Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr7a5 |
A |
T |
4: 139,044,079 (GRCm39) |
H225L |
possibly damaging |
Het |
Arhgap32 |
C |
A |
9: 32,168,655 (GRCm39) |
H879Q |
probably benign |
Het |
Axin2 |
A |
G |
11: 108,833,128 (GRCm39) |
I438V |
possibly damaging |
Het |
Btbd18 |
T |
A |
2: 84,491,920 (GRCm39) |
C34S |
probably damaging |
Het |
Carns1 |
G |
T |
19: 4,216,256 (GRCm39) |
T642N |
possibly damaging |
Het |
Casp8 |
T |
C |
1: 58,883,542 (GRCm39) |
I283T |
probably benign |
Het |
Ccdc136 |
T |
A |
6: 29,421,982 (GRCm39) |
|
probably benign |
Het |
Ccnk |
C |
A |
12: 108,161,946 (GRCm39) |
Q284K |
unknown |
Het |
Ceacam12 |
T |
A |
7: 17,801,177 (GRCm39) |
L52H |
probably damaging |
Het |
Cit |
G |
A |
5: 116,065,970 (GRCm39) |
D540N |
probably damaging |
Het |
Cntnap1 |
T |
C |
11: 101,072,121 (GRCm39) |
V458A |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,758,976 (GRCm39) |
I2077F |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,409,104 (GRCm39) |
K425E |
probably benign |
Het |
Eya2 |
A |
G |
2: 165,529,631 (GRCm39) |
S125G |
probably benign |
Het |
Gabrg1 |
T |
G |
5: 70,934,599 (GRCm39) |
M260L |
probably benign |
Het |
Greb1 |
T |
C |
12: 16,732,153 (GRCm39) |
S1603G |
probably damaging |
Het |
Isx |
A |
G |
8: 75,600,434 (GRCm39) |
T56A |
probably benign |
Het |
Kif2b |
A |
T |
11: 91,467,975 (GRCm39) |
S103T |
probably benign |
Het |
Krtap26-1 |
T |
C |
16: 88,444,342 (GRCm39) |
H93R |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mdm4 |
G |
A |
1: 132,924,416 (GRCm39) |
T236M |
probably damaging |
Het |
Mgat5 |
T |
A |
1: 127,325,348 (GRCm39) |
L405Q |
probably damaging |
Het |
Msantd1 |
A |
G |
5: 35,080,885 (GRCm39) |
I272V |
probably benign |
Het |
Ocstamp |
A |
G |
2: 165,237,768 (GRCm39) |
*499Q |
probably null |
Het |
Or11h6 |
A |
G |
14: 50,880,493 (GRCm39) |
K252E |
possibly damaging |
Het |
Or1e16 |
G |
A |
11: 73,279,789 (GRCm39) |
P21L |
probably benign |
Het |
Or2n1d |
G |
A |
17: 38,646,414 (GRCm39) |
R122Q |
probably damaging |
Het |
Or4c100 |
A |
G |
2: 88,356,211 (GRCm39) |
M95V |
probably benign |
Het |
Or5b12 |
A |
T |
19: 12,897,309 (GRCm39) |
Y121* |
probably null |
Het |
Pcdh15 |
T |
A |
10: 74,461,756 (GRCm39) |
|
probably benign |
Het |
Pkdrej |
C |
T |
15: 85,700,834 (GRCm39) |
G1701S |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,113,757 (GRCm39) |
T754A |
probably damaging |
Het |
Prss8 |
C |
A |
7: 127,527,082 (GRCm39) |
Q55H |
probably damaging |
Het |
Psg20 |
G |
T |
7: 18,416,670 (GRCm39) |
R149S |
probably benign |
Het |
Ptprz1 |
T |
G |
6: 23,002,444 (GRCm39) |
N1511K |
probably benign |
Het |
Rbbp8nl |
C |
T |
2: 179,920,894 (GRCm39) |
|
probably null |
Het |
Sgk2 |
A |
G |
2: 162,854,975 (GRCm39) |
D362G |
probably benign |
Het |
Sim1 |
T |
C |
10: 50,859,796 (GRCm39) |
Y553H |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,208,896 (GRCm39) |
D504G |
probably damaging |
Het |
Smad7 |
T |
C |
18: 75,502,547 (GRCm39) |
V174A |
possibly damaging |
Het |
Smarcc1 |
T |
A |
9: 109,996,792 (GRCm39) |
N303K |
possibly damaging |
Het |
Snai3 |
T |
C |
8: 123,183,038 (GRCm39) |
H169R |
possibly damaging |
Het |
Tecpr2 |
T |
A |
12: 110,895,505 (GRCm39) |
S331T |
possibly damaging |
Het |
Tenm2 |
G |
A |
11: 35,959,303 (GRCm39) |
T1082I |
probably benign |
Het |
Tle4 |
A |
T |
19: 14,429,890 (GRCm39) |
I627N |
probably damaging |
Het |
Tnxb |
A |
T |
17: 34,898,088 (GRCm39) |
N912I |
possibly damaging |
Het |
Vmn1r238 |
A |
T |
18: 3,122,994 (GRCm39) |
V140E |
probably damaging |
Het |
Vmn1r65 |
G |
A |
7: 6,011,988 (GRCm39) |
T82I |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,572,290 (GRCm39) |
K969R |
probably damaging |
Het |
Zfp943 |
A |
G |
17: 22,209,832 (GRCm39) |
R35G |
possibly damaging |
Het |
|
Other mutations in Ube2q2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00667:Ube2q2l
|
APN |
6 |
136,377,996 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01701:Ube2q2l
|
APN |
6 |
136,377,804 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02194:Ube2q2l
|
APN |
6 |
136,378,056 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03266:Ube2q2l
|
APN |
6 |
136,377,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1270:Ube2q2l
|
UTSW |
6 |
136,378,785 (GRCm39) |
missense |
probably damaging |
0.97 |
R1893:Ube2q2l
|
UTSW |
6 |
136,378,825 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4192:Ube2q2l
|
UTSW |
6 |
136,378,435 (GRCm39) |
missense |
probably benign |
0.06 |
R5371:Ube2q2l
|
UTSW |
6 |
136,378,371 (GRCm39) |
missense |
probably benign |
0.02 |
R6418:Ube2q2l
|
UTSW |
6 |
136,378,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6999:Ube2q2l
|
UTSW |
6 |
136,378,272 (GRCm39) |
missense |
probably benign |
0.01 |
R7035:Ube2q2l
|
UTSW |
6 |
136,378,347 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7316:Ube2q2l
|
UTSW |
6 |
136,378,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8125:Ube2q2l
|
UTSW |
6 |
136,378,184 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8179:Ube2q2l
|
UTSW |
6 |
136,378,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R8222:Ube2q2l
|
UTSW |
6 |
136,377,882 (GRCm39) |
missense |
probably damaging |
0.97 |
R8225:Ube2q2l
|
UTSW |
6 |
136,378,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8421:Ube2q2l
|
UTSW |
6 |
136,378,350 (GRCm39) |
missense |
probably damaging |
0.97 |
R8784:Ube2q2l
|
UTSW |
6 |
136,378,729 (GRCm39) |
nonsense |
probably null |
|
R9080:Ube2q2l
|
UTSW |
6 |
136,377,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R9103:Ube2q2l
|
UTSW |
6 |
136,378,011 (GRCm39) |
missense |
probably benign |
0.39 |
|