Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl1 |
G |
T |
8: 84,663,886 (GRCm39) |
G1118W |
probably damaging |
Het |
Ajap1 |
T |
A |
4: 153,516,661 (GRCm39) |
T227S |
possibly damaging |
Het |
Ankmy1 |
A |
G |
1: 92,804,740 (GRCm39) |
F851S |
probably damaging |
Het |
Blvrb |
C |
T |
7: 27,158,894 (GRCm39) |
P98L |
probably benign |
Het |
Bmpr1b |
C |
A |
3: 141,563,283 (GRCm39) |
M220I |
possibly damaging |
Het |
Cacna1e |
T |
A |
1: 154,347,086 (GRCm39) |
N1027I |
probably benign |
Het |
Cacng4 |
A |
T |
11: 107,625,610 (GRCm39) |
V327E |
probably damaging |
Het |
Casp1 |
T |
C |
9: 5,303,143 (GRCm39) |
V199A |
probably damaging |
Het |
Cdh13 |
A |
T |
8: 119,484,213 (GRCm39) |
D158V |
probably benign |
Het |
Cenpe |
C |
A |
3: 134,940,837 (GRCm39) |
S662* |
probably null |
Het |
Ctnna1 |
A |
G |
18: 35,382,795 (GRCm39) |
D647G |
probably benign |
Het |
Dennd5a |
C |
A |
7: 109,518,630 (GRCm39) |
E480* |
probably null |
Het |
Exoc6 |
T |
A |
19: 37,566,977 (GRCm39) |
V258D |
probably benign |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
G |
A |
1: 174,437,377 (GRCm39) |
C1116Y |
probably damaging |
Het |
H2-Aa |
T |
C |
17: 34,502,816 (GRCm39) |
T117A |
possibly damaging |
Het |
Ktn1 |
TTGTTGTCTTTGTGTT |
TTGTT |
14: 47,971,554 (GRCm39) |
|
probably benign |
Het |
Lig1 |
C |
A |
7: 13,039,933 (GRCm39) |
T715N |
probably damaging |
Het |
Lrrc31 |
C |
A |
3: 30,743,994 (GRCm39) |
|
probably null |
Het |
Mcm6 |
T |
C |
1: 128,283,326 (GRCm39) |
T60A |
probably damaging |
Het |
Mex3c |
T |
A |
18: 73,723,014 (GRCm39) |
M369K |
possibly damaging |
Het |
Mmp14 |
T |
C |
14: 54,676,869 (GRCm39) |
Y428H |
probably damaging |
Het |
Msh6 |
A |
G |
17: 88,294,329 (GRCm39) |
D1028G |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,771,227 (GRCm39) |
V933A |
probably damaging |
Het |
Nepn |
A |
T |
10: 52,277,233 (GRCm39) |
D323V |
probably benign |
Het |
Nrf1 |
C |
T |
6: 30,126,245 (GRCm39) |
A150V |
probably damaging |
Het |
Obscn |
T |
G |
11: 59,013,674 (GRCm39) |
K1150Q |
probably benign |
Het |
Or12j5 |
A |
C |
7: 140,084,318 (GRCm39) |
V18G |
probably benign |
Het |
Or52s1b |
T |
C |
7: 102,822,056 (GRCm39) |
T263A |
probably damaging |
Het |
Or52z12 |
G |
A |
7: 103,233,506 (GRCm39) |
W92* |
probably null |
Het |
Or7a38 |
A |
G |
10: 78,752,933 (GRCm39) |
I86M |
possibly damaging |
Het |
Or7e170 |
T |
A |
9: 19,795,272 (GRCm39) |
M110L |
probably benign |
Het |
Otop1 |
G |
A |
5: 38,451,848 (GRCm39) |
G184S |
possibly damaging |
Het |
Pkp2 |
G |
T |
16: 16,078,239 (GRCm39) |
D494Y |
probably damaging |
Het |
Pop5 |
G |
A |
5: 115,378,260 (GRCm39) |
R68Q |
probably damaging |
Het |
Ppp1r13b |
T |
C |
12: 111,800,223 (GRCm39) |
D518G |
probably benign |
Het |
Preb |
G |
T |
5: 31,117,307 (GRCm39) |
|
probably benign |
Het |
Qrfpr |
A |
G |
3: 36,235,114 (GRCm39) |
V292A |
possibly damaging |
Het |
Rag1 |
G |
A |
2: 101,474,137 (GRCm39) |
T335I |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 122,596,309 (GRCm39) |
V617E |
probably damaging |
Het |
Sf3a3 |
A |
T |
4: 124,608,746 (GRCm39) |
D20V |
probably damaging |
Het |
Slco1b2 |
A |
G |
6: 141,631,312 (GRCm39) |
N649D |
probably benign |
