Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
A |
G |
11: 58,876,769 (GRCm38) |
K31E |
probably damaging |
Het |
4930548H24Rik |
T |
C |
5: 31,487,383 (GRCm38) |
V160A |
possibly damaging |
Het |
9130011E15Rik |
G |
T |
19: 45,891,285 (GRCm38) |
P543Q |
probably damaging |
Het |
Abcc10 |
G |
C |
17: 46,303,565 (GRCm38) |
N1477K |
probably benign |
Het |
Ablim2 |
G |
A |
5: 35,798,513 (GRCm38) |
C24Y |
probably damaging |
Het |
Ankle1 |
T |
C |
8: 71,409,344 (GRCm38) |
F497S |
probably damaging |
Het |
Ash1l |
C |
G |
3: 88,966,203 (GRCm38) |
P98A |
probably damaging |
Het |
Atad5 |
A |
T |
11: 80,098,052 (GRCm38) |
|
probably null |
Het |
B3gnt4 |
A |
T |
5: 123,511,370 (GRCm38) |
H266L |
probably benign |
Het |
Bmi1 |
A |
G |
2: 18,684,040 (GRCm38) |
I207V |
probably benign |
Het |
Bnip3l |
A |
G |
14: 66,989,222 (GRCm38) |
M174T |
probably damaging |
Het |
Bora |
T |
C |
14: 99,062,278 (GRCm38) |
S229P |
probably damaging |
Het |
Ccdc27 |
T |
A |
4: 154,041,813 (GRCm38) |
N73I |
unknown |
Het |
Cdc42bpg |
T |
A |
19: 6,320,488 (GRCm38) |
C1204S |
probably damaging |
Het |
Cdsn |
A |
T |
17: 35,554,694 (GRCm38) |
D40V |
probably damaging |
Het |
Cilp |
T |
A |
9: 65,279,095 (GRCm38) |
V824D |
probably damaging |
Het |
Cmtr1 |
A |
G |
17: 29,694,783 (GRCm38) |
|
probably null |
Het |
Cntnap1 |
A |
G |
11: 101,182,979 (GRCm38) |
Y652C |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,647,696 (GRCm38) |
I2033M |
probably benign |
Het |
Cwh43 |
T |
C |
5: 73,421,517 (GRCm38) |
L289P |
probably damaging |
Het |
Ddhd1 |
T |
C |
14: 45,610,624 (GRCm38) |
D529G |
probably damaging |
Het |
Defb28 |
T |
A |
2: 152,520,144 (GRCm38) |
S75T |
probably benign |
Het |
Dennd2a |
A |
T |
6: 39,465,119 (GRCm38) |
V939D |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,136,635 (GRCm38) |
R1866G |
probably damaging |
Het |
Dsc1 |
C |
T |
18: 20,088,296 (GRCm38) |
|
probably null |
Het |
Ecscr |
T |
G |
18: 35,715,437 (GRCm38) |
N184T |
probably damaging |
Het |
Eif4ebp1 |
G |
T |
8: 27,273,344 (GRCm38) |
R55L |
probably damaging |
Het |
Eml1 |
G |
T |
12: 108,512,999 (GRCm38) |
V344L |
probably damaging |
Het |
Fam161b |
T |
A |
12: 84,356,428 (GRCm38) |
I143F |
probably benign |
Het |
Fam180a |
A |
G |
6: 35,325,911 (GRCm38) |
S2P |
probably benign |
Het |
Fam57b |
T |
C |
7: 126,819,840 (GRCm38) |
L4P |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,999,370 (GRCm38) |
I1779F |
probably benign |
Het |
Fat4 |
A |
G |
3: 39,010,655 (GRCm38) |
K4920R |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,976,355 (GRCm38) |
V1006E |
probably damaging |
Het |
Glcci1 |
A |
G |
6: 8,558,566 (GRCm38) |
S30G |
probably damaging |
