Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
A |
G |
8: 111,768,881 (GRCm39) |
D227G |
possibly damaging |
Het |
Actl11 |
T |
A |
9: 107,806,065 (GRCm39) |
D129E |
probably benign |
Het |
Adam12 |
T |
A |
7: 133,491,929 (GRCm39) |
E877D |
possibly damaging |
Het |
Adarb2 |
T |
A |
13: 8,807,395 (GRCm39) |
V732E |
probably damaging |
Het |
Adcy1 |
T |
C |
11: 7,111,328 (GRCm39) |
I873T |
probably damaging |
Het |
Adgrg1 |
C |
T |
8: 95,736,276 (GRCm39) |
H477Y |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,623,321 (GRCm39) |
E99G |
possibly damaging |
Het |
Ankk1 |
T |
A |
9: 49,329,292 (GRCm39) |
M93L |
|
Het |
Ankmy1 |
A |
T |
1: 92,812,972 (GRCm39) |
L446M |
possibly damaging |
Het |
Anxa10 |
T |
A |
8: 62,510,825 (GRCm39) |
Y309F |
probably damaging |
Het |
Arg2 |
C |
T |
12: 79,196,794 (GRCm39) |
Q172* |
probably null |
Het |
Atp6v0a4 |
T |
A |
6: 38,025,926 (GRCm39) |
*834L |
probably null |
Het |
Avl9 |
T |
A |
6: 56,730,378 (GRCm39) |
S574T |
probably benign |
Het |
AW551984 |
G |
A |
9: 39,511,005 (GRCm39) |
T194I |
possibly damaging |
Het |
Azin1 |
G |
A |
15: 38,493,775 (GRCm39) |
L283F |
probably damaging |
Het |
Birc6 |
G |
A |
17: 74,916,114 (GRCm39) |
A1677T |
possibly damaging |
Het |
Carm1 |
A |
T |
9: 21,497,464 (GRCm39) |
D342V |
possibly damaging |
Het |
Ccr4 |
T |
C |
9: 114,321,216 (GRCm39) |
D283G |
probably damaging |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Cntn2 |
A |
T |
1: 132,450,731 (GRCm39) |
L548Q |
probably damaging |
Het |
Copg1 |
A |
G |
6: 87,869,637 (GRCm39) |
D172G |
probably damaging |
Het |
Dapk3 |
T |
C |
10: 81,026,069 (GRCm39) |
L120P |
probably damaging |
Het |
Dclre1b |
A |
C |
3: 103,711,298 (GRCm39) |
S204R |
probably damaging |
Het |
Dennd2a |
G |
A |
6: 39,500,137 (GRCm39) |
R143* |
probably null |
Het |
Dnah5 |
A |
T |
15: 28,289,367 (GRCm39) |
E1185D |
probably benign |
Het |
Dop1b |
C |
T |
16: 93,568,699 (GRCm39) |
T1587I |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,570,809 (GRCm39) |
T1603A |
probably benign |
Het |
Dym |
T |
A |
18: 75,363,089 (GRCm39) |
V531E |
probably damaging |
Het |
Dync2i1 |
G |
T |
12: 116,193,262 (GRCm39) |
D563E |
probably benign |
Het |
Ecpas |
T |
C |
4: 58,834,515 (GRCm39) |
S788G |
probably benign |
Het |
Eif2b4 |
A |
T |
5: 31,345,274 (GRCm39) |
F453L |
probably damaging |
Het |
Entpd8 |
G |
A |
2: 24,974,992 (GRCm39) |
G441D |
probably damaging |
Het |
Galnt6 |
A |
T |
15: 100,592,603 (GRCm39) |
Y535N |
probably damaging |
Het |
Garin2 |
TGATGTCACAGATGTCAC |
TGATGTCAC |
12: 78,762,057 (GRCm39) |
|
probably benign |
Het |
Gm10340 |
T |
A |
14: 14,826,748 (GRCm39) |
D72E |
possibly damaging |
Het |
Gm13102 |
T |
A |
4: 143,835,680 (GRCm39) |
D449E |
probably damaging |
Het |
Hdac9 |
T |
A |
12: 34,440,220 (GRCm39) |
K386N |
