Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
A |
T |
15: 64,576,638 (GRCm39) |
S975T |
probably damaging |
Het |
Adgrg1 |
C |
G |
8: 95,729,936 (GRCm39) |
T46S |
probably damaging |
Het |
Akip1 |
T |
A |
7: 109,306,697 (GRCm39) |
D131E |
probably benign |
Het |
Arhgef39 |
A |
G |
4: 43,498,015 (GRCm39) |
V163A |
probably benign |
Het |
Atg2a |
T |
C |
19: 6,301,433 (GRCm39) |
|
probably null |
Het |
Bcam |
A |
T |
7: 19,494,325 (GRCm39) |
L357* |
probably null |
Het |
Bcat2 |
A |
G |
7: 45,237,075 (GRCm39) |
N194S |
probably damaging |
Het |
Bcl2l14 |
T |
C |
6: 134,400,720 (GRCm39) |
L47P |
probably benign |
Het |
Cbln1 |
C |
T |
8: 88,198,673 (GRCm39) |
A66T |
possibly damaging |
Het |
Ccdc191 |
G |
T |
16: 43,710,262 (GRCm39) |
|
probably benign |
Het |
Cd70 |
C |
T |
17: 57,456,468 (GRCm39) |
S45N |
possibly damaging |
Het |
Cfap43 |
G |
A |
19: 47,886,363 (GRCm39) |
A84V |
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,710,792 (GRCm39) |
N804Y |
possibly damaging |
Het |
Cmah |
A |
T |
13: 24,601,350 (GRCm39) |
N52I |
probably damaging |
Het |
Crot |
A |
G |
5: 9,043,518 (GRCm39) |
Y35H |
probably damaging |
Het |
Cyp3a59 |
C |
A |
5: 146,041,487 (GRCm39) |
P344T |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,247,978 (GRCm39) |
E705G |
probably benign |
Het |
Dnm2 |
A |
G |
9: 21,377,016 (GRCm39) |
Y125C |
probably damaging |
Het |
Dst |
A |
G |
1: 34,208,266 (GRCm39) |
Y739C |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,767,929 (GRCm39) |
M203K |
possibly damaging |
Het |
Enpep |
C |
T |
3: 129,113,076 (GRCm39) |
V283M |
probably damaging |
Het |
Ephx3 |
A |
G |
17: 32,407,219 (GRCm39) |
S240P |
probably damaging |
Het |
Evi5l |
T |
C |
8: 4,260,784 (GRCm39) |
H1011R |
possibly damaging |
Het |
Fig4 |
A |
T |
10: 41,108,170 (GRCm39) |
F677I |
probably benign |
Het |
Gramd1b |
A |
G |
9: 40,287,207 (GRCm39) |
|
probably null |
Het |
Gse1 |
C |
T |
8: 121,295,123 (GRCm39) |
|
probably benign |
Het |
Hoxa9 |
A |
G |
6: 52,202,506 (GRCm39) |
|
probably null |
Het |
Ice1 |
A |
T |
13: 70,752,566 (GRCm39) |
S1173R |
probably benign |
Het |
Ifi207 |
G |
A |
1: 173,556,605 (GRCm39) |
T718I |
possibly damaging |
Het |
Ifit1bl1 |
A |
G |
19: 34,572,262 (GRCm39) |
L65P |
probably damaging |
Het |
Lrp1 |
A |
G |
10: 127,375,572 (GRCm39) |
C4409R |
probably damaging |
Het |
Mark1 |
A |
G |
1: 184,651,783 (GRCm39) |
W131R |
probably damaging |
Het |
Mindy3 |
T |
C |
2: 12,404,839 (GRCm39) |
T190A |
probably damaging |
Het |
Mybbp1a |
A |
G |
11: 72,338,563 (GRCm39) |
D721G |
probably benign |
Het |
Myo1d |
A |
G |
11: 80,561,745 (GRCm39) |
V466A |
possibly damaging |
Het |
Myo5b |
A |
C |
18: 74,903,411 (GRCm39) |
D1809A |
probably damaging |
Het |
Nudcd2 |
C |
T |
11: 40,624,850 (GRCm39) |
Q20* |
probably null |
Het |
Or4f62 |
T |
C |
2: 111,986,320 (GRCm39) |
M8T |
probably benign |
Het |
Or5b101 |
A |
G |
19: 13,005,357 (GRCm39) |
