Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
T |
7: 120,032,796 (GRCm39) |
I272F |
possibly damaging |
Het |
Adcy10 |
G |
T |
1: 165,337,939 (GRCm39) |
M184I |
probably benign |
Het |
Aldoa |
G |
T |
7: 126,396,034 (GRCm39) |
T124N |
possibly damaging |
Het |
Ap4e1 |
T |
A |
2: 126,853,727 (GRCm39) |
I55N |
probably damaging |
Het |
Arhgap21 |
T |
C |
2: 20,870,198 (GRCm39) |
T913A |
probably benign |
Het |
Atrnl1 |
G |
A |
19: 58,030,784 (GRCm39) |
E1309K |
probably damaging |
Het |
BC034090 |
A |
T |
1: 155,117,777 (GRCm39) |
C114S |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,122,994 (GRCm39) |
|
probably null |
Het |
Ccn4 |
T |
A |
15: 66,784,879 (GRCm39) |
V184E |
probably damaging |
Het |
Ccna1 |
G |
T |
3: 54,953,120 (GRCm39) |
H408Q |
probably benign |
Het |
Cd209g |
T |
G |
8: 4,185,189 (GRCm39) |
|
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,219,905 (GRCm39) |
I433V |
probably benign |
Het |
Cdk2ap1 |
G |
A |
5: 124,492,421 (GRCm39) |
P5L |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,260,933 (GRCm39) |
E310G |
probably damaging |
Het |
Cflar |
G |
T |
1: 58,793,007 (GRCm39) |
V458F |
|
Het |
Clec4b2 |
A |
G |
6: 123,158,343 (GRCm39) |
T70A |
probably benign |
Het |
Cntnap5c |
A |
G |
17: 58,593,883 (GRCm39) |
T741A |
probably benign |
Het |
Csf3r |
A |
T |
4: 125,937,515 (GRCm39) |
T800S |
probably benign |
Het |
Csnk1g2 |
T |
C |
10: 80,473,733 (GRCm39) |
Y67H |
probably damaging |
Het |
Cyp2c67 |
A |
T |
19: 39,604,138 (GRCm39) |
V406E |
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,900,006 (GRCm39) |
D3868G |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,737,867 (GRCm39) |
|
probably null |
Het |
Dst |
A |
G |
1: 34,191,324 (GRCm39) |
N208S |
probably damaging |
Het |
Echdc3 |
A |
G |
2: 6,211,224 (GRCm39) |
|
probably null |
Het |
Edrf1 |
T |
C |
7: 133,239,578 (GRCm39) |
S13P |
probably benign |
Het |
Ephb1 |
T |
C |
9: 101,841,276 (GRCm39) |
Y734C |
probably damaging |
Het |
Eps8l1 |
A |
G |
7: 4,475,184 (GRCm39) |
Y325C |
probably damaging |
Het |
Evc2 |
A |
G |
5: 37,544,183 (GRCm39) |
D644G |
probably damaging |
Het |
Eya4 |
A |
C |
10: 23,048,943 (GRCm39) |
D54E |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,495 (GRCm39) |
S375G |
possibly damaging |
Het |
Fmo9 |
A |
G |
1: 166,505,189 (GRCm39) |
M68T |
probably benign |
Het |
Gemin5 |
G |
C |
11: 58,032,489 (GRCm39) |
P772A |
probably benign |
Het |
Gle1 |
T |
G |
2: 29,833,805 (GRCm39) |
C401G |
probably damaging |
Het |
Gm7298 |
A |
T |
6: 121,738,546 (GRCm39) |
I376F |
probably damaging |
Het |
Gpr35 |
A |
C |
1: 92,910,353 (GRCm39) |
I22L |
probably benign |
Het |
Grin2b |
T |
G |
6: 135,710,474 (GRCm39) |
D1024A |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,539,624 (GRCm39) |
N2956D |
probably damaging |
Het |
Htt |
T |
C |
5: 35,003,350 (GRCm39) |
L1275P |
probably damaging |
Het |
Ibtk |
T |
C |
9: 85,625,744 (GRCm39) |
D2G |
probably benign |
Het |
Il16 |
T |
A |
7: 83,295,659 (GRCm39) |
D1170V |
probably damaging |
Het |
Iqgap3 |
T |
A |
3: 88,024,217 (GRCm39) |
I1513N |
probably damaging |
Het |
Kiz |
T |
G |
2: 146,792,430 (GRCm39) |
|
probably null |
Het |
Krt12 |
A |
T |
11: 99,306,839 (GRCm39) |
*488K |
probably null |
Het |
Lap3 |
A |
T |
5: 45,654,290 (GRCm39) |
T83S |
probably benign |
Het |
Lars2 |
T |
A |
9: 123,261,058 (GRCm39) |
S410T |
