Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001C19Rik |
G |
A |
17: 47,413,890 |
S102L |
probably benign |
Het |
A430105I19Rik |
T |
A |
2: 118,761,760 |
|
probably null |
Het |
Adam11 |
T |
C |
11: 102,775,113 |
|
probably null |
Het |
AI314180 |
T |
C |
4: 58,832,701 |
|
probably null |
Het |
Amd1 |
A |
T |
10: 40,290,505 |
M194K |
probably benign |
Het |
Ap1b1 |
T |
G |
11: 5,039,547 |
F793C |
probably damaging |
Het |
Arfgef3 |
G |
A |
10: 18,613,222 |
R1292* |
probably null |
Het |
Arhgef5 |
C |
A |
6: 43,279,515 |
H1186N |
probably damaging |
Het |
Atad1 |
A |
G |
19: 32,706,921 |
F26L |
probably benign |
Het |
Atg2b |
C |
T |
12: 105,661,133 |
V532I |
probably benign |
Het |
Atp2b4 |
A |
G |
1: 133,717,988 |
F943L |
probably damaging |
Het |
Atp7b |
G |
A |
8: 22,028,724 |
L21F |
possibly damaging |
Het |
Cenpf |
A |
T |
1: 189,660,038 |
D532E |
probably benign |
Het |
Ckmt2 |
A |
T |
13: 91,861,201 |
D202E |
probably benign |
Het |
Crim1 |
A |
C |
17: 78,367,954 |
K864T |
probably benign |
Het |
Ctnnd2 |
A |
G |
15: 30,887,121 |
R765G |
possibly damaging |
Het |
Ddx10 |
T |
A |
9: 53,117,199 |
R802* |
probably null |
Het |
Dnah7b |
T |
A |
1: 46,177,281 |
F1152L |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,282,023 |
L659P |
probably damaging |
Het |
Dzank1 |
A |
G |
2: 144,482,188 |
F577L |
probably benign |
Het |
Eci3 |
T |
C |
13: 34,956,920 |
D93G |
probably benign |
Het |
Ep400 |
C |
A |
5: 110,739,445 |
V591L |
probably benign |
Het |
Fam126b |
A |
T |
1: 58,539,607 |
D261E |
probably benign |
Het |
Fgd3 |
T |
C |
13: 49,266,694 |
N569S |
probably benign |
Het |
Ghsr |
T |
A |
3: 27,372,482 |
V229E |
probably damaging |
Het |
Gm8298 |
T |
C |
3: 59,861,112 |
I21T |
probably benign |
Het |
Gna15 |
T |
A |
10: 81,509,342 |
I230F |
probably damaging |
Het |
Gnl2 |
A |
G |
4: 125,046,306 |
S324G |
probably damaging |
Het |
Grid1 |
T |
C |
14: 35,309,293 |
V281A |
probably benign |
Het |
Hebp2 |
G |
A |
10: 18,545,761 |
A12V |
possibly damaging |
Het |
Hfm1 |
T |
C |
5: 106,853,123 |
D1254G |
probably benign |
Het |
Hif3a |
A |
C |
7: 17,042,639 |
S459A |
probably benign |
Het |
Hnrnpl |
T |
A |
7: 28,813,923 |
N149K |
possibly damaging |
Het |
Hoxc10 |
A |
T |
15: 102,967,200 |
S115C |
probably damaging |
Het |
Ifnab |
T |
C |
4: 88,691,055 |
D58G |
possibly damaging |
Het |
Itfg1 |
T |
C |
8: 85,810,614 |
T195A |
probably benign |
Het |
Itpr3 |
T |
A |
17: 27,105,485 |
|
probably null |
Het |
Iws1 |
A |
G |
18: 32,080,281 |
D254G |
probably benign |
Het |
Kl |
C |
A |
5: 150,988,941 |
D718E |
probably benign |
Het |
Lrit2 |
A |
G |
14: 37,068,827 |
I154M |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,523,182 |
D578G |
