Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730455P16Rik |
G |
A |
11: 80,254,838 (GRCm39) |
Q328* |
probably null |
Het |
Aadacl4fm4 |
T |
A |
4: 144,396,994 (GRCm39) |
K246I |
possibly damaging |
Het |
Adamts1 |
G |
A |
16: 85,595,399 (GRCm39) |
Q260* |
probably null |
Het |
Add2 |
A |
T |
6: 86,075,628 (GRCm39) |
Y259F |
probably benign |
Het |
Bora |
T |
C |
14: 99,305,840 (GRCm39) |
V403A |
probably benign |
Het |
Ccnl1 |
G |
A |
3: 65,854,191 (GRCm39) |
R477W |
probably damaging |
Het |
Cdc25a |
CG |
CGG |
9: 109,708,961 (GRCm39) |
|
probably null |
Het |
Cdr2l |
T |
C |
11: 115,284,203 (GRCm39) |
S180P |
probably damaging |
Het |
Cep290 |
T |
A |
10: 100,385,191 (GRCm39) |
L1889Q |
probably damaging |
Het |
Ces4a |
T |
C |
8: 105,869,453 (GRCm39) |
V208A |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,877,131 (GRCm39) |
D1049G |
probably damaging |
Het |
Coro1a |
A |
T |
7: 126,300,864 (GRCm39) |
N154K |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,474,600 (GRCm39) |
R401S |
probably benign |
Het |
Cul7 |
A |
T |
17: 46,974,017 (GRCm39) |
Q1434L |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dars1 |
G |
T |
1: 128,301,709 (GRCm39) |
D308E |
probably benign |
Het |
Dna2 |
T |
A |
10: 62,797,436 (GRCm39) |
F604I |
probably damaging |
Het |
Dnah1 |
T |
G |
14: 31,023,219 (GRCm39) |
I1033L |
probably benign |
Het |
Erlin1 |
T |
C |
19: 44,036,112 (GRCm39) |
E206G |
probably damaging |
Het |
Esrp2 |
T |
A |
8: 106,859,905 (GRCm39) |
E345D |
probably damaging |
Het |
Foxa1 |
T |
C |
12: 57,589,473 (GRCm39) |
D249G |
possibly damaging |
Het |
Ghsr |
C |
A |
3: 27,426,426 (GRCm39) |
L161M |
probably benign |
Het |
Gm57858 |
C |
T |
3: 36,073,146 (GRCm39) |
A379T |
probably damaging |
Het |
Gpr155 |
C |
A |
2: 73,200,434 (GRCm39) |
V358F |
probably damaging |
Het |
H2-Eb2 |
A |
T |
17: 34,553,348 (GRCm39) |
N178I |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,137,306 (GRCm39) |
I703N |
possibly damaging |
Het |
Kctd15 |
A |
G |
7: 34,341,417 (GRCm39) |
V170A |
probably damaging |
Het |
Klhl31 |
A |
T |
9: 77,558,298 (GRCm39) |
Y338F |
possibly damaging |
Het |
Krt5 |
C |
T |
15: 101,620,876 (GRCm39) |
A124T |
probably benign |
Het |
Krt72 |
T |
A |
15: 101,688,688 (GRCm39) |
I331F |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,401,490 (GRCm39) |
D388V |
probably damaging |
Het |
Ly9 |
A |
G |
1: 171,424,075 (GRCm39) |
V382A |
probably benign |
Het |
Mon2 |
T |
C |
10: 122,852,301 (GRCm39) |
Y1024C |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,287,818 (GRCm39) |
F572L |
probably damaging |
Het |
Myh3 |
A |
T |
11: 66,983,997 (GRCm39) |
D987V |
probably damaging |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Nphp4 |
A |
G |
4: 152,646,547 (GRCm39) |
T1360A |
probably benign |
Het |
Oog4 |
A |
G |
4: 143,164,571 (GRCm39) |
L320P |
probably damaging |
Het |
Or4k49 |
G |
T |
2: 111,495,099 (GRCm39) |
S176I |
probably damaging |
Het |
Or5m9 |
C |
T |
2: 85,877,657 (GRCm39) |
T277I |
probably damaging |
Het |
Or5w8 |
T |
A |
2: 87,688,095 (GRCm39) |
I192K |
probably benign |
Het |
Pcnx2 |
T |
C |
8: 126,498,825 (GRCm39) |
N1558S |
probably benign |
Het |
Pde10a |
A |
G |
17: 9,147,976 (GRCm39) |
E147G |
probably damaging |
Het |
Pgbd5 |
T |
A |
8: 125,101,026 (GRCm39) |
H410L |
probably benign |
Het |
Psg25 |
G |
A |
7: 18,265,928 (GRCm39) |
Q16* |
probably null |
Het |
Psmd9 |
T |
A |
5: 123,379,980 (GRCm39) |
V133E |
probably damaging |
Het |
Rabgap1 |
C |
T |
2: 37,451,911 (GRCm39) |
S937F |
probably damaging |
Het |
Rbck1 |
A |
G |
2: 152,165,090 (GRCm39) |
|
probably null |
Het |
Rprd2 |
C |
G |
3: 95,726,051 (GRCm39) |
|
probably benign |
Het |
Rrs1 |
A |
G |
1: 9,616,137 (GRCm39) |
N130S |
probably benign |
Het |
Scmh1 |
A |
T |
4: 120,372,327 (GRCm39) |
I377F |
possibly damaging |
Het |
Skor1 |
G |
T |
9: 63,053,286 (GRCm39) |
R228S |
probably damaging |