Het |
Gm13078 |
T |
G |
4: 143,726,902 (GRCm38) |
Y193* |
probably null |
Het |
Gm5414 |
A |
T |
15: 101,628,060 (GRCm38) |
S43R |
possibly damaging |
Het |
Hao1 |
T |
C |
2: 134,530,615 (GRCm38) |
T158A |
probably damaging |
Het |
Hic1 |
T |
C |
11: 75,169,059 (GRCm38) |
H154R |
possibly damaging |
Het |
Hmgxb3 |
T |
C |
18: 61,171,359 (GRCm38) |
Y53C |
probably damaging |
Het |
Ipmk |
A |
T |
10: 71,372,749 (GRCm38) |
K122* |
probably null |
Het |
Jakmip2 |
T |
C |
18: 43,563,330 (GRCm38) |
E518G |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,501,995 (GRCm38) |
T1519A |
probably benign |
Het |
Lfng |
T |
C |
5: 140,612,595 (GRCm38) |
I224T |
possibly damaging |
Het |
Magel2 |
G |
A |
7: 62,379,096 (GRCm38) |
V583I |
unknown |
Het |
Map4k5 |
C |
T |
12: 69,816,337 (GRCm38) |
V629I |
probably damaging |
Het |
Med12l |
A |
G |
3: 59,244,905 (GRCm38) |
D1037G |
probably damaging |
Het |
Morc1 |
C |
T |
16: 48,592,611 (GRCm38) |
T705I |
probably benign |
Het |
Mptx2 |
A |
T |
1: 173,274,578 (GRCm38) |
Y181* |
probably null |
Het |
Mrpl24 |
T |
C |
3: 87,923,067 (GRCm38) |
|
probably null |
Het |
Myo5a |
A |
G |
9: 75,181,984 (GRCm38) |
E1132G |
probably benign |
Het |
Nedd4l |
T |
G |
18: 65,212,820 (GRCm38) |
F814L |
probably damaging |
Het |
Nmral1 |
T |
A |
16: 4,716,347 (GRCm38) |
I77F |
probably damaging |
Het |
Oit3 |
T |
G |
10: 59,431,013 (GRCm38) |
I224L |
probably benign |
Het |
Oxsm |
A |
G |
14: 16,241,983 (GRCm38) |
L262P |
probably benign |
Het |
Pacs2 |
C |
T |
12: 113,061,111 (GRCm38) |
T407I |
probably damaging |
Het |
Pard6g |
T |
C |
18: 80,117,725 (GRCm38) |
I351T |
probably benign |
Het |
Pdcl2 |
A |
T |
5: 76,324,991 (GRCm38) |
|
probably null |
Het |
Pdzph1 |
T |
C |
17: 58,974,097 (GRCm38) |
R397G |
probably benign |
Het |
Phip |
T |
A |
9: 82,875,299 (GRCm38) |
I1607L |
probably benign |
Het |
Plekhd1 |
C |
A |
12: 80,692,907 (GRCm38) |
S10* |
probably null |
Het |
Prdm1 |
C |
T |
10: 44,441,412 (GRCm38) |
D505N |
possibly damaging |
Het |
Psmd13 |
T |
C |
7: 140,897,648 (GRCm38) |
V320A |
probably damaging |
Het |
Rbak |
A |
G |
5: 143,176,584 (GRCm38) |
L8P |
probably damaging |
Het |
Rere |
C |
A |
4: 150,614,590 (GRCm38) |
|
probably benign |
Het |
Rint1 |
T |
C |
5: 23,810,929 (GRCm38) |
S456P |
possibly damaging |
Het |
Scn3a |
T |
C |
2: 65,520,866 (GRCm38) |
Q446R |
possibly damaging |
Het |
Slitrk5 |
A |
G |
14: 111,680,189 (GRCm38) |
Y415C |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,212,403 (GRCm38) |
E210G |
possibly damaging |
Het |
Snrnp200 |
A |
G |
2: 127,237,883 (GRCm38) |
T1891A |
probably benign |
Het |
Sohlh2 |
A |
G |
3: 55,207,622 (GRCm38) |
I343V |
probably benign |