probably damaging |
Het |
Limch1 |
A |
G |
5: 67,175,001 (GRCm39) |
T518A |
probably benign |
Het |
Lrrc49 |
A |
T |
9: 60,522,439 (GRCm39) |
S381T |
probably damaging |
Het |
Lrrk2 |
A |
G |
15: 91,618,258 (GRCm39) |
D919G |
possibly damaging |
Het |
Mmp1a |
A |
T |
9: 7,475,319 (GRCm39) |
S363C |
probably damaging |
Het |
Mrps22 |
A |
C |
9: 98,483,524 (GRCm39) |
|
probably null |
Het |
Mybpc3 |
T |
C |
2: 90,964,949 (GRCm39) |
I1066T |
probably benign |
Het |
Myo10 |
A |
T |
15: 25,724,011 (GRCm39) |
N215I |
probably damaging |
Het |
Myocd |
A |
C |
11: 65,109,474 (GRCm39) |
L99R |
probably damaging |
Het |
Nadk |
T |
G |
4: 155,673,793 (GRCm39) |
I394S |
probably damaging |
Het |
Nadsyn1 |
T |
C |
7: 143,364,952 (GRCm39) |
N251S |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Ncapd2 |
G |
A |
6: 125,153,633 (GRCm39) |
P694L |
probably benign |
Het |
Or2ag1 |
T |
A |
7: 106,473,075 (GRCm39) |
I126F |
probably damaging |
Het |
Or2w3b |
A |
C |
11: 58,623,571 (GRCm39) |
L140R |
probably damaging |
Het |
Or4a71 |
T |
C |
2: 89,357,901 (GRCm39) |
I284M |
probably damaging |
Het |
Or5t16 |
G |
T |
2: 86,819,164 (GRCm39) |
R119S |
probably damaging |
Het |
Pcdhb13 |
T |
A |
18: 37,576,309 (GRCm39) |
I229K |
probably damaging |
Het |
Pgbd5 |
A |
T |
8: 125,101,056 (GRCm39) |
M400K |
possibly damaging |
Het |
Phactr3 |
A |
G |
2: 177,944,529 (GRCm39) |
N409S |
probably damaging |
Het |
Pik3c2g |
C |
A |
6: 139,606,868 (GRCm39) |
P305Q |
probably damaging |
Het |
Pira12 |
A |
G |
7: 3,900,615 (GRCm39) |
V45A |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,802,870 (GRCm39) |
C250* |
probably null |
Het |
Pramel14 |
A |
C |
4: 143,718,103 (GRCm39) |
S447A |
probably benign |
Het |
Rapgef6 |
A |
C |
11: 54,548,191 (GRCm39) |
T792P |
possibly damaging |
Het |
Rexo5 |
A |
G |
7: 119,404,414 (GRCm39) |
D170G |
probably damaging |
Het |
Rnf17 |
G |
A |
14: 56,749,789 (GRCm39) |
|
probably null |
Het |
Septin11 |
A |
G |
5: 93,304,725 (GRCm39) |
I181V |
probably benign |
Het |
Serpina1e |
T |
G |
12: 103,913,277 (GRCm39) |
*414C |
probably null |
Het |
Serpine1 |
C |
A |
5: 137,099,918 (GRCm39) |
Q80H |
probably damaging |
Het |
Sh3bp2 |
A |
G |
5: 34,718,975 (GRCm39) |
N560S |
probably benign |
Het |
Slc25a25 |
A |
G |
2: 32,309,178 (GRCm39) |
F221S |
probably damaging |
Het |
Spag17 |
G |
T |
3: 99,934,717 (GRCm39) |
|
probably null |
Het |
Sspn |
T |
C |
6: 145,906,881 (GRCm39) |
L104P |
probably damaging |
Het |
St18 |
A |
C |
1: 6,903,818 (GRCm39) |
E693A |
probably damaging |
Het |
St6galnac3 |
T |
C |
3: 153,117,169 (GRCm39) |
I185V |
possibly damaging |
Het |
St8sia1 |
T |
C |
6: 142,822,395 (GRCm39) |
D156G |
probably damaging |
Het |
Syne2 |
C |
A |
12: 76,052,152 (GRCm39) |
S4092R |
probably benign |
Het |
Tll1 |
T |
A |
8: 64,577,979 (GRCm39) |
D76V |
possibly damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,022 (GRCm39) |
|
probably benign |
Het |
Tnfaip3 |
T |
A |
10: 18,883,029 (GRCm39) |
T179S |
probably benign |
Het |
Trav16 |
T |
C |
14: 53,981,096 (GRCm39) |
I95T |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,771,435 (GRCm39) |
S280T |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,108,885 (GRCm39) |
M2166V |
probably benign |
Het |
Vmn2r1 |
A |
G |
3: 63,997,362 (GRCm39) |
I339M |
probably damaging |
Het |
Vwa5b1 |
A |
G |
4: 138,332,742 (GRCm39) |
|
probably null |
