Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
A |
G |
8: 43,570,420 |
F11S |
probably benign |
Het |
Adipor2 |
T |
A |
6: 119,357,221 |
I343F |
probably damaging |
Het |
Ahdc1 |
C |
T |
4: 133,062,798 |
P450L |
possibly damaging |
Het |
Akna |
A |
C |
4: 63,368,203 |
V1353G |
possibly damaging |
Het |
Baz2b |
G |
A |
2: 59,962,614 |
T390I |
probably benign |
Het |
Btbd7 |
T |
C |
12: 102,838,392 |
K130E |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 180,137,850 |
Y1101C |
probably damaging |
Het |
Crlf2 |
T |
G |
5: 109,557,635 |
|
probably benign |
Het |
Ddx59 |
A |
T |
1: 136,419,448 |
R281S |
probably damaging |
Het |
Dgcr8 |
T |
G |
16: 18,283,771 |
T216P |
probably benign |
Het |
Dsg4 |
A |
T |
18: 20,446,839 |
I34F |
probably benign |
Het |
Enpp3 |
A |
G |
10: 24,809,916 |
S194P |
probably damaging |
Het |
Entpd8 |
C |
T |
2: 25,085,045 |
R463W |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,118,496 |
T407A |
probably benign |
Het |
Fam98b |
G |
T |
2: 117,259,298 |
V99F |
possibly damaging |
Het |
Foxn3 |
T |
A |
12: 99,196,428 |
K405* |
probably null |
Het |
Gm340 |
T |
A |
19: 41,585,039 |
H744Q |
probably damaging |
Het |
Gsdmc |
T |
C |
15: 63,801,957 |
T160A |
probably benign |
Het |
Hdac1 |
T |
C |
4: 129,528,923 |
|
probably null |
Het |
Igfbp1 |
A |
C |
11: 7,201,892 |
T232P |
probably damaging |
Het |
Mertk |
G |
C |
2: 128,801,314 |
G878R |
possibly damaging |
Het |
Metap2 |
G |
T |
10: 93,868,922 |
P281H |
possibly damaging |
Het |
Metap2 |
T |
A |
10: 93,868,932 |
T278S |
probably benign |
Het |
Mfn1 |
T |
C |
3: 32,564,205 |
V169A |
probably benign |
Het |
Mms22l |
A |
G |
4: 24,578,774 |
D751G |
probably damaging |
Het |
Mpl |
A |
G |
4: 118,455,721 |
V138A |
probably benign |
Het |
Myef2 |
T |
A |
2: 125,095,721 |
K533N |
probably damaging |
Het |
Mylk3 |
C |
T |
8: 85,355,442 |
G309E |
probably damaging |
Het |
Nid1 |
T |
C |
13: 13,468,572 |
V365A |
probably damaging |
Het |
Olfr27 |
T |
C |
9: 39,144,315 |
C72R |
probably damaging |
Het |
Olfr463 |
A |
T |
11: 87,893,192 |
I244N |
probably damaging |
Het |
Olfr480 |
A |
T |
7: 108,066,216 |
L164* |
probably null |
Het |
Olfr77 |
C |
A |
9: 19,920,621 |
N137K |
possibly damaging |
Het |
Pbrm1 |
A |
G |
14: 31,106,184 |
K1323E |
probably damaging |
Het |
Pcdhga12 |
G |
A |
18: 37,766,675 |
D187N |
possibly damaging |
Het |
Phrf1 |
T |
C |
7: 141,259,283 |
|
probably benign |
Het |
Phtf2 |
A |
G |
5: 20,772,197 |
V608A |
probably benign |
Het |
Plec |
G |
A |
15: 76,173,438 |
R4122W |
probably damaging |
Het |
Polm |
A |
G |
11: 5,829,393 |
S441P |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,214,722 |
V1404E |
probably benign |
Het |
Ptger1 |
T |
G |
8: 83,669,345 |
S344A |
possibly damaging |
Het |
Rasef |
A |
T |
4: 73,735,767 |
D401E |
probably null |
Het |
Rbfox3 |
T |
C |
11: 118,496,352 |
Y312C |
probably damaging |
Het |
Rbm48 |
A |
G |
5: 3,584,759 |
C402R |
probably benign |
Het |
Rhbdl3 |
G |
A |
11: 80,319,666 |
A82T |
probably benign |
Het |
Rnf123 |
AT |
ATT |
9: 108,064,003 |
|
probably null |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,153,384 |
|
probably benign |
Homo |
Sidt2 |
T |
A |
9: 45,954,777 |
N44Y |
probably damaging |
Het |
Slf2 |
T |
A |
19: 44,935,161 |
L138Q |
possibly damaging |
Het |
Spag16 |
T |
C |
1: 69,896,583 |
|
probably null |
Het |
Sspo |
C |
T |
6: 48,490,467 |
P4188S |
probably damaging |
Het |
Synm |
C |
T |
7: 67,734,689 |
S1075N |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,729,317 |
D2151Y |
probably damaging |
Het |
Tbc1d32 |
C |
A |
10: 56,151,818 |
L729F |
probably damaging |
Het |
Tnfsf4 |
A |
G |
1: 161,417,013 |
N91S |
possibly damaging |
Het |
Trim63 |
G |
A |
4: 134,323,133 |
E243K |
probably benign |
Het |
Trim72 |
T |
G |
7: 128,004,542 |
L20R |
probably damaging |
Het |
Tubb1 |
A |
G |
2: 174,457,424 |
M300V |
probably damaging |
Het |
Ubfd1 |
C |
T |
7: 122,068,868 |
A207V |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,470,451 |
|
probably null |
Het |
Vmn2r72 |
T |
A |
7: 85,738,254 |
I701F |
possibly damaging |
Het |
Wdfy4 |
A |
G |
14: 33,047,275 |
Y2078H |
probably damaging |
Het |
Wdr41 |
T |
C |
13: 95,017,450 |
|
probably null |
Het |
Zfp955b |
A |
G |
17: 33,303,057 |
Y500C |
probably damaging |
Het |
|