Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
A |
G |
2: 152,284,376 (GRCm39) |
E323G |
probably damaging |
Het |
A4gnt |
T |
C |
9: 99,502,601 (GRCm39) |
S254P |
probably damaging |
Het |
Actn4 |
A |
G |
7: 28,601,407 (GRCm39) |
L447P |
probably damaging |
Het |
Agbl2 |
C |
A |
2: 90,627,907 (GRCm39) |
S237R |
probably damaging |
Het |
Apc |
G |
A |
18: 34,431,527 (GRCm39) |
D309N |
probably damaging |
Het |
Arhgef3 |
A |
G |
14: 27,123,814 (GRCm39) |
M492V |
probably damaging |
Het |
Atp10b |
T |
A |
11: 43,121,442 (GRCm39) |
M1035K |
probably null |
Het |
Cfap69 |
T |
A |
5: 5,636,436 (GRCm39) |
|
probably benign |
Het |
Ctf1 |
A |
G |
7: 127,313,166 (GRCm39) |
N24S |
probably benign |
Het |
Cx3cr1 |
T |
A |
9: 119,880,503 (GRCm39) |
K300* |
probably null |
Het |
Ddx25 |
A |
T |
9: 35,453,299 (GRCm39) |
Y484N |
probably damaging |
Het |
Eif4g1 |
A |
G |
16: 20,499,734 (GRCm39) |
E506G |
possibly damaging |
Het |
Ficd |
G |
T |
5: 113,876,800 (GRCm39) |
R325L |
probably benign |
Het |
G6pc2 |
A |
G |
2: 69,051,239 (GRCm39) |
|
probably benign |
Het |
Gm11168 |
C |
A |
9: 3,004,767 (GRCm39) |
P103T |
probably benign |
Het |
Hbb-y |
A |
T |
7: 103,501,976 (GRCm39) |
H98Q |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,577,720 (GRCm39) |
S2014P |
probably benign |
Het |
Hoxc5 |
T |
C |
15: 102,922,568 (GRCm39) |
Y19H |
probably damaging |
Het |
Igfbpl1 |
A |
G |
4: 45,813,555 (GRCm39) |
|
probably benign |
Het |
Ighg2c |
A |
C |
12: 113,251,614 (GRCm39) |
V171G |
unknown |
Het |
Kctd13 |
A |
G |
7: 126,544,190 (GRCm39) |
D296G |
probably benign |
Het |
Mfsd2b |
A |
C |
12: 4,924,335 (GRCm39) |
M1R |
probably null |
Het |
Nipbl |
A |
G |
15: 8,380,360 (GRCm39) |
S811P |
probably benign |
Het |
Or10al2 |
G |
A |
17: 37,983,448 (GRCm39) |
C178Y |
possibly damaging |
Het |
Or10al3 |
G |
T |
17: 38,011,682 (GRCm39) |
M40I |
probably damaging |
Het |
Or52r1 |
G |
A |
7: 102,536,989 (GRCm39) |
R124C |
probably benign |
Het |
Or5b122 |
T |
G |
19: 13,563,439 (GRCm39) |
M257R |
probably damaging |
Het |
Pcolce2 |
T |
C |
9: 95,560,393 (GRCm39) |
|
probably benign |
Het |
Ppp1r18 |
A |
G |
17: 36,178,938 (GRCm39) |
D271G |
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,333,830 (GRCm39) |
I3013T |
probably damaging |
Het |
Rock1 |
A |
T |
18: 10,097,493 (GRCm39) |
M765K |
probably benign |
Het |
Sec16a |
T |
C |
2: 26,325,945 (GRCm39) |
Y1244C |
probably benign |
Het |
Taar7d |
T |
C |
10: 23,903,204 (GRCm39) |
C29R |
possibly damaging |
Het |
Tlcd4 |
C |
T |
3: 121,022,489 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
C |
2: 76,572,264 (GRCm39) |
F26210V |
probably damaging |
Het |
Ube2b |
A |
T |
11: 51,877,534 (GRCm39) |
V145D |
probably damaging |
Het |
Vmn1r219 |
T |
G |
13: 23,347,580 (GRCm39) |
S256R |
possibly damaging |
Het |
|
Other mutations in Pik3c2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Pik3c2a
|
APN |
7 |
115,975,518 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL00732:Pik3c2a
|
APN |
7 |
115,963,735 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01303:Pik3c2a
|
APN |
7 |
115,973,038 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01443:Pik3c2a
|
APN |
7 |
116,017,429 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01462:Pik3c2a
|
APN |
7 |
115,975,485 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01641:Pik3c2a
|
APN |
7 |
115,950,000 (GRCm39) |
intron |
probably benign |
|
IGL01695:Pik3c2a
|
APN |
7 |
116,016,753 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02095:Pik3c2a
|
APN |
7 |
115,945,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02137:Pik3c2a
|
APN |
7 |
115,950,039 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02160:Pik3c2a
|
APN |
7 |
115,987,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02224:Pik3c2a
|
APN |
7 |
115,962,575 (GRCm39) |
