Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7b |
A |
T |
4: 56,741,022 (GRCm39) |
L112Q |
probably damaging |
Het |
Agap3 |
A |
C |
5: 24,688,399 (GRCm39) |
I396L |
probably benign |
Het |
AI987944 |
G |
T |
7: 41,023,880 (GRCm39) |
S366R |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,215,714 (GRCm39) |
T1049A |
probably damaging |
Het |
Ap1g2 |
A |
T |
14: 55,340,111 (GRCm39) |
L407* |
probably null |
Het |
Baiap3 |
G |
A |
17: 25,462,814 (GRCm39) |
R1075C |
probably benign |
Het |
Brd3 |
T |
C |
2: 27,346,929 (GRCm39) |
K402E |
probably damaging |
Het |
Cc2d2b |
A |
T |
19: 40,790,845 (GRCm39) |
D935V |
probably damaging |
Het |
Cfap74 |
G |
T |
4: 155,538,565 (GRCm39) |
|
probably null |
Het |
Chrdl2 |
A |
G |
7: 99,677,879 (GRCm39) |
T261A |
probably damaging |
Het |
Cyp4a14 |
G |
A |
4: 115,348,278 (GRCm39) |
R400C |
probably benign |
Het |
Dhfr |
G |
A |
13: 92,491,791 (GRCm39) |
V9I |
probably benign |
Het |
Epha4 |
A |
G |
1: 77,483,422 (GRCm39) |
S196P |
probably damaging |
Het |
Evc2 |
T |
A |
5: 37,579,232 (GRCm39) |
L1115Q |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,287,561 (GRCm39) |
E654V |
probably damaging |
Het |
Fcgbpl1 |
G |
A |
7: 27,839,573 (GRCm39) |
R462Q |
possibly damaging |
Het |
Fer1l4 |
C |
T |
2: 155,878,650 (GRCm39) |
V14I |
probably benign |
Het |
Frmd5 |
A |
T |
2: 121,378,128 (GRCm39) |
|
probably benign |
Het |
Helz |
T |
C |
11: 107,510,144 (GRCm39) |
|
probably null |
Het |
Igkv6-13 |
T |
C |
6: 70,434,498 (GRCm39) |
S116G |
probably benign |
Het |
Iscu |
T |
C |
5: 113,914,833 (GRCm39) |
V115A |
possibly damaging |
Het |
Jade2 |
C |
A |
11: 51,719,186 (GRCm39) |
K253N |
probably damaging |
Het |
Katnal2 |
A |
G |
18: 77,134,868 (GRCm39) |
|
probably null |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Magi3 |
T |
C |
3: 103,958,699 (GRCm39) |
D462G |
probably damaging |
Het |
Map3k14 |
T |
C |
11: 103,111,861 (GRCm39) |
N940S |
probably damaging |
Het |
Masp2 |
A |
T |
4: 148,687,043 (GRCm39) |
M1L |
probably benign |
Het |
Mga |
G |
A |
2: 119,763,159 (GRCm39) |
V1272I |
probably benign |
Het |
Mib2 |
T |
C |
4: 155,744,158 (GRCm39) |
D168G |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Msto1 |
A |
C |
3: 88,818,697 (GRCm39) |
V287G |
probably damaging |
Het |
Myo5b |
T |
A |
18: 74,834,599 (GRCm39) |
D886E |
probably benign |
Het |
Nek10 |
T |
C |
14: 14,826,946 (GRCm38) |
I48T |
possibly damaging |
Het |
Nek10 |
A |
T |
14: 14,986,700 (GRCm38) |
R1013W |
probably damaging |
Het |
Nipsnap3a |
T |
C |
4: 53,000,130 (GRCm39) |
V194A |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,267,367 (GRCm39) |
T766S |
probably benign |
Het |
Nol10 |
T |
A |
12: 17,479,185 (GRCm39) |
S672T |
possibly damaging |
Het |
Or4a80 |