Het |
Washc4 |
A |
T |
10: 83,409,638 (GRCm39) |
|
probably null |
Het |
Wiz |
A |
G |
17: 32,576,602 (GRCm39) |
S642P |
possibly damaging |
Het |
Zeb2 |
T |
A |
2: 45,000,053 (GRCm39) |
K60N |
possibly damaging |
Het |
Zfat |
T |
A |
15: 68,050,631 (GRCm39) |
T797S |
probably benign |
Het |
Zfp74 |
T |
C |
7: 29,634,590 (GRCm39) |
K373E |
probably damaging |
Het |
Zswim5 |
T |
C |
4: 116,833,173 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Pik3r4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01375:Pik3r4
|
APN |
9 |
105,521,803 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01617:Pik3r4
|
APN |
9 |
105,532,164 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01764:Pik3r4
|
APN |
9 |
105,562,321 (GRCm39) |
splice site |
probably benign |
|
IGL01817:Pik3r4
|
APN |
9 |
105,528,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01830:Pik3r4
|
APN |
9 |
105,522,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01905:Pik3r4
|
APN |
9 |
105,522,077 (GRCm39) |
nonsense |
probably null |
|
IGL01947:Pik3r4
|
APN |
9 |
105,563,349 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01985:Pik3r4
|
APN |
9 |
105,540,244 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02321:Pik3r4
|
APN |
9 |
105,521,677 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02389:Pik3r4
|
APN |
9 |
105,527,530 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02898:Pik3r4
|
APN |
9 |
105,527,605 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03037:Pik3r4
|
APN |
9 |
105,528,012 (GRCm39) |
missense |
probably damaging |
1.00 |
boteh
|
UTSW |
9 |
105,545,137 (GRCm39) |
splice site |
probably null |
|
truth
|
UTSW |
9 |
105,527,805 (GRCm39) |
missense |
probably damaging |
0.98 |
verisimilitude
|
UTSW |
9 |
105,555,352 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02835:Pik3r4
|
UTSW |
9 |
105,549,905 (GRCm39) |
missense |
probably benign |
0.07 |
R0011:Pik3r4
|
UTSW |
9 |
105,521,836 (GRCm39) |
missense |
probably benign |
0.01 |
R0312:Pik3r4
|
UTSW |
9 |
105,563,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R0321:Pik3r4
|
UTSW |
9 |
105,525,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Pik3r4
|
UTSW |
9 |
105,546,244 (GRCm39) |
missense |
probably benign |
0.04 |
R0645:Pik3r4
|
UTSW |
9 |
105,546,386 (GRCm39) |
splice site |
probably benign |
|
R0690:Pik3r4
|
UTSW |
9 |
105,531,175 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0789:Pik3r4
|
UTSW |
9 |
105,562,366 (GRCm39) |
missense |
probably benign |
0.14 |
R0894:Pik3r4
|
UTSW |
9 |
105,544,970 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0988:Pik3r4
|
UTSW |
9 |
105,564,404 (GRCm39) |
missense |
probably damaging |
0.97 |
R1123:Pik3r4
|
UTSW |
9 |
105,540,328 (GRCm39) |
missense |
probably benign |
|
R1172:Pik3r4
|
UTSW |
9 |
105,540,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1174:Pik3r4
|
UTSW |
9 |
105,540,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1342:Pik3r4
|
UTSW |
9 |
105,528,100 (GRCm39) |
critical splice donor site |
probably null |
|
R1387:Pik3r4
|
UTSW |
9 |
105,521,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1480:Pik3r4
|
UTSW |
9 |
105,564,443 (GRCm39) |
missense |
probably benign |
0.39 |
R1638:Pik3r4
|
UTSW |
9 |
105,564,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1643:Pik3r4
|
UTSW |
9 |
105,564,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1995:Pik3r4