L112P |
probably damaging |
Het |
Or8g2b |
T |
A |
9: 39,751,048 (GRCm39) |
L106H |
possibly damaging |
Het |
Pcif1 |
A |
T |
2: 164,730,272 (GRCm39) |
D335V |
probably damaging |
Het |
Pebp4 |
T |
A |
14: 70,085,136 (GRCm39) |
C65S |
possibly damaging |
Het |
Ptger1 |
C |
T |
8: 84,395,267 (GRCm39) |
A248V |
probably benign |
Het |
Qki |
A |
T |
17: 10,537,747 (GRCm39) |
M19K |
probably benign |
Het |
Ralgapa2 |
C |
G |
2: 146,266,750 (GRCm39) |
A609P |
probably damaging |
Het |
Robo2 |
C |
T |
16: 73,745,150 (GRCm39) |
G875D |
probably damaging |
Het |
Runx2 |
A |
G |
17: 44,919,147 (GRCm39) |
V375A |
probably damaging |
Het |
Sis |
A |
T |
3: 72,836,730 (GRCm39) |
F841I |
probably damaging |
Het |
Slc5a8 |
A |
G |
10: 88,757,552 (GRCm39) |
D514G |
possibly damaging |
Het |
Spag17 |
A |
T |
3: 99,934,586 (GRCm39) |
T623S |
probably benign |
Het |
Sppl2c |
A |
G |
11: 104,078,963 (GRCm39) |
S588G |
probably benign |
Het |
Stxbp6 |
A |
C |
12: 44,949,704 (GRCm39) |
V75G |
possibly damaging |
Het |
Tmc3 |
G |
A |
7: 83,259,122 (GRCm39) |
R531Q |
probably damaging |
Het |
Tmem258 |
T |
C |
19: 10,184,550 (GRCm39) |
Y41H |
probably damaging |
Het |
Tsks |
A |
T |
7: 44,600,263 (GRCm39) |
T91S |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,681,599 (GRCm39) |
V169A |
probably benign |
Het |
Wdr54 |
T |
C |
6: 83,129,985 (GRCm39) |
N282S |
probably benign |
Het |
Yme1l1 |
T |
A |
2: 23,052,584 (GRCm39) |
N79K |
probably benign |
Het |
|
Other mutations in Impact |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01531:Impact
|
APN |
18 |
13,109,076 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01960:Impact
|
APN |
18 |
13,107,815 (GRCm39) |
missense |
probably benign |
0.13 |
R1056:Impact
|
UTSW |
18 |
13,109,581 (GRCm39) |
missense |
probably benign |
0.14 |
R1552:Impact
|
UTSW |
18 |
13,117,337 (GRCm39) |
missense |
probably benign |
0.25 |
R4111:Impact
|
UTSW |
18 |
13,109,090 (GRCm39) |
critical splice donor site |
probably null |
|
R4734:Impact
|
UTSW |
18 |
13,118,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Impact
|
UTSW |
18 |
13,119,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Impact
|
UTSW |
18 |
13,107,819 (GRCm39) |
missense |
probably damaging |
0.98 |
R5601:Impact
|
UTSW |
18 |
13,109,064 (GRCm39) |
missense |
probably benign |
0.44 |
R5966:Impact
|
UTSW |
18 |
13,123,601 (GRCm39) |
missense |
probably benign |
0.00 |
R6974:Impact
|
UTSW |
18 |
13,115,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:Impact
|
UTSW |
18 |
13,119,370 (GRCm39) |
splice site |
probably null |
|
R8108:Impact
|
UTSW |
18 |
13,117,388 (GRCm39) |
missense |
probably benign |
0.00 |
R8460:Impact
|
UTSW |
18 |
13,109,564 (GRCm39) |
missense |
probably benign |
0.00 |
R8897:Impact
|
UTSW |
18 |
13,123,551 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Impact
|
UTSW |
18 |
13,121,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|