Het |
Slc2a4 |
A |
G |
11: 69,835,844 (GRCm39) |
V335A |
probably benign |
Het |
Slc4a9 |
G |
A |
18: 36,661,424 (GRCm39) |
W62* |
probably null |
Het |
Styxl2 |
G |
A |
1: 165,937,828 (GRCm39) |
T77I |
probably benign |
Het |
Taar9 |
G |
T |
10: 23,985,305 (GRCm39) |
A43D |
possibly damaging |
Het |
Tns4 |
T |
C |
11: 98,961,243 (GRCm39) |
Y645C |
probably damaging |
Het |
Tpcn2 |
G |
T |
7: 144,830,957 (GRCm39) |
Y129* |
probably null |
Het |
Trpm3 |
T |
C |
19: 22,710,388 (GRCm39) |
S278P |
possibly damaging |
Het |
Ttc3 |
T |
C |
16: 94,223,156 (GRCm39) |
W615R |
probably damaging |
Het |
Ttll5 |
T |
C |
12: 85,910,372 (GRCm39) |
V207A |
probably damaging |
Het |
Ubr7 |
G |
T |
12: 102,736,153 (GRCm39) |
M358I |
probably damaging |
Het |
Urb1 |
C |
A |
16: 90,574,328 (GRCm39) |
V918F |
possibly damaging |
Het |
Vmn2r51 |
G |
A |
7: 9,839,432 (GRCm39) |
T52I |
probably benign |
Het |
Vmn2r95 |
A |
T |
17: 18,672,575 (GRCm39) |
I771F |
probably benign |
Het |
Wfdc16 |
T |
C |
2: 164,477,350 (GRCm39) |
S107G |
probably benign |
Het |
Zmym2 |
A |
G |
14: 57,140,226 (GRCm39) |
T22A |
possibly damaging |
Het |
Zmym2 |
G |
A |
14: 57,151,524 (GRCm39) |
G470R |
probably damaging |
Het |
|
Other mutations in Plce1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Plce1
|
APN |
19 |
38,734,232 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00336:Plce1
|
APN |
19 |
38,640,350 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00430:Plce1
|
APN |
19 |
38,713,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00466:Plce1
|
APN |
19 |
38,709,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00477:Plce1
|
APN |
19 |
38,513,576 (GRCm39) |
missense |
probably benign |
0.39 |
IGL00839:Plce1
|
APN |
19 |
38,687,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01292:Plce1
|
APN |
19 |
38,640,229 (GRCm39) |
splice site |
probably benign |
|
IGL01665:Plce1
|
APN |
19 |
38,513,331 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01826:Plce1
|
APN |
19 |
38,727,682 (GRCm39) |
splice site |
probably benign |
|
IGL01833:Plce1
|
APN |
19 |
38,709,425 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02201:Plce1
|
APN |
19 |
38,757,890 (GRCm39) |
splice site |
probably benign |
|
IGL02276:Plce1
|
APN |
19 |
38,513,201 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02477:Plce1
|
APN |
19 |
38,707,997 (GRCm39) |
splice site |
probably benign |
|
IGL02746:Plce1
|
APN |
19 |
38,686,916 (GRCm39) |
missense |
probably damaging |
1.00 |
Angel_food
|
UTSW |
19 |
38,715,457 (GRCm39) |
splice site |
probably benign |
|
Heavenly
|
UTSW |
19 |
38,766,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Plce1
|
UTSW |
19 |
38,513,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0058:Plce1
|
UTSW |
19 |
38,513,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0064:Plce1
|
UTSW |
19 |
38,769,228 (GRCm39) |
critical splice donor site |
probably null |
|
R0116:Plce1
|
UTSW |
19 |
38,710,265 (GRCm39) |
missense |
probably benign |
|
R0138:Plce1
|
UTSW |
19 |
38,512,863 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0240:Plce1
|
UTSW |
19 |
38,717,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Plce1
|
UTSW |
19 |
38,717,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Plce1
|
UTSW |
19 |
38,766,465 (GRCm39) |
splice site |
probably benign |
|
R0506:Plce1
|
UTSW |
19 |
38,748,582 (GRCm39) |
missense |
probably benign |
0.04 |
R0578:Plce1
|
UTSW |
19 |
38,766,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Plce1
|
UTSW |
19 |
38,766,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Plce1
|
UTSW |
19 |
38,705,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R0920:Plce1
|
UTSW |
19 |
38,724,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Plce1
|
UTSW |
19 |
38,755,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Plce1
|
UTSW |
19 |
38,690,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Plce1
