Other mutations in this stock |
Total: 135 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
T |
12: 55,104,090 (GRCm39) |
N176K |
possibly damaging |
Het |
3110009E18Rik |
T |
A |
1: 120,097,006 (GRCm39) |
V134E |
|
Het |
Abca8a |
T |
A |
11: 109,965,010 (GRCm39) |
H429L |
probably benign |
Het |
Acsf2 |
T |
A |
11: 94,463,891 (GRCm39) |
I98F |
possibly damaging |
Het |
Actr5 |
A |
G |
2: 158,470,135 (GRCm39) |
D255G |
probably damaging |
Het |
Adam21 |
C |
T |
12: 81,605,833 (GRCm39) |
C643Y |
probably damaging |
Het |
Adcy7 |
TGG |
TG |
8: 89,053,053 (GRCm39) |
|
probably null |
Het |
AI429214 |
A |
G |
8: 37,461,067 (GRCm39) |
S72G |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,259,161 (GRCm39) |
V595A |
probably benign |
Het |
Akt3 |
T |
C |
1: 176,907,769 (GRCm39) |
T209A |
possibly damaging |
Het |
Alpk2 |
C |
T |
18: 65,439,014 (GRCm39) |
G793D |
probably damaging |
Het |
Amotl1 |
T |
C |
9: 14,473,513 (GRCm39) |
K562R |
possibly damaging |
Het |
Ankib1 |
T |
A |
5: 3,805,733 (GRCm39) |
N178I |
possibly damaging |
Het |
Arfgef1 |
A |
T |
1: 10,217,758 (GRCm39) |
D1560E |
probably benign |
Het |
Arhgap20 |
AAGAGAG |
AAGAG |
9: 51,761,413 (GRCm39) |
|
probably null |
Het |
Arpc5l |
A |
G |
2: 38,905,124 (GRCm39) |
T152A |
probably benign |
Het |
Asic3 |
C |
G |
5: 24,620,875 (GRCm39) |
D252E |
possibly damaging |
Het |
Atf7 |
T |
A |
15: 102,442,712 (GRCm39) |
M466L |
probably benign |
Het |
Bcl9l |
A |
G |
9: 44,420,554 (GRCm39) |
D1320G |
probably damaging |
Het |
Bdkrb1 |
G |
A |
12: 105,571,078 (GRCm39) |
V215I |
probably benign |
Het |
Brpf3 |
T |
G |
17: 29,026,152 (GRCm39) |
D408E |
probably benign |
Het |
Btn2a2 |
C |
A |
13: 23,662,848 (GRCm39) |
K367N |
possibly damaging |
Het |
Btnl10 |
T |
A |
11: 58,813,189 (GRCm39) |
F273I |
probably benign |
Het |
C1qtnf12 |
C |
T |
4: 156,049,473 (GRCm39) |
T145I |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,516 (GRCm39) |
C1763R |
probably benign |
Het |
Ccdc154 |
C |
A |
17: 25,387,381 (GRCm39) |
Q372K |
possibly damaging |
Het |
Cd300ld2 |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
11: 114,903,257 (GRCm39) |
|
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,321,834 (GRCm39) |
Y326C |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,231,471 (GRCm39) |
V914E |
|
Het |
Coil |
T |
A |
11: 88,872,626 (GRCm39) |
V329E |
possibly damaging |
Het |
Copb1 |
A |
G |
7: 113,836,034 (GRCm39) |
I449T |
possibly damaging |
Het |
Copg1 |
T |
G |
6: 87,869,683 (GRCm39) |
S187R |
probably damaging |
Het |
Cps1 |
T |
A |
1: 67,198,048 (GRCm39) |
F371Y |
probably benign |