Het |
Spin1 |
T |
C |
13: 51,144,537 (GRCm38) |
|
probably null |
Het |
St14 |
T |
A |
9: 31,091,373 (GRCm38) |
I745F |
probably damaging |
Het |
Sv2a |
G |
A |
3: 96,193,875 (GRCm38) |
A730T |
possibly damaging |
Het |
Tars2 |
C |
A |
3: 95,747,638 (GRCm38) |
G113C |
probably damaging |
Het |
Trp53 |
A |
G |
11: 69,589,632 (GRCm38) |
D278G |
probably damaging |
Het |
Ubxn7 |
T |
A |
16: 32,372,469 (GRCm38) |
C160S |
possibly damaging |
Het |
Uty |
T |
C |
Y: 1,169,193 (GRCm38) |
E414G |
probably benign |
Het |
Wrap73 |
T |
A |
4: 154,148,743 (GRCm38) |
S125T |
possibly damaging |
Het |
Wwc2 |
T |
C |
8: 47,868,321 (GRCm38) |
D586G |
unknown |
Het |
Zfp106 |
T |
C |
2: 120,523,529 (GRCm38) |
H1490R |
probably benign |
Het |
Zswim5 |
T |
C |
4: 116,979,912 (GRCm38) |
V731A |
probably benign |
Het |
Zyg11b |
G |
C |
4: 108,250,819 (GRCm38) |
N463K |
possibly damaging |
Het |
|
Other mutations in Exoc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Exoc2
|
APN |
13 |
30,820,626 (GRCm38) |
missense |
probably benign |
0.17 |
IGL01839:Exoc2
|
APN |
13 |
30,906,799 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02092:Exoc2
|
APN |
13 |
30,875,277 (GRCm38) |
missense |
probably benign |
0.09 |
IGL02245:Exoc2
|
APN |
13 |
30,906,859 (GRCm38) |
missense |
probably benign |
0.10 |
IGL02267:Exoc2
|
APN |
13 |
30,815,321 (GRCm38) |
missense |
probably benign |
|
IGL02478:Exoc2
|
APN |
13 |
30,927,420 (GRCm38) |
missense |
probably benign |
|
IGL02500:Exoc2
|
APN |
13 |
30,911,196 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03081:Exoc2
|
APN |
13 |
30,900,902 (GRCm38) |
missense |
probably benign |
0.28 |
IGL03112:Exoc2
|
APN |
13 |
30,906,587 (GRCm38) |
splice site |
probably benign |
|
IGL03409:Exoc2
|
APN |
13 |
30,940,737 (GRCm38) |
utr 5 prime |
probably benign |
|
R0284:Exoc2
|
UTSW |
13 |
30,877,625 (GRCm38) |
splice site |
probably benign |
|
R0452:Exoc2
|
UTSW |
13 |
30,886,327 (GRCm38) |
splice site |
probably benign |
|
R0826:Exoc2
|
UTSW |
13 |
30,856,797 (GRCm38) |
critical splice acceptor site |
probably null |
|
R1251:Exoc2
|
UTSW |
13 |
30,886,276 (GRCm38) |
missense |
probably benign |
0.03 |
R1367:Exoc2
|
UTSW |
13 |
30,882,273 (GRCm38) |
nonsense |
probably null |
|
R1501:Exoc2
|
UTSW |
13 |
30,935,502 (GRCm38) |
missense |
probably benign |
0.01 |
R1593:Exoc2
|
UTSW |
13 |
30,856,761 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1839:Exoc2
|
UTSW |
13 |
30,906,497 (GRCm38) |
splice site |
probably benign |
|
R1872:Exoc2
|
UTSW |
13 |
30,822,661 (GRCm38) |
missense |
probably benign |
0.17 |
R2064:Exoc2
|
UTSW |
13 |
30,935,561 (GRCm38) |
missense |
probably benign |
0.00 |
R2227:Exoc2
|
