Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,207,267 (GRCm39) |
N308S |
possibly damaging |
Het |
Acot5 |
A |
T |
12: 84,122,643 (GRCm39) |
H409L |
possibly damaging |
Het |
Ang4 |
A |
G |
14: 52,001,955 (GRCm39) |
|
probably benign |
Het |
Ap3d1 |
A |
G |
10: 80,556,966 (GRCm39) |
S315P |
probably benign |
Het |
Arhgap15 |
G |
A |
2: 44,276,359 (GRCm39) |
G437R |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,562,287 (GRCm39) |
C810R |
probably damaging |
Het |
Capn5 |
A |
G |
7: 97,785,082 (GRCm39) |
W131R |
probably damaging |
Het |
Cd177 |
A |
G |
7: 24,455,661 (GRCm39) |
V287A |
possibly damaging |
Het |
Cdk5r2 |
T |
C |
1: 74,895,059 (GRCm39) |
L268P |
probably damaging |
Het |
Cfap251 |
C |
G |
5: 123,421,411 (GRCm39) |
|
probably null |
Het |
Clrn2 |
A |
G |
5: 45,611,304 (GRCm39) |
D51G |
probably benign |
Het |
Cntd1 |
T |
C |
11: 101,175,682 (GRCm39) |
S174P |
probably damaging |
Het |
Col11a2 |
A |
G |
17: 34,258,651 (GRCm39) |
H8R |
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,669,816 (GRCm39) |
|
probably null |
Het |
Cyp2a5 |
A |
G |
7: 26,536,528 (GRCm39) |
D169G |
possibly damaging |
Het |
Cyp2c37 |
A |
G |
19: 39,984,303 (GRCm39) |
I264V |
possibly damaging |
Het |
Cyp2j12 |
A |
G |
4: 96,021,315 (GRCm39) |
I97T |
probably damaging |
Het |
Dipk1b |
T |
C |
2: 26,525,162 (GRCm39) |
L157P |
probably damaging |
Het |
Eif3b |
T |
C |
5: 140,413,258 (GRCm39) |
F354L |
possibly damaging |
Het |
Eif4a3l1 |
A |
T |
6: 136,305,559 (GRCm39) |
M7L |
probably benign |
Het |
Entpd2 |
C |
T |
2: 25,288,099 (GRCm39) |
P108S |
probably damaging |
Het |
F5 |
T |
A |
1: 164,019,750 (GRCm39) |
S742T |
probably damaging |
Het |
Fam187a |
A |
G |
11: 102,776,124 (GRCm39) |
|
probably benign |
Het |
Fam43b |
G |
C |
4: 138,122,409 (GRCm39) |
R304G |
probably benign |
Het |
Flnc |
G |
A |
6: 29,438,665 (GRCm39) |
W186* |
probably null |
Het |
Fndc3b |
G |
T |
3: 27,494,309 (GRCm39) |
Q939K |
possibly damaging |
Het |
Gja4 |
C |
A |
4: 127,206,623 (GRCm39) |
D47Y |
probably damaging |
Het |
Gm11565 |
T |
G |
11: 99,805,844 (GRCm39) |
C79G |
possibly damaging |
Het |
Gpbar1 |
T |
C |
1: 74,318,164 (GRCm39) |
F136L |
probably benign |
Het |
Gsn |
G |
A |
2: 35,180,349 (GRCm39) |
G130E |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,490,723 (GRCm39) |
D756E |
probably benign |
Het |
Hrc |
C |
A |
7: 44,986,105 (GRCm39) |
R419S |
possibly damaging |
Het |
Inpp4a |
T |
A |
1: 37,416,777 (GRCm39) |
S433T |
probably damaging |
Het |
Ism2 |
C |
A |
12: 87,326,848 (GRCm39) |
V320L |
possibly damaging |
Het |
Krt8 |
G |
T |
15: 101,907,257 (GRCm39) |
D275E |
probably benign |
Het |
Lgalsl2 |
A |
G |
7: 5,362,401 (GRCm39) |
M11V |
probably benign |
Het |
Lyg2 |
A |
C |
1: 37,948,077 (GRCm39) |
N132K |
probably benign |
Het |
Lyst |
G |
A |
13: 13,812,243 (GRCm39) |
R885Q |
probably benign |
Het |
Marveld2 |
A |
G |
13: 100,748,978 (GRCm39) |
S34P |
probably benign |
Het |
Mcc |
C |
A |
18: 44,608,203 (GRCm39) |
G355W |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,555,802 (GRCm39) |
V44A |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,239,842 (GRCm39) |
M28K |
probably benign |
Het |
Ms4a15 |
A |
G |
19: 10,962,159 (GRCm39) |
C47R |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,344,745 (GRCm39) |
N72S |
probably benign |
Het |
Myo18b |
C |
T |
5: 113,022,529 (GRCm39) |
|
probably benign |
Het |
Nat8f4 |
A |
T |
6: 85,878,207 (GRCm39) |
H105Q |
possibly damaging |
Het |
Ncapd3 |
A |
G |
9: 26,967,368 (GRCm39) |
D568G |
probably benign |
Het |
Nptx1 |
T |
G |
11: 119,434,142 (GRCm39) |
I315L |
probably benign |
Het |
Nrap |
T |
C |
19: 56,310,394 (GRCm39) |
R1534G |