probably damaging |
Het |
Hgs |
T |
A |
11: 120,366,044 (GRCm39) |
C212* |
probably null |
Het |
Hoxa2 |
C |
A |
6: 52,141,540 (GRCm39) |
A29S |
possibly damaging |
Het |
Ifnar1 |
T |
A |
16: 91,296,332 (GRCm39) |
W278R |
probably damaging |
Het |
Irf7 |
C |
T |
7: 140,843,422 (GRCm39) |
G389R |
probably null |
Het |
Lipo3 |
G |
A |
19: 33,759,604 (GRCm39) |
L211F |
probably benign |
Het |
Mars2 |
C |
T |
1: 55,277,741 (GRCm39) |
T448I |
probably benign |
Het |
Mcm4 |
C |
A |
16: 15,453,138 (GRCm39) |
G184C |
probably damaging |
Het |
Mmaa |
C |
T |
8: 79,994,598 (GRCm39) |
A403T |
probably damaging |
Het |
Mmel1 |
A |
G |
4: 154,973,985 (GRCm39) |
I342V |
probably benign |
Het |
Myb |
T |
C |
10: 21,026,405 (GRCm39) |
T188A |
possibly damaging |
Het |
Myo1g |
C |
T |
11: 6,467,569 (GRCm39) |
|
probably null |
Het |
Npas2 |
A |
G |
1: 39,386,708 (GRCm39) |
Q659R |
probably benign |
Het |
Npr1 |
A |
G |
3: 90,362,497 (GRCm39) |
V941A |
probably benign |
Het |
Numa1 |
T |
G |
7: 101,626,617 (GRCm39) |
M1R |
probably null |
Het |
Obscn |
T |
C |
11: 58,967,705 (GRCm39) |
S2700G |
probably benign |
Het |
Or2t35 |
T |
A |
14: 14,407,480 (GRCm38) |
L84H |
probably benign |
Het |
Or4k2 |
A |
T |
14: 50,424,203 (GRCm39) |
M157K |
possibly damaging |
Het |
Or5g25 |
A |
T |
2: 85,478,410 (GRCm39) |
I85N |
probably benign |
Het |
Pdpr |
T |
A |
8: 111,850,492 (GRCm39) |
H476Q |
probably damaging |
Het |
Pkd1l1 |
A |
T |
11: 8,821,805 (GRCm39) |
S1630T |
|
Het |
Prdm16 |
A |
G |
4: 154,613,161 (GRCm39) |
S89P |
probably damaging |
Het |
Ptgdr2 |
T |
A |
19: 10,917,893 (GRCm39) |
W137R |
possibly damaging |
Het |
Ptpra |
A |
G |
2: 130,394,187 (GRCm39) |
I784V |
possibly damaging |
Het |
Rabepk |
G |
T |
2: 34,685,188 (GRCm39) |
D77E |
possibly damaging |
Het |
Sh2b1 |
GGGGACCAGCTCAGCCACGGGGACCAGCTC |
GGGGACCAGCTCAGCCACAGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,743 (GRCm39) |
|
probably benign |
Het |
Smc3 |
T |
A |
19: 53,629,616 (GRCm39) |
S994T |
possibly damaging |
Het |
Sparc |
A |
G |
11: 55,292,783 (GRCm39) |
C147R |
probably damaging |
Het |
Supt6 |
A |
T |
11: 78,108,727 (GRCm39) |
D1191E |
probably benign |
Het |
Susd4 |
T |
C |
1: 182,719,832 (GRCm39) |
|
probably null |
Het |
Tbc1d5 |
A |
G |
17: 51,291,631 (GRCm39) |
|
probably null |
Het |
Tecta |
T |
G |
9: 42,278,268 (GRCm39) |
D1080A |
probably damaging |
Het |
Tenm4 |
G |
T |
7: 96,552,064 (GRCm39) |
W2538L |
probably damaging |
Het |
Trappc9 |
A |
G |
15: 72,884,664 (GRCm39) |
F439L |
probably benign |
Het |
Tsbp1 |
A |
T |
17: 34,667,782 (GRCm39) |
Q158L |
possibly damaging |
Het |
Vegfa |
A |
T |
17: 46,342,396 (GRCm39) |
S141T |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,996,873 (GRCm39) |
D132V |
probably benign |
Het |
|
Other mutations in Cyp2j12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Cyp2j12
