Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930518I15Rik |
A |
G |
2: 156,699,133 (GRCm39) |
M1T |
probably null |
Het |
Abca13 |
A |
G |
11: 9,227,847 (GRCm39) |
E630G |
probably benign |
Het |
Abcf2 |
T |
A |
5: 24,778,504 (GRCm39) |
H218L |
possibly damaging |
Het |
Abo |
A |
T |
2: 26,733,395 (GRCm39) |
M268K |
probably benign |
Het |
Ankrd33 |
G |
T |
15: 101,014,029 (GRCm39) |
|
probably benign |
Het |
Apc |
G |
C |
18: 34,446,251 (GRCm39) |
R1049T |
probably damaging |
Het |
Atg16l2 |
T |
C |
7: 100,941,338 (GRCm39) |
K412E |
probably damaging |
Het |
Cachd1 |
G |
A |
4: 100,809,202 (GRCm39) |
|
probably null |
Het |
Ccdc152 |
T |
G |
15: 3,330,643 (GRCm39) |
K11Q |
probably damaging |
Het |
Ccdc38 |
T |
A |
10: 93,401,735 (GRCm39) |
W232R |
probably damaging |
Het |
Cluh |
C |
T |
11: 74,551,192 (GRCm39) |
P347L |
possibly damaging |
Het |
Cntn3 |
A |
G |
6: 102,314,288 (GRCm39) |
L142P |
probably damaging |
Het |
Ctnnd2 |
T |
A |
15: 30,806,884 (GRCm39) |
M601K |
probably damaging |
Het |
D930048N14Rik |
G |
A |
11: 51,545,734 (GRCm39) |
D209N |
unknown |
Het |
Dcaf6 |
A |
T |
1: 165,164,332 (GRCm39) |
N814K |
probably damaging |
Het |
Dhx8 |
A |
T |
11: 101,632,406 (GRCm39) |
D455V |
possibly damaging |
Het |
Fcna |
A |
C |
2: 25,514,956 (GRCm39) |
L301W |
possibly damaging |
Het |
Garin1b |
C |
T |
6: 29,323,902 (GRCm39) |
T209I |
probably benign |
Het |
Gdf9 |
T |
G |
11: 53,324,269 (GRCm39) |
C13G |
probably damaging |
Het |
Hells |
T |
A |
19: 38,933,858 (GRCm39) |
N226K |
probably damaging |
Het |
Hes6 |
A |
G |
1: 91,340,061 (GRCm39) |
S132P |
probably damaging |
Het |
Ifi207 |
A |
T |
1: 173,564,153 (GRCm39) |
|
probably benign |
Het |
Ighv16-1 |
A |
T |
12: 114,032,504 (GRCm39) |
Y99* |
probably null |
Het |
Kirrel2 |
T |
C |
7: 30,150,305 (GRCm39) |
I508V |
probably benign |
Het |
Klhl38 |
T |
A |
15: 58,186,022 (GRCm39) |
I236F |
probably damaging |
Het |
Klk15 |
C |
T |
7: 43,587,790 (GRCm39) |
H73Y |
possibly damaging |
Het |
Lamc1 |
A |
T |
1: 153,126,870 (GRCm39) |
C425* |
probably null |
Het |
Letm1 |
A |
G |
5: 33,918,213 (GRCm39) |
F311L |
probably damaging |
Het |
Lypd11 |
A |
T |
7: 24,422,173 (GRCm39) |
I192N |
possibly damaging |
Het |
Mybpc1 |
C |
T |
10: 88,391,501 (GRCm39) |
C318Y |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,393,692 (GRCm39) |
Y1141C |
|
Het |
Ndufv2 |
T |
A |
17: 66,390,475 (GRCm39) |
D165V |
probably damaging |
Het |
Nrde2 |
T |
C |
12: 100,110,123 (GRCm39) |
K303E |
probably benign |
Het |
Nup205 |
T |
A |
6: 35,196,808 (GRCm39) |
|
probably benign |
Het |
Or1j12 |
A |
G |
2: 36,342,897 (GRCm39) |
Q100R |
probably damaging |
Het |
Or2f2 |
A |
T |
6: 42,767,141 (GRCm39) |
H56L |
probably damaging |
Het |
Or5b118 |
A |
G |
19: 13,448,523 (GRCm39) |
N21S |
probably damaging |
Het |
Otof |
C |
T |
5: 30,546,001 (GRCm39) |
V451I |
possibly damaging |
Het |
Pask |
G |
A |
1: 93,253,191 (GRCm39) |
Q399* |
probably null |
Het |
Pbk |
T |
A |
14: 66,049,439 (GRCm39) |
F39I |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,374,753 (GRCm39) |
K1794R |
possibly damaging |
Het |
Pibf1 |
T |
C |
14: 99,424,069 (GRCm39) |
|
probably null |
Het |
Ppip5k2 |
G |
A |
1: 97,645,187 (GRCm39) |
T1089I |
probably damaging |
Het |
Ppp1cb |
T |
A |
5: 32,635,492 (GRCm39) |
F45L |
possibly damaging |
Het |
Pramel21 |
T |
G |
4: 143,342,741 (GRCm39) |
S283A |
