Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts15 |
T |
A |
9: 30,833,433 (GRCm39) |
D34V |
probably benign |
Het |
Adgrf1 |
A |
T |
17: 43,632,112 (GRCm39) |
R884* |
probably null |
Het |
Adgrg7 |
T |
C |
16: 56,582,236 (GRCm39) |
T301A |
probably benign |
Het |
Arhgef17 |
A |
G |
7: 100,530,988 (GRCm39) |
I1366T |
probably damaging |
Het |
C1s2 |
A |
T |
6: 124,612,048 (GRCm39) |
L112H |
probably damaging |
Het |
C2cd6 |
A |
T |
1: 59,042,391 (GRCm39) |
|
noncoding transcript |
Het |
Cfap74 |
G |
A |
4: 155,504,724 (GRCm39) |
R103H |
possibly damaging |
Het |
Col7a1 |
A |
T |
9: 108,797,943 (GRCm39) |
|
probably null |
Het |
Dmp1 |
A |
G |
5: 104,360,706 (GRCm39) |
S461G |
probably damaging |
Het |
Eif4g2 |
A |
T |
7: 110,673,405 (GRCm39) |
D753E |
probably benign |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Etv4 |
T |
C |
11: 101,665,063 (GRCm39) |
D130G |
probably damaging |
Het |
Gabbr2 |
A |
T |
4: 46,734,119 (GRCm39) |
I533N |
probably damaging |
Het |
Gne |
T |
C |
4: 44,055,273 (GRCm39) |
E234G |
probably benign |
Het |
Itga6 |
C |
A |
2: 71,647,025 (GRCm39) |
N78K |
probably benign |
Het |
Lap3 |
C |
T |
5: 45,650,899 (GRCm39) |
T33M |
probably benign |
Het |
Limd1 |
A |
G |
9: 123,308,564 (GRCm39) |
S88G |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,380,385 (GRCm39) |
T3922K |
probably damaging |
Het |
Map4k3 |
A |
G |
17: 80,971,517 (GRCm39) |
|
probably benign |
Het |
Mib1 |
T |
C |
18: 10,812,118 (GRCm39) |
L263S |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,216,427 (GRCm39) |
S1474G |
probably benign |
Het |
Nkapl |
A |
C |
13: 21,651,607 (GRCm39) |
S335R |
probably damaging |
Het |
Nrg3 |
A |
G |
14: 38,092,771 (GRCm39) |
S605P |
probably damaging |
Het |
Or10x4 |
G |
T |
1: 174,218,995 (GRCm39) |
R120L |
possibly damaging |
Het |
Or52b3 |
A |
G |
7: 102,204,151 (GRCm39) |
Y220C |
probably damaging |
Het |
Patj |
G |
A |
4: 98,344,406 (GRCm39) |
D577N |
probably damaging |
Het |
Pfpl |
A |
C |
19: 12,407,319 (GRCm39) |
K523N |
possibly damaging |
Het |
Pkd2l1 |
C |
A |
19: 44,144,403 (GRCm39) |
R278L |
probably benign |
Het |
Prss2 |
A |
T |
6: 41,500,910 (GRCm39) |
I108F |
probably damaging |
Het |
Rnase2b |
A |
G |
14: 51,400,347 (GRCm39) |
T143A |
possibly damaging |
Het |
Sgk1 |
C |
T |
10: 21,872,500 (GRCm39) |
R171W |
probably damaging |
Het |
Sphk2 |
A |
T |
7: 45,360,437 (GRCm39) |
H522Q |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,235,261 (GRCm39) |
|
probably null |
Het |
Tmem88 |
C |
A |
11: 69,288,602 (GRCm39) |
A106S |
probably damaging |
Het |
Trappc14 |
C |
A |
5: 138,259,191 (GRCm39) |
C434F |
probably damaging |
Het |
Trim39 |
A |
G |
17: 36,574,646 (GRCm39) |
L252S |
possibly damaging |
Het |
Trim60 |
T |
A |
8: 65,453,975 (GRCm39) |
E91D |
probably damaging |
Het |
Trpm5 |
A |
G |
7: 142,641,475 (GRCm39) |
I145T |
possibly damaging |
Het |
Vmn2r107 |
A |
T |
17: 20,595,729 (GRCm39) |
M761L |
probably benign |
Het |
Wdr4 |
G |
A |
17: 31,719,584 (GRCm39) |
|
probably benign |
Het |
Wfs1 |
A |
T |
5: 37,125,653 (GRCm39) |
S413T |
probably damaging |
Het |
Wnt2 |
A |
T |
6: 18,030,208 (GRCm39) |
W27R |
probably damaging |
Het |
Zc3h3 |
A |
T |
15: 75,651,158 (GRCm39) |
H687Q |
probably damaging |
Het |
Zfp750 |
G |
A |
11: 121,403,951 (GRCm39) |
P308L |
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 |
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 |
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 |
|