Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
T |
A |
8: 88,309,238 (GRCm39) |
S134T |
possibly damaging |
Het |
Aadacl4 |
T |
A |
4: 144,349,790 (GRCm39) |
L349Q |
probably damaging |
Het |
Ankrd29 |
T |
C |
18: 12,428,970 (GRCm39) |
N33S |
probably damaging |
Het |
Arid3b |
T |
C |
9: 57,699,900 (GRCm39) |
S536G |
possibly damaging |
Het |
Art5 |
A |
C |
7: 101,748,699 (GRCm39) |
M1R |
probably null |
Het |
Arvcf |
T |
A |
16: 18,218,452 (GRCm39) |
C545S |
probably damaging |
Het |
Atpsckmt |
A |
G |
15: 31,617,101 (GRCm39) |
T189A |
probably benign |
Het |
Axin2 |
T |
A |
11: 108,833,794 (GRCm39) |
N580K |
probably benign |
Het |
Cdh23 |
T |
G |
10: 60,151,478 (GRCm39) |
D2469A |
probably benign |
Het |
Cep350 |
T |
A |
1: 155,773,228 (GRCm39) |
T1781S |
probably damaging |
Het |
Cfap65 |
T |
A |
1: 74,943,847 (GRCm39) |
T1555S |
possibly damaging |
Het |
Chga |
G |
A |
12: 102,529,054 (GRCm39) |
E344K |
possibly damaging |
Het |
Ckap2l |
A |
T |
2: 129,126,892 (GRCm39) |
L429M |
probably damaging |
Het |
Cpne7 |
C |
T |
8: 123,856,951 (GRCm39) |
P402L |
probably damaging |
Het |
Cyp2g1 |
A |
G |
7: 26,509,256 (GRCm39) |
N110S |
probably benign |
Het |
Cyp3a11 |
T |
C |
5: 145,805,995 (GRCm39) |
D124G |
probably benign |
Het |
Dgkq |
A |
T |
5: 108,801,061 (GRCm39) |
V527D |
probably damaging |
Het |
Dnah3 |
T |
C |
7: 119,551,272 (GRCm39) |
I37V |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,845,680 (GRCm39) |
E3068V |
|
Het |
Dusp23 |
T |
C |
1: 172,460,184 (GRCm39) |
E89G |
probably null |
Het |
Fam187a |
A |
G |
11: 102,776,685 (GRCm39) |
Y163C |
possibly damaging |
Het |
Gabrg2 |
T |
A |
11: 41,865,662 (GRCm39) |
I106F |
probably damaging |
Het |
Gpc2 |
A |
G |
5: 138,277,193 (GRCm39) |
I78T |
probably benign |
Het |
Gpr149 |
A |
C |
3: 62,511,360 (GRCm39) |
L213R |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,565,056 (GRCm39) |
L1084* |
probably null |
Het |
Gypa |
A |
G |
8: 81,222,946 (GRCm39) |
T17A |
unknown |
Het |
Gys2 |
A |
T |
6: 142,376,059 (GRCm39) |
F534L |
probably damaging |
Het |
Iqce |
A |
T |
5: 140,651,810 (GRCm39) |
M721K |
probably benign |
Het |
Klrc2 |
T |
A |
6: 129,635,741 (GRCm39) |
Y129F |
probably damaging |
Het |
Krt14 |
T |
C |
11: 100,095,464 (GRCm39) |
S314G |
possibly damaging |
Het |
L3mbtl3 |
T |
C |
10: 26,156,152 (GRCm39) |
Q685R |
unknown |
Het |
Lamb3 |
A |
T |
1: 193,007,919 (GRCm39) |
K206* |
probably null |
Het |
Lgr5 |
A |
G |
10: 115,314,343 (GRCm39) |
I198T |
probably damaging |
Het |
Mapk10 |
A |
T |
5: 103,074,025 (GRCm39) |
|
probably benign |
Het |
Mcm6 |
C |
T |
1: 128,271,231 (GRCm39) |
D463N |
probably damaging |
Het |
Med15 |
A |
T |
16: 17,470,582 (GRCm39) |
W742R |
probably benign |
Het |
Meis1 |
T |
A |
11: 18,831,916 (GRCm39) |
Q374L |
possibly damaging |
Het |
Nrxn3 |
T |
C |
12: 89,227,252 (GRCm39) |
C296R |
probably damaging |
Het |
Ntaq1 |
A |
G |
15: 58,014,004 (GRCm39) |
Y67C |
possibly damaging |
Het |
Oaf |
C |
T |
9: 43,135,308 (GRCm39) |
A157T |
probably damaging |
Het |
Oca2 |
T |
A |
7: 55,927,189 (GRCm39) |
|
probably null |
Het |
Or5b110-ps1 |
A |
T |
19: 13,260,074 (GRCm39) |
M116K |