possibly damaging |
Het |
Samd4 |
T |
C |
14: 47,301,728 (GRCm39) |
F344S |
probably damaging |
Het |
Slc2a13 |
C |
T |
15: 91,234,333 (GRCm39) |
M334I |
possibly damaging |
Het |
Slc37a1 |
C |
T |
17: 31,556,365 (GRCm39) |
A363V |
probably damaging |
Het |
Slc8a3 |
T |
A |
12: 81,263,540 (GRCm39) |
I616F |
probably damaging |
Het |
Srcin1 |
A |
G |
11: 97,427,206 (GRCm39) |
L257P |
probably damaging |
Het |
Tarbp1 |
A |
G |
8: 127,173,880 (GRCm39) |
F945L |
probably damaging |
Het |
Thbs4 |
A |
T |
13: 92,911,187 (GRCm39) |
|
probably null |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Trim62 |
G |
A |
4: 128,802,963 (GRCm39) |
V338M |
probably damaging |
Het |
Ttll9 |
C |
T |
2: 152,818,113 (GRCm39) |
H20Y |
possibly damaging |
Het |
Uevld |
A |
T |
7: 46,587,806 (GRCm39) |
I298N |
probably damaging |
Het |
Zan |
T |
C |
5: 137,462,653 (GRCm39) |
E842G |
probably damaging |
Het |
Zdbf2 |
T |
G |
1: 63,346,296 (GRCm39) |
S1558R |
|
Het |
|
Other mutations in Mapk8ip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01942:Mapk8ip2
|
APN |
15 |
89,341,220 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02720:Mapk8ip2
|
APN |
15 |
89,341,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Mapk8ip2
|
APN |
15 |
89,341,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Mapk8ip2
|
APN |
15 |
89,342,310 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Mapk8ip2
|
UTSW |
15 |
89,344,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Mapk8ip2
|
UTSW |
15 |
89,340,861 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2355:Mapk8ip2
|
UTSW |
15 |
89,343,168 (GRCm39) |
missense |
probably benign |
0.04 |
R3026:Mapk8ip2
|
UTSW |
15 |
89,345,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Mapk8ip2
|
UTSW |
15 |
89,341,485 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4275:Mapk8ip2
|
UTSW |
15 |
89,343,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Mapk8ip2
|
UTSW |
15 |
89,343,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Mapk8ip2
|
UTSW |
15 |
89,341,431 (GRCm39) |
missense |
probably benign |
|
R5209:Mapk8ip2
|
UTSW |
15 |
89,343,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R5417:Mapk8ip2
|
UTSW |
15 |
89,341,642 (GRCm39) |
missense |
probably benign |
0.16 |
R5521:Mapk8ip2
|
UTSW |
15 |
89,343,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Mapk8ip2
|
UTSW |
15 |
89,344,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7145:Mapk8ip2
|
UTSW |
15 |
89,343,201 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7231:Mapk8ip2
|
UTSW |
15 |
89,342,279 (GRCm39) |
missense |
probably benign |
|
R7369:Mapk8ip2
|
UTSW |
15 |
89,338,454 (GRCm39) |
missense |
probably benign |
0.01 |
R7753:Mapk8ip2
|
UTSW |
15 |
89,345,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7827:Mapk8ip2
|
UTSW |
15 |
89,342,322 (GRCm39) |
missense |
probably damaging |
0.98 |
R7834:Mapk8ip2
|
UTSW |
15 |
89,345,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Mapk8ip2
|
UTSW |
15 |
89,344,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8433:Mapk8ip2
|
UTSW |
15 |
89,342,069 (GRCm39) |
missense |
probably benign |
0.01 |
R8528:Mapk8ip2
|
UTSW |
15 |
89,339,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Mapk8ip2
|
UTSW |
15 |
89,341,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R9768:Mapk8ip2
|
UTSW |
15 |
89,343,160 (GRCm39) |
missense |
probably damaging |
1.00 |
|