Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700007K13Rik |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,466,110 |
|
probably benign |
Het |
1700010I14Rik |
T |
A |
17: 8,997,029 |
C322* |
probably null |
Het |
1700019N19Rik |
A |
T |
19: 58,789,107 |
Y90* |
probably null |
Het |
2310035C23Rik |
G |
T |
1: 105,721,416 |
|
probably null |
Het |
4930553M12Rik |
G |
A |
4: 88,868,331 |
R17C |
unknown |
Het |
Abcc8 |
G |
A |
7: 46,135,526 |
T726I |
probably benign |
Het |
Adamts18 |
T |
C |
8: 113,709,645 |
T981A |
probably benign |
Het |
Adgrb3 |
A |
G |
1: 25,531,876 |
C507R |
probably damaging |
Het |
Bloc1s6 |
T |
A |
2: 122,742,695 |
D63E |
probably damaging |
Het |
Cdc25b |
C |
T |
2: 131,191,173 |
R135W |
probably damaging |
Het |
Cdca2 |
G |
T |
14: 67,677,877 |
Y644* |
probably null |
Het |
Ceacam10 |
G |
T |
7: 24,778,350 |
G97C |
probably damaging |
Het |
Cenpf |
G |
A |
1: 189,650,694 |
L2668F |
probably damaging |
Het |
Cog4 |
A |
G |
8: 110,881,828 |
D774G |
probably damaging |
Het |
Col11a2 |
G |
A |
17: 34,051,508 |
G511E |
unknown |
Het |
Col19a1 |
T |
A |
1: 24,530,008 |
I220F |
unknown |
Het |
Cubn |
G |
T |
2: 13,424,739 |
T1317K |
probably damaging |
Het |
Dnaaf5 |
T |
C |
5: 139,150,317 |
L24P |
unknown |
Het |
Fan1 |
T |
A |
7: 64,372,486 |
N340Y |
probably damaging |
Het |
Foxn4 |
C |
A |
5: 114,258,655 |
E256* |
probably null |
Het |
Gm4869 |
A |
G |
5: 140,471,670 |
D398G |
probably benign |
Het |
Gm5580 |
G |
A |
6: 116,551,477 |
R105Q |
probably damaging |
Het |
Gm5930 |
A |
G |
14: 44,336,557 |
S108P |
probably damaging |
Het |
Gnl3 |
A |
G |
14: 31,013,232 |
S468P |
probably benign |
Het |
Gzmb |
A |
T |
14: 56,262,119 |
S11T |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,733,129 |
|
probably null |
Het |
Ifi206 |
A |
G |
1: 173,473,862 |
L750P |
unknown |
Het |
Ifi213 |
T |
A |
1: 173,595,125 |
E58V |
probably damaging |
Het |
Igkv4-78 |
A |
T |
6: 69,059,768 |
Y94N |
probably damaging |
Het |
Igsf9 |
G |
T |
1: 172,491,757 |
|
probably null |
Het |
Itpr2 |
G |
T |
6: 146,158,949 |
L2490M |
possibly damaging |
Het |
Kdm2b |
A |
G |
5: 122,880,791 |
F862S |
probably damaging |
Het |
Meis1 |
A |
G |
11: 19,011,351 |
I174T |
probably damaging |
Het |
Micu3 |
A |
G |
8: 40,382,125 |
Q507R |
probably benign |
Het |
Mpp4 |
C |
T |
1: 59,143,810 |
E313K |
possibly damaging |
Het |
Nfatc4 |
G |
A |
14: 55,825,055 |
E7K |
probably damaging |
Het |
Olfr466 |
T |
A |
13: 65,152,842 |
V206D |
possibly damaging |
Het |
Olfr828 |
A |
T |
9: 18,816,190 |
Y35N |
probably damaging |
Het |
Osbpl5 |
G |
A |
7: 143,701,278 |
P470S |
probably damaging |
Het |
Pak6 |
A |
G |
2: 118,693,591 |
D409G |
possibly damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,498,590 |
M553K |
probably benign |
Het |
Ppp2r3a |
T |
C |
9: 101,212,672 |
N151D |
probably damaging |
Het |
Prdm12 |
T |
C |
2: 31,643,850 |
W160R |
probably damaging |
Het |
Prdm2 |
G |
A |
4: 143,132,901 |
T1273M |
possibly damaging |
Het |
Prl2a1 |
A |
G |
13: 27,807,370 |
|
probably null |
Het |
Prob1 |
G |
A |
18: 35,654,550 |
P217L |
possibly damaging |
Het |
Ramp1 |
A |
C |
1: 91,196,777 |
H20P |
probably benign |
Het |
Rbm47 |
T |
A |
5: 66,026,750 |
E170V |
possibly damaging |
Het |
Rpn1 |
C |
T |
6: 88,090,084 |
P142L |
probably damaging |
Het |
Rsu1 |
C |
T |
2: 13,170,016 |
R238H |
probably damaging |
Het |
Sh3rf3 |
C |
T |
10: 59,071,973 |
P441L |
probably damaging |
Het |
Slc1a6 |
A |
G |
10: 78,814,604 |
S559G |
possibly damaging |
Het |
Slc35f5 |
C |
A |
1: 125,572,485 |
S245R |
probably damaging |
Het |
Spcs3 |
T |
C |
8: 54,526,519 |
N76D |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,111,395 |
T1075A |
possibly damaging |
Het |
Sympk |
A |
T |
7: 19,036,030 |
I211F |
probably benign |
Het |
Tk1 |
C |
T |
11: 117,825,777 |
M1I |
probably null |
Het |
Tln2 |
A |
G |
9: 67,346,461 |
V776A |
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,786,256 |
R118L |
possibly damaging |
Het |
Tnk2 |
T |
C |
16: 32,680,800 |
V977A |
probably benign |
Het |
Toporsl |
A |
T |
4: 52,611,630 |
S508C |
probably benign |
Het |
Trio |
T |
A |
15: 27,828,351 |
Q1409L |
possibly damaging |
Het |
Vit |
T |
C |
17: 78,605,498 |
F287L |
probably benign |
Het |
Vmn2r109 |
G |
C |
17: 20,541,438 |
D552E |
probably benign |
Het |
Zw10 |
T |
C |
9: 49,061,191 |
V186A |
probably benign |
Het |
|