Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
A |
G |
8: 84,730,008 (GRCm39) |
Y165C |
probably damaging |
Het |
Abcb11 |
T |
A |
2: 69,095,840 (GRCm39) |
K833N |
possibly damaging |
Het |
Abcb1a |
T |
A |
5: 8,736,171 (GRCm39) |
M188K |
probably benign |
Het |
Akap1 |
A |
T |
11: 88,727,966 (GRCm39) |
V672D |
probably damaging |
Het |
Anapc4 |
A |
G |
5: 53,021,867 (GRCm39) |
T650A |
possibly damaging |
Het |
Ash1l |
C |
A |
3: 88,890,297 (GRCm39) |
S725R |
possibly damaging |
Het |
Axdnd1 |
T |
A |
1: 156,247,917 (GRCm39) |
K28* |
probably null |
Het |
C8b |
C |
A |
4: 104,644,192 (GRCm39) |
H286Q |
probably benign |
Het |
Cacna2d1 |
A |
G |
5: 16,217,396 (GRCm39) |
K34E |
probably damaging |
Het |
Ccdc14 |
T |
A |
16: 34,517,728 (GRCm39) |
H154Q |
probably damaging |
Het |
Ccdc184 |
A |
G |
15: 98,066,393 (GRCm39) |
D66G |
probably damaging |
Het |
Ccdc62 |
A |
G |
5: 124,092,772 (GRCm39) |
I586V |
possibly damaging |
Het |
Cfap20dc |
A |
G |
14: 8,578,361 (GRCm38) |
I127T |
possibly damaging |
Het |
Chadl |
A |
T |
15: 81,578,691 (GRCm39) |
C313S |
probably damaging |
Het |
Clec14a |
C |
A |
12: 58,315,536 (GRCm39) |
A29S |
probably damaging |
Het |
Col26a1 |
C |
T |
5: 136,786,608 (GRCm39) |
G161D |
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,232,811 (GRCm39) |
V1110A |
probably benign |
Het |
Ctbp2 |
A |
G |
7: 132,615,961 (GRCm39) |
S325P |
probably damaging |
Het |
Dcaf13 |
A |
G |
15: 38,993,687 (GRCm39) |
D260G |
possibly damaging |
Het |
Dhx37 |
G |
A |
5: 125,499,736 (GRCm39) |
P575L |
probably benign |
Het |
Dnajc6 |
T |
C |
4: 101,408,054 (GRCm39) |
|
probably null |
Het |
Eapp |
T |
C |
12: 54,737,061 (GRCm39) |
T145A |
unknown |
Het |
Efcab3 |
A |
G |
11: 104,722,126 (GRCm39) |
I1913V |
probably benign |
Het |
Efcab5 |
A |
G |
11: 77,012,064 (GRCm39) |
M730T |
probably benign |
Het |
Eif4g3 |
T |
A |
4: 137,917,968 (GRCm39) |
D1305E |
probably damaging |
Het |
Endou |
A |
T |
15: 97,609,946 (GRCm39) |
V450E |
probably benign |
Het |
F10 |
A |
T |
8: 13,098,177 (GRCm39) |
K127* |
probably null |
Het |
Fbxw21 |
A |
G |
9: 108,972,830 (GRCm39) |
F368S |
probably damaging |
Het |
Fezf1 |
A |
T |
6: 23,245,797 (GRCm39) |
L456Q |
possibly damaging |
Het |
Foxo3 |
C |
T |
10: 42,073,021 (GRCm39) |
V499M |
probably damaging |
Het |
Fyco1 |
A |
C |
9: 123,623,878 (GRCm39) |
C1384G |
probably damaging |
Het |
Galnt6 |
G |
T |
15: 100,602,032 (GRCm39) |
S258R |
possibly damaging |
Het |
Gemin5 |
A |
G |
11: 58,028,574 (GRCm39) |
V882A |
probably benign |
Het |
Gm10750 |
A |
G |
2: 148,858,107 (GRCm39) |
L48P |
unknown |
Het |
Gm16503 |
T |
A |
4: 147,625,571 (GRCm39) |
F22I |
unknown |
Het |
Hdac10 |
A |
G |
15: 89,010,480 (GRCm39) |
C281R |
probably damaging |
Het |
Hikeshi |
T |
C |
7: 89,584,968 (GRCm39) |
S79G |
probably damaging |
Het |
Ifitm2 |
AG |
A |
7: 140,535,814 (GRCm39) |
|
probably null |
Het |
Itpr3 |
A |
G |
17: 27,330,191 (GRCm39) |
E1603G |
probably damaging |
Het |
Lrrc37a |
A |
T |
11: 103,395,359 (GRCm39) |
V22E |
probably benign |
Het |
Man1a |
C |
T |
10: 53,809,587 (GRCm39) |
|
probably null |
Het |
Mdga1 |
A |
G |
17: 30,058,871 (GRCm39) |
L5P |
probably damaging |
Het |
Mup6 |
A |
G |
4: 60,004,838 (GRCm39) |
I76M |
probably benign |
Het |
Nbea |
A |
T |
