Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921513I03Rik |
T |
C |
10: 120,614,533 (GRCm39) |
|
probably benign |
Het |
4930447C04Rik |
C |
T |
12: 72,931,992 (GRCm39) |
|
probably null |
Het |
Abca16 |
A |
G |
7: 120,119,307 (GRCm39) |
H1017R |
probably damaging |
Het |
Actl11 |
A |
G |
9: 107,807,207 (GRCm39) |
Y510C |
probably damaging |
Het |
Agbl2 |
A |
G |
2: 90,631,664 (GRCm39) |
T341A |
probably damaging |
Het |
Agbl5 |
A |
G |
5: 31,050,726 (GRCm39) |
Y458C |
probably damaging |
Het |
Akap5 |
C |
T |
12: 76,376,698 (GRCm39) |
S710L |
probably damaging |
Het |
Akr1c21 |
A |
G |
13: 4,625,177 (GRCm39) |
E36G |
probably damaging |
Het |
Arhgap44 |
A |
G |
11: 64,944,023 (GRCm39) |
S163P |
probably damaging |
Het |
Armc1 |
A |
G |
3: 19,189,050 (GRCm39) |
V205A |
possibly damaging |
Het |
Asph |
A |
G |
4: 9,610,869 (GRCm39) |
L102P |
probably damaging |
Het |
Brca1 |
T |
C |
11: 101,422,925 (GRCm39) |
E74G |
probably damaging |
Het |
Brms1l |
A |
G |
12: 55,888,385 (GRCm39) |
R58G |
probably damaging |
Het |
C1qbp |
G |
T |
11: 70,869,073 (GRCm39) |
|
probably null |
Het |
Calcrl |
A |
T |
2: 84,169,631 (GRCm39) |
L350H |
probably damaging |
Het |
Ceacam10 |
T |
A |
7: 24,480,491 (GRCm39) |
N87K |
probably benign |
Het |
Cfap206 |
G |
T |
4: 34,719,058 (GRCm39) |
T316K |
probably damaging |
Het |
Col4a3 |
A |
T |
1: 82,668,384 (GRCm39) |
|
probably null |
Het |
Comtd1 |
A |
G |
14: 21,897,398 (GRCm39) |
V183A |
probably damaging |
Het |
Crygs |
A |
T |
16: 22,625,425 (GRCm39) |
|
probably null |
Het |
Dact1 |
C |
A |
12: 71,359,551 (GRCm39) |
T139K |
probably damaging |
Het |
Dlx6 |
T |
C |
6: 6,867,173 (GRCm39) |
W259R |
probably damaging |
Het |
Dnah9 |
G |
T |
11: 65,845,650 (GRCm39) |
S627* |
probably null |
Het |
Dnajc11 |
T |
A |
4: 152,063,730 (GRCm39) |
V442D |
probably damaging |
Het |
Dnajc21 |
A |
T |
15: 10,451,649 (GRCm39) |
S393T |
probably benign |
Het |
Dpysl3 |
C |
A |
18: 43,461,439 (GRCm39) |
C584F |
possibly damaging |
Het |
Efcab14 |
A |
G |
4: 115,603,736 (GRCm39) |
K138R |
possibly damaging |
Het |
Ephb3 |
A |
G |
16: 21,040,495 (GRCm39) |
E577G |
probably damaging |
Het |
Exoc3 |
C |
T |
13: 74,338,184 (GRCm39) |
|
probably null |
Het |
Fam171a1 |
A |
G |
2: 3,226,660 (GRCm39) |
S473G |
probably benign |
Het |
Fbxl2 |
A |
T |
9: 113,832,239 (GRCm39) |
F58L |
probably damaging |
Het |
Fmo6 |
T |
C |
1: 162,750,241 (GRCm39) |
M272V |
probably benign |
Het |
Gm10000 |
T |
C |
12: 104,442,859 (GRCm39) |
|
probably benign |
Het |
Grik1 |
T |
A |
16: 87,746,956 (GRCm39) |
D442V |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,791,375 (GRCm39) |
Y2588H |
probably damaging |
Het |
Insrr |
A |
C |
3: 87,711,369 (GRCm39) |
T430P |
probably benign |
Het |
Lats1 |
T |
C |
10: 7,577,709 (GRCm39) |
S278P |
probably benign |
Het |
Lrch4 |
A |
G |
5: 137,636,723 (GRCm39) |
T463A |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,532,280 (GRCm39) |
Q118R |
possibly damaging |
Het |
Lyst |
T |
G |
13: 13,835,746 (GRCm39) |
F1809L |
probably damaging |
Het |
Mad2l1bp |
A |
G |
17: 46,463,770 (GRCm39) |
Y85H |
possibly damaging |
Het |
Magoh |
G |
T |
4: 107,740,362 (GRCm39) |
R82L |
probably benign |
Het |
Mdfic2 |
A |
C |
6: 98,215,100 (GRCm39) |
S174R |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,057,543 (GRCm39) |
V756A |
probably damaging |
Het |
Mlh3 |
T |
C |
12: 85,313,915 (GRCm39) |
E757G |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,464,947 (GRCm39) |
T1339A |
probably damaging |
Het |
Myh7b |
A |
T |
2: 155,455,113 (GRCm39) |
E46V |
probably damaging |
Het |
Naalad2 |
T |
A |
9: 18,238,683 (GRCm39) |
R677S |
probably damaging |
Het |
Nadsyn1 |