Het |
Cpt1b |
A |
T |
15: 89,303,472 (GRCm39) |
F554L |
probably damaging |
Het |
Ctdsp2 |
A |
G |
10: 126,832,040 (GRCm39) |
D216G |
probably damaging |
Het |
Ctla2b |
A |
T |
13: 61,043,856 (GRCm39) |
Y104* |
probably null |
Het |
Ddi1 |
T |
A |
9: 6,265,730 (GRCm39) |
D213V |
probably damaging |
Het |
Degs1l |
G |
T |
1: 180,882,810 (GRCm39) |
V191F |
possibly damaging |
Het |
Dennd2b |
G |
T |
7: 109,125,536 (GRCm39) |
D980E |
probably damaging |
Het |
Dlgap1 |
T |
G |
17: 70,964,458 (GRCm39) |
N400K |
probably benign |
Het |
Dnah5 |
G |
A |
15: 28,290,422 (GRCm39) |
V1271M |
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,932,021 (GRCm39) |
V1463E |
probably benign |
Het |
Dstyk |
G |
A |
1: 132,362,023 (GRCm39) |
R151H |
probably damaging |
Het |
Ehd3 |
T |
G |
17: 74,137,361 (GRCm39) |
V510G |
probably benign |
Het |
Enthd1 |
G |
T |
15: 80,444,235 (GRCm39) |
Q107K |
probably damaging |
Het |
Entpd7 |
A |
G |
19: 43,705,889 (GRCm39) |
E237G |
probably benign |
Het |
Fadd |
A |
T |
7: 144,136,048 (GRCm39) |
C27S |
probably damaging |
Het |
Fan1 |
A |
G |
7: 63,999,240 (GRCm39) |
L874P |
possibly damaging |
Het |
Fbxw17 |
T |
C |
13: 50,579,605 (GRCm39) |
W141R |
probably damaging |
Het |
Fig4 |
A |
G |
10: 41,161,387 (GRCm39) |
V63A |
probably benign |
Het |
Fmo3 |
T |
C |
1: 162,786,021 (GRCm39) |
D323G |
probably damaging |
Het |
Gas8 |
T |
A |
8: 124,263,179 (GRCm39) |
V452E |
possibly damaging |
Het |
Gdf9 |
T |
A |
11: 53,327,511 (GRCm39) |
S156T |
probably damaging |
Het |
Hlcs |
T |
C |
16: 93,935,580 (GRCm39) |
S571G |
probably benign |
Het |
Hmox2 |
A |
G |
16: 4,582,870 (GRCm39) |
Y201C |
probably damaging |
Het |
Ikzf3 |
T |
A |
11: 98,358,032 (GRCm39) |
D435V |
probably damaging |
Het |
Kank2 |
T |
C |
9: 21,705,852 (GRCm39) |
T389A |
possibly damaging |
Het |
Kank2 |
A |
G |
9: 21,706,631 (GRCm39) |
L129P |
probably damaging |
Het |
Kdr |
T |
A |
5: 76,125,565 (GRCm39) |
K339N |
probably benign |
Het |
Lmntd2 |
A |
G |
7: 140,790,701 (GRCm39) |
S516P |
|
Het |
Lrrc37 |
T |
C |
11: 103,503,822 (GRCm39) |
I2715M |
unknown |
Het |
Lrrc40 |
T |
A |
3: 157,746,078 (GRCm39) |
V51D |
probably benign |
Het |
Lrrtm1 |
A |
G |
6: 77,221,536 (GRCm39) |
N331S |
probably benign |
Het |
Lvrn |
T |
G |
18: 47,017,506 (GRCm39) |
I612S |
probably damaging |
Het |
Map3k3 |
T |
A |
11: 106,041,860 (GRCm39) |
I413N |
probably damaging |
Het |
Mcm9 |
C |
T |
10: 53,506,104 (GRCm39) |
A57T |
possibly damaging |
Het |
Met |
T |
A |
6: 17,531,425 (GRCm39) |
F568I |
probably benign |
Het |
Mkx |
A |
G |
18: 7,002,457 (GRCm39) |
