Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
A |
T |
8: 41,206,844 (GRCm39) |
I37L |
probably benign |
Het |
Alpk1 |
A |
G |
3: 127,474,968 (GRCm39) |
|
probably null |
Het |
Ankrd33 |
T |
C |
15: 101,014,488 (GRCm39) |
F8L |
probably damaging |
Het |
Avil |
A |
G |
10: 126,852,222 (GRCm39) |
K669R |
probably benign |
Het |
Bcor |
G |
T |
X: 11,914,749 (GRCm39) |
L1165I |
probably damaging |
Het |
C7 |
A |
G |
15: 5,088,871 (GRCm39) |
|
probably benign |
Het |
Cc2d2a |
A |
G |
5: 43,875,896 (GRCm39) |
I958V |
probably benign |
Het |
Chrna7 |
G |
A |
7: 62,755,842 (GRCm39) |
L235F |
probably damaging |
Het |
Col6a3 |
C |
A |
1: 90,706,919 (GRCm39) |
V2065L |
unknown |
Het |
Copb1 |
A |
T |
7: 113,846,020 (GRCm39) |
N183K |
probably benign |
Het |
Cpn2 |
G |
A |
16: 30,079,653 (GRCm39) |
A16V |
probably benign |
Het |
Cul1 |
A |
G |
6: 47,502,542 (GRCm39) |
K769E |
possibly damaging |
Het |
Deup1 |
C |
T |
9: 15,503,656 (GRCm39) |
V302M |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,927,176 (GRCm39) |
K3871E |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,004,431 (GRCm39) |
V3844A |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,657,487 (GRCm39) |
L763* |
probably null |
Het |
Donson |
A |
T |
16: 91,478,064 (GRCm39) |
W461R |
probably damaging |
Het |
Dpp10 |
T |
C |
1: 123,269,418 (GRCm39) |
I664V |
probably benign |
Het |
Dusp8 |
T |
A |
7: 141,636,484 (GRCm39) |
T369S |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,117,422 (GRCm39) |
L56Q |
probably damaging |
Het |
Ecd |
A |
T |
14: 20,374,545 (GRCm39) |
S532T |
probably benign |
Het |
Frg2f1 |
G |
A |
4: 119,388,154 (GRCm39) |
T115I |
probably damaging |
Het |
Gpatch2l |
A |
G |
12: 86,335,735 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
T |
A |
5: 31,316,867 (GRCm39) |
|
probably null |
Het |
Haghl |
T |
C |
17: 26,002,470 (GRCm39) |
|
probably benign |
Het |
Hoxc8 |
A |
T |
15: 102,901,181 (GRCm39) |
N208I |
probably damaging |
Het |
Igf2 |
T |
C |
7: 142,207,785 (GRCm39) |
D115G |
probably benign |
Het |
Jag2 |
T |
A |
12: 112,879,613 (GRCm39) |
D385V |
probably damaging |
Het |
Laptm4b |
A |
G |
15: 34,258,888 (GRCm39) |
H54R |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,352,117 (GRCm39) |
S640P |
probably damaging |
Het |
Map3k8 |
A |
C |
18: 4,334,660 (GRCm39) |
V328G |
probably damaging |
Het |
Mfsd13a |
A |
G |
19: 46,360,686 (GRCm39) |
E388G |
probably damaging |
Het |
Ms4a13 |
G |
A |
19: 11,149,292 (GRCm39) |
T168I |
probably benign |
Het |
Mtg1 |
C |
A |
7: 139,730,085 (GRCm39) |
Q294K |
probably benign |
Het |
Myh3 |
C |
T |
11: 66,987,766 (GRCm39) |
A1413V |
possibly damaging |
Het |
Neo1 |
A |
T |
9: 58,801,150 (GRCm39) |
|
probably benign |
Het |
Ogfod3 |
T |
C |
11: 121,091,749 (GRCm39) |
E119G |
probably benign |
Het |
Or10ak9 |
A |
G |
4: 118,726,497 (GRCm39) |
N173S |
possibly damaging |
Het |
Or2t49 |
A |
T |
11: 58,393,073 (GRCm39) |
M109K |
probably benign |
Het |
Or4a77 |
A |
G |
2: 89,487,692 (GRCm39) |
L31P |
probably damaging |
Het |
Or5ak20 |
G |
A |
2: 85,184,006 (GRCm39) |
T88I |
probably benign |
Het |
Or6c210 |
A |
T |
10: 129,496,475 (GRCm39) |
I267F |
probably benign |
Het |
Parvb |
G |
T |
15: 84,187,635 (GRCm39) |
D248Y |
probably damaging |
Het |
Pcdh11x |
A |
T |
X: 119,310,315 (GRCm39) |
H586L |
possibly damaging |
Het |
Phactr2 |
T |
C |
10: 13,137,572 (GRCm39) |
E120G |
probably damaging |
Het |
Ppfibp2 |
A |
T |
7: 107,342,171 (GRCm39) |
Q775L |
probably damaging |
Het |
Rcbtb1 |
A |
G |
14: 59,467,443 (GRCm39) |
Y427C |
probably damaging |
Het |
Rftn2 |
A |
T |
1: 55,250,351 (GRCm39) |
C131* |
probably null |
Het |
Rigi |
A |
G |
4: 40,229,536 (GRCm39) |
S83P |
probably damaging |
Het |
Rps6ka2 |
A |
G |
17: 7,556,402 (GRCm39) |
D474G |
probably benign |
Het |
Rsbn1l |
T |
C |
5: 21,156,734 (GRCm39) |
E17G |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,720,585 (GRCm39) |
M2688V |
probably benign |
Het |
Slc22a18 |
C |
A |
7: 143,046,574 (GRCm39) |
|
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,961,194 (GRCm39) |
|
probably benign |
Het |
Soat2 |
T |
C |
15: 102,070,550 (GRCm39) |
V451A |
probably damaging |
Het |
Sptlc2 |
A |
T |
12: 87,356,667 (GRCm39) |
|
probably benign |
Het |
Tada1 |
C |
T |
1: 166,220,203 (GRCm39) |
L308F |
probably damaging |
Het |
Tango2 |
A |
T |
16: 18,128,731 (GRCm39) |
|
probably null |
Het |
Tbc1d15 |
A |
T |
10: 115,065,111 (GRCm39) |
V158D |
probably damaging |
Het |
Tmx2 |
A |
T |
2: 84,503,588 (GRCm39) |
|
probably benign |
Het |
Tpte |
T |
A |
8: 22,795,874 (GRCm39) |
I79K |
probably benign |
Het |
Trav6-1 |
A |
G |
14: 52,876,199 (GRCm39) |
I40V |
probably benign |
Het |
Trgv3 |
A |
G |
13: 19,427,423 (GRCm39) |
Y102C |
probably damaging |
Het |
Ubash3a |
T |
C |
17: 31,450,455 (GRCm39) |
S377P |
possibly damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,600,446 (GRCm39) |
D575G |
probably damaging |
Het |
Vps41 |
A |
G |
13: 19,037,649 (GRCm39) |
D704G |
possibly damaging |
Het |
Vwa5a |
T |
C |
9: 38,638,259 (GRCm39) |
S261P |
possibly damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,317,264 (GRCm39) |
V112A |
probably damaging |
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 |
|
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 |
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 |
|