Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,854,394 (GRCm39) |
D216V |
possibly damaging |
Het |
2610021A01Rik |
C |
T |
7: 41,276,081 (GRCm39) |
R595* |
probably null |
Het |
Adgrl3 |
A |
G |
5: 81,836,414 (GRCm39) |
D724G |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,187,578 (GRCm39) |
F1664S |
possibly damaging |
Het |
Akt1 |
T |
C |
12: 112,621,585 (GRCm39) |
I404V |
probably benign |
Het |
Anxa13 |
T |
A |
15: 58,205,344 (GRCm39) |
|
noncoding transcript |
Het |
Atoh1 |
T |
C |
6: 64,706,617 (GRCm39) |
V104A |
probably benign |
Het |
Brwd1 |
T |
C |
16: 95,822,437 (GRCm39) |
D1256G |
probably damaging |
Het |
C9 |
ATTTT |
ATTT |
15: 6,512,619 (GRCm39) |
|
probably null |
Het |
Cd164 |
A |
G |
10: 41,399,177 (GRCm39) |
T89A |
probably benign |
Het |
Cep350 |
G |
C |
1: 155,808,850 (GRCm39) |
N575K |
possibly damaging |
Het |
Chrm5 |
A |
G |
2: 112,310,597 (GRCm39) |
V173A |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,468,572 (GRCm39) |
V1417A |
possibly damaging |
Het |
Cntnap3 |
T |
C |
13: 64,906,204 (GRCm39) |
T801A |
probably damaging |
Het |
Cntnap5b |
A |
C |
1: 99,999,865 (GRCm39) |
K208Q |
possibly damaging |
Het |
Crx |
A |
T |
7: 15,603,272 (GRCm39) |
V107D |
possibly damaging |
Het |
Csrnp2 |
A |
G |
15: 100,387,321 (GRCm39) |
F49S |
probably damaging |
Het |
Ctbp1 |
A |
G |
5: 33,408,248 (GRCm39) |
L228P |
possibly damaging |
Het |
Ctdp1 |
A |
T |
18: 80,492,616 (GRCm39) |
D626E |
possibly damaging |
Het |
Dnah3 |
T |
A |
7: 119,566,793 (GRCm39) |
T2478S |
possibly damaging |
Het |
Dnah3 |
T |
G |
7: 119,567,182 (GRCm39) |
D2348A |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,343,737 (GRCm39) |
I2379T |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,069,175 (GRCm39) |
I2504T |
probably damaging |
Het |
Dnase1l2 |
A |
C |
17: 24,660,625 (GRCm39) |
W138G |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,563,061 (GRCm39) |
I855N |
probably damaging |
Het |
Dsc3 |
T |
A |
18: 20,098,903 (GRCm39) |
N759Y |
possibly damaging |
Het |
Dtx2 |
C |
T |
5: 136,061,147 (GRCm39) |
R510* |
probably null |
Het |
Fat4 |
G |
T |
3: 38,941,264 (GRCm39) |
M52I |
probably benign |
Het |
Fat4 |
G |
A |
3: 39,050,239 (GRCm39) |
E4034K |
probably damaging |
Het |
Fezf2 |
T |
C |
14: 12,344,350 (GRCm38) |
K279R |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,806,861 (GRCm39) |
W1060L |
possibly damaging |
Het |
G6pc1 |
T |
A |
11: 101,258,768 (GRCm39) |
I49N |
probably damaging |
Het |
Gars1 |
A |
G |
6: 55,054,757 (GRCm39) |
E688G |
probably null |
Het |
Gdf11 |
T |
C |
10: 128,721,111 (GRCm39) |
N361S |
probably benign |
Het |
Gli3 |
A |
C |
13: 15,900,965 (GRCm39) |
M1451L |
probably benign |
Het |
Heatr3 |
T |
C |
8: 88,876,945 (GRCm39) |
I329T |
probably benign |
Het |
Herc3 |
T |
G |
6: 58,861,960 (GRCm39) |
|
probably null |
Het |
Hrnr |
A |
G |
3: 93,239,911 (GRCm39) |
N3383S |
unknown |
Het |
Igsf3 |
A |
T |
3: 101,338,612 (GRCm39) |
I309F |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,080,002 (GRCm39) |
