Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,774,002 (GRCm39) |
E1137G |
probably damaging |
Het |
Adcy9 |
T |
C |
16: 4,105,818 (GRCm39) |
I1099V |
probably benign |
Het |
Angptl4 |
A |
T |
17: 33,996,015 (GRCm39) |
N320K |
probably benign |
Het |
Atp6v0a2 |
G |
A |
5: 124,767,268 (GRCm39) |
M10I |
probably benign |
Het |
Bltp1 |
C |
T |
3: 37,042,318 (GRCm39) |
T2768I |
probably benign |
Het |
Cbfa2t3 |
A |
G |
8: 123,361,135 (GRCm39) |
S395P |
probably benign |
Het |
Chsy1 |
T |
C |
7: 65,820,625 (GRCm39) |
Y287H |
probably benign |
Het |
Col4a4 |
G |
T |
1: 82,462,151 (GRCm39) |
P1075T |
probably damaging |
Het |
Cryab |
T |
A |
9: 50,665,813 (GRCm39) |
M68K |
probably damaging |
Het |
Cybrd1 |
T |
A |
2: 70,967,858 (GRCm39) |
L143Q |
probably null |
Het |
Dcaf7 |
T |
C |
11: 105,942,584 (GRCm39) |
V177A |
probably damaging |
Het |
Dclk2 |
T |
C |
3: 86,722,457 (GRCm39) |
Y392C |
probably damaging |
Het |
Ddx20 |
T |
C |
3: 105,586,036 (GRCm39) |
T770A |
probably benign |
Het |
Dennd1b |
T |
A |
1: 139,095,456 (GRCm39) |
D501E |
probably benign |
Het |
Dgkh |
A |
T |
14: 78,865,504 (GRCm39) |
Y26* |
probably null |
Het |
Dnajc2 |
A |
G |
5: 21,973,646 (GRCm39) |
V196A |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,806,362 (GRCm39) |
K827E |
probably damaging |
Het |
Fam8a1 |
C |
T |
13: 46,823,099 (GRCm39) |
P13L |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,582 (GRCm39) |
S139G |
possibly damaging |
Het |
Ggnbp1 |
G |
A |
17: 27,248,847 (GRCm39) |
V139I |
possibly damaging |
Het |
Gja1 |
T |
A |
10: 56,264,330 (GRCm39) |
Y230N |
probably damaging |
Het |
Gldc |
A |
G |
19: 30,111,172 (GRCm39) |
S535P |
probably damaging |
Het |
Gm45871 |
A |
G |
18: 90,610,357 (GRCm39) |
T532A |
probably benign |
Het |
Gm5431 |
T |
A |
11: 48,785,220 (GRCm39) |
D107V |
probably benign |
Het |
Herc2 |
C |
T |
7: 55,857,510 (GRCm39) |
T4031M |
probably damaging |
Het |
Iffo2 |
G |
A |
4: 139,333,769 (GRCm39) |
A282T |
probably damaging |
Het |
Ifi44 |
T |
G |
3: 151,451,276 (GRCm39) |
|
probably null |
Het |
Igkv4-53 |
C |
T |
6: 69,625,915 (GRCm39) |
R62H |
possibly damaging |
Het |
Lrp11 |
A |
C |
10: 7,474,454 (GRCm39) |
|
probably null |
Het |
Lrp4 |
A |
G |
2: 91,338,833 (GRCm39) |
T1755A |
probably benign |
Het |
Mcm3ap |
A |
T |
10: 76,336,934 (GRCm39) |
K1316M |
probably damaging |
Het |
Mctp1 |
T |
G |
13: 76,971,082 (GRCm39) |
|
probably null |
Het |
Mroh5 |
A |
T |
15: 73,662,630 (GRCm39) |
I396N |
probably damaging |
Het |
Mrps5 |
T |
A |
2: 127,443,305 (GRCm39) |
H294Q |
probably damaging |
Het |
Muc16 |
A |
T |
9: 18,569,985 (GRCm39) |
S845T |
unknown |
Het |
Mycbpap |
A |
T |
11: 94,398,557 (GRCm39) |
V474E |
probably damaging |
Het |
Mzt2 |
G |
C |
16: 15,666,551 (GRCm39) |
S122W |
probably benign |
Het |
Neb |
T |
C |
2: 52,146,802 (GRCm39) |
I2821V |
probably benign |
Het |
Ngef |
A |
T |
1: 87,415,622 (GRCm39) |
D347E |
probably damaging |
Het |
Nlrp14 |
T |
C |
7: 106,781,646 (GRCm39) |
V281A |
probably benign |
Het |
Obscn |
A |
T |
11: 58,888,864 (GRCm39) |
Y7597N |
unknown |
Het |
Or4k47 |
T |
C |
2: 111,451,520 (GRCm39) |
R300G |
possibly damaging |
Het |
Patj |
G |
T |
4: 98,344,394 (GRCm39) |
G569W |
probably damaging |
Het |
Pdzrn4 |
A |
T |
15: 92,655,562 (GRCm39) |
E485V |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,973,583 (GRCm39) |
T361S |
unknown |
Het |
Pik3r6 |
A |
G |
11: 68,434,455 (GRCm39) |
E552G |
probably damaging |
Het |
Pitx2 |
A |
G |
3: 129,009,521 (GRCm39) |
T147A |
probably benign |
Het |
Pkmyt1 |
G |
A |
17: 23,953,167 (GRCm39) |
G241D |
probably damaging |
Het |
Pola2 |
A |
T |
19: 6,003,802 (GRCm39) |
V191D |
possibly damaging |
Het |
Ralgapb |
T |
A |