3: 55,998,513 (GRCm39) |
M98K |
probably benign |
Het |
Nckap1l |
A |
G |
15: 103,381,966 (GRCm39) |
E454G |
probably damaging |
Het |
Notch3 |
A |
T |
17: 32,362,665 (GRCm39) |
L1320Q |
probably benign |
Het |
Nrn1 |
A |
T |
13: 36,910,648 (GRCm39) |
L128H |
probably damaging |
Het |
Numa1 |
T |
C |
7: 101,644,623 (GRCm39) |
S200P |
possibly damaging |
Het |
Numa1 |
A |
G |
7: 101,662,003 (GRCm39) |
D1898G |
probably damaging |
Het |
Or10ag58 |
G |
A |
2: 87,265,010 (GRCm39) |
A60T |
probably benign |
Het |
Or1af1 |
T |
C |
2: 37,110,122 (GRCm39) |
I207T |
possibly damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,605 (GRCm39) |
S21R |
possibly damaging |
Het |
Or5i1 |
A |
C |
2: 87,612,867 (GRCm39) |
|
probably null |
Het |
P2ry6 |
A |
T |
7: 100,588,133 (GRCm39) |
Y75* |
probably null |
Het |
Pbrm1 |
T |
A |
14: 30,806,760 (GRCm39) |
C1062* |
probably null |
Het |
Pcdh15 |
A |
G |
10: 74,479,560 (GRCm39) |
E557G |
unknown |
Het |
Pcdh7 |
T |
C |
5: 57,878,677 (GRCm39) |
L744P |
probably benign |
Het |
Plekhg3 |
A |
T |
12: 76,609,052 (GRCm39) |
I142L |
possibly damaging |
Het |
Plk4 |
C |
T |
3: 40,766,326 (GRCm39) |
H695Y |
probably damaging |
Het |
Pms1 |
T |
C |
1: 53,247,216 (GRCm39) |
H243R |
probably benign |
Het |
Prdm14 |
T |
C |
1: 13,192,707 (GRCm39) |
D344G |
possibly damaging |
Het |
R3hdml |
A |
G |
2: 163,344,252 (GRCm39) |
I214V |
probably benign |
Het |
Rab11fip5 |
T |
C |
6: 85,325,692 (GRCm39) |
N238S |
probably benign |
Het |
Resf1 |
T |
A |
6: 149,227,930 (GRCm39) |
N325K |
probably benign |
Het |
Sacs |
T |
A |
14: 61,477,768 (GRCm39) |
Y732N |
possibly damaging |
Het |
Scfd1 |
T |
A |
12: 51,440,649 (GRCm39) |
M187K |
possibly damaging |
Het |
Serpina1d |
A |
G |
12: 103,734,257 (GRCm39) |
C16R |
probably damaging |
Het |
Slc2a12 |
T |
C |
10: 22,540,994 (GRCm39) |
I283T |
possibly damaging |
Het |
Smarca5 |
A |
G |
8: 81,446,432 (GRCm39) |
Y423H |
probably damaging |
Het |
Srrm3 |
C |
A |
5: 135,897,115 (GRCm39) |
A366E |
unknown |
Het |
St7 |
A |
T |
6: 17,844,913 (GRCm39) |
K134* |
probably null |
Het |
St8sia5 |
T |
G |
18: 77,342,525 (GRCm39) |
C412G |
probably damaging |
Het |
Tanc2 |
A |
T |
11: 105,777,284 (GRCm39) |
I821F |
probably damaging |
Het |
Tbrg4 |
A |
G |
11: 6,574,204 (GRCm39) |
M6T |
probably benign |
Het |
Tcf20 |
A |
T |
15: 82,736,897 (GRCm39) |
I1518N |
probably benign |
Het |
Tctn3 |
A |
G |
19: 40,595,720 (GRCm39) |
V355A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,915,327 (GRCm39) |
F2070Y |
probably damaging |
Het |
Tex2 |
A |
G |
11: 106,459,361 (GRCm39) |
V23A |
probably damaging |
Het |
Thrsp |
C |
G |
7: 97,066,281 (GRCm39) |
E144Q |
probably damaging |
Het |
Tmt1a |
A |
G |
15: 100,211,014 (GRCm39) |
E213G |
probably damaging |
Het |
Top2a |
A |
C |
11: 98,891,904 (GRCm39) |
S1114A |
probably benign |
Het |
Tpm1 |
A |
G |
9: 66,936,998 (GRCm39) |
Y267H |
probably benign |
Het |
Txndc2 |
G |
T |
17: 65,946,019 (GRCm39) |
P53T |
unknown |
Het |
Ugt2b36 |
A |
T |
5: 87,228,876 (GRCm39) |
I389N |
probably damaging |
Het |
Virma |
C |
T |
4: 11,513,507 (GRCm39) |
R454* |
probably null |
Het |
Vwa3b |
T |
A |
1: 37,074,882 (GRCm39) |
H16Q |
probably damaging |
Het |
Zbp1 |
A |
G |
2: 173,052,436 (GRCm39) |
M240T |
possibly damaging |
Het |
|