Het |
Smarcal1 |
A |
G |
1: 72,625,372 (GRCm39) |
D173G |
probably benign |
Het |
Smg7 |
A |
G |
1: 152,718,985 (GRCm39) |
L914P |
probably damaging |
Het |
Tbc1d32 |
A |
T |
10: 56,005,246 (GRCm39) |
S796T |
possibly damaging |
Het |
Tex14 |
A |
G |
11: 87,413,404 (GRCm39) |
T1052A |
probably benign |
Het |
Tspan1 |
A |
G |
4: 116,021,277 (GRCm39) |
V109A |
possibly damaging |
Het |
Ttbk2 |
A |
G |
2: 120,637,305 (GRCm39) |
V51A |
possibly damaging |
Het |
Tubgcp6 |
A |
G |
15: 88,995,353 (GRCm39) |
V419A |
probably benign |
Het |
Ubr2 |
G |
T |
17: 47,245,126 (GRCm39) |
C1633* |
probably null |
Het |
Uggt2 |
C |
T |
14: 119,326,611 (GRCm39) |
G200D |
possibly damaging |
Het |
Vmn2r25 |
T |
C |
6: 123,805,318 (GRCm39) |
E513G |
possibly damaging |
Het |
Zscan22 |
G |
A |
7: 12,640,919 (GRCm39) |
G388S |
probably damaging |
Het |
|
Other mutations in Nxpe5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Nxpe5
|
APN |
5 |
138,247,096 (GRCm39) |
missense |
probably benign |
0.00 |
FR4737:Nxpe5
|
UTSW |
5 |
138,228,196 (GRCm39) |
start gained |
probably benign |
|
R0049:Nxpe5
|
UTSW |
5 |
138,249,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Nxpe5
|
UTSW |
5 |
138,249,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Nxpe5
|
UTSW |
5 |
138,238,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Nxpe5
|
UTSW |
5 |
138,237,658 (GRCm39) |
missense |
probably benign |
0.04 |
R1774:Nxpe5
|
UTSW |
5 |
138,237,797 (GRCm39) |
missense |
probably benign |
|
R1895:Nxpe5
|
UTSW |
5 |
138,249,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R3717:Nxpe5
|
UTSW |
5 |
138,249,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Nxpe5
|
UTSW |
5 |
138,228,795 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5268:Nxpe5
|
UTSW |
5 |
138,238,200 (GRCm39) |
nonsense |
probably null |
|
R5342:Nxpe5
|
UTSW |
5 |
138,237,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R6966:Nxpe5
|
UTSW |
5 |
138,237,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Nxpe5
|
UTSW |
5 |
138,237,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R7196:Nxpe5
|
UTSW |
5 |
138,237,586 (GRCm39) |
missense |
probably benign |
0.30 |
R7427:Nxpe5
|
UTSW |
5 |
138,238,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R7428:Nxpe5
|
UTSW |
5 |
138,238,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R7548:Nxpe5
|
UTSW |
5 |
138,249,493 (GRCm39) |
missense |
probably benign |
0.29 |
R7823:Nxpe5
|
UTSW |
5 |
138,237,844 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8058:Nxpe5
|
UTSW |
5 |
138,237,573 (GRCm39) |
nonsense |
probably null |
|
R8094:Nxpe5
|
UTSW |
5 |
138,249,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R8293:Nxpe5
|
UTSW |
5 |
138,228,804 (GRCm39) |
missense |
probably benign |
0.20 |
R8303:Nxpe5
|
UTSW |
5 |
138,239,264 (GRCm39) |
unclassified |
probably benign |
|
R9372:Nxpe5
|
UTSW |
5 |
138,249,445 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:Nxpe5
|
UTSW |
5 |
138,228,591 (GRCm39) |
start gained |
probably benign |
|
Z1088:Nxpe5
|
UTSW |
5 |
138,239,176 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Nxpe5
|
UTSW |
5 |
138,228,088 (GRCm39) |
start gained |
probably benign |
|
|