Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
A |
8: 25,157,639 (GRCm39) |
I104F |
probably benign |
Het |
Adgrg7 |
C |
T |
16: 56,590,674 (GRCm39) |
V166I |
probably benign |
Het |
Agfg1 |
G |
T |
1: 82,859,966 (GRCm39) |
V278L |
probably benign |
Het |
Alpk3 |
A |
G |
7: 80,742,328 (GRCm39) |
E715G |
possibly damaging |
Het |
Ap2m1 |
A |
G |
16: 20,362,095 (GRCm39) |
Y401C |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,101,960 (GRCm39) |
S838N |
probably benign |
Het |
Ash2l |
A |
T |
8: 26,317,233 (GRCm39) |
Y373* |
probably null |
Het |
Best2 |
C |
T |
8: 85,734,393 (GRCm39) |
V442I |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,475,542 (GRCm39) |
|
probably null |
Het |
Fat2 |
T |
A |
11: 55,175,856 (GRCm39) |
D1619V |
probably damaging |
Het |
Fer1l6 |
A |
T |
15: 58,499,446 (GRCm39) |
N1272I |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,417,995 (GRCm39) |
*779C |
probably null |
Het |
Gm12216 |
G |
A |
11: 53,750,077 (GRCm39) |
|
probably benign |
Het |
Grm2 |
C |
T |
9: 106,524,370 (GRCm39) |
V311I |
|
Het |
Immt |
T |
A |
6: 71,851,689 (GRCm39) |
D683E |
probably benign |
Het |
Itga8 |
T |
G |
2: 12,237,712 (GRCm39) |
D336A |
probably damaging |
Het |
Jhy |
T |
C |
9: 40,872,453 (GRCm39) |
T19A |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,776,885 (GRCm39) |
M1V |
probably null |
Het |
Kctd17 |
A |
T |
15: 78,317,214 (GRCm39) |
I117F |
probably damaging |
Het |
Lrp6 |
T |
C |
6: 134,484,364 (GRCm39) |
T420A |
probably damaging |
Het |
Manba |
T |
C |
3: 135,223,673 (GRCm39) |
S187P |
probably damaging |
Het |
Mef2b |
A |
T |
8: 70,616,938 (GRCm39) |
D13V |
probably damaging |
Het |
Mical2 |
T |
C |
7: 111,902,963 (GRCm39) |
F145L |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,922,497 (GRCm39) |
D551E |
possibly damaging |
Het |
Mplkipl1 |
A |
G |
19: 61,163,973 (GRCm39) |
V154A |
possibly damaging |
Het |
Myo10 |
C |
G |
15: 25,783,067 (GRCm39) |
R1170G |
probably damaging |
Het |
Myo16 |
A |
C |
8: 10,322,687 (GRCm39) |
Q39P |
unknown |
Het |
Myo1f |
A |
G |
17: 33,820,668 (GRCm39) |
E837G |
probably benign |
Het |
Nell2 |
T |
A |
15: 95,333,274 (GRCm39) |
I128F |
possibly damaging |
Het |
Or1i2 |
A |
G |
10: 78,448,448 (GRCm39) |
V9A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,215,222 (GRCm39) |
R659* |
probably null |
Het |
Pcdhga1 |
A |
G |
18: 37,973,028 (GRCm39) |
Q881R |
possibly damaging |
Het |
Plekhm2 |
T |
G |
4: 141,369,770 (GRCm39) |
E75A |
possibly damaging |
Het |
Prc1 |
A |
G |
7: 79,957,405 (GRCm39) |
K357E |
possibly damaging |
Het |
Pxk |
T |
A |
14: 8,146,220 (GRCm38) |
C377S |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,176,488 (GRCm39) |
E1696G |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 122,600,590 (GRCm39) |
S1532R |
unknown |
Het |
Scn5a |
G |
T |
9: 119,391,626 (GRCm39) |
A22E |
probably benign |
Het |
Sctr |
G |
A |
1: 119,949,955 (GRCm39) |
R48Q |
probably benign |
Het |
Siae |
T |
C |
9: 37,534,309 (GRCm39) |
V115A |
probably damaging |
Het |
Slc16a6 |
A |
G |
11: 109,344,107 (GRCm39) |
C563R |
probably benign |
Het |
Sntg1 |
A |
C |
1: 8,752,243 (GRCm39) |
V58G |
possibly damaging |
Het |
Snx11 |
C |
T |
11: 96,663,985 (GRCm39) |
V36M |
probably damaging |
Het |
Synpo |
A |
G |
18: 60,762,631 (GRCm39) |
F92S |
probably benign |
Het |
Tle1 |
A |
G |
4: 72,057,924 (GRCm39) |
|
probably null |
Het |
Tmem117 |
A |
G |
15: 94,829,684 (GRCm39) |
D173G |
possibly damaging |
Het |
Tmem217b |
C |
A |
17: 29,738,347 (GRCm39) |
V140L |
probably benign |
Het |
Tmprss5 |
T |
C |
9: 49,025,841 (GRCm39) |
W338R |
probably benign |
Het |
Tnfrsf19 |
T |
C |
14: 61,212,147 (GRCm39) |
T168A |
possibly damaging |
