Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts3 |
C |
A |
5: 89,840,909 (GRCm39) |
V805F |
probably damaging |
Het |
Adgrb3 |
G |
A |
1: 25,865,165 (GRCm39) |
T226M |
probably damaging |
Het |
Ak5 |
A |
G |
3: 152,187,270 (GRCm39) |
S406P |
probably damaging |
Het |
Akt3 |
C |
G |
1: 177,076,254 (GRCm39) |
V12L |
probably benign |
Het |
Arhgef40 |
A |
C |
14: 52,227,146 (GRCm39) |
S397R |
probably damaging |
Het |
Atp5f1c |
A |
G |
2: 10,068,323 (GRCm39) |
V144A |
probably benign |
Het |
Ccser1 |
A |
G |
6: 61,289,144 (GRCm39) |
S436G |
probably benign |
Het |
Clgn |
G |
T |
8: 84,137,152 (GRCm39) |
V290F |
possibly damaging |
Het |
Dis3l |
T |
A |
9: 64,226,498 (GRCm39) |
D261V |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,981,435 (GRCm39) |
Y2577F |
probably damaging |
Het |
Evi5l |
A |
G |
8: 4,243,317 (GRCm39) |
E371G |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,201,530 (GRCm39) |
S515P |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,822,329 (GRCm39) |
I6021V |
probably benign |
Het |
Ftdc1 |
A |
C |
16: 58,434,227 (GRCm39) |
N163K |
probably benign |
Het |
Gstm5 |
A |
T |
3: 107,803,258 (GRCm39) |
|
probably benign |
Het |
H2-Oa |
G |
A |
17: 34,312,809 (GRCm39) |
D29N |
probably damaging |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Ireb2 |
A |
G |
9: 54,802,668 (GRCm39) |
I434M |
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Micall1 |
A |
G |
15: 79,014,078 (GRCm39) |
T658A |
probably benign |
Het |
Mitf |
C |
T |
6: 97,973,423 (GRCm39) |
A252V |
possibly damaging |
Het |
Mpzl1 |
A |
G |
1: 165,433,285 (GRCm39) |
I122T |
probably damaging |
Het |
Mtus2 |
G |
A |
5: 148,232,392 (GRCm39) |
V146I |
probably damaging |
Het |
Myh11 |
C |
T |
16: 14,023,770 (GRCm39) |
|
probably null |
Het |
Myrfl |
A |
G |
10: 116,653,609 (GRCm39) |
I486T |
probably damaging |
Het |
N4bp2 |
T |
C |
5: 65,974,561 (GRCm39) |
V1477A |
probably damaging |
Het |
Ndc1 |
T |
A |
4: 107,231,358 (GRCm39) |
S100T |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,857,851 (GRCm38) |
N433K |
probably benign |
Het |
Noc4l |
C |
T |
5: 110,799,212 (GRCm39) |
S190N |
probably benign |
Het |
Nprl2 |
A |
G |
9: 107,420,731 (GRCm39) |
E122G |
probably damaging |
Het |
Or13a19 |
A |
G |
7: 139,903,008 (GRCm39) |
Y132C |
probably damaging |
Het |
Or1e16 |
G |
C |
11: 73,286,119 (GRCm39) |
S243C |
probably damaging |
Het |
Or6n2 |
C |
T |
1: 173,897,095 (GRCm39) |
T77I |
probably benign |
Het |
Osbpl1a |
T |
C |
18: 12,896,594 (GRCm39) |
I324V |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Peg3 |
C |
T |
7: 6,713,026 (GRCm39) |
R732H |
probably damaging |
Het |
Rfc4 |
A |
G |
16: 22,933,046 (GRCm39) |
I297T |
possibly damaging |
Het |
Rpl3l |
T |
A |
17: 24,952,435 (GRCm39) |
D218E |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Syt11 |
C |
T |
3: 88,655,231 (GRCm39) |
V51I |
probably benign |
Het |
Tas2r115 |
A |
C |
6: 132,714,216 (GRCm39) |
L245R |
probably damaging |
Het |
Tmem115 |
G |
A |
9: 107,412,059 (GRCm39) |
V128I |
probably benign |
Het |
Trim47 |
A |
G |
11: 115,997,260 (GRCm39) |
V499A |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,638,256 (GRCm39) |
|
probably null |
Het |
Zfp143 |
A |
G |
7: 109,687,998 (GRCm39) |
D479G |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,839,878 (GRCm39) |
T91A |
possibly damaging |
Het |
|
Other mutations in Sesn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Sesn2
|
APN |
4 |
132,227,124 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01319:Sesn2
|
APN |
4 |
132,227,278 (GRCm39) |
splice site |
probably benign |
|
IGL01336:Sesn2
|
APN |
4 |
132,226,678 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01800:Sesn2
|
APN |
4 |
132,226,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Sesn2
|
APN |
4 |
132,224,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02882:Sesn2
|
APN |
4 |
132,221,104 (GRCm39) |
missense |
probably benign |
0.16 |
R1845:Sesn2
|
UTSW |
4 |
132,224,381 (GRCm39) |
nonsense |
probably null |
|
R4732:Sesn2
|
UTSW |
4 |
132,221,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Sesn2
|
UTSW |
4 |
132,221,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R5261:Sesn2
|
UTSW |
4 |
132,226,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R5385:Sesn2
|
UTSW |
4 |
132,226,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R6011:Sesn2
|
UTSW |
4 |
132,226,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6224:Sesn2
|
UTSW |
4 |
132,229,881 (GRCm39) |
missense |
probably benign |
0.01 |
R6852:Sesn2
|
UTSW |
4 |
132,221,113 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7224:Sesn2
|
UTSW |
4 |
132,224,724 (GRCm39) |
missense |
probably benign |
0.22 |
R7546:Sesn2
|
UTSW |
4 |
132,227,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Sesn2
|
UTSW |
4 |
132,224,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R8213:Sesn2
|
UTSW |
4 |
132,225,364 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9041:Sesn2
|
UTSW |
4 |
132,225,272 (GRCm39) |
missense |
probably benign |
0.44 |
R9072:Sesn2
|
UTSW |
4 |
132,224,195 (GRCm39) |
critical splice donor site |
probably null |
|
R9073:Sesn2
|
UTSW |
4 |
132,224,195 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Sesn2
|
UTSW |
4 |
132,226,623 (GRCm39) |
missense |
probably damaging |
0.99 |
|