2: 158,291,367 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
T |
C |
2: 71,811,661 (GRCm39) |
S11P |
probably benign |
Het |
Rnf10 |
G |
A |
5: 115,395,136 (GRCm39) |
R151C |
probably damaging |
Het |
Rpl34 |
G |
A |
3: 130,522,716 (GRCm39) |
P50L |
probably benign |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 79,895,850 (GRCm39) |
L977Q |
probably damaging |
Het |
Sec14l3 |
G |
A |
11: 4,025,566 (GRCm39) |
|
probably null |
Het |
Serping1 |
A |
T |
2: 84,600,612 (GRCm39) |
N243K |
possibly damaging |
Het |
Slco2b1 |
T |
A |
7: 99,334,779 (GRCm39) |
I231F |
probably damaging |
Het |
Spag8 |
A |
G |
4: 43,652,458 (GRCm39) |
F294S |
probably damaging |
Het |
Speer4f1 |
G |
A |
5: 17,684,493 (GRCm39) |
A174T |
probably damaging |
Het |
Spred3 |
T |
C |
7: 28,862,402 (GRCm39) |
D147G |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,527,241 (GRCm39) |
D1166G |
probably damaging |
Het |
Svep1 |
G |
T |
4: 58,104,536 (GRCm39) |
T1229K |
possibly damaging |
Het |
Tanc1 |
T |
A |
2: 59,669,305 (GRCm39) |
|
probably null |
Het |
Tmem232 |
T |
C |
17: 65,737,800 (GRCm39) |
Y420C |
probably damaging |
Het |
Tubd1 |
A |
T |
11: 86,448,619 (GRCm39) |
M311L |
probably benign |
Het |
Tulp3 |
G |
A |
6: 128,332,703 (GRCm39) |
|
probably null |
Het |
Usp42 |
T |
C |
5: 143,702,942 (GRCm39) |
T560A |
possibly damaging |
Het |
Vmn1r170 |
A |
T |
7: 23,305,934 (GRCm39) |
Y112F |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,322,699 (GRCm39) |
C7S |
probably benign |
Het |
Wrn |
A |
G |
8: 33,774,682 (GRCm39) |
M652T |
probably benign |
Het |
Wsb1 |
G |
A |
11: 79,139,336 (GRCm39) |
P120L |
possibly damaging |
Het |
Zfp142 |
T |
C |
1: 74,609,667 (GRCm39) |
E1376G |
probably damaging |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cenpe |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00655:Cenpe
|
APN |
3 |
134,937,216 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00799:Cenpe
|
APN |
3 |
134,934,678 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00815:Cenpe
|
APN |
3 |
134,965,112 (GRCm39) |
missense |
probably benign |
|
IGL01446:Cenpe
|
APN |
3 |
134,943,300 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01469:Cenpe
|
APN |
3 |
134,934,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01843:Cenpe
|
APN |
3 |
134,924,268 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02254:Cenpe
|
APN |
3 |
134,961,238 (GRCm39) |
missense |
probably benign |
|
IGL02337:Cenpe
|
APN |
3 |
134,926,037 (GRCm39) |
splice site |
probably benign |
|
IGL02382:Cenpe
|
APN |
3 |
134,953,147 (GRCm39) |
missense |
probably benign |
|
IGL02458:Cenpe
|
APN |
3 |
134,935,869 (GRCm39) |
nonsense |
probably null |
|
IGL02934:Cenpe
|
APN |
3 |
134,970,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03335:Cenpe
|
APN |
3 |
134,949,386 (GRCm39) |
missense |
probably benign |
|
R0086:Cenpe
|
UTSW |
3 |
134,970,185 (GRCm39) |
splice site |
probably benign |
|
R0173:Cenpe
|
UTSW |
3 |
134,965,744 (GRCm39) |
missense |
probably benign |
0.00 |
R0394:Cenpe
|
UTSW |
3 |
134,922,186 (GRCm39) |
splice site |
probably benign |
|
R0411:Cenpe
|
UTSW |
3 |
134,928,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Cenpe
|
UTSW |
3 |
134,952,347 (GRCm39) |
missense |
probably benign |
0.00 |
R0634:Cenpe
|
UTSW |
3 |
134,952,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Cenpe
|
UTSW |
3 |
134,935,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Cenpe
|
UTSW |
3 |
134,923,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Cenpe
|
UTSW |
3 |
134,970,183 (GRCm39) |
critical splice donor site |
probably null |
|
R1530:Cenpe
|
UTSW |
3 |
134,952,663 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1559:Cenpe