Het |
Trhde |
C |
T |
10: 114,636,776 (GRCm39) |
G144S |
possibly damaging |
Het |
Trim56 |
G |
T |
5: 137,143,097 (GRCm39) |
Q140K |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,562,918 (GRCm39) |
V28679M |
probably damaging |
Het |
Ubxn8 |
G |
A |
8: 34,113,231 (GRCm39) |
R208C |
probably damaging |
Het |
Vmn2r72 |
G |
T |
7: 85,387,482 (GRCm39) |
S694* |
probably null |
Het |
Wdr38 |
T |
A |
2: 38,890,276 (GRCm39) |
W137R |
probably damaging |
Het |
Zdhhc6 |
G |
T |
19: 55,292,932 (GRCm39) |
N271K |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,575,744 (GRCm39) |
S446P |
possibly damaging |
Het |
Zmynd8 |
T |
C |
2: 165,649,492 (GRCm39) |
Q867R |
possibly damaging |
Het |
Zswim3 |
T |
C |
2: 164,662,402 (GRCm39) |
I294T |
probably benign |
Het |
|
Other mutations in Stk3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Stk3
|
APN |
15 |
35,114,768 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02133:Stk3
|
APN |
15 |
35,099,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03121:Stk3
|
APN |
15 |
35,099,572 (GRCm39) |
splice site |
probably benign |
|
IGL03309:Stk3
|
APN |
15 |
35,099,697 (GRCm39) |
splice site |
probably benign |
|
R0276:Stk3
|
UTSW |
15 |
35,099,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0416:Stk3
|
UTSW |
15 |
35,114,778 (GRCm39) |
missense |
probably benign |
0.07 |
R1352:Stk3
|
UTSW |
15 |
35,008,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Stk3
|
UTSW |
15 |
34,959,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Stk3
|
UTSW |
15 |
35,008,454 (GRCm39) |
splice site |
probably null |
|
R1917:Stk3
|
UTSW |
15 |
35,073,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Stk3
|
UTSW |
15 |
35,073,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Stk3
|
UTSW |
15 |
35,072,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Stk3
|
UTSW |
15 |
34,959,195 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2073:Stk3
|
UTSW |
15 |
34,959,195 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2075:Stk3
|
UTSW |
15 |
34,959,195 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3158:Stk3
|
UTSW |
15 |
35,008,387 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3402:Stk3
|
UTSW |
15 |
34,945,144 (GRCm39) |
splice site |
probably benign |
|
R4633:Stk3
|
UTSW |
15 |
34,959,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R4672:Stk3
|
UTSW |
15 |
35,099,603 (GRCm39) |
missense |
probably benign |
0.06 |
R4687:Stk3
|
UTSW |
15 |
35,114,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R4825:Stk3
|
UTSW |
15 |
35,000,054 (GRCm39) |
missense |
probably benign |
0.14 |
R4903:Stk3
|
UTSW |
15 |
34,959,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R5390:Stk3
|
UTSW |
15 |
35,114,706 (GRCm39) |
nonsense |
probably null |
|
R5834:Stk3
|
UTSW |
15 |
34,959,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R7208:Stk3
|
UTSW |
15 |
35,073,262 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7862:Stk3
|
UTSW |
15 |
35,115,732 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8354:Stk3
|
UTSW |
15 |
34,876,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Stk3
|
UTSW |
15 |
34,876,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R8996:Stk3
|
UTSW |
15 |
34,945,208 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9160:Stk3
|
UTSW |
15 |
35,099,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R9366:Stk3
|
UTSW |
15 |
35,072,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Stk3
|
UTSW |
15 |
35,114,791 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Stk3
|
UTSW |
15 |
35,072,701 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Stk3
|
UTSW |
15 |
35,114,679 (GRCm39) |
missense |
probably damaging |
0.99 |
|