Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
T |
5: 114,379,982 (GRCm39) |
|
probably null |
Het |
Acsm3 |
G |
T |
7: 119,373,094 (GRCm39) |
W199L |
probably damaging |
Het |
Arap1 |
T |
A |
7: 101,034,778 (GRCm39) |
D236E |
probably benign |
Het |
Arhgap1 |
T |
C |
2: 91,498,582 (GRCm39) |
Y160H |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,045,247 (GRCm39) |
|
probably benign |
Het |
Cdc25a |
A |
G |
9: 109,718,801 (GRCm39) |
E334G |
probably damaging |
Het |
Ciz1 |
C |
T |
2: 32,260,111 (GRCm39) |
T219M |
possibly damaging |
Het |
Cluap1 |
A |
C |
16: 3,751,586 (GRCm39) |
D315A |
possibly damaging |
Het |
Cps1 |
T |
C |
1: 67,210,154 (GRCm39) |
|
probably null |
Het |
Cul2 |
T |
C |
18: 3,434,856 (GRCm39) |
S668P |
probably damaging |
Het |
Fah |
T |
A |
7: 84,248,344 (GRCm39) |
T125S |
probably damaging |
Het |
Fam221a |
G |
A |
6: 49,355,366 (GRCm39) |
C156Y |
probably damaging |
Het |
Gm6158 |
G |
T |
14: 24,120,362 (GRCm39) |
|
noncoding transcript |
Het |
Hbq1b |
T |
A |
11: 32,237,295 (GRCm39) |
V63E |
probably damaging |
Het |
Ighv6-5 |
G |
A |
12: 114,380,337 (GRCm39) |
T79I |
possibly damaging |
Het |
Kif12 |
G |
A |
4: 63,089,455 (GRCm39) |
T99M |
probably damaging |
Het |
Kif1a |
T |
A |
1: 92,996,272 (GRCm39) |
K298M |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lama1 |
A |
G |
17: 68,080,707 (GRCm39) |
Q1245R |
probably benign |
Het |
Marchf4 |
G |
A |
1: 72,467,973 (GRCm39) |
P353L |
probably benign |
Het |
Nadk |
A |
T |
4: 155,667,032 (GRCm39) |
|
probably benign |
Het |
Ncoa2 |
T |
C |
1: 13,247,389 (GRCm39) |
T345A |
probably damaging |
Het |
Niban3 |
A |
G |
8: 72,060,155 (GRCm39) |
|
probably benign |
Het |
Nsun6 |
T |
A |
2: 15,001,333 (GRCm39) |
M408L |
probably benign |
Het |
Nuak1 |
T |
A |
10: 84,229,908 (GRCm39) |
E155V |
probably damaging |
Het |
Oosp1 |
C |
T |
19: 11,645,158 (GRCm39) |
V169I |
possibly damaging |
Het |
Or13c7c |
C |
T |
4: 43,836,124 (GRCm39) |
R122H |
probably benign |
Het |
Or2t26 |
T |
A |
11: 49,039,842 (GRCm39) |
Y253N |
probably damaging |
Het |
Or5ae2 |
T |
C |
7: 84,505,756 (GRCm39) |
Y60H |
probably damaging |
Het |
Or5p81 |
T |
A |
7: 108,267,460 (GRCm39) |
V279E |
probably damaging |
Het |
Pabpc2 |
T |
C |
18: 39,908,238 (GRCm39) |
V501A |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,484,516 (GRCm39) |
V2013A |
probably benign |
Het |
Psmd1 |
T |
A |
1: 86,055,914 (GRCm39) |
S759T |
possibly damaging |
Het |
Scgb1b2 |
T |
A |
7: 30,990,089 (GRCm39) |
K86N |
possibly damaging |
Het |
Sdk1 |
T |
C |
5: 142,080,381 (GRCm39) |
I1291T |
probably damaging |
Het |
Skint5 |
T |
C |
4: 113,341,090 (GRCm39) |
Y1396C |
probably benign |
Het |
Slc24a3 |
A |
G |
2: 145,448,746 (GRCm39) |
E380G |
probably benign |
Het |
Spock1 |
A |
G |
13: 57,588,263 (GRCm39) |
S270P |
probably damaging |
Het |
Tmem128 |
T |
C |
5: 38,419,418 (GRCm39) |
S57P |
probably damaging |
Het |
Tmem186 |
G |
A |
16: 8,453,887 (GRCm39) |
R125W |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 18,882,758 (GRCm39) |
S220P |
probably damaging |
Het |
Usp45 |
T |
C |
4: 21,830,505 (GRCm39) |
|
probably null |
Het |
Usp5 |
C |
T |
6: 124,795,437 (GRCm39) |
|
probably null |
Het |
Vmn1r35 |
A |
T |
6: 66,656,573 (GRCm39) |
C32* |
probably null |
Het |
Vmn2r112 |
T |
A |
17: 22,820,303 (GRCm39) |
F59I |
probably benign |
Het |
Wfdc9 |
A |
T |
2: 164,492,458 (GRCm39) |
S56R |
probably benign |
Het |
Zfp369 |
A |
G |
13: 65,444,806 (GRCm39) |
I650V |
probably benign |
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 |
IGL03339:Pik3c2a
|
APN |
7 |
116,017,256 (GRCm39) |
missense |
possibly damaging |
0.57 |
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 |
|
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 |
|