G |
A |
7: 143,361,749 (GRCm39) |
T324I |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,787,886 (GRCm39) |
L1389Q |
probably damaging |
Het |
Nlrp1b |
A |
G |
11: 71,107,681 (GRCm39) |
|
probably null |
Het |
Nup210 |
A |
C |
6: 91,039,785 (GRCm39) |
I690S |
probably benign |
Het |
Or55b3 |
A |
T |
7: 102,126,547 (GRCm39) |
S177T |
probably benign |
Het |
Or5an11 |
T |
A |
19: 12,246,281 (GRCm39) |
I229N |
probably damaging |
Het |
Or9r7 |
T |
A |
10: 129,962,123 (GRCm39) |
I268F |
possibly damaging |
Het |
Otud7a |
C |
A |
7: 63,383,458 (GRCm39) |
H316N |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,429,995 (GRCm39) |
S1241P |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,570,977 (GRCm39) |
K121E |
probably damaging |
Het |
Pcmtd1 |
A |
T |
1: 7,217,872 (GRCm39) |
I107L |
probably benign |
Het |
Pde6c |
A |
G |
19: 38,168,673 (GRCm39) |
I755V |
probably damaging |
Het |
Pes1 |
CGGAGGAGGAGGAGGAGGAGGAGG |
CGGAGGAGGAGGAGGAGGAGG |
11: 3,927,719 (GRCm39) |
|
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,113,240 (GRCm39) |
I1532N |
probably damaging |
Het |
Pla2r1 |
A |
G |
2: 60,271,428 (GRCm39) |
|
probably null |
Het |
Plb1 |
A |
G |
5: 32,474,621 (GRCm39) |
N661S |
probably null |
Het |
Plekhd1 |
A |
G |
12: 80,769,095 (GRCm39) |
K452E |
possibly damaging |
Het |
Prr12 |
C |
A |
7: 44,678,003 (GRCm39) |
V2003F |
unknown |
Het |
Ptger1 |
G |
A |
8: 84,395,107 (GRCm39) |
G195R |
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,711,240 (GRCm39) |
Q67R |
probably damaging |
Het |
Rgsl1 |
C |
T |
1: 153,680,422 (GRCm39) |
R760H |
probably damaging |
Het |
Rock1 |
A |
G |
18: 10,136,094 (GRCm39) |
|
probably null |
Het |
Rtn1 |
T |
C |
12: 72,270,298 (GRCm39) |
Y71C |
probably damaging |
Het |
Rtp4 |
T |
C |
16: 23,431,870 (GRCm39) |
*62Q |
probably null |
Het |
Scaf4 |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTG |
16: 90,026,745 (GRCm39) |
|
probably benign |
Het |
Scimp |
G |
T |
11: 70,684,618 (GRCm39) |
P78H |
probably damaging |
Het |
Scn8a |
C |
A |
15: 100,853,409 (GRCm39) |
S132* |
probably null |
Het |
Set |
A |
G |
2: 29,959,436 (GRCm39) |
I124M |
probably damaging |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Sgce |
A |
G |
6: 4,689,709 (GRCm39) |
S375P |
probably damaging |
Het |
Slc4a1ap |
G |
C |
5: 31,701,098 (GRCm39) |
E600Q |
probably damaging |
Het |
Slit1 |
A |
G |
19: 41,626,031 (GRCm39) |
V577A |
possibly damaging |
Het |
Sqstm1 |
A |
G |
11: 50,098,307 (GRCm39) |
V153A |
probably benign |
Het |
Src |
A |
G |
2: 157,311,675 (GRCm39) |
M468V |
possibly damaging |
Het |
Srrm3 |
A |
G |
5: 135,902,079 (GRCm39) |
|
probably benign |
Het |
Stk11ip |
C |
T |
1: 75,504,030 (GRCm39) |
R257W |
probably damaging |
Het |
Tfrc |
T |
A |
16: 32,433,443 (GRCm39) |
D32E |
probably damaging |
Het |
Tor1aip2 |
A |
T |
1: 155,941,031 (GRCm39) |
I446L |
probably benign |
Het |
Trmt11 |
T |
C |
10: 30,411,221 (GRCm39) |
H424R |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,563,928 (GRCm39) |
Y1612H |
probably benign |
Het |
Vcan |
A |
T |
13: 89,836,602 (GRCm39) |
S2981T |
probably damaging |
Het |
Vdac1 |
G |
C |
11: 52,265,190 (GRCm39) |
G21A |
probably damaging |
Het |
Vmn2r76 |
A |
G |
7: 85,879,356 (GRCm39) |
S315P |
probably benign |
Het |
Xpo1 |
A |
G |
11: 23,231,399 (GRCm39) |
T328A |
probably benign |
Het |
Xrcc5 |
C |
T |
1: 72,358,255 (GRCm39) |
L197F |
possibly damaging |
Het |
Zfhx2 |
G |
C |
14: 55,311,401 (GRCm39) |
S431C |
possibly damaging |
Het |
Zfp410 |
C |
T |
12: 84,372,494 (GRCm39) |
P54S |
probably benign |
Het |
Zfp560 |
C |
A |
9: 20,259,282 (GRCm39) |
G527* |
probably null |
Het |
Zfp775 |
A |
G |
6: 48,596,389 (GRCm39) |