|
UTSW |
9 |
105,546,364 (GRCm39) |
missense |
probably benign |
0.12 |
R2037:Pik3r4
|
UTSW |
9 |
105,527,534 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Pik3r4
|
UTSW |
9 |
105,549,984 (GRCm39) |
missense |
probably benign |
0.05 |
R4210:Pik3r4
|
UTSW |
9 |
105,527,957 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4515:Pik3r4
|
UTSW |
9 |
105,549,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4519:Pik3r4
|
UTSW |
9 |
105,549,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4630:Pik3r4
|
UTSW |
9 |
105,532,098 (GRCm39) |
missense |
probably benign |
0.06 |
R4632:Pik3r4
|
UTSW |
9 |
105,532,098 (GRCm39) |
missense |
probably benign |
0.06 |
R4732:Pik3r4
|
UTSW |
9 |
105,555,375 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4733:Pik3r4
|
UTSW |
9 |
105,555,375 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4940:Pik3r4
|
UTSW |
9 |
105,546,193 (GRCm39) |
missense |
probably benign |
0.20 |
R5120:Pik3r4
|
UTSW |
9 |
105,546,208 (GRCm39) |
missense |
probably benign |
0.30 |
R5169:Pik3r4
|
UTSW |
9 |
105,555,360 (GRCm39) |
missense |
probably benign |
0.14 |
R5183:Pik3r4
|
UTSW |
9 |
105,559,507 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5353:Pik3r4
|
UTSW |
9 |
105,545,137 (GRCm39) |
splice site |
probably null |
|
R5463:Pik3r4
|
UTSW |
9 |
105,525,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Pik3r4
|
UTSW |
9 |
105,545,024 (GRCm39) |
missense |
probably benign |
0.01 |
R5763:Pik3r4
|
UTSW |
9 |
105,546,974 (GRCm39) |
missense |
probably benign |
0.01 |
R5830:Pik3r4
|
UTSW |
9 |
105,522,023 (GRCm39) |
nonsense |
probably null |
|
R6251:Pik3r4
|
UTSW |
9 |
105,531,247 (GRCm39) |
missense |
probably benign |
|
R6468:Pik3r4
|
UTSW |
9 |
105,562,389 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6611:Pik3r4
|
UTSW |
9 |
105,521,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R6642:Pik3r4
|
UTSW |
9 |
105,521,845 (GRCm39) |
missense |
probably benign |
0.11 |
R6821:Pik3r4
|
UTSW |
9 |
105,527,805 (GRCm39) |
missense |
probably damaging |
0.98 |
R7039:Pik3r4
|
UTSW |
9 |
105,554,089 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7410:Pik3r4
|
UTSW |
9 |
105,527,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R7559:Pik3r4
|
UTSW |
9 |
105,555,352 (GRCm39) |
missense |
probably benign |
0.17 |
R7561:Pik3r4
|
UTSW |
9 |
105,564,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7658:Pik3r4
|
UTSW |
9 |
105,521,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R7727:Pik3r4
|
UTSW |
9 |
105,547,081 (GRCm39) |
missense |
probably damaging |
0.99 |
R7871:Pik3r4
|
UTSW |
9 |
105,540,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7957:Pik3r4
|
UTSW |
9 |
105,564,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8138:Pik3r4
|
UTSW |
9 |
105,546,234 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8686:Pik3r4
|
UTSW |
9 |
105,535,728 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8719:Pik3r4
|
UTSW |
9 |
105,559,394 (GRCm39) |
missense |
probably benign |
0.00 |
R9091:Pik3r4
|
UTSW |
9 |
105,547,108 (GRCm39) |
missense |
probably benign |
0.35 |
R9189:Pik3r4
|
UTSW |
9 |
105,547,038 (GRCm39) |
missense |
probably benign |
0.22 |
R9270:Pik3r4
|
UTSW |
9 |
105,547,108 (GRCm39) |
missense |
probably benign |
0.35 |
R9439:Pik3r4
|
UTSW |
9 |
105,528,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|