probably damaging |
Het |
Lss |
T |
G |
10: 76,536,289 |
Y159* |
probably null |
Het |
Mab21l1 |
C |
A |
3: 55,783,833 |
Y280* |
probably null |
Het |
Maf |
A |
T |
8: 115,693,170 |
S378T |
probably benign |
Het |
Mast2 |
C |
T |
4: 116,430,519 |
V59I |
probably benign |
Het |
Nisch |
C |
T |
14: 31,180,938 |
|
probably benign |
Het |
Nova2 |
A |
T |
7: 18,957,554 |
N139Y |
probably damaging |
Het |
Nup210 |
C |
A |
6: 91,036,376 |
D434Y |
probably damaging |
Het |
Nvl |
C |
T |
1: 181,109,159 |
|
probably null |
Het |
Olfr1049 |
A |
T |
2: 86,255,241 |
Y151N |
probably damaging |
Het |
Olfr1087 |
A |
G |
2: 86,690,333 |
V214A |
possibly damaging |
Het |
Olfr577 |
A |
G |
7: 102,973,879 |
Y38H |
probably damaging |
Het |
Olfr657 |
A |
G |
7: 104,636,489 |
T272A |
probably benign |
Het |
Olfr743 |
T |
C |
14: 50,533,702 |
S97P |
possibly damaging |
Het |
Pbx3 |
T |
C |
2: 34,204,859 |
Y255C |
probably damaging |
Het |
Pcyt1a |
G |
A |
16: 32,451,793 |
E27K |
possibly damaging |
Het |
Pex6 |
A |
T |
17: 46,714,064 |
T348S |
probably benign |
Het |
Phf21b |
A |
G |
15: 84,797,396 |
I251T |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,430,702 |
I490T |
probably damaging |
Het |
Pla2g12a |
T |
A |
3: 129,878,885 |
L56Q |
probably damaging |
Het |
Plk4 |
A |
G |
3: 40,806,536 |
T434A |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,564,132 |
N1632S |
probably benign |
Het |
Rfpl4 |
C |
T |
7: 5,110,712 |
V151M |
probably damaging |
Het |
Rpain |
G |
C |
11: 70,974,915 |
E169Q |
probably damaging |
Het |
Samd8 |
T |
A |
14: 21,775,159 |
V124D |
possibly damaging |
Het |
Sdk2 |
C |
T |
11: 113,838,646 |
|
silent |
Het |
Slc12a1 |
C |
T |
2: 125,190,295 |
T622I |
probably damaging |
Het |
Slc17a3 |
T |
A |
13: 23,845,445 |
V67D |
probably damaging |
Het |
Slc41a3 |
G |
T |
6: 90,644,216 |
V387L |
probably damaging |
Het |
Slitrk1 |
T |
A |
14: 108,913,277 |
M1L |
probably benign |
Het |
Stat4 |
T |
C |
1: 52,011,793 |
W4R |
probably damaging |
Het |
Tbc1d24 |
A |
G |
17: 24,185,979 |
C64R |
probably damaging |
Het |
Tcaf2 |
T |
C |
6: 42,629,506 |
S505G |
probably benign |
Het |
Tiam2 |
T |
C |
17: 3,516,703 |
V1506A |
probably benign |
Het |
Tmem9b |
A |
C |
7: 109,736,949 |
S163A |
probably benign |
Het |
Tmtc2 |
G |
A |
10: 105,303,658 |
S669L |
probably damaging |
Het |
Tnpo3 |
A |
T |
6: 29,560,221 |
I641K |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,735,367 |
A28214T |
probably damaging |
Het |
Utp11 |
G |
A |
4: 124,683,239 |
A113V |
probably benign |
Het |
Utp20 |
G |
A |
10: 88,753,006 |
R2434C |
probably damaging |
Het |
Vmn1r60 |
A |
T |
7: 5,544,903 |
I66N |
probably benign |
Het |
Zeb2 |
T |
C |
2: 44,997,194 |
E572G |
probably damaging |
Het |
|