T88A |
possibly damaging |
Het |
Zfp780b |
T |
A |
7: 27,663,808 (GRCm39) |
H249L |
possibly damaging |
Het |
|
Other mutations in Casr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Casr
|
APN |
16 |
36,316,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01587:Casr
|
APN |
16 |
36,330,127 (GRCm39) |
missense |
probably benign |
|
IGL02323:Casr
|
APN |
16 |
36,330,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02369:Casr
|
APN |
16 |
36,315,051 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02514:Casr
|
APN |
16 |
36,320,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02547:Casr
|
APN |
16 |
36,336,036 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02633:Casr
|
APN |
16 |
36,336,017 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Casr
|
APN |
16 |
36,316,250 (GRCm39) |
missense |
probably benign |
0.07 |
R1163:Casr
|
UTSW |
16 |
36,315,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Casr
|
UTSW |
16 |
36,315,499 (GRCm39) |
missense |
probably benign |
0.10 |
R1643:Casr
|
UTSW |
16 |
36,320,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Casr
|
UTSW |
16 |
36,330,327 (GRCm39) |
nonsense |
probably null |
|
R2040:Casr
|
UTSW |
16 |
36,330,728 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2092:Casr
|
UTSW |
16 |
36,330,405 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2125:Casr
|
UTSW |
16 |
36,315,614 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2190:Casr
|
UTSW |
16 |
36,315,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Casr
|
UTSW |
16 |
36,336,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R4409:Casr
|
UTSW |
16 |
36,320,703 (GRCm39) |
missense |
probably benign |
0.01 |
R4410:Casr
|
UTSW |
16 |
36,320,703 (GRCm39) |
missense |
probably benign |
0.01 |
R4591:Casr
|
UTSW |
16 |
36,320,732 (GRCm39) |
missense |
probably benign |
0.05 |
R5451:Casr
|
UTSW |
16 |
36,330,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R5469:Casr
|
UTSW |
16 |
36,330,392 (GRCm39) |
missense |
probably benign |
0.29 |
R5581:Casr
|
UTSW |
16 |
36,315,106 (GRCm39) |
missense |
probably benign |
0.01 |
R5700:Casr
|
UTSW |
16 |
36,329,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R6258:Casr
|
UTSW |
16 |
36,337,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6447:Casr
|
UTSW |
16 |
36,315,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Casr
|
UTSW |
16 |
36,335,950 (GRCm39) |
missense |
probably benign |
0.00 |
R6938:Casr
|
UTSW |
16 |
36,316,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Casr
|
UTSW |
16 |
36,314,936 (GRCm39) |
missense |
probably benign |
0.00 |
R7313:Casr
|
UTSW |
16 |
36,330,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7789:Casr
|
UTSW |
16 |
36,315,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Casr
|
UTSW |
16 |
36,330,006 (GRCm39) |
missense |
probably benign |
0.22 |
R8026:Casr
|
UTSW |
16 |
36,315,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Casr
|
UTSW |
16 |
36,315,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Casr
|
UTSW |
16 |
36,330,108 (GRCm39) |
missense |
probably benign |
|
R8278:Casr
|
UTSW |
16 |
36,336,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8386:Casr
|
UTSW |
16 |
36,335,950 (GRCm39) |
missense |
probably damaging |
0.96 |
R8393:Casr
|
UTSW |
16 |
36,330,566 (GRCm39) |
missense |
probably benign |
0.02 |
R8682:Casr
|
UTSW |
16 |
36,315,784 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9020:Casr
|
UTSW |
16 |
36,315,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Casr
|
UTSW |
16 |
36,330,414 (GRCm39) |
missense |
probably benign |
0.00 |
R9260:Casr
|
UTSW |
16 |
36,330,326 (GRCm39) |
missense |
probably benign |
0.01 |
|