F30L |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,266,117 (GRCm39) |
N345S |
probably benign |
Het |
Mstn |
T |
A |
1: 53,103,367 (GRCm39) |
N234K |
probably benign |
Het |
Mtmr3 |
A |
T |
11: 4,440,992 (GRCm39) |
S554T |
possibly damaging |
Het |
Mug1 |
G |
A |
6: 121,861,587 (GRCm39) |
V1350I |
probably benign |
Het |
Myh8 |
T |
C |
11: 67,177,215 (GRCm39) |
V427A |
probably benign |
Het |
Nr4a2 |
A |
T |
2: 57,000,190 (GRCm39) |
I365N |
probably damaging |
Het |
Nrxn2 |
A |
G |
19: 6,559,887 (GRCm39) |
D1215G |
probably damaging |
Het |
Or2d3c |
A |
G |
7: 106,525,847 (GRCm39) |
M273T |
probably benign |
Het |
Or6c33 |
T |
C |
10: 129,853,287 (GRCm39) |
I19T |
probably benign |
Het |
Or7g18 |
G |
A |
9: 18,786,640 (GRCm39) |
V3I |
probably benign |
Het |
Osbpl6 |
T |
A |
2: 76,426,321 (GRCm39) |
W967R |
probably damaging |
Het |
Pcdhb21 |
T |
C |
18: 37,646,972 (GRCm39) |
S34P |
possibly damaging |
Het |
Pibf1 |
G |
T |
14: 99,374,610 (GRCm39) |
D350Y |
possibly damaging |
Het |
Pira1 |
C |
T |
7: 3,742,646 (GRCm39) |
V21M |
possibly damaging |
Het |
Plekhs1 |
A |
T |
19: 56,461,628 (GRCm39) |
I123F |
probably damaging |
Het |
Pold2 |
C |
T |
11: 5,824,163 (GRCm39) |
G214D |
probably benign |
Het |
Pomc |
A |
G |
12: 4,009,971 (GRCm39) |
T71A |
probably benign |
Het |
Pot1b |
A |
G |
17: 55,969,465 (GRCm39) |
S568P |
possibly damaging |
Het |
Prkd2 |
C |
A |
7: 16,591,744 (GRCm39) |
Q592K |
possibly damaging |
Het |
Prss28 |
C |
T |
17: 25,528,911 (GRCm39) |
A84V |
probably damaging |
Het |
Prtg |
T |
A |
9: 72,766,153 (GRCm39) |
Y649N |
probably damaging |
Het |
Psip1 |
T |
C |
4: 83,386,888 (GRCm39) |
E161G |
possibly damaging |
Het |
Rab3gap2 |
A |
G |
1: 185,014,691 (GRCm39) |
D1280G |
probably damaging |
Het |
Rab3ip |
A |
T |
10: 116,751,780 (GRCm39) |
I329N |
probably damaging |
Het |
Rarres2 |
C |
T |
6: 48,549,164 (GRCm39) |
G13D |
possibly damaging |
Het |
Rbp3 |
A |
G |
14: 33,677,477 (GRCm39) |
D475G |
probably damaging |
Het |
Ric3 |
A |
G |
7: 108,638,018 (GRCm39) |
V246A |
probably damaging |
Het |
Robo3 |
A |
G |
9: 37,340,900 (GRCm39) |
F124S |
probably damaging |
Het |
Rpl27a |
C |
A |
7: 109,118,837 (GRCm39) |
H17N |
probably benign |
Het |
Rptn |
A |
G |
3: 93,304,536 (GRCm39) |
D623G |
probably benign |
Het |
Rtl1 |
G |
T |
12: 109,556,713 (GRCm39) |
Q1709K |
probably benign |
Het |
Sacs |
T |
A |
14: 61,449,046 (GRCm39) |
D3697E |
probably damaging |
Het |
Sec61b |
A |
G |
4: 47,483,049 (GRCm39) |
Y93C |
probably damaging |
Het |
Serpina3a |
A |
T |
12: 104,084,886 (GRCm39) |
I94L |
probably benign |
Het |
Skic2 |
C |
T |
17: 35,063,758 (GRCm39) |