R513W |
probably damaging |
Het |
Kif7 |
G |
T |
7: 79,348,989 (GRCm39) |
H1195Q |
probably benign |
Het |
Lpcat4 |
T |
C |
2: 112,072,887 (GRCm39) |
V182A |
possibly damaging |
Het |
Map3k21 |
T |
A |
8: 126,654,294 (GRCm39) |
I371N |
probably benign |
Het |
Mns1 |
G |
A |
9: 72,356,041 (GRCm39) |
|
probably null |
Het |
Myo3a |
A |
G |
2: 22,468,140 (GRCm39) |
T465A |
possibly damaging |
Het |
Nlrc4 |
A |
T |
17: 74,733,938 (GRCm39) |
S992T |
probably benign |
Het |
Notch4 |
G |
A |
17: 34,806,562 (GRCm39) |
G1833E |
possibly damaging |
Het |
Or52ad1 |
T |
A |
7: 102,995,316 (GRCm39) |
Y273F |
possibly damaging |
Het |
Or52n2 |
T |
C |
7: 104,542,110 (GRCm39) |
T242A |
probably damaging |
Het |
Or5g29 |
G |
A |
2: 85,420,985 (GRCm39) |
V34I |
probably benign |
Het |
Or5p5 |
A |
T |
7: 107,413,907 (GRCm39) |
I39L |
probably benign |
Het |
Or8a1b |
A |
T |
9: 37,622,993 (GRCm39) |
I194K |
possibly damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,741 (GRCm39) |
P143L |
probably damaging |
Het |
Pik3cd |
T |
A |
4: 149,747,660 (GRCm39) |
T28S |
probably damaging |
Het |
Pkd1 |
G |
T |
17: 24,795,566 (GRCm39) |
|
probably null |
Het |
Plk4 |
A |
T |
3: 40,760,252 (GRCm39) |
S383C |
possibly damaging |
Het |
Plxna2 |
T |
C |
1: 194,326,297 (GRCm39) |
L77P |
probably damaging |
Het |
Ppm1f |
T |
C |
16: 16,741,530 (GRCm39) |
S335P |
probably damaging |
Het |
Prr16 |
C |
T |
18: 51,436,349 (GRCm39) |
P276L |
probably damaging |
Het |
Rilp |
A |
G |
11: 75,401,759 (GRCm39) |
|
probably null |
Het |
Rspry1 |
A |
G |
8: 95,358,682 (GRCm39) |
|
probably null |
Het |
Serpinb9b |
T |
C |
13: 33,213,542 (GRCm39) |
V33A |
probably benign |
Het |
Slc4a10 |
C |
A |
2: 62,098,548 (GRCm39) |
Q561K |
probably damaging |
Het |
Smyd5 |
T |
C |
6: 85,415,118 (GRCm39) |
I42T |
possibly damaging |
Het |
Stk17b |
T |
C |
1: 53,800,241 (GRCm39) |
N246D |
probably damaging |
Het |
Suco |
T |
C |
1: 161,646,380 (GRCm39) |
|
probably null |
Het |
Tecpr1 |
C |
T |
5: 144,141,515 (GRCm39) |
V785M |
possibly damaging |
Het |
Telo2 |
C |
T |
17: 25,320,642 (GRCm39) |
V756I |
probably benign |
Het |
Tgm1 |
C |
T |
14: 55,943,034 (GRCm39) |
R602H |
probably benign |
Het |
Timeless |
A |
G |
10: 128,080,056 (GRCm39) |
T402A |
probably damaging |
Het |
Tnfaip2 |
T |
A |
12: 111,416,325 (GRCm39) |
|
probably null |
Het |
Trgc3 |
C |
A |
13: 19,445,164 (GRCm39) |
F37L |
probably damaging |
Het |
Trim5 |
A |
G |
7: 103,914,828 (GRCm39) |
S414P |
probably damaging |
Het |
Txnip |
A |
G |
3: 96,467,066 (GRCm39) |
T247A |
possibly damaging |
Het |
Vmn1r174 |
A |
T |
7: 23,454,050 (GRCm39) |
T239S |
probably damaging |
Het |
Vmn1r231 |
T |
A |
17: 21,110,212 (GRCm39) |
E234D |
probably damaging |
Het |
Zranb3 |
A |
T |
1: 127,887,480 (GRCm39) |
N982K |
probably benign |
Het |
|
Other mutations in Cyp1a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Cyp1a2
|
APN |
9 |
57,589,352 (GRCm39) |
nonsense |
probably null |
|
IGL01161:Cyp1a2
|
APN |
9 |
57,587,176 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01583:Cyp1a2
