Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c18 |
T |
A |
13: 4,195,276 (GRCm39) |
I61L |
probably benign |
Het |
Angptl2 |
T |
C |
2: 33,118,277 (GRCm39) |
V17A |
probably benign |
Het |
Casp14 |
T |
C |
10: 78,550,975 (GRCm39) |
D70G |
possibly damaging |
Het |
Cckbr |
A |
G |
7: 105,083,773 (GRCm39) |
M234V |
possibly damaging |
Het |
Cd93 |
T |
C |
2: 148,284,044 (GRCm39) |
N434S |
probably benign |
Het |
Col6a3 |
A |
C |
1: 90,731,810 (GRCm39) |
V1481G |
probably damaging |
Het |
Dnah5 |
G |
T |
15: 28,233,384 (GRCm39) |
E248* |
probably null |
Het |
Dnah5 |
G |
A |
15: 28,451,609 (GRCm39) |
R4349Q |
probably damaging |
Het |
F11 |
A |
G |
8: 45,706,092 (GRCm39) |
Y98H |
probably benign |
Het |
Fen1 |
A |
G |
19: 10,178,067 (GRCm39) |
F126L |
probably benign |
Het |
Gpr146 |
G |
A |
5: 139,378,795 (GRCm39) |
G199D |
possibly damaging |
Het |
Gramd1b |
A |
G |
9: 40,219,702 (GRCm39) |
I324T |
probably benign |
Het |
H2bc12 |
A |
T |
13: 22,220,259 (GRCm39) |
N68I |
probably benign |
Het |
Hivep1 |
C |
A |
13: 42,310,557 (GRCm39) |
S932R |
probably benign |
Het |
Hk3 |
A |
T |
13: 55,158,644 (GRCm39) |
|
probably null |
Het |
Hspbp1 |
T |
A |
7: 4,663,781 (GRCm39) |
M355L |
possibly damaging |
Het |
Jaml |
T |
C |
9: 45,000,058 (GRCm39) |
C77R |
probably damaging |
Het |
Kmt2e |
A |
G |
5: 23,687,505 (GRCm39) |
N452D |
possibly damaging |
Het |
Krt5 |
T |
C |
15: 101,621,076 (GRCm39) |
Y57C |
unknown |
Het |
Lipn |
A |
T |
19: 34,058,160 (GRCm39) |
M294L |
probably benign |
Het |
Magel2 |
A |
G |
7: 62,029,907 (GRCm39) |
E937G |
unknown |
Het |
Med13l |
G |
A |
5: 118,897,329 (GRCm39) |
|
probably null |
Het |
Mrgprb8 |
G |
A |
7: 48,038,892 (GRCm39) |
V188I |
probably benign |
Het |
Ocln |
T |
C |
13: 100,676,223 (GRCm39) |
D90G |
probably damaging |
Het |
Ofcc1 |
C |
T |
13: 40,241,423 (GRCm39) |
R695Q |
possibly damaging |
Het |
Or11h23 |
T |
A |
14: 50,948,563 (GRCm39) |
Y259N |
probably damaging |
Het |
Or52ab7 |
G |
A |
7: 102,978,328 (GRCm39) |
V212I |
probably benign |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Pak5 |
A |
T |
2: 135,939,454 (GRCm39) |
H560Q |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,480,694 (GRCm39) |
S493P |
probably damaging |
Het |
Ppp6r3 |
A |
G |
19: 3,564,719 (GRCm39) |
W185R |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,450,522 (GRCm39) |
D4189E |
probably damaging |
Het |
Serpinb9b |
A |
G |
13: 33,213,467 (GRCm39) |
N8S |
possibly damaging |
Het |
Slit3 |
A |
G |
11: 35,524,779 (GRCm39) |
T730A |
possibly damaging |
Het |
Srgap3 |
A |
T |
6: 112,806,503 (GRCm39) |
F53I |
probably damaging |
Het |
Stc2 |
T |
A |
11: 31,315,351 (GRCm39) |
K163* |
probably null |
Het |
Tasor2 |
T |
C |
13: 3,626,769 (GRCm39) |
I1060M |
probably benign |
Het |
Tlk1 |
T |
A |
2: 70,568,770 (GRCm39) |
K411* |
probably null |
Het |
Ttc27 |
G |
T |
17: 75,036,883 (GRCm39) |
L185F |
probably benign |
Het |
Vmn2r102 |
C |
T |
17: 19,880,694 (GRCm39) |
Q12* |
probably null |
Het |
Vmn2r95 |
C |
T |
17: 18,672,551 (GRCm39) |
|
probably benign |
Het |
Vopp1 |
A |
G |
6: 57,739,492 (GRCm39) |
Y19H |
possibly damaging |
Het |
Wdr64 |
T |
A |
1: 175,638,176 (GRCm39) |
|
probably null |
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 |
R6192:Cenpe
|
UTSW |
3 |
134,954,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
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 |
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 |
|