|
UTSW |
3 |
134,976,661 (GRCm39) |
missense |
probably benign |
0.07 |
R1562:Cenpe
|
UTSW |
3 |
134,944,155 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1568:Cenpe
|
UTSW |
3 |
134,945,519 (GRCm39) |
missense |
probably benign |
0.01 |
R1712:Cenpe
|
UTSW |
3 |
134,971,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R1828:Cenpe
|
UTSW |
3 |
134,952,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R1846:Cenpe
|
UTSW |
3 |
134,945,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Cenpe
|
UTSW |
3 |
134,974,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Cenpe
|
UTSW |
3 |
134,953,240 (GRCm39) |
missense |
probably damaging |
0.98 |
R1961:Cenpe
|
UTSW |
3 |
134,948,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Cenpe
|
UTSW |
3 |
134,928,082 (GRCm39) |
splice site |
probably benign |
|
R2118:Cenpe
|
UTSW |
3 |
134,952,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2127:Cenpe
|
UTSW |
3 |
134,945,541 (GRCm39) |
missense |
probably benign |
0.08 |
R2156:Cenpe
|
UTSW |
3 |
134,953,235 (GRCm39) |
missense |
probably benign |
0.34 |
R2265:Cenpe
|
UTSW |
3 |
134,967,397 (GRCm39) |
missense |
probably benign |
0.02 |
R2268:Cenpe
|
UTSW |
3 |
134,967,397 (GRCm39) |
missense |
probably benign |
0.02 |
R2392:Cenpe
|
UTSW |
3 |
134,953,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Cenpe
|
UTSW |
3 |
134,946,834 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3084:Cenpe
|
UTSW |
3 |
134,946,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R3779:Cenpe
|
UTSW |
3 |
134,962,337 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3833:Cenpe
|
UTSW |
3 |
134,928,083 (GRCm39) |
splice site |
probably benign |
|
R3974:Cenpe
|
UTSW |
3 |
134,940,986 (GRCm39) |
splice site |
probably null |
|
R3975:Cenpe
|
UTSW |
3 |
134,944,233 (GRCm39) |
critical splice donor site |
probably null |
|
R3975:Cenpe
|
UTSW |
3 |
134,940,986 (GRCm39) |
splice site |
probably null |
|
R4151:Cenpe
|
UTSW |
3 |
134,920,914 (GRCm39) |
missense |
probably benign |
0.36 |
R4166:Cenpe
|
UTSW |
3 |
134,949,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R4581:Cenpe
|
UTSW |
3 |
134,952,761 (GRCm39) |
missense |
probably benign |
0.30 |
R4622:Cenpe
|
UTSW |
3 |
134,949,469 (GRCm39) |
missense |
probably benign |
0.22 |
R4692:Cenpe
|
UTSW |
3 |
134,922,140 (GRCm39) |
missense |
probably benign |
0.29 |
R4769:Cenpe
|
UTSW |
3 |
134,953,912 (GRCm39) |
missense |
probably benign |
|
R4976:Cenpe
|
UTSW |
3 |
134,940,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Cenpe
|
UTSW |
3 |
134,940,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Cenpe
|
UTSW |
3 |
134,962,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5002:Cenpe
|
UTSW |
3 |
134,952,842 (GRCm39) |
missense |
probably benign |
|
R5057:Cenpe
|
UTSW |
3 |
134,926,074 (GRCm39) |
missense |
probably benign |
0.14 |
R5063:Cenpe
|
UTSW |
3 |
134,976,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R5181:Cenpe
|
UTSW |
3 |
134,948,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R5281:Cenpe
|
UTSW |
3 |
134,935,911 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5389:Cenpe
|
UTSW |
3 |
134,965,149 (GRCm39) |
critical splice donor site |
probably null |
|
R5517:Cenpe
|
UTSW |
3 |
134,929,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Cenpe
|
UTSW |
3 |
134,974,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R5607:Cenpe
|
UTSW |
3 |
134,940,837 (GRCm39) |
nonsense |
probably null |
|
R5608:Cenpe
|
UTSW |
3 |
134,940,837 (GRCm39) |
nonsense |
probably null |
|
R5627:Cenpe
|
UTSW |
3 |
134,941,234 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5766:Cenpe
|
UTSW |
3 |
134,954,174 (GRCm39) |
missense |
probably damaging |
0.96 |