splice site |
probably benign |
|
IGL02345:Pik3c2a
|
APN |
7 |
116,005,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02644:Pik3c2a
|
APN |
7 |
115,972,049 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02756:Pik3c2a
|
APN |
7 |
115,963,748 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03412:Pik3c2a
|
APN |
7 |
116,017,074 (GRCm39) |
missense |
probably benign |
0.21 |
R0046:Pik3c2a
|
UTSW |
7 |
115,953,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Pik3c2a
|
UTSW |
7 |
115,972,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R0501:Pik3c2a
|
UTSW |
7 |
115,953,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Pik3c2a
|
UTSW |
7 |
115,945,482 (GRCm39) |
splice site |
probably benign |
|
R0991:Pik3c2a
|
UTSW |
7 |
115,961,280 (GRCm39) |
critical splice donor site |
probably null |
|
R1074:Pik3c2a
|
UTSW |
7 |
115,950,160 (GRCm39) |
nonsense |
probably null |
|
R1485:Pik3c2a
|
UTSW |
7 |
116,016,908 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1495:Pik3c2a
|
UTSW |
7 |
115,987,300 (GRCm39) |
missense |
probably benign |
0.01 |
R1510:Pik3c2a
|
UTSW |
7 |
115,987,280 (GRCm39) |
missense |
probably benign |
0.00 |
R1654:Pik3c2a
|
UTSW |
7 |
115,968,083 (GRCm39) |
missense |
probably benign |
0.02 |
R1711:Pik3c2a
|
UTSW |
7 |
116,017,162 (GRCm39) |
nonsense |
probably null |
|
R1733:Pik3c2a
|
UTSW |
7 |
116,017,755 (GRCm39) |
start codon destroyed |
possibly damaging |
0.96 |
R1751:Pik3c2a
|
UTSW |
7 |
115,945,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R1812:Pik3c2a
|
UTSW |
7 |
116,016,899 (GRCm39) |
missense |
probably damaging |
0.98 |
R1817:Pik3c2a
|
UTSW |
7 |
115,975,747 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Pik3c2a
|
UTSW |
7 |
115,967,352 (GRCm39) |
missense |
probably benign |
|
R1875:Pik3c2a
|
UTSW |
7 |
116,017,206 (GRCm39) |
missense |
probably benign |
0.35 |
R1995:Pik3c2a
|
UTSW |
7 |
115,953,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Pik3c2a
|
UTSW |
7 |
115,941,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Pik3c2a
|
UTSW |
7 |
115,963,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Pik3c2a
|
UTSW |
7 |
115,950,166 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2014:Pik3c2a
|
UTSW |
7 |
115,950,166 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2015:Pik3c2a
|
UTSW |
7 |
115,950,166 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2027:Pik3c2a
|
UTSW |
7 |
115,950,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Pik3c2a
|
UTSW |
7 |
116,016,686 (GRCm39) |
critical splice donor site |
probably null |
|
R2068:Pik3c2a
|
UTSW |
7 |
115,972,126 (GRCm39) |
nonsense |
probably null |
|
R3814:Pik3c2a
|
UTSW |
7 |
115,947,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Pik3c2a
|
UTSW |
7 |
115,963,785 (GRCm39) |
nonsense |
probably null |
|
R4386:Pik3c2a
|
UTSW |
7 |
115,953,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Pik3c2a
|
UTSW |
7 |
115,957,923 (GRCm39) |
missense |
probably benign |
0.16 |
R4783:Pik3c2a
|
UTSW |
7 |
116,017,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Pik3c2a
|
UTSW |
7 |
115,939,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Pik3c2a
|
UTSW |
7 |
115,939,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Pik3c2a
|
UTSW |
7 |
115,975,518 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5080:Pik3c2a
|
UTSW |
7 |
115,947,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R5083:Pik3c2a
|
UTSW |
7 |
115,941,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R5144:Pik3c2a
|
UTSW |
7 |
115,950,021 (GRCm39) |
missense |
probably benign |
0.01 |
R5589:Pik3c2a
|
UTSW |
7 |
116,016,893 (GRCm39) |
missense |
probably benign |
0.02 |
R5646:Pik3c2a
|
UTSW |
7 |
116,005,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Pik3c2a
|
UTSW |
7 |
115,972,049 (GRCm39) |
missense |