|
APN |
4 |
95,994,826 (GRCm39) |
splice site |
probably benign |
|
IGL01655:Cyp2j12
|
APN |
4 |
96,003,814 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01723:Cyp2j12
|
APN |
4 |
95,990,363 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01737:Cyp2j12
|
APN |
4 |
96,010,895 (GRCm39) |
makesense |
probably null |
|
IGL01936:Cyp2j12
|
APN |
4 |
96,021,306 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01962:Cyp2j12
|
APN |
4 |
95,987,999 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02691:Cyp2j12
|
APN |
4 |
96,021,231 (GRCm39) |
critical splice donor site |
probably null |
|
R0255:Cyp2j12
|
UTSW |
4 |
96,029,262 (GRCm39) |
missense |
probably benign |
0.38 |
R0613:Cyp2j12
|
UTSW |
4 |
95,990,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Cyp2j12
|
UTSW |
4 |
96,001,099 (GRCm39) |
splice site |
probably benign |
|
R1016:Cyp2j12
|
UTSW |
4 |
96,001,102 (GRCm39) |
critical splice donor site |
probably null |
|
R1251:Cyp2j12
|
UTSW |
4 |
96,003,903 (GRCm39) |
nonsense |
probably null |
|
R1753:Cyp2j12
|
UTSW |
4 |
96,009,669 (GRCm39) |
splice site |
probably null |
|
R2258:Cyp2j12
|
UTSW |
4 |
96,021,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Cyp2j12
|
UTSW |
4 |
96,021,306 (GRCm39) |
missense |
probably benign |
0.01 |
R4559:Cyp2j12
|
UTSW |
4 |
96,001,194 (GRCm39) |
missense |
probably damaging |
0.99 |
R4702:Cyp2j12
|
UTSW |
4 |
96,021,230 (GRCm39) |
critical splice donor site |
probably null |
|
R4923:Cyp2j12
|
UTSW |
4 |
95,990,346 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4928:Cyp2j12
|
UTSW |
4 |
95,990,388 (GRCm39) |
splice site |
probably null |
|
R5591:Cyp2j12
|
UTSW |
4 |
96,029,359 (GRCm39) |
start gained |
probably benign |
|
R5897:Cyp2j12
|
UTSW |
4 |
95,990,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R6176:Cyp2j12
|
UTSW |
4 |
96,029,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R6942:Cyp2j12
|
UTSW |
4 |
96,001,101 (GRCm39) |
critical splice donor site |
probably null |
|
R7422:Cyp2j12
|
UTSW |
4 |
96,029,222 (GRCm39) |
missense |
probably benign |
0.05 |
R7453:Cyp2j12
|
UTSW |
4 |
95,990,363 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7839:Cyp2j12
|
UTSW |
4 |
95,987,893 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8437:Cyp2j12
|
UTSW |
4 |
95,987,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8445:Cyp2j12
|
UTSW |
4 |
96,021,259 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8701:Cyp2j12
|
UTSW |
4 |
96,009,810 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8864:Cyp2j12
|
UTSW |
4 |
96,009,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Cyp2j12
|
UTSW |
4 |
95,994,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R9330:Cyp2j12
|
UTSW |
4 |
95,994,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|