|
APN |
9 |
57,589,655 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01726:Cyp1a2
|
APN |
9 |
57,589,485 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01973:Cyp1a2
|
APN |
9 |
57,589,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02995:Cyp1a2
|
APN |
9 |
57,584,511 (GRCm39) |
makesense |
probably null |
|
IGL03349:Cyp1a2
|
APN |
9 |
57,587,158 (GRCm39) |
missense |
possibly damaging |
0.82 |
broadway
|
UTSW |
9 |
57,584,516 (GRCm39) |
nonsense |
probably null |
|
PIT4515001:Cyp1a2
|
UTSW |
9 |
57,589,242 (GRCm39) |
missense |
probably benign |
0.14 |
R0025:Cyp1a2
|
UTSW |
9 |
57,589,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Cyp1a2
|
UTSW |
9 |
57,589,308 (GRCm39) |
missense |
probably benign |
0.00 |
R0582:Cyp1a2
|
UTSW |
9 |
57,587,529 (GRCm39) |
splice site |
probably benign |
|
R0589:Cyp1a2
|
UTSW |
9 |
57,586,345 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1239:Cyp1a2
|
UTSW |
9 |
57,589,050 (GRCm39) |
missense |
probably benign |
0.02 |
R2156:Cyp1a2
|
UTSW |
9 |
57,589,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Cyp1a2
|
UTSW |
9 |
57,584,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Cyp1a2
|
UTSW |
9 |
57,587,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R3944:Cyp1a2
|
UTSW |
9 |
57,589,151 (GRCm39) |
missense |
probably benign |
|
R5225:Cyp1a2
|
UTSW |
9 |
57,584,516 (GRCm39) |
nonsense |
probably null |
|
R5419:Cyp1a2
|
UTSW |
9 |
57,589,794 (GRCm39) |
missense |
probably benign |
0.17 |
R5471:Cyp1a2
|
UTSW |
9 |
57,586,303 (GRCm39) |
missense |
probably damaging |
0.96 |
R5816:Cyp1a2
|
UTSW |
9 |
57,588,336 (GRCm39) |
missense |
probably benign |
|
R6017:Cyp1a2
|
UTSW |
9 |
57,588,313 (GRCm39) |
missense |
probably damaging |
0.98 |
R6825:Cyp1a2
|
UTSW |
9 |
57,584,543 (GRCm39) |
missense |
probably benign |
0.01 |
R6931:Cyp1a2
|
UTSW |
9 |
57,589,439 (GRCm39) |
missense |
probably benign |
0.02 |
R7058:Cyp1a2
|
UTSW |
9 |
57,584,525 (GRCm39) |
missense |
probably damaging |
0.99 |
R7079:Cyp1a2
|
UTSW |
9 |
57,589,161 (GRCm39) |
missense |
probably benign |
|
R7081:Cyp1a2
|
UTSW |
9 |
57,586,272 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7400:Cyp1a2
|
UTSW |
9 |
57,589,223 (GRCm39) |
missense |
probably benign |
0.37 |
R7672:Cyp1a2
|
UTSW |
9 |
57,589,620 (GRCm39) |
missense |
probably benign |
0.05 |
R8097:Cyp1a2
|
UTSW |
9 |
57,586,836 (GRCm39) |
splice site |
probably null |
|
R8879:Cyp1a2
|
UTSW |
9 |
57,589,168 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8926:Cyp1a2
|
UTSW |
9 |
57,588,361 (GRCm39) |
missense |
probably benign |
0.00 |
R9083:Cyp1a2
|
UTSW |
9 |
57,587,572 (GRCm39) |
missense |
probably benign |
0.01 |
R9206:Cyp1a2
|
UTSW |
9 |
57,589,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Cyp1a2
|
UTSW |
9 |
57,589,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:Cyp1a2
|
UTSW |
9 |
57,587,562 (GRCm39) |
missense |
probably benign |
0.07 |
RF007:Cyp1a2
|
UTSW |
9 |
57,589,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|