Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530064D06Rik |
C |
T |
17: 48,166,390 |
V120M |
possibly damaging |
Het |
Abca6 |
T |
C |
11: 110,218,967 |
D646G |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 30,903,059 |
R141Q |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,314,018 |
T554A |
possibly damaging |
Het |
Atp2a3 |
G |
T |
11: 72,982,826 |
V824L |
probably null |
Het |
Bet1 |
T |
C |
6: 4,077,895 |
I115V |
possibly damaging |
Het |
Cdc23 |
C |
A |
18: 34,651,689 |
V7L |
unknown |
Het |
Cfap65 |
A |
G |
1: 74,906,441 |
S1373P |
probably damaging |
Het |
Chd9 |
T |
C |
8: 90,984,374 |
L353P |
probably damaging |
Het |
Chil3 |
C |
A |
3: 106,164,089 |
|
probably null |
Het |
Comp |
C |
T |
8: 70,381,300 |
T655M |
probably damaging |
Het |
Dctd |
T |
C |
8: 48,111,716 |
Y18H |
probably damaging |
Het |
Ddx39b |
G |
A |
17: 35,253,029 |
G348D |
possibly damaging |
Het |
Dhx36 |
A |
T |
3: 62,471,999 |
S889R |
probably benign |
Het |
Dtx2 |
T |
C |
5: 136,012,190 |
Y150H |
probably damaging |
Het |
Epx |
A |
G |
11: 87,872,680 |
F238S |
probably damaging |
Het |
Ergic2 |
T |
C |
6: 148,196,014 |
T154A |
probably benign |
Het |
Esco1 |
A |
G |
18: 10,594,734 |
I184T |
probably benign |
Het |
Esf1 |
G |
T |
2: 140,157,071 |
A495E |
possibly damaging |
Het |
Esf1 |
T |
C |
2: 140,158,579 |
Y429C |
possibly damaging |
Het |
Fcho1 |
C |
A |
8: 71,717,176 |
R101L |
probably benign |
Het |
Foxn4 |
T |
A |
5: 114,256,927 |
D313V |
probably damaging |
Het |
Gm11568 |
T |
C |
11: 99,857,972 |
M1T |
probably null |
Het |
Gm14409 |
A |
G |
2: 177,265,571 |
F45L |
probably damaging |
Het |
Gphn |
T |
A |
12: 78,623,289 |
|
probably null |
Het |
Grid2 |
C |
T |
6: 64,320,152 |
Q500* |
probably null |
Het |
Igsf10 |
A |
G |
3: 59,326,273 |
S1680P |
probably damaging |
Het |
Ints12 |
T |
C |
3: 133,100,777 |
M155T |
possibly damaging |
Het |
Invs |
A |
T |
4: 48,396,307 |
M327L |
possibly damaging |
Het |
Kdm3a |
T |
C |
6: 71,621,362 |
E180G |
probably damaging |
Het |
Mgat3 |
G |
A |
15: 80,211,298 |
V109M |
possibly damaging |
Het |
Mroh7 |
A |
T |
4: 106,690,318 |
V1109D |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,866,656 |
T1111S |
probably benign |
Het |
Myo19 |
G |
T |
11: 84,903,211 |
A654S |
possibly damaging |
Het |
Mypn |
A |
T |
10: 63,118,528 |
V1224D |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,323,294 |
|
probably null |
Het |
Olfr250 |
G |
A |
9: 38,368,062 |
C172Y |
possibly damaging |
Het |
Olfr437 |
G |
T |
6: 43,167,339 |
A94S |
probably benign |
Het |
Olfr676 |
A |
T |
7: 105,035,411 |
Y71F |
probably damaging |
Het |
Pdcd2 |
A |
G |
17: 15,522,822 |
I247T |
possibly damaging |
Het |
Pik3c2a |
A |
T |
7: 116,342,401 |
N1571K |
probably damaging |
Het |
Plagl2 |
T |
C |
2: 153,236,044 |
T6A |
probably benign |
Het |
Ros1 |
T |
A |
10: 52,163,941 |
Y318F |
possibly damaging |
Het |
Sdccag8 |
C |
A |
1: 176,824,892 |
H70N |
probably damaging |
Het |
Skint1 |
A |
G |
4: 112,029,433 |
R359G |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 154,247,787 |
I269L |
probably benign |
Het |
Slfn10-ps |
T |
A |
11: 83,030,515 |
|
noncoding transcript |
Het |
Suclg1 |
C |
A |
6: 73,263,980 |
T164K |
probably benign |
Het |
Tgds |
C |
A |
14: 118,116,079 |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,813,533 |
D13117G |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,870,737 |
|
probably benign |
Het |
Vmn2r28 |
A |
T |
7: 5,480,672 |
I843N |
possibly damaging |
Het |
Vmn2r52 |
A |
T |
7: 10,159,465 |
Y582* |
probably null |
Het |
Vps33b |
G |
T |
7: 80,274,641 |
K65N |
probably damaging |
Het |
|