Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
T |
A |
7: 119,130,983 (GRCm39) |
|
probably null |
Het |
Alb |
T |
A |
5: 90,610,665 (GRCm39) |
S82T |
probably benign |
Het |
Arf4 |
A |
G |
14: 26,374,248 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
T |
C |
14: 33,084,500 (GRCm39) |
C260R |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,081,441 (GRCm39) |
E153G |
probably benign |
Het |
Arhgef18 |
T |
A |
8: 3,484,897 (GRCm39) |
M200K |
probably damaging |
Het |
Atp1a4 |
T |
A |
1: 172,062,567 (GRCm39) |
N647Y |
probably benign |
Het |
Atp5f1c |
A |
T |
2: 10,064,428 (GRCm39) |
L226Q |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,226,245 (GRCm39) |
K310R |
probably damaging |
Het |
Cadm3 |
T |
A |
1: 173,174,013 (GRCm39) |
T67S |
probably damaging |
Het |
Cartpt |
C |
T |
13: 100,036,588 (GRCm39) |
|
probably null |
Het |
Cenpj |
A |
T |
14: 56,790,840 (GRCm39) |
V403E |
possibly damaging |
Het |
Chst7 |
C |
A |
X: 19,927,110 (GRCm39) |
R386S |
probably damaging |
Het |
Dnah7b |
A |
T |
1: 46,117,684 (GRCm39) |
D50V |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 98,945,160 (GRCm39) |
D295G |
possibly damaging |
Het |
Gin1 |
C |
T |
1: 97,712,565 (GRCm39) |
P154S |
probably damaging |
Het |
Gm6471 |
G |
A |
7: 142,385,360 (GRCm39) |
|
noncoding transcript |
Het |
Gm6818 |
T |
A |
7: 38,101,981 (GRCm39) |
|
noncoding transcript |
Het |
Gm9271 |
T |
A |
7: 39,013,734 (GRCm39) |
|
noncoding transcript |
Het |
Gpam |
A |
G |
19: 55,084,551 (GRCm39) |
|
probably null |
Het |
Gpr183 |
T |
C |
14: 122,192,149 (GRCm39) |
D124G |
probably damaging |
Het |
Ift140 |
C |
A |
17: 25,317,935 (GRCm39) |
|
probably benign |
Het |
Itih5 |
A |
C |
2: 10,195,180 (GRCm39) |
I191L |
probably benign |
Het |
Jcad |
A |
G |
18: 4,674,175 (GRCm39) |
T646A |
probably benign |
Het |
Kank1 |
T |
C |
19: 25,387,944 (GRCm39) |
M511T |
probably benign |
Het |
Krt74 |
A |
T |
15: 101,667,304 (GRCm39) |
|
noncoding transcript |
Het |
Lrrc37a |
A |
G |
11: 103,395,363 (GRCm39) |
S21P |
probably benign |
Het |
Lrrc8c |
G |
A |
5: 105,756,240 (GRCm39) |
V672I |
probably benign |
Het |
Lypd4 |
T |
C |
7: 24,566,151 (GRCm39) |
R58G |
probably benign |
Het |
Magi1 |
A |
T |
6: 93,663,624 (GRCm39) |
|
probably null |
Het |
Mefv |
T |
A |
16: 3,526,071 (GRCm39) |
L745F |
possibly damaging |
Het |
Myh13 |
A |
T |
11: 67,255,564 (GRCm39) |
K1645* |
probably null |
Het |
Naip6 |
A |
G |
13: 100,431,239 (GRCm39) |
|
probably null |
Het |
Nlrp1c-ps |
T |
C |
11: 71,171,382 (GRCm39) |
|
noncoding transcript |
Het |
Nsmce3 |
A |
T |
7: 64,522,530 (GRCm39) |
L46Q |
probably benign |
Het |
Or51aa2 |
A |
G |
7: 103,188,393 (GRCm39) |
V16A |
possibly damaging |
Het |
Or6k6 |
T |
A |
1: 173,945,427 (GRCm39) |
M52L |
probably benign |
Het |
Or8k37 |
T |
C |
2: 86,469,512 (GRCm39) |
D180G |
possibly damaging |
Het |
P2ry12 |
T |
C |
3: 59,125,325 (GRCm39) |
|
probably null |
Het |
Pcx |
T |
A |
19: 4,669,916 (GRCm39) |
V861E |
probably damaging |
Het |
Pkp3 |
C |
T |
7: 140,662,612 (GRCm39) |
P75S |
probably benign |
Het |
Plscr4 |
T |
C |
9: 92,364,920 (GRCm39) |
|
probably null |
Het |
Pole |
A |
G |
5: 110,454,253 (GRCm39) |
T923A |
probably benign |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Rhot2 |
A |
C |
17: 26,060,305 (GRCm39) |
|
probably benign |
Het |
Rsrp1 |
A |
G |
4: 134,651,488 (GRCm39) |
Y84C |
unknown |
Het |
Sbf2 |
T |
C |
7: 109,934,606 (GRCm39) |
K1348E |
probably damaging |
Het |
Sgip1 |
A |
T |
4: 102,726,951 (GRCm39) |
N53Y |
probably damaging |
Het |
Snapc2 |
A |
G |
8: 4,304,998 (GRCm39) |
T127A |
possibly damaging |
Het |
Snx8 |
A |
G |
5: 140,341,713 (GRCm39) |
|
probably null |
Het |
Spag8 |
A |
G |
4: 43,653,378 (GRCm39) |
|
probably benign |
Het |
Srebf2 |
T |
C |
15: 82,076,503 (GRCm39) |
F718L |