R5783:Cenpe
|
UTSW |
3 |
134,967,341 (GRCm39) |
missense |
probably benign |
0.00 |
R5933:Cenpe
|
UTSW |
3 |
134,967,389 (GRCm39) |
missense |
probably benign |
0.03 |
R6073:Cenpe
|
UTSW |
3 |
134,965,834 (GRCm39) |
nonsense |
probably null |
|
R6163:Cenpe
|
UTSW |
3 |
134,974,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R6224:Cenpe
|
UTSW |
3 |
134,949,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6313:Cenpe
|
UTSW |
3 |
134,935,936 (GRCm39) |
missense |
probably benign |
0.26 |
R6326:Cenpe
|
UTSW |
3 |
134,945,539 (GRCm39) |
missense |
probably benign |
0.15 |
R6383:Cenpe
|
UTSW |
3 |
134,957,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R6418:Cenpe
|
UTSW |
3 |
134,957,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R6797:Cenpe
|
UTSW |
3 |
134,943,899 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6810:Cenpe
|
UTSW |
3 |
134,949,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6989:Cenpe
|
UTSW |
3 |
134,940,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Cenpe
|
UTSW |
3 |
134,940,963 (GRCm39) |
missense |
probably benign |
0.02 |
R7009:Cenpe
|
UTSW |
3 |
134,940,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R7039:Cenpe
|
UTSW |
3 |
134,961,217 (GRCm39) |
missense |
probably benign |
0.28 |
R7387:Cenpe
|
UTSW |
3 |
134,952,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7470:Cenpe
|
UTSW |
3 |
134,947,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Cenpe
|
UTSW |
3 |
134,949,523 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7562:Cenpe
|
UTSW |
3 |
134,954,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Cenpe
|
UTSW |
3 |
134,953,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R7613:Cenpe
|
UTSW |
3 |
134,948,063 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7741:Cenpe
|
UTSW |
3 |
134,953,096 (GRCm39) |
splice site |
probably null |
|
R7771:Cenpe
|
UTSW |
3 |
134,946,702 (GRCm39) |
splice site |
probably null |
|
R7843:Cenpe
|
UTSW |
3 |
134,938,720 (GRCm39) |
nonsense |
probably null |
|
R7973:Cenpe
|
UTSW |
3 |
134,929,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8036:Cenpe
|
UTSW |
3 |
134,945,609 (GRCm39) |
frame shift |
probably null |
|
R8069:Cenpe
|
UTSW |
3 |
134,949,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Cenpe
|
UTSW |
3 |
134,952,783 (GRCm39) |
missense |
probably benign |
0.28 |
R8176:Cenpe
|
UTSW |
3 |
134,935,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Cenpe
|
UTSW |
3 |
134,957,375 (GRCm39) |
missense |
probably benign |
|
R8251:Cenpe
|
UTSW |
3 |
134,957,445 (GRCm39) |
critical splice donor site |
probably null |
|
R8425:Cenpe
|
UTSW |
3 |
134,948,388 (GRCm39) |
nonsense |
probably null |
|
R8488:Cenpe
|
UTSW |
3 |
134,965,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R8811:Cenpe
|
UTSW |
3 |
134,929,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R8850:Cenpe
|
UTSW |
3 |
134,930,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Cenpe
|
UTSW |
3 |
134,965,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R8899:Cenpe
|
UTSW |
3 |
134,945,644 (GRCm39) |
missense |
probably benign |
0.18 |
R9035:Cenpe
|
UTSW |
3 |
134,976,572 (GRCm39) |
missense |
probably benign |
0.01 |
R9038:Cenpe
|
UTSW |
3 |
134,923,797 (GRCm39) |
missense |
probably benign |
0.00 |
R9093:Cenpe
|
UTSW |
3 |
134,945,641 (GRCm39) |
nonsense |
probably null |
|
R9221:Cenpe
|
UTSW |
3 |
134,935,839 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9365:Cenpe
|
UTSW |
3 |
134,954,207 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9443:Cenpe
|
UTSW |
3 |
134,976,609 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cenpe
|
UTSW |
3 |
134,922,146 (GRCm39) |
missense |
possibly damaging |
0.83 |
|