Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
T |
C |
19: 8,989,090 (GRCm39) |
M3458T |
possibly damaging |
Het |
Akap9 |
T |
G |
5: 4,010,491 (GRCm39) |
L398R |
probably damaging |
Het |
Anks3 |
A |
T |
16: 4,759,840 (GRCm39) |
C635S |
probably benign |
Het |
Ankzf1 |
C |
A |
1: 75,175,196 (GRCm39) |
Q649K |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,245,829 (GRCm39) |
E621G |
probably damaging |
Het |
Bscl2 |
A |
G |
19: 8,817,110 (GRCm39) |
T13A |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,611,074 (GRCm39) |
L1230P |
possibly damaging |
Het |
Celsr2 |
T |
A |
3: 108,301,551 (GRCm39) |
S2678C |
probably damaging |
Het |
Cnot10 |
A |
G |
9: 114,420,715 (GRCm39) |
L709P |
probably damaging |
Het |
Col5a1 |
G |
A |
2: 27,842,994 (GRCm39) |
R449Q |
unknown |
Het |
Cyp3a25 |
T |
A |
5: 145,931,732 (GRCm39) |
E125D |
probably benign |
Het |
Ddx50 |
T |
G |
10: 62,476,524 (GRCm39) |
I250L |
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,852,249 (GRCm39) |
N1859S |
probably damaging |
Het |
Dnajc13 |
A |
G |
9: 104,042,211 (GRCm39) |
L2008P |
probably damaging |
Het |
Dock4 |
C |
T |
12: 40,686,097 (GRCm39) |
L111F |
probably damaging |
Het |
Ffar3 |
C |
G |
7: 30,555,119 (GRCm39) |
R67P |
probably damaging |
Het |
Gdap2 |
C |
T |
3: 100,109,441 (GRCm39) |
A486V |
probably benign |
Het |
Gm45871 |
G |
A |
18: 90,610,111 (GRCm39) |
V450M |
possibly damaging |
Het |
Golgb1 |
T |
A |
16: 36,718,996 (GRCm39) |
S342T |
probably damaging |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Grm5 |
T |
C |
7: 87,723,903 (GRCm39) |
I731T |
probably damaging |
Het |
Gxylt2 |
A |
T |
6: 100,760,109 (GRCm39) |
T215S |
probably damaging |
Het |
Jakmip2 |
A |
T |
18: 43,673,685 (GRCm39) |
I793N |
probably damaging |
Het |
Kcnc1 |
C |
A |
7: 46,076,955 (GRCm39) |
C252* |
probably null |
Het |
Kdr |
T |
A |
5: 76,129,521 (GRCm39) |
D122V |
probably damaging |
Het |
Kmt2a |
G |
A |
9: 44,731,557 (GRCm39) |
P2920L |
unknown |
Het |
Lrrc31 |
T |
C |
3: 30,741,617 (GRCm39) |
E264G |
probably damaging |
Het |
Mbnl1 |
A |
G |
3: 60,529,614 (GRCm39) |
T256A |
probably benign |
Het |
Myh3 |
A |
G |
11: 66,991,921 (GRCm39) |
E1822G |
possibly damaging |
Het |
Ndst4 |
A |
G |
3: 125,518,344 (GRCm39) |
N155S |
unknown |
Het |
Negr1 |
T |
C |
3: 156,267,898 (GRCm39) |
C23R |
probably damaging |
Het |
Nfia |
T |
A |
4: 97,671,465 (GRCm39) |
D58E |
probably damaging |
Het |
Nrp1 |
A |
T |
8: 129,202,650 (GRCm39) |
N545I |
probably damaging |
Het |
Nrtn |
T |
A |
17: 57,059,480 (GRCm39) |
|
probably benign |
Het |
Or2a14 |
A |
G |
6: 43,130,629 (GRCm39) |
H130R |
probably benign |
Het |
Or4c100 |
T |
C |
2: 88,356,421 (GRCm39) |
F165L |
probably benign |
Het |
Or5an11 |
C |
T |
19: 12,246,379 (GRCm39) |
R262* |
probably null |
Het |
Pclo |
G |
A |
5: 14,727,558 (GRCm39) |
D2139N |
unknown |
Het |
Phlpp1 |
C |
T |
1: 106,246,699 (GRCm39) |
Q630* |
probably null |
Het |
Pkd1 |
T |
C |
17: 24,796,812 (GRCm39) |
V2429A |
possibly damaging |
Het |
Pramel20 |
T |
A |
4: 143,299,328 (GRCm39) |
H330Q |
probably benign |
Het |
Pramel30 |
T |
C |
4: 144,056,844 (GRCm39) |
L9P |
probably damaging |
Het |
Prkch |
A |
G |
12: 73,805,730 (GRCm39) |
K502E |
probably damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,509,413 (GRCm39) |
K930E |
possibly damaging |
Het |
Rin2 |
T |
C |
2: 145,690,764 (GRCm39) |
L144P |
probably damaging |
Het |
Scfd2 |
T |
C |
5: 74,691,611 (GRCm39) |
S224G |
possibly damaging |
Het |
Srprb |
A |
G |
9: 103,069,481 (GRCm39) |
Y158H |
probably damaging |
Het |
Thbs4 |
T |
A |
13: 92,890,896 (GRCm39) |
H857L |
probably damaging |
Het |
Tmem184a |
A |
G |
5: 139,798,790 (GRCm39) |
L77P |
possibly damaging |
Het |
Trbv26 |
G |
T |
6: 41,204,478 (GRCm39) |
C7F |
probably benign |
Het |
Trip11 |
A |
G |
12: 101,850,123 (GRCm39) |
S1314P |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,431,879 (GRCm39) |
T1951S |
probably benign |
Het |
Ttc29 |
A |
C |
8: 78,972,895 (GRCm39) |
D115A |
possibly damaging |
Het |
Upf2 |
G |
A |
2: 6,032,024 (GRCm39) |
V857I |
unknown |
Het |
Vmn2r43 |
A |
G |
7: 8,247,787 (GRCm39) |
V792A |
probably damaging |
Het |
Washc5 |
A |
T |
15: 59,218,706 (GRCm39) |
I687N |
probably damaging |
Het |
Wwc2 |
G |
A |
8: 48,281,799 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
G |
A |
2: 67,340,539 (GRCm39) |
E927K |
possibly damaging |
Het |
Zc3hav1l |
A |
G |
6: 38,276,112 (GRCm39) |
F22L |
probably benign |
Het |
Zfp407 |
C |
T |
18: 84,578,312 (GRCm39) |
A934T |
probably benign |
Het |
Zfp986 |
T |
A |
4: 145,626,070 (GRCm39) |
S243R |
probably benign |
Het |
Zfyve9 |
T |
C |
4: 108,576,305 (GRCm39) |
T259A |
probably benign |
Het |
|