probably benign |
0.00 |
R5951:Pik3c2a
|
UTSW |
7 |
115,967,419 (GRCm39) |
missense |
probably damaging |
0.96 |
R5958:Pik3c2a
|
UTSW |
7 |
115,961,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6356:Pik3c2a
|
UTSW |
7 |
115,947,440 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6551:Pik3c2a
|
UTSW |
7 |
116,016,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R6641:Pik3c2a
|
UTSW |
7 |
115,939,460 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6661:Pik3c2a
|
UTSW |
7 |
115,967,993 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6789:Pik3c2a
|
UTSW |
7 |
115,961,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6874:Pik3c2a
|
UTSW |
7 |
115,993,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R6985:Pik3c2a
|
UTSW |
7 |
116,017,223 (GRCm39) |
missense |
probably damaging |
0.98 |
R7106:Pik3c2a
|
UTSW |
7 |
116,017,368 (GRCm39) |
nonsense |
probably null |
|
R7153:Pik3c2a
|
UTSW |
7 |
115,941,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Pik3c2a
|
UTSW |
7 |
115,987,331 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7265:Pik3c2a
|
UTSW |
7 |
115,987,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Pik3c2a
|
UTSW |
7 |
116,005,178 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Pik3c2a
|
UTSW |
7 |
115,973,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Pik3c2a
|
UTSW |
7 |
115,975,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R7406:Pik3c2a
|
UTSW |
7 |
115,953,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Pik3c2a
|
UTSW |
7 |
115,972,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R7528:Pik3c2a
|
UTSW |
7 |
115,993,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Pik3c2a
|
UTSW |
7 |
115,939,331 (GRCm39) |
missense |
probably damaging |
0.97 |
R7684:Pik3c2a
|
UTSW |
7 |
115,987,312 (GRCm39) |
nonsense |
probably null |
|
R7737:Pik3c2a
|
UTSW |
7 |
115,955,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R7739:Pik3c2a
|
UTSW |
7 |
115,993,529 (GRCm39) |
missense |
probably benign |
0.26 |
R7852:Pik3c2a
|
UTSW |
7 |
116,016,693 (GRCm39) |
missense |
probably benign |
|
R7922:Pik3c2a
|
UTSW |
7 |
115,990,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7956:Pik3c2a
|
UTSW |
7 |
115,949,350 (GRCm39) |
missense |
probably benign |
0.01 |
R8005:Pik3c2a
|
UTSW |
7 |
116,017,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Pik3c2a
|
UTSW |
7 |
115,942,232 (GRCm39) |
missense |
probably benign |
0.00 |
R8329:Pik3c2a
|
UTSW |
7 |
116,017,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Pik3c2a
|
UTSW |
7 |
116,017,584 (GRCm39) |
missense |
probably damaging |
0.96 |
R8736:Pik3c2a
|
UTSW |
7 |
115,975,464 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8812:Pik3c2a
|
UTSW |
7 |
115,951,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Pik3c2a
|
UTSW |
7 |
116,017,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Pik3c2a
|
UTSW |
7 |
115,987,320 (GRCm39) |
missense |
probably benign |
0.19 |
R9105:Pik3c2a
|
UTSW |
7 |
115,972,049 (GRCm39) |
missense |
probably benign |
0.00 |
R9111:Pik3c2a
|
UTSW |
7 |
115,993,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R9152:Pik3c2a
|
UTSW |
7 |
116,017,004 (GRCm39) |
missense |
probably benign |
0.30 |
R9241:Pik3c2a
|
UTSW |
7 |
116,017,115 (GRCm39) |
missense |
probably benign |
0.02 |
R9301:Pik3c2a
|
UTSW |
7 |
115,945,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R9325:Pik3c2a
|
UTSW |
7 |
115,990,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R9482:Pik3c2a
|
UTSW |
7 |
115,961,289 (GRCm39) |
missense |
probably benign |
0.04 |
R9513:Pik3c2a
|
UTSW |
7 |
115,939,321 (GRCm39) |
missense |
probably benign |
0.06 |
R9569:Pik3c2a
|
UTSW |
7 |
115,957,939 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9758:Pik3c2a
|
UTSW |
7 |
115,945,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|