Het |
Plin1 |
A |
T |
7: 79,373,192 (GRCm39) |
L259Q |
probably damaging |
Het |
Pmpca |
G |
C |
2: 26,285,046 (GRCm39) |
E424Q |
possibly damaging |
Het |
Pou6f2 |
T |
A |
13: 18,414,379 (GRCm39) |
Q132L |
unknown |
Het |
Ppa2 |
A |
T |
3: 133,036,199 (GRCm39) |
N118Y |
possibly damaging |
Het |
Prickle2 |
T |
C |
6: 92,387,959 (GRCm39) |
E537G |
possibly damaging |
Het |
Prl3d1 |
A |
G |
13: 27,282,684 (GRCm39) |
I141V |
possibly damaging |
Het |
Prl8a1 |
A |
T |
13: 27,758,172 (GRCm39) |
V179D |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,984,489 (GRCm39) |
F1669L |
probably benign |
Het |
Prrg4 |
T |
A |
2: 104,669,787 (GRCm39) |
E110V |
possibly damaging |
Het |
Rfx5 |
C |
A |
3: 94,866,187 (GRCm39) |
H495Q |
unknown |
Het |
Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
Rpe65 |
A |
G |
3: 159,328,491 (GRCm39) |
Y433C |
probably damaging |
Het |
Rpl35rt |
A |
T |
1: 156,193,657 (GRCm39) |
I4F |
probably damaging |
Het |
Rtn4rl1 |
C |
T |
11: 75,156,576 (GRCm39) |
S336F |
possibly damaging |
Het |
Scn2a |
A |
G |
2: 65,578,663 (GRCm39) |
D1446G |
probably benign |
Het |
Sdk1 |
C |
A |
5: 142,031,931 (GRCm39) |
T1002K |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,036,422 (GRCm39) |
S409P |
probably benign |
Het |
Sowahc |
A |
G |
10: 59,058,100 (GRCm39) |
T79A |
probably benign |
Het |
Spata31h1 |
G |
A |
10: 82,129,248 (GRCm39) |
T1254I |
probably benign |
Het |
Stk35 |
T |
A |
2: 129,643,513 (GRCm39) |
C166S |
probably benign |
Het |
Tarbp2 |
A |
G |
15: 102,430,922 (GRCm39) |
H225R |
probably benign |
Het |
Tdrd12 |
T |
A |
7: 35,188,648 (GRCm39) |
K530* |
probably null |
Het |
Terf2ip |
A |
G |
8: 112,744,618 (GRCm39) |
I312V |
probably benign |
Het |
Tgfb1 |
T |
C |
7: 25,391,964 (GRCm39) |
|
probably null |
Het |
Thbs2 |
T |
C |
17: 14,891,720 (GRCm39) |
D939G |
probably damaging |
Het |
Ube4b |
A |
T |
4: 149,483,067 (GRCm39) |
I67K |
probably benign |
Het |
Ubn1 |
G |
T |
16: 4,895,080 (GRCm39) |
V709F |
possibly damaging |
Het |
Ugt2b5 |
T |
C |
5: 87,276,258 (GRCm39) |
K339E |
possibly damaging |
Het |
Vax2 |
T |
C |
6: 83,714,882 (GRCm39) |
S266P |
probably damaging |
Het |
Vmn2r108 |
A |
G |
17: 20,683,038 (GRCm39) |
I722T |
probably benign |
Het |
Vmn2r95 |
A |
G |
17: 18,661,577 (GRCm39) |
K441R |
probably benign |
Het |
Wapl |
C |
A |
14: 34,458,648 (GRCm39) |
D903E |
probably benign |
Het |
Wee1 |
T |
A |
7: 109,734,001 (GRCm39) |
V442D |
probably benign |
Het |
Zan |
T |
C |
5: 137,432,358 (GRCm39) |
N2313S |
unknown |
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 |
R6704:Nlrp2
|
UTSW |
7 |
5,328,040 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|