Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,660,951 |
Y1019F |
probably benign |
Het |
4930455H04Rik |
T |
G |
3: 116,968,551 |
|
probably benign |
Het |
4930548H24Rik |
A |
T |
5: 31,487,427 |
I175L |
probably benign |
Het |
4932415D10Rik |
C |
A |
10: 82,284,734 |
K4147N |
probably damaging |
Het |
9830107B12Rik |
A |
T |
17: 48,128,583 |
|
probably benign |
Het |
Abcc8 |
A |
G |
7: 46,135,493 |
V737A |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,331,448 |
Y930F |
probably damaging |
Het |
Alkbh8 |
T |
A |
9: 3,369,825 |
F365I |
probably damaging |
Het |
App |
G |
A |
16: 85,103,239 |
H108Y |
probably damaging |
Het |
Bfsp1 |
T |
C |
2: 143,827,644 |
|
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,742,429 |
N478S |
probably damaging |
Het |
Camsap3 |
G |
A |
8: 3,604,795 |
V796I |
probably damaging |
Het |
Carns1 |
A |
T |
19: 4,166,499 |
|
probably null |
Het |
Clca1 |
C |
T |
3: 145,007,778 |
M697I |
probably benign |
Het |
Cltc |
C |
T |
11: 86,702,248 |
M1600I |
probably benign |
Het |
Cnot1 |
T |
A |
8: 95,741,009 |
N1499Y |
probably damaging |
Het |
Crebbp |
T |
A |
16: 4,124,768 |
I196L |
probably damaging |
Het |
Drc3 |
C |
A |
11: 60,358,649 |
|
probably benign |
Het |
Fam161a |
T |
A |
11: 23,020,702 |
Y234* |
probably null |
Het |
Il1r1 |
C |
A |
1: 40,313,170 |
P500Q |
probably damaging |
Het |
Katnal1 |
G |
T |
5: 148,893,797 |
|
probably benign |
Het |
Klhdc2 |
A |
G |
12: 69,297,053 |
N20S |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,502,019 |
T1527S |
possibly damaging |
Het |
Magi1 |
C |
T |
6: 93,747,224 |
G270D |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,715,922 |
S2035T |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,699,546 |
M1253K |
probably benign |
Het |
Myh7 |
T |
C |
14: 54,988,879 |
M435V |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,292,679 |
I739V |
probably benign |
Het |
Npnt |
T |
C |
3: 132,885,982 |
K430R |
probably damaging |
Het |
Nrd1 |
A |
G |
4: 109,047,660 |
N696S |
probably benign |
Het |
Oit3 |
T |
C |
10: 59,425,484 |
|
probably benign |
Het |
Olfr1350 |
A |
G |
7: 6,570,212 |
T74A |
probably benign |
Het |
Olfr478 |
A |
T |
7: 108,032,121 |
I74K |
possibly damaging |
Het |
Olfr571 |
A |
G |
7: 102,909,719 |
I40T |
possibly damaging |
Het |
Olfr642 |
A |
G |
7: 104,050,169 |
Y62H |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,594,821 |
|
probably null |
Het |
Plat |
A |
G |
8: 22,776,828 |
M279V |
probably benign |
Het |
Prkd1 |
A |
T |
12: 50,392,910 |
L378* |
probably null |
Het |
Rasgef1a |
C |
T |
6: 118,084,545 |
T157I |
probably benign |
Het |
Rbm22 |
A |
G |
18: 60,560,857 |
N11S |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,046,330 |
|
probably benign |
Het |
Sema6d |
T |
A |
2: 124,653,642 |
F3Y |
unknown |
Het |
Sis |
T |
C |
3: 72,961,021 |
D112G |
probably benign |
Het |
Slit1 |
C |
A |
19: 41,611,044 |
G1023C |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,612,555 |
|
probably benign |
Het |
Sspo |
T |
C |
6: 48,498,343 |
I4881T |
probably benign |
Het |
Supt6 |
C |
A |
11: 78,221,143 |
D1038Y |
probably damaging |
Het |
Tbc1d2b |
A |
T |
9: 90,205,091 |
L945Q |
probably damaging |
Het |
Tgfbr3 |
G |
T |
5: 107,149,898 |
A212E |
probably damaging |
Het |
Tipin |
A |
G |
9: 64,304,408 |
T259A |
probably benign |
Het |
Traip |
T |
C |
9: 107,970,472 |
S365P |
probably benign |
Het |
Tst |
T |
C |
15: 78,399,767 |
T287A |
probably benign |
Het |
Tube1 |
C |
T |
10: 39,145,722 |
|
probably benign |
Het |
Uhrf1bp1l |
T |
C |
10: 89,805,762 |
S932P |
probably benign |
Het |
Vmn1r37 |
T |
A |
6: 66,731,409 |
N6K |
probably damaging |
Het |
Vmn2r17 |
C |
T |
5: 109,453,032 |
T732I |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,406,628 |
D767E |
possibly damaging |
Het |
|