Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Ahi1 |
G |
A |
10: 20,848,035 (GRCm39) |
R481Q |
probably damaging |
Het |
Arhgef3 |
T |
C |
14: 27,101,555 (GRCm39) |
I77T |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,889,207 (GRCm39) |
V362E |
possibly damaging |
Het |
Bcat2 |
T |
A |
7: 45,225,294 (GRCm39) |
F57L |
probably damaging |
Het |
Ccdc73 |
C |
T |
2: 104,738,011 (GRCm39) |
L36F |
probably damaging |
Het |
Ccl19 |
C |
T |
4: 42,756,288 (GRCm39) |
V15I |
probably benign |
Het |
Ces1a |
A |
T |
8: 93,774,727 (GRCm39) |
F4I |
probably benign |
Het |
Chchd6 |
G |
A |
6: 89,551,413 (GRCm39) |
P83S |
probably benign |
Het |
Cnr1 |
T |
C |
4: 33,943,798 (GRCm39) |
M62T |
probably benign |
Het |
Colec12 |
T |
C |
18: 9,848,146 (GRCm39) |
L108P |
probably damaging |
Het |
Cyb5a |
T |
C |
18: 84,894,979 (GRCm39) |
|
probably benign |
Het |
Dhrs4 |
C |
T |
14: 55,724,776 (GRCm39) |
T181I |
probably benign |
Het |
Disc1 |
T |
C |
8: 125,851,285 (GRCm39) |
S392P |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,566,859 (GRCm39) |
F69L |
|
Het |
Ehmt1 |
T |
C |
2: 24,728,722 (GRCm39) |
D726G |
probably damaging |
Het |
Epg5 |
T |
A |
18: 77,997,957 (GRCm39) |
L462I |
probably damaging |
Het |
Exoc2 |
A |
T |
13: 31,040,697 (GRCm39) |
S774T |
probably benign |
Het |
Fam135b |
A |
G |
15: 71,334,813 (GRCm39) |
S794P |
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,606,973 (GRCm39) |
V646A |
probably benign |
Het |
Gm3543 |
G |
T |
14: 41,804,093 (GRCm39) |
D57E |
possibly damaging |
Het |
Golgb1 |
T |
A |
16: 36,736,124 (GRCm39) |
D1831E |
probably damaging |
Het |
Hace1 |
T |
G |
10: 45,586,092 (GRCm39) |
|
probably null |
Het |
Irgc |
T |
C |
7: 24,131,872 (GRCm39) |
E315G |
possibly damaging |
Het |
Ism1 |
A |
G |
2: 139,582,321 (GRCm39) |
Y211C |
probably damaging |
Het |
Kpna1 |
T |
G |
16: 35,833,287 (GRCm39) |
V121G |
probably damaging |
Het |
Lifr |
T |
A |
15: 7,198,521 (GRCm39) |
F250L |
probably damaging |
Het |
Llgl2 |
A |
G |
11: 115,740,407 (GRCm39) |
T368A |
probably benign |
Het |
Lmln |
T |
A |
16: 32,925,169 (GRCm39) |
C467* |
probably null |
Het |
Lrrtm3 |
T |
C |
10: 63,923,943 (GRCm39) |
E408G |
probably benign |
Het |
Melk |
C |
T |
4: 44,340,693 (GRCm39) |
A330V |
probably null |
Het |
Mmp13 |
T |
G |
9: 7,277,921 (GRCm39) |
D271E |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,052,297 (GRCm39) |
T390A |
|
Het |
Myh8 |
A |
G |
11: 67,174,632 (GRCm39) |
K249R |
probably benign |
Het |
Nr1h4 |
T |
A |
10: 89,319,315 (GRCm39) |
M184L |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,885,337 (GRCm39) |
|
probably null |
Het |
Otog |
T |
G |
7: 45,920,688 (GRCm39) |
C964G |
probably damaging |
Het |
Oxct2b |
T |
C |
4: 123,010,589 (GRCm39) |
S170P |
probably benign |
Het |
Pcdha4 |
T |
C |
18: 37,087,112 (GRCm39) |
S432P |
possibly damaging |
Het |
Prb1a |
T |
A |
6: 132,184,201 (GRCm39) |
R477S |
unknown |
Het |
Prh1 |
G |
A |
6: 132,549,108 (GRCm39) |
G205D |
unknown |
Het |
Psg23 |
C |
T |
7: 18,344,393 (GRCm39) |
G354D |
probably damaging |
Het |
Pura |
T |
G |
18: 36,420,913 (GRCm39) |
D233E |
possibly damaging |
Het |
Rb1cc1 |
G |
T |
1: 6,315,117 (GRCm39) |
L423F |
probably damaging |
Het |
Rimbp3 |
T |
C |
16: 17,026,620 (GRCm39) |
S15P |
possibly damaging |
Het |
Scn1a |
A |
G |
2: 66,148,465 (GRCm39) |
F7L |
probably benign |
Het |
Sftpb |
A |
T |
6: 72,284,189 (GRCm39) |
R203* |
probably null |
Het |
Slc30a9 |
A |
G |
5: 67,507,142 (GRCm39) |
K478R |
probably damaging |
Het |
Slc35f5 |
T |
A |
1: 125,496,333 (GRCm39) |
M156K |
probably benign |
Het |
Slc41a3 |
A |
G |
6: 90,612,327 (GRCm39) |
I232V |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,461,534 (GRCm39) |
D1527G |
probably benign |
Het |
Srfbp1 |
T |
G |
18: 52,623,540 (GRCm39) |
V389G |
possibly damaging |
Het |
Sun2 |
C |
T |
15: 79,622,720 (GRCm39) |
|
probably null |
Het |
Tep1 |
G |
T |
14: 51,064,597 (GRCm39) |
A2386D |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,064,564 (GRCm39) |
S1331R |
possibly damaging |
Het |
Tgm1 |
A |
T |
14: 55,942,349 (GRCm39) |
N667K |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tsen54 |
T |
C |
11: 115,713,410 (GRCm39) |
F438L |
probably damaging |
Het |
Ube4a |
T |
C |
9: 44,862,191 (GRCm39) |
H150R |
probably benign |
Het |
Uty |
T |
C |
Y: 1,099,712 (GRCm39) |
N1161S |
possibly damaging |
Het |
Vmn2r16 |
T |
A |
5: 109,488,064 (GRCm39) |
D312E |
probably damaging |
Het |
Wdr55 |
T |
G |
18: 36,893,354 (GRCm39) |
C5W |
probably damaging |
Het |
Zbtb24 |
C |
A |
10: 41,332,540 (GRCm39) |
P405Q |
probably damaging |
Het |
Zkscan2 |
T |
A |
7: 123,079,591 (GRCm39) |
I789F |
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 |
|
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 |
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 |
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 |
|