Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
T |
C |
3: 97,075,891 (GRCm39) |
|
probably null |
Het |
Adam33 |
C |
A |
2: 130,896,399 (GRCm39) |
G437C |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,579,377 (GRCm39) |
M1K |
probably null |
Het |
Amotl2 |
C |
A |
9: 102,597,718 (GRCm39) |
P126Q |
probably damaging |
Het |
Ap1g1 |
T |
A |
8: 110,580,275 (GRCm39) |
M576K |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,040,406 (GRCm39) |
A581E |
probably damaging |
Het |
Asb7 |
A |
T |
7: 66,328,907 (GRCm39) |
D44E |
probably damaging |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
C9orf72 |
G |
A |
4: 35,193,257 (GRCm39) |
T232I |
probably benign |
Het |
Ccdc65 |
A |
T |
15: 98,615,348 (GRCm39) |
H118L |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,039,204 (GRCm39) |
E523G |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,731,999 (GRCm39) |
|
probably benign |
Het |
Cilk1 |
G |
T |
9: 78,062,799 (GRCm39) |
|
probably null |
Het |
Clec1b |
A |
G |
6: 129,378,570 (GRCm39) |
|
probably benign |
Het |
Cntrl |
A |
G |
2: 35,017,392 (GRCm39) |
T400A |
probably benign |
Het |
Cpne4 |
T |
G |
9: 104,899,481 (GRCm39) |
|
probably null |
Het |
Dock2 |
T |
C |
11: 34,579,380 (GRCm39) |
I678V |
probably benign |
Het |
Dqx1 |
C |
T |
6: 83,036,407 (GRCm39) |
|
probably benign |
Het |
Dsp |
A |
T |
13: 38,377,326 (GRCm39) |
K1704* |
probably null |
Het |
Eif2b2 |
T |
C |
12: 85,266,957 (GRCm39) |
F121S |
probably benign |
Het |
Ephx4 |
T |
C |
5: 107,561,379 (GRCm39) |
V69A |
possibly damaging |
Het |
Epn2 |
T |
C |
11: 61,426,134 (GRCm39) |
Q281R |
probably damaging |
Het |
Fgf3 |
A |
C |
7: 144,396,547 (GRCm39) |
D187A |
probably damaging |
Het |
Galnt18 |
C |
A |
7: 111,378,506 (GRCm39) |
|
probably benign |
Het |
Gm4871 |
C |
T |
5: 144,968,402 (GRCm39) |
|
probably benign |
Het |
Inpp4b |
T |
C |
8: 82,768,528 (GRCm39) |
I679T |
possibly damaging |
Het |
Itpkb |
A |
G |
1: 180,245,820 (GRCm39) |
E779G |
probably damaging |
Het |
Itsn1 |
G |
A |
16: 91,696,477 (GRCm39) |
V27M |
probably damaging |
Het |
Lrp2 |
C |
A |
2: 69,355,578 (GRCm39) |
R422L |
probably damaging |
Het |
Mmp25 |
G |
A |
17: 23,858,858 (GRCm39) |
A231V |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,650,561 (GRCm39) |
S1422P |
probably damaging |
Het |
Mro |
A |
T |
18: 74,009,860 (GRCm39) |
Q176L |
probably benign |
Het |
Mrpl12 |
A |
G |
11: 120,379,229 (GRCm39) |
E192G |
probably damaging |
Het |
Myo5b |
A |
T |
18: 74,862,025 (GRCm39) |
|
probably benign |
Het |
Ncam2 |
G |
T |
16: 80,997,772 (GRCm39) |
|
probably benign |
Het |
Nip7 |
T |
C |
8: 107,783,949 (GRCm39) |
L63P |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,138,450 (GRCm39) |
|
probably benign |
Het |
Nup98 |
A |
T |
7: 101,788,004 (GRCm39) |
V1022D |
probably benign |
Het |
Or2y1e |
T |
A |
11: 49,218,744 (GRCm39) |
C169S |
probably damaging |
Het |
Or5d43 |
A |
G |
2: 88,104,559 (GRCm39) |
V278A |
possibly damaging |
Het |
Or5h22 |
A |
G |
16: 58,894,633 (GRCm39) |
I270T |
probably benign |
Het |
Or7g28 |
A |
T |
9: 19,272,177 (GRCm39) |
L158* |
probably null |
Het |
P4ha2 |
T |
C |
11: 54,008,434 (GRCm39) |
Y214H |
possibly damaging |
Het |
Pacrg |
A |
T |
17: 10,795,407 (GRCm39) |
F184L |
possibly damaging |
Het |
Parpbp |
T |
A |
10: 87,929,569 (GRCm39) |
R426S |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,359 (GRCm39) |
Y246* |
probably null |
Het |
Pik3cg |
T |
A |
12: 32,244,770 (GRCm39) |
T895S |
probably damaging |
Het |
Prkch |
T |
C |
12: 73,738,426 (GRCm39) |
Y178H |
probably benign |
Het |
Rusc2 |
G |
T |
4: 43,425,486 (GRCm39) |
R1197L |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,054,700 (GRCm39) |
E3296G |
possibly damaging |
Het |
Svs3a |
A |
G |
2: 164,131,801 (GRCm39) |
K123R |
probably benign |
Het |
Sycp2l |
A |
G |
13: 41,304,006 (GRCm39) |
|
probably null |
Het |
Syne3 |
T |
C |
12: 104,909,685 (GRCm39) |
H717R |
probably benign |
Het |
Tiprl |
A |
G |
1: 165,050,092 (GRCm39) |
|
probably null |
Het |
Trim24 |
T |
G |
6: 37,892,130 (GRCm39) |
V151G |
possibly damaging |
Het |
Trim33 |
T |
C |
3: 103,234,217 (GRCm39) |
V56A |
possibly damaging |
Het |
Trim67 |
C |
A |
8: 125,521,397 (GRCm39) |
T253K |
probably benign |
Het |
Trip12 |
T |
C |
1: 84,703,928 (GRCm39) |
E698G |
probably damaging |
Het |
Tspan14 |
T |
C |
14: 40,637,353 (GRCm39) |
D145G |
probably damaging |
Het |
Ushbp1 |
G |
A |
8: 71,847,021 (GRCm39) |
Q204* |
probably null |
Het |
Vmn1r71 |
G |
C |
7: 10,482,019 (GRCm39) |
S223C |