|
UTSW |
19 |
38,693,783 (GRCm39) |
nonsense |
probably null |
|
R1488:Plce1
|
UTSW |
19 |
38,705,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1624:Plce1
|
UTSW |
19 |
38,713,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Plce1
|
UTSW |
19 |
38,705,282 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1778:Plce1
|
UTSW |
19 |
38,769,234 (GRCm39) |
splice site |
probably benign |
|
R1797:Plce1
|
UTSW |
19 |
38,747,392 (GRCm39) |
critical splice donor site |
probably null |
|
R1872:Plce1
|
UTSW |
19 |
38,748,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Plce1
|
UTSW |
19 |
38,769,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Plce1
|
UTSW |
19 |
38,766,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Plce1
|
UTSW |
19 |
38,715,457 (GRCm39) |
splice site |
probably benign |
|
R2103:Plce1
|
UTSW |
19 |
38,766,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2376:Plce1
|
UTSW |
19 |
38,766,430 (GRCm39) |
missense |
probably benign |
0.02 |
R2471:Plce1
|
UTSW |
19 |
38,768,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Plce1
|
UTSW |
19 |
38,748,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Plce1
|
UTSW |
19 |
38,512,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Plce1
|
UTSW |
19 |
38,766,328 (GRCm39) |
missense |
probably damaging |
0.98 |
R3104:Plce1
|
UTSW |
19 |
38,608,963 (GRCm39) |
missense |
probably benign |
0.00 |
R3700:Plce1
|
UTSW |
19 |
38,693,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Plce1
|
UTSW |
19 |
38,766,343 (GRCm39) |
missense |
probably benign |
|
R3753:Plce1
|
UTSW |
19 |
38,640,278 (GRCm39) |
missense |
probably benign |
0.09 |
R4027:Plce1
|
UTSW |
19 |
38,512,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4057:Plce1
|
UTSW |
19 |
38,748,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4376:Plce1
|
UTSW |
19 |
38,693,891 (GRCm39) |
critical splice donor site |
probably null |
|
R4433:Plce1
|
UTSW |
19 |
38,755,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4521:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4522:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4524:Plce1
|
UTSW |
19 |
38,512,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4650:Plce1
|
UTSW |
19 |
38,513,088 (GRCm39) |
missense |
probably benign |
0.30 |
R4673:Plce1
|
UTSW |
19 |
38,737,840 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4701:Plce1
|
UTSW |
19 |
38,713,451 (GRCm39) |
missense |
probably benign |
0.33 |
R4828:Plce1
|
UTSW |
19 |
38,757,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R5103:Plce1
|
UTSW |
19 |
38,755,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Plce1
|
UTSW |
19 |
38,640,277 (GRCm39) |
missense |
probably benign |
0.00 |
R5236:Plce1
|
UTSW |
19 |
38,758,791 (GRCm39) |
missense |
probably benign |
0.11 |
R5268:Plce1
|
UTSW |
19 |
38,747,279 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5288:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Plce1
|
UTSW |
19 |
38,748,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Plce1
|
UTSW |
19 |
38,768,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Plce1
|
UTSW |
19 |
38,608,926 (GRCm39) |
missense |
probably benign |
0.01 |
R6004:Plce1
|
UTSW |
19 |
38,710,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Plce1
|
UTSW |
19 |
38,513,195 (GRCm39) |
missense |
probably benign |
|
R6147:Plce1
|
UTSW |
19 |
38,690,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Plce1
|
UTSW |
19 |
38,734,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R6278:Plce1
|
UTSW |
19 |
38,713,495 (GRCm39) |
splice site |
probably null |
|
R6306:Plce1
|
UTSW |
19 |
38,757,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Plce1
|
UTSW |
19 |
38,512,974 (GRCm39) |
nonsense |
probably null |
|
R6437:Plce1
|
UTSW |
19 |
38,513,576 (GRCm39) |
missense |
probably benign |
0.39 |
R6522:Plce1
|
UTSW |
19 |
38,736,965 (GRCm39) |