A562T |
probably benign |
Het |
Skor2 |
C |
T |
18: 76,946,376 (GRCm39) |
H33Y |
unknown |
Het |
Slc12a3 |
G |
A |
8: 95,082,983 (GRCm39) |
V874I |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,591,861 (GRCm39) |
M1254L |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,812,208 (GRCm39) |
S52P |
unknown |
Het |
Sorl1 |
A |
G |
9: 41,957,893 (GRCm39) |
Y584H |
probably damaging |
Het |
Spata32 |
T |
A |
11: 103,099,779 (GRCm39) |
Q242L |
possibly damaging |
Het |
Sptbn4 |
T |
G |
7: 27,117,504 (GRCm39) |
E415A |
probably damaging |
Het |
St6galnac5 |
T |
C |
3: 152,545,782 (GRCm39) |
R259G |
probably damaging |
Het |
Stat3 |
T |
C |
11: 100,784,614 (GRCm39) |
I589V |
probably benign |
Het |
Tecta |
T |
A |
9: 42,249,123 (GRCm39) |
K1913M |
probably damaging |
Het |
Tek |
C |
A |
4: 94,762,172 (GRCm39) |
N1103K |
probably damaging |
Het |
Telo2 |
A |
G |
17: 25,334,199 (GRCm39) |
I16T |
probably benign |
Het |
Tmem207 |
G |
T |
16: 26,335,499 (GRCm39) |
C79* |
probably null |
Het |
Topaz1 |
C |
T |
9: 122,579,219 (GRCm39) |
H710Y |
probably benign |
Het |
Trim33 |
T |
A |
3: 103,238,965 (GRCm39) |
S648T |
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,851,240 (GRCm39) |
T1734A |
possibly damaging |
Het |
Trpm8 |
A |
G |
1: 88,254,158 (GRCm39) |
E127G |
possibly damaging |
Het |
Ttc3 |
T |
A |
16: 94,248,918 (GRCm39) |
C1139S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,580,330 (GRCm39) |
E23521G |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,268,551 (GRCm39) |
I1669T |
possibly damaging |
Het |
Vcpip1 |
C |
A |
1: 9,817,456 (GRCm39) |
S309I |
possibly damaging |
Het |
Vmn1r208 |
A |
G |
13: 22,956,789 (GRCm39) |
V236A |
probably damaging |
Het |
Vmn1r74 |
T |
C |
7: 11,581,534 (GRCm39) |
F278S |
probably damaging |
Het |
Vmn2r33 |
T |
C |
7: 7,557,081 (GRCm39) |
S540G |
probably benign |
Het |
Vmn2r52 |
T |
C |
7: 9,905,182 (GRCm39) |
D219G |
probably benign |
Het |
Wiz |
G |
T |
17: 32,575,939 (GRCm39) |
D812E |
probably benign |
Het |
Ylpm1 |
C |
T |
12: 85,091,176 (GRCm39) |
P1787S |
probably benign |
Het |
Zan |
T |
C |
5: 137,404,688 (GRCm39) |
E3858G |
unknown |
Het |
Zfp760 |
T |
G |
17: 21,942,272 (GRCm39) |
H482Q |
possibly damaging |
Het |
Zfp78 |
A |
G |
7: 6,381,390 (GRCm39) |
T147A |
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,320,661 (GRCm39) |
I630K |
possibly damaging |
Het |
Zpld1 |
T |
A |
16: 55,061,701 (GRCm39) |
R227* |
probably null |
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 |
|
R0471:Cyp2j6
|
UTSW |
4 |
96,419,985 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|
|