A |
T |
2: 89,583,095 (GRCm39) |
F26I |
probably benign |
Het |
Or4c121 |
A |
T |
2: 89,023,790 (GRCm39) |
I196N |
probably damaging |
Het |
Or8d1b |
T |
A |
9: 38,887,283 (GRCm39) |
F104I |
probably damaging |
Het |
Or8j3c |
A |
T |
2: 86,253,177 (GRCm39) |
I281K |
possibly damaging |
Het |
Patj |
T |
A |
4: 98,457,315 (GRCm39) |
N1272K |
probably damaging |
Het |
Peak1 |
T |
C |
9: 56,165,093 (GRCm39) |
E945G |
probably benign |
Het |
Peg3 |
C |
T |
7: 6,720,858 (GRCm39) |
D16N |
probably damaging |
Het |
Pik3r4 |
T |
G |
9: 105,554,089 (GRCm39) |
I1082M |
possibly damaging |
Het |
Plekhg5 |
T |
A |
4: 152,192,242 (GRCm39) |
M472K |
possibly damaging |
Het |
Plekhm1 |
T |
C |
11: 103,286,054 (GRCm39) |
D127G |
probably damaging |
Het |
Ppfia4 |
G |
A |
1: 134,239,853 (GRCm39) |
S908L |
probably damaging |
Het |
Psmc3 |
A |
G |
2: 90,885,391 (GRCm39) |
N60S |
probably benign |
Het |
Rapgef1 |
T |
A |
2: 29,616,226 (GRCm39) |
D697E |
probably damaging |
Het |
Rapgef3 |
T |
A |
15: 97,659,449 (GRCm39) |
H54L |
probably benign |
Het |
Rhobtb3 |
G |
A |
13: 76,020,572 (GRCm39) |
R577* |
probably null |
Het |
Safb2 |
T |
C |
17: 56,871,594 (GRCm39) |
E218G |
possibly damaging |
Het |
Scaf1 |
C |
T |
7: 44,657,850 (GRCm39) |
R343H |
probably damaging |
Het |
Snx24 |
G |
A |
18: 53,473,307 (GRCm39) |
|
probably null |
Het |
Tbc1d1 |
T |
C |
5: 64,442,100 (GRCm39) |
F707L |
probably benign |
Het |
Tcaf2 |
T |
C |
6: 42,603,074 (GRCm39) |
T829A |
probably damaging |
Het |
Tcea2 |
C |
T |
2: 181,328,711 (GRCm39) |
Q248* |
probably null |
Het |
Tcirg1 |
A |
T |
19: 3,946,666 (GRCm39) |
L729Q |
probably damaging |
Het |
Thap3 |
A |
G |
4: 152,070,149 (GRCm39) |
F82L |
probably damaging |
Het |
Ttk |
T |
A |
9: 83,750,145 (GRCm39) |
M700K |
probably damaging |
Het |
Ubap2l |
G |
T |
3: 89,909,662 (GRCm39) |
P56H |
probably damaging |
Het |
Ubr2 |
A |
G |
17: 47,321,139 (GRCm39) |
S3P |
probably benign |
Het |
Uchl3 |
C |
T |
14: 101,923,128 (GRCm39) |
|
probably benign |
Het |
Vmn2r111 |
T |
A |
17: 22,767,165 (GRCm39) |
E777D |
probably damaging |
Het |
Vmn2r20 |
A |
T |
6: 123,363,082 (GRCm39) |
D567E |
probably damaging |
Het |
Vps13c |
T |
G |
9: 67,845,045 (GRCm39) |
L2043R |
probably damaging |
Het |
Zan |
T |
G |
5: 137,398,396 (GRCm39) |
D4212A |
unknown |
Het |
Zap70 |
C |
T |
1: 36,817,832 (GRCm39) |
P278S |
probably benign |
Het |
Zbtb8b |
A |
T |
4: 129,321,478 (GRCm39) |
M461K |
possibly damaging |
Het |
Zfat |
T |
G |
15: 68,052,211 (GRCm39) |
I528L |
probably benign |
Het |
Zfp532 |
T |
G |
18: 65,771,834 (GRCm39) |
V784G |
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 |
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 |
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 |
|