probably damaging |
Het |
Or5b12 |
T |
A |
19: 12,897,667 (GRCm39) |
E2V |
probably benign |
Het |
Or5d36 |
T |
A |
2: 87,900,983 (GRCm39) |
T248S |
possibly damaging |
Het |
Or9k2b |
A |
T |
10: 130,016,154 (GRCm39) |
H198Q |
probably benign |
Het |
Pacs1 |
A |
G |
19: 5,188,964 (GRCm39) |
I806T |
probably benign |
Het |
Pax2 |
T |
A |
19: 44,804,499 (GRCm39) |
S257T |
probably benign |
Het |
Pbxip1 |
A |
T |
3: 89,350,794 (GRCm39) |
T72S |
probably benign |
Het |
Pcdhb14 |
T |
C |
18: 37,581,851 (GRCm39) |
I319T |
probably damaging |
Het |
Pcdhga2 |
C |
A |
18: 37,802,963 (GRCm39) |
A269E |
possibly damaging |
Het |
Pdzph1 |
A |
C |
17: 59,280,535 (GRCm39) |
N582K |
probably benign |
Het |
Plk2 |
A |
T |
13: 110,533,194 (GRCm39) |
I186F |
probably damaging |
Het |
Pzp |
A |
T |
6: 128,471,742 (GRCm39) |
C895S |
probably damaging |
Het |
Rasa2 |
A |
T |
9: 96,484,770 (GRCm39) |
V148D |
probably damaging |
Het |
Rgsl1 |
A |
T |
1: 153,717,567 (GRCm39) |
I14N |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,349,739 (GRCm39) |
R3867G |
|
Het |
Rpap3 |
A |
G |
15: 97,584,443 (GRCm39) |
Y334H |
possibly damaging |
Het |
Scara3 |
A |
C |
14: 66,169,070 (GRCm39) |
N182K |
probably damaging |
Het |
Sh3bp1 |
A |
G |
15: 78,791,449 (GRCm39) |
E412G |
possibly damaging |
Het |
Sh3tc2 |
T |
A |
18: 62,122,961 (GRCm39) |
I574N |
possibly damaging |
Het |
Slc16a11 |
T |
C |
11: 70,106,520 (GRCm39) |
Y253H |
probably damaging |
Het |
Slc38a4 |
A |
T |
15: 96,906,805 (GRCm39) |
V311E |
possibly damaging |
Het |
Slc4a7 |
T |
C |
14: 14,775,048 (GRCm38) |
L826P |
probably damaging |
Het |
Spag9 |
T |
G |
11: 93,951,085 (GRCm39) |
V83G |
|
Het |
Sspo |
T |
G |
6: 48,470,214 (GRCm39) |
V4560G |
probably benign |
Het |
Stxbp2 |
T |
A |
8: 3,684,478 (GRCm39) |
F144I |
|
Het |
Tafa2 |
T |
C |
10: 123,540,294 (GRCm39) |
V50A |
probably damaging |
Het |
Tdh |
T |
C |
14: 63,730,278 (GRCm39) |
I334V |
probably benign |
Het |
Tesk2 |
C |
A |
4: 116,660,148 (GRCm39) |
S451Y |
probably benign |
Het |
Tjp1 |
A |
T |
7: 64,962,679 (GRCm39) |
V1166E |
probably benign |
Het |
Tmeff2 |
G |
A |
1: 51,018,779 (GRCm39) |
V254M |
unknown |
Het |
Tmem126a |
A |
G |
7: 90,100,749 (GRCm39) |
|
probably null |
Het |
Togaram2 |
C |
G |
17: 71,993,699 (GRCm39) |
P2A |
probably benign |
Het |
Trappc14 |
G |
A |
5: 138,259,889 (GRCm39) |
T389I |
possibly damaging |
Het |
Tssk4 |
C |
T |
14: 55,889,211 (GRCm39) |
R246W |
probably damaging |
Het |
Tubal3 |
C |
T |
13: 3,982,708 (GRCm39) |
R163* |
probably null |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Vezt |
T |
C |
10: 93,820,027 (GRCm39) |
N446S |
probably damaging |
Het |
Vim |
A |
T |
2: 13,579,249 (GRCm39) |
T3S |
unknown |
Het |
Vmn2r45 |
A |
G |
7: 8,474,904 (GRCm39) |
L708P |
possibly damaging |
Het |
Yes1 |
A |
G |
5: 32,810,312 (GRCm39) |
Y157C |
probably damaging |
Het |
Zfp358 |
A |
G |
8: 3,545,810 (GRCm39) |
T131A |
probably benign |
Het |
Zfp426 |
C |
T |
9: 20,386,308 (GRCm39) |
V58M |
probably damaging |
Het |
Zfp692 |
T |
C |
11: 58,198,550 (GRCm39) |
S47P |
probably damaging |
Het |
Zfp719 |
A |
T |
7: 43,239,605 (GRCm39) |
T398S |
possibly damaging |
Het |
|