splice site |
probably null |
|
R7034:Plce1
|
UTSW |
19 |
38,727,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7036:Plce1
|
UTSW |
19 |
38,727,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Plce1
|
UTSW |
19 |
38,690,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7069:Plce1
|
UTSW |
19 |
38,747,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Plce1
|
UTSW |
19 |
38,768,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Plce1
|
UTSW |
19 |
38,748,581 (GRCm39) |
missense |
probably damaging |
0.97 |
R7227:Plce1
|
UTSW |
19 |
38,715,346 (GRCm39) |
missense |
probably benign |
0.00 |
R7253:Plce1
|
UTSW |
19 |
38,686,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Plce1
|
UTSW |
19 |
38,768,340 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7287:Plce1
|
UTSW |
19 |
38,690,347 (GRCm39) |
missense |
probably benign |
0.02 |
R7422:Plce1
|
UTSW |
19 |
38,640,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:Plce1
|
UTSW |
19 |
38,753,848 (GRCm39) |
missense |
probably benign |
0.30 |
R7607:Plce1
|
UTSW |
19 |
38,513,196 (GRCm39) |
missense |
probably benign |
|
R7615:Plce1
|
UTSW |
19 |
38,513,109 (GRCm39) |
missense |
probably benign |
0.18 |
R7653:Plce1
|
UTSW |
19 |
38,737,763 (GRCm39) |
missense |
probably benign |
0.20 |
R7685:Plce1
|
UTSW |
19 |
38,736,877 (GRCm39) |
missense |
probably benign |
0.00 |
R7716:Plce1
|
UTSW |
19 |
38,705,295 (GRCm39) |
missense |
probably benign |
|
R7744:Plce1
|
UTSW |
19 |
38,608,899 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7790:Plce1
|
UTSW |
19 |
38,769,140 (GRCm39) |
missense |
probably damaging |
0.97 |
R7921:Plce1
|
UTSW |
19 |
38,608,997 (GRCm39) |
missense |
probably benign |
0.03 |
R8070:Plce1
|
UTSW |
19 |
38,690,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R8087:Plce1
|
UTSW |
19 |
38,724,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Plce1
|
UTSW |
19 |
38,513,262 (GRCm39) |
missense |
probably benign |
0.32 |
R8178:Plce1
|
UTSW |
19 |
38,761,423 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8321:Plce1
|
UTSW |
19 |
38,640,380 (GRCm39) |
missense |
probably benign |
0.00 |
R8416:Plce1
|
UTSW |
19 |
38,761,441 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8544:Plce1
|
UTSW |
19 |
38,512,903 (GRCm39) |
missense |
probably benign |
0.00 |
R8713:Plce1
|
UTSW |
19 |
38,513,345 (GRCm39) |
missense |
probably benign |
0.01 |
R8850:Plce1
|
UTSW |
19 |
38,512,811 (GRCm39) |
missense |
probably benign |
|
R9217:Plce1
|
UTSW |
19 |
38,748,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Plce1
|
UTSW |
19 |
38,705,040 (GRCm39) |
missense |
probably benign |
0.13 |
R9232:Plce1
|
UTSW |
19 |
38,705,423 (GRCm39) |
missense |
probably benign |
0.16 |
R9332:Plce1
|
UTSW |
19 |
38,726,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9473:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9474:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9475:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9476:Plce1
|
UTSW |
19 |
38,766,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9751:Plce1
|
UTSW |
19 |
38,717,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9780:Plce1
|
UTSW |
19 |
38,609,134 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9781:Plce1
|
UTSW |
19 |
38,513,654 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Plce1
|
UTSW |
19 |
38,705,651 (GRCm39) |
missense |
probably damaging |
0.99 |
X0022:Plce1
|
UTSW |
19 |
38,715,443 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Plce1
|
UTSW |
19 |
38,766,358 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Plce1
|
UTSW |
19 |
38,757,904 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Plce1
|
UTSW |
19 |
38,713,424 (GRCm39) |
nonsense |
probably null |
|
Z1176:Plce1
|
UTSW |
19 |
38,690,338 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Plce1
|
UTSW |
19 |
38,640,286 (GRCm39) |
missense |
probably null |
0.48 |
|