UTSW |
13 |
30,864,884 (GRCm38) |
missense |
probably benign |
|
R2507:Exoc2
|
UTSW |
13 |
30,882,365 (GRCm38) |
missense |
possibly damaging |
0.55 |
R3965:Exoc2
|
UTSW |
13 |
30,877,582 (GRCm38) |
missense |
probably benign |
0.00 |
R4601:Exoc2
|
UTSW |
13 |
30,882,268 (GRCm38) |
missense |
probably benign |
0.05 |
R4914:Exoc2
|
UTSW |
13 |
30,876,813 (GRCm38) |
missense |
probably benign |
0.21 |
R5299:Exoc2
|
UTSW |
13 |
30,871,918 (GRCm38) |
splice site |
probably null |
|
R5410:Exoc2
|
UTSW |
13 |
30,864,856 (GRCm38) |
missense |
probably damaging |
0.98 |
R5461:Exoc2
|
UTSW |
13 |
30,925,755 (GRCm38) |
missense |
possibly damaging |
0.66 |
R5956:Exoc2
|
UTSW |
13 |
30,820,623 (GRCm38) |
missense |
probably benign |
0.03 |
R6056:Exoc2
|
UTSW |
13 |
30,900,829 (GRCm38) |
missense |
probably benign |
0.03 |
R6107:Exoc2
|
UTSW |
13 |
30,876,797 (GRCm38) |
missense |
probably benign |
|
R6548:Exoc2
|
UTSW |
13 |
30,826,064 (GRCm38) |
missense |
possibly damaging |
0.86 |
R6692:Exoc2
|
UTSW |
13 |
30,935,507 (GRCm38) |
missense |
probably benign |
0.09 |
R6969:Exoc2
|
UTSW |
13 |
30,911,178 (GRCm38) |
missense |
probably benign |
|
R7386:Exoc2
|
UTSW |
13 |
30,906,663 (GRCm38) |
splice site |
probably null |
|
R7461:Exoc2
|
UTSW |
13 |
30,882,272 (GRCm38) |
missense |
probably benign |
0.32 |
R7467:Exoc2
|
UTSW |
13 |
30,925,733 (GRCm38) |
missense |
probably damaging |
0.98 |
R7473:Exoc2
|
UTSW |
13 |
30,822,630 (GRCm38) |
critical splice donor site |
probably null |
|
R7613:Exoc2
|
UTSW |
13 |
30,882,272 (GRCm38) |
missense |
probably benign |
0.32 |
R7767:Exoc2
|
UTSW |
13 |
30,876,769 (GRCm38) |
missense |
probably benign |
0.01 |
R7793:Exoc2
|
UTSW |
13 |
30,911,178 (GRCm38) |
missense |
probably benign |
0.00 |
R7795:Exoc2
|
UTSW |
13 |
30,876,773 (GRCm38) |
nonsense |
probably null |
|
R7993:Exoc2
|
UTSW |
13 |
30,906,730 (GRCm38) |
critical splice donor site |
probably null |
|
R8085:Exoc2
|
UTSW |
13 |
30,940,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R8330:Exoc2
|
UTSW |
13 |
30,877,573 (GRCm38) |
missense |
probably benign |
|
R8716:Exoc2
|
UTSW |
13 |
30,911,244 (GRCm38) |
missense |
probably damaging |
1.00 |
R8735:Exoc2
|
UTSW |
13 |
30,906,839 (GRCm38) |
missense |
probably damaging |
1.00 |
R8922:Exoc2
|
UTSW |
13 |
30,871,855 (GRCm38) |
missense |
probably benign |
0.05 |
R9237:Exoc2
|
UTSW |
13 |
30,864,875 (GRCm38) |
missense |
probably benign |
|
R9243:Exoc2
|
UTSW |
13 |
30,925,795 (GRCm38) |
missense |
probably benign |
0.03 |
R9365:Exoc2
|
UTSW |
13 |
30,856,714 (GRCm38) |
missense |
probably benign |
0.00 |
R9731:Exoc2
|
UTSW |
13 |
30,877,250 (GRCm38) |
missense |
probably benign |
0.06 |
|