possibly damaging |
Het |
Nwd2 |
C |
A |
5: 63,962,499 (GRCm39) |
N694K |
probably benign |
Het |
Oas1c |
G |
A |
5: 120,941,082 (GRCm39) |
A35V |
probably null |
Het |
Or2d3b |
A |
G |
7: 106,514,113 (GRCm39) |
K236R |
probably damaging |
Het |
Or5bw2 |
A |
T |
7: 6,573,022 (GRCm39) |
I11F |
probably damaging |
Het |
Or5p58 |
C |
T |
7: 107,694,402 (GRCm39) |
R125H |
possibly damaging |
Het |
Or8d1b |
T |
C |
9: 38,887,296 (GRCm39) |
V108A |
probably benign |
Het |
Pate8 |
C |
A |
9: 36,493,161 (GRCm39) |
V54L |
probably benign |
Het |
Pde2a |
A |
T |
7: 101,133,774 (GRCm39) |
D85V |
probably damaging |
Het |
Plaat5 |
C |
T |
19: 7,590,111 (GRCm39) |
R46C |
probably damaging |
Het |
Polr1f |
A |
G |
12: 33,483,587 (GRCm39) |
H113R |
probably damaging |
Het |
Prex1 |
C |
T |
2: 166,429,077 (GRCm39) |
V839I |
probably benign |
Het |
Psmd3 |
T |
A |
11: 98,581,790 (GRCm39) |
M305K |
probably benign |
Het |
Rbm20 |
T |
C |
19: 53,840,172 (GRCm39) |
S1054P |
probably benign |
Het |
Rhox13 |
G |
C |
X: 37,210,221 (GRCm39) |
E19Q |
unknown |
Het |
Ryr2 |
A |
G |
13: 11,753,102 (GRCm39) |
F1740L |
possibly damaging |
Het |
Sox1 |
C |
A |
8: 12,446,927 (GRCm39) |
N189K |
possibly damaging |
Het |
Spta1 |
C |
A |
1: 174,001,907 (GRCm39) |
S12R |
possibly damaging |
Het |
Stard13 |
A |
G |
5: 150,963,196 (GRCm39) |
L971P |
probably damaging |
Het |
Tigd4 |
T |
A |
3: 84,501,600 (GRCm39) |
N172K |
probably benign |
Het |
Tmt1a |
A |
T |
15: 100,211,049 (GRCm39) |
I174F |
probably benign |
Het |
Ttyh1 |
T |
C |
7: 4,131,183 (GRCm39) |
V218A |
probably damaging |
Het |
Unc45b |
T |
A |
11: 82,808,625 (GRCm39) |
M237K |
probably benign |
Het |
Vldlr |
A |
G |
19: 27,215,786 (GRCm39) |
D220G |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,861,142 (GRCm39) |
N2891S |
probably benign |
Het |
Wdr25 |
T |
A |
12: 108,864,100 (GRCm39) |
S82T |
possibly damaging |
Het |
Wnk4 |
C |
A |
11: 101,165,861 (GRCm39) |
P796Q |
probably damaging |
Het |
Xpo5 |
C |
T |
17: 46,551,822 (GRCm39) |
Q1050* |
probably null |
Het |
Zc3h15 |
G |
A |
2: 83,487,360 (GRCm39) |
V60I |
probably benign |
Het |
Zfp629 |
G |
A |
7: 127,210,963 (GRCm39) |
T282M |
probably damaging |
Het |
Zscan22 |
T |
G |
7: 12,637,887 (GRCm39) |
V93G |
probably damaging |
Het |
|
Other mutations in Ccnj |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01903:Ccnj
|
APN |
19 |
40,834,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02584:Ccnj
|
APN |
19 |
40,833,185 (GRCm39) |
missense |
probably benign |
0.04 |
R0220:Ccnj
|
UTSW |
19 |
40,833,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:Ccnj
|
UTSW |
19 |
40,833,508 (GRCm39) |
splice site |
probably null |
|
R0693:Ccnj
|
UTSW |
19 |
40,825,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1600:Ccnj
|
UTSW |
19 |
40,833,101 (GRCm39) |
splice site |
probably benign |
|
R2237:Ccnj
|
UTSW |
19 |
40,834,219 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Ccnj
|
UTSW |
19 |
40,833,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Ccnj
|
UTSW |
19 |
40,833,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R6384:Ccnj
|
UTSW |
19 |
40,834,451 (GRCm39) |
missense |
probably benign |
0.09 |
R6528:Ccnj
|
UTSW |
19 |
40,820,529 (GRCm39) |
splice site |
probably null |
|
R6830:Ccnj
|
UTSW |
19 |
40,833,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R7338:Ccnj
|
UTSW |
19 |
40,825,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Ccnj
|
UTSW |
19 |
40,833,394 (GRCm39) |
missense |
probably benign |
0.28 |
R8472:Ccnj
|
UTSW |
19 |
40,833,608 (GRCm39) |
missense |
probably damaging |
0.97 |
R8977:Ccnj
|
UTSW |
19 |
40,833,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|