probably damaging |
Het |
Szt2 |
C |
G |
4: 118,233,026 (GRCm39) |
|
probably benign |
Het |
Traf3ip2 |
C |
T |
10: 39,515,256 (GRCm39) |
P345S |
possibly damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,004,146 (GRCm39) |
Y62* |
probably null |
Het |
Usp29 |
T |
A |
7: 6,965,914 (GRCm39) |
S586T |
possibly damaging |
Het |
Vasp |
T |
C |
7: 18,998,350 (GRCm39) |
N108S |
probably benign |
Het |
Vmn1r214 |
A |
G |
13: 23,219,141 (GRCm39) |
M212V |
probably benign |
Het |
Wipi2 |
G |
C |
5: 142,645,345 (GRCm39) |
A194P |
probably benign |
Het |
Zbtb4 |
T |
A |
11: 69,667,355 (GRCm39) |
I220N |
probably damaging |
Het |
Zcchc2 |
A |
T |
1: 105,917,996 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
A |
13: 67,769,534 (GRCm39) |
K232* |
probably null |
Het |
Zfp995 |
A |
T |
17: 22,106,320 (GRCm39) |
M1K |
probably null |
Het |
|
Other mutations in Cyp4f37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Cyp4f37
|
APN |
17 |
32,848,027 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01994:Cyp4f37
|
APN |
17 |
32,844,150 (GRCm39) |
nonsense |
probably null |
|
IGL02073:Cyp4f37
|
APN |
17 |
32,846,825 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02145:Cyp4f37
|
APN |
17 |
32,849,009 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02814:Cyp4f37
|
APN |
17 |
32,853,645 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02873:Cyp4f37
|
APN |
17 |
32,844,142 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02937:Cyp4f37
|
APN |
17 |
32,844,163 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03170:Cyp4f37
|
APN |
17 |
32,844,093 (GRCm39) |
splice site |
probably benign |
|
R0625:Cyp4f37
|
UTSW |
17 |
32,853,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Cyp4f37
|
UTSW |
17 |
32,848,864 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1871:Cyp4f37
|
UTSW |
17 |
32,853,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Cyp4f37
|
UTSW |
17 |
32,853,244 (GRCm39) |
missense |
probably benign |
0.23 |
R2847:Cyp4f37
|
UTSW |
17 |
32,848,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Cyp4f37
|
UTSW |
17 |
32,848,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Cyp4f37
|
UTSW |
17 |
32,850,646 (GRCm39) |
missense |
probably benign |
0.00 |
R4463:Cyp4f37
|
UTSW |
17 |
32,846,710 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4517:Cyp4f37
|
UTSW |
17 |
32,850,566 (GRCm39) |
missense |
probably benign |
0.00 |
R4573:Cyp4f37
|
UTSW |
17 |
32,848,061 (GRCm39) |
missense |
probably benign |
0.23 |
R5752:Cyp4f37
|
UTSW |
17 |
32,850,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Cyp4f37
|
UTSW |
17 |
32,848,957 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6248:Cyp4f37
|
UTSW |
17 |
32,848,864 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7412:Cyp4f37
|
UTSW |
17 |
32,848,818 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7969:Cyp4f37
|
UTSW |
17 |
32,844,181 (GRCm39) |
missense |
probably benign |
0.00 |
R8066:Cyp4f37
|
UTSW |
17 |
32,854,047 (GRCm39) |
missense |
probably benign |
0.21 |
R8187:Cyp4f37
|
UTSW |
17 |
32,854,171 (GRCm39) |
missense |
probably benign |
|
R8303:Cyp4f37
|
UTSW |
17 |
32,853,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8309:Cyp4f37
|
UTSW |
17 |
32,853,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Cyp4f37
|
UTSW |
17 |
32,853,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Cyp4f37
|
UTSW |
17 |
32,844,096 (GRCm39) |
missense |
probably benign |
0.01 |
R9054:Cyp4f37
|
UTSW |
17 |
32,853,253 (GRCm39) |
missense |
probably benign |
0.25 |
R9565:Cyp4f37
|
UTSW |
17 |
32,844,205 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9674:Cyp4f37
|
UTSW |
17 |
32,846,841 (GRCm39) |
critical splice donor site |
probably null |
|
X0057:Cyp4f37
|
UTSW |
17 |
32,844,198 (GRCm39) |
missense |
probably benign |
0.01 |
|