possibly damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,814,721 (GRCm39) |
N257K |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,394,598 (GRCm39) |
|
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,666,169 (GRCm39) |
D560N |
probably damaging |
Het |
Zscan21 |
T |
C |
5: 138,123,402 (GRCm39) |
V27A |
probably benign |
Het |
Zzef1 |
A |
C |
11: 72,813,937 (GRCm39) |
E2842A |
probably damaging |
Het |
|
Other mutations in Cyp2j6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Cyp2j6
|
APN |
4 |
96,424,283 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01543:Cyp2j6
|
APN |
4 |
96,414,161 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02324:Cyp2j6
|
APN |
4 |
96,414,170 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02727:Cyp2j6
|
APN |
4 |
96,434,001 (GRCm39) |
missense |
probably benign |
|
IGL02963:Cyp2j6
|
APN |
4 |
96,406,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03099:Cyp2j6
|
APN |
4 |
96,424,328 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0109:Cyp2j6
|
UTSW |
4 |
96,406,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R0109:Cyp2j6
|
UTSW |
4 |
96,406,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R0376:Cyp2j6
|
UTSW |
4 |
96,414,260 (GRCm39) |
missense |
probably damaging |
0.99 |
R0448:Cyp2j6
|
UTSW |
4 |
96,433,965 (GRCm39) |
missense |
probably benign |
|
R0734:Cyp2j6
|
UTSW |
4 |
96,412,081 (GRCm39) |
splice site |
probably benign |
|
R1497:Cyp2j6
|
UTSW |
4 |
96,419,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R1686:Cyp2j6
|
UTSW |
4 |
96,412,014 (GRCm39) |
missense |
probably benign |
0.08 |
R2079:Cyp2j6
|
UTSW |
4 |
96,419,962 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2293:Cyp2j6
|
UTSW |
4 |
96,417,670 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2350:Cyp2j6
|
UTSW |
4 |
96,417,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Cyp2j6
|
UTSW |
4 |
96,420,018 (GRCm39) |
missense |
probably benign |
0.06 |
R3927:Cyp2j6
|
UTSW |
4 |
96,441,525 (GRCm39) |
missense |
probably benign |
0.15 |
R4020:Cyp2j6
|
UTSW |
4 |
96,406,407 (GRCm39) |
missense |
probably benign |
0.03 |
R5087:Cyp2j6
|
UTSW |
4 |
96,419,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R5309:Cyp2j6
|
UTSW |
4 |
96,423,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Cyp2j6
|
UTSW |
4 |
96,434,040 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5882:Cyp2j6
|
UTSW |
4 |
96,423,839 (GRCm39) |
missense |
probably benign |
0.00 |
R6123:Cyp2j6
|
UTSW |
4 |
96,406,266 (GRCm39) |
makesense |
probably null |
|
R6180:Cyp2j6
|
UTSW |
4 |
96,424,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Cyp2j6
|
UTSW |
4 |
96,424,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Cyp2j6
|
UTSW |
4 |
96,424,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6185:Cyp2j6
|
UTSW |
4 |
96,424,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6186:Cyp2j6
|
UTSW |
4 |
96,424,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6217:Cyp2j6
|
UTSW |
4 |
96,406,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Cyp2j6
|
UTSW |
4 |
96,423,741 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7038:Cyp2j6
|
UTSW |
4 |
96,423,708 (GRCm39) |
missense |
probably benign |
|
R7146:Cyp2j6
|
UTSW |
4 |
96,434,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Cyp2j6
|
UTSW |
4 |
96,414,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R7470:Cyp2j6
|
UTSW |
4 |
96,423,708 (GRCm39) |
missense |
probably benign |
|
R7536:Cyp2j6
|
UTSW |
4 |
96,423,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7789:Cyp2j6
|
UTSW |
4 |
96,433,953 (GRCm39) |
missense |
probably benign |
0.00 |
R8321:Cyp2j6
|
UTSW |
4 |
96,441,684 (GRCm39) |
missense |
probably benign |
0.07 |
R8836:Cyp2j6
|
UTSW |
4 |
96,411,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Cyp2j6
|
UTSW |
4 |
96,414,087 (GRCm39) |
missense |
probably benign |
0.23 |
R9315:Cyp2j6
|
UTSW |
4 |
96,420,035 (GRCm39) |
missense |
probably benign |
0.05 |
R9507:Cyp2j6
|
UTSW |
4 |
96,406,344 (GRCm39) |
nonsense |
probably null |
|
R9563:Cyp2j6
|
UTSW |
4 |
96,414,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Cyp2j6
|
UTSW |
4 |
96,414,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Cyp2j6
|
UTSW |
4 |
96,414,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9618:Cyp2j6
|
UTSW |
4 |
96,414,085 (GRCm39) |
missense |
probably benign |
0.36 |
R9745:Cyp2j6
|
UTSW |
4 |
96,441,621 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1176:Cyp2j6
|
UTSW |
4 |
96,424,305 (GRCm39) |
nonsense |
probably null |
|
|