Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110002H16Rik |
C |
T |
18: 12,179,177 |
T158M |
probably benign |
Het |
Abl1 |
T |
A |
2: 31,797,047 |
S519T |
probably damaging |
Het |
Acap2 |
A |
G |
16: 31,108,126 |
S524P |
probably benign |
Het |
Acot1 |
T |
A |
12: 84,017,168 |
I350N |
probably damaging |
Het |
Adam8 |
A |
G |
7: 139,987,639 |
V397A |
probably benign |
Het |
Ankar |
A |
G |
1: 72,670,151 |
M735T |
possibly damaging |
Het |
B020031M17Rik |
A |
T |
13: 119,949,848 |
V74E |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,656,536 |
|
probably null |
Het |
Cdc25b |
A |
G |
2: 131,192,596 |
S222G |
probably benign |
Het |
Celsr3 |
T |
C |
9: 108,832,124 |
S1390P |
probably damaging |
Het |
Clca4a |
T |
G |
3: 144,970,461 |
D104A |
probably damaging |
Het |
Clcn6 |
A |
T |
4: 148,038,749 |
|
probably benign |
Het |
Coq8b |
A |
G |
7: 27,250,348 |
T320A |
probably benign |
Het |
Cspg5 |
A |
T |
9: 110,246,630 |
M145L |
probably benign |
Het |
Cyp2c67 |
T |
A |
19: 39,626,232 |
I284F |
probably benign |
Het |
Eya4 |
T |
C |
10: 23,110,048 |
I565V |
probably benign |
Het |
Fbxw11 |
A |
G |
11: 32,738,471 |
N410S |
probably damaging |
Het |
Gabrb2 |
C |
T |
11: 42,626,809 |
A448V |
possibly damaging |
Het |
Gm11487 |
A |
T |
4: 73,401,277 |
W77R |
probably damaging |
Het |
Itsn2 |
T |
C |
12: 4,672,783 |
V1073A |
probably damaging |
Het |
Kif5c |
A |
G |
2: 49,723,066 |
T139A |
probably benign |
Het |
L1td1 |
G |
A |
4: 98,736,447 |
G293D |
probably damaging |
Het |
Lama1 |
A |
G |
17: 67,817,563 |
M2873V |
probably benign |
Het |
Myo15 |
A |
G |
11: 60,497,538 |
R1960G |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,328,210 |
|
probably null |
Het |
Ndufb4 |
A |
G |
16: 37,654,178 |
|
probably null |
Het |
Nup153 |
A |
T |
13: 46,686,865 |
L1089* |
probably null |
Het |
Olfr1107 |
A |
G |
2: 87,071,492 |
V214A |
possibly damaging |
Het |
Olfr1512 |
G |
A |
14: 52,372,268 |
R262* |
probably null |
Het |
Olfr168 |
T |
A |
16: 19,530,777 |
I48F |
probably damaging |
Het |
P2rx1 |
A |
G |
11: 73,009,230 |
T158A |
probably damaging |
Het |
Park7 |
A |
G |
4: 150,908,423 |
|
probably benign |
Het |
Parl |
A |
T |
16: 20,298,142 |
F102I |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,849,969 |
H720L |
probably benign |
Het |
Ptpn4 |
A |
G |
1: 119,765,477 |
S140P |
probably benign |
Het |
Rel |
A |
G |
11: 23,742,462 |
S524P |
probably benign |
Het |
Ripply2 |
A |
G |
9: 87,019,726 |
|
probably null |
Het |
Rps4l-ps |
T |
C |
7: 114,927,198 |
|
noncoding transcript |
Het |
Rtn4ip1 |
T |
C |
10: 43,932,470 |
L81P |
probably damaging |
Het |
Sap130 |
T |
C |
18: 31,648,198 |
L138P |
probably benign |
Het |
Scp2 |
A |
T |
4: 108,055,579 |
|
probably null |
Het |
Sec24c |
T |
A |
14: 20,693,220 |
M970K |
probably benign |
Het |
Setd5 |
C |
T |
6: 113,116,007 |
P340L |
probably damaging |
Het |
Sgcg |
A |
T |
14: 61,245,769 |
M61K |
probably damaging |
Het |
Slc22a27 |
C |
G |
19: 7,865,938 |
A359P |
probably damaging |
Het |
Slc34a1 |
A |
G |
13: 55,400,518 |
R21G |
probably benign |
Het |
Slc7a14 |
A |
C |
3: 31,223,857 |
L533W |
probably damaging |
Het |
Srsf9 |
A |
G |
5: 115,330,536 |
D77G |
probably benign |
Het |
Tab1 |
A |
T |
15: 80,149,813 |
E119V |
possibly damaging |
Het |
Tnrc6c |
C |
T |
11: 117,723,287 |
A757V |
possibly damaging |
Het |
Tradd |
A |
T |
8: 105,259,924 |
I72N |
probably damaging |
Het |
Trbv12-1 |
C |
T |
6: 41,113,847 |
T51M |
probably benign |
Het |
Tsga10 |
T |
C |
1: 37,763,311 |
K605E |
probably damaging |
Het |
Vwc2l |
A |
G |
1: 70,728,918 |
D47G |
probably damaging |
Het |
Zfp647 |
T |
A |
15: 76,911,495 |
T322S |
possibly damaging |
Het |
Zscan20 |
A |
C |
4: 128,588,121 |
S583A |
probably benign |
Het |
|