Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
T |
C |
9: 53,319,365 (GRCm39) |
S2P |
probably benign |
Het |
Abca16 |
A |
C |
7: 120,035,116 (GRCm39) |
T301P |
probably damaging |
Het |
Acer2 |
A |
G |
4: 86,805,399 (GRCm39) |
D121G |
possibly damaging |
Het |
Adgrd1 |
T |
C |
5: 129,248,995 (GRCm39) |
|
probably null |
Het |
Arhgap11a |
T |
C |
2: 113,672,056 (GRCm39) |
I249V |
probably benign |
Het |
Arhgap22 |
A |
G |
14: 33,088,671 (GRCm39) |
E219G |
probably benign |
Het |
C2cd4b |
T |
A |
9: 67,667,033 (GRCm39) |
S10T |
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,573,998 (GRCm39) |
I224N |
probably damaging |
Het |
Ctrc |
T |
C |
4: 141,568,829 (GRCm39) |
T125A |
probably damaging |
Het |
Cxxc5 |
T |
G |
18: 35,991,642 (GRCm39) |
S14R |
unknown |
Het |
Dcbld1 |
T |
G |
10: 52,188,946 (GRCm39) |
I186S |
probably benign |
Het |
Dmxl2 |
T |
C |
9: 54,289,986 (GRCm39) |
T2510A |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,671,110 (GRCm39) |
I591T |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 68,078,612 (GRCm39) |
I204N |
probably benign |
Het |
Dysf |
G |
A |
6: 84,088,969 (GRCm39) |
|
probably null |
Het |
Erich5 |
A |
G |
15: 34,471,515 (GRCm39) |
E248G |
probably damaging |
Het |
Fhip1a |
A |
G |
3: 85,637,807 (GRCm39) |
V164A |
possibly damaging |
Het |
Foxm1 |
A |
G |
6: 128,350,834 (GRCm39) |
S712G |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,284,055 (GRCm39) |
T959A |
probably benign |
Het |
Gfra4 |
C |
T |
2: 130,882,176 (GRCm39) |
V277I |
probably null |
Het |
Hacd4 |
T |
C |
4: 88,353,247 (GRCm39) |
I82V |
probably benign |
Het |
Itih2 |
C |
T |
2: 10,128,225 (GRCm39) |
V159I |
possibly damaging |
Het |
Itpr2 |
T |
A |
6: 146,068,149 (GRCm39) |
M2410L |
probably benign |
Het |
Marchf11 |
A |
G |
15: 26,311,129 (GRCm39) |
I202V |
probably damaging |
Het |
Marchf3 |
A |
G |
18: 56,944,902 (GRCm39) |
|
probably null |
Het |
Med12l |
G |
A |
3: 59,154,858 (GRCm39) |
E1135K |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,743,917 (GRCm39) |
G42S |
probably damaging |
Het |
Mlx |
T |
C |
11: 100,978,608 (GRCm39) |
L78P |
possibly damaging |
Het |
Muc5b |
T |
C |
7: 141,400,164 (GRCm39) |
C473R |
unknown |
Het |
N4bp2l1 |
T |
A |
5: 150,500,210 (GRCm39) |
R66* |
probably null |
Het |
Nes |
A |
G |
3: 87,884,479 (GRCm39) |
T913A |
possibly damaging |
Het |
Oas1a |
T |
C |
5: 121,037,322 (GRCm39) |
E235G |
probably damaging |
Het |
Or5p56 |
T |
C |
7: 107,590,396 (GRCm39) |
S275P |
probably damaging |
Het |
Or8b1c |
T |
C |
9: 38,384,504 (GRCm39) |
S154P |
possibly damaging |
Het |
Or8i2 |
T |
A |
2: 86,851,964 (GRCm39) |
H308L |
probably benign |
Het |
Parn |
C |
T |
16: 13,458,158 (GRCm39) |
V286I |
probably benign |
Het |
Paxip1 |
G |
A |
5: 27,970,940 (GRCm39) |
Q470* |
probably null |
Het |
Phc2 |
C |
G |
4: 128,617,503 (GRCm39) |
H510D |
possibly damaging |
Het |
Pla2g4f |
T |
A |
2: 120,135,522 (GRCm39) |
D384V |
probably damaging |
Het |
Plpbp |
A |
T |
8: 27,535,159 (GRCm39) |
N68I |
probably damaging |
Het |
Podxl2 |
G |
A |
6: 88,826,937 (GRCm39) |
A123V |
possibly damaging |
Het |
Pole |
A |
T |
5: 110,473,416 (GRCm39) |
T1737S |
possibly damaging |
Het |
Ppp3cc |
T |
C |
14: 70,462,476 (GRCm39) |
E396G |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,321,352 (GRCm39) |
I228F |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,894,123 (GRCm39) |
C149S |
probably benign |
Het |
Qtrt1 |
G |
T |
9: 21,329,584 (GRCm39) |
M217I |
probably benign |
Het |
Sec24a |
T |
A |
11: 51,620,281 (GRCm39) |
D456V |
probably damaging |
Het |
Shox2 |
T |
G |
3: 66,888,877 (GRCm39) |
|
probably null |
Het |
Skint2 |
T |
A |
4: 112,481,283 (GRCm39) |
S49T |
probably damaging |
Het |
Smarca5 |
A |
G |
8: 81,447,315 (GRCm39) |
|
probably null |
Het |
Sorcs2 |
T |
A |
5: 36,181,916 (GRCm39) |
D1068V |
possibly damaging |
Het |
Tmem114 |
T |
C |
16: 8,229,966 (GRCm39) |
|
probably null |
Het |
Ttc7b |
T |
A |
12: 100,321,305 (GRCm39) |
M24L |
probably benign |
Het |
Ttll3 |
A |
G |
6: 113,385,864 (GRCm39) |
|
probably null |
Het |
Usp7 |
C |
T |
16: 8,522,846 (GRCm39) |
D102N |
probably benign |
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 |
|
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 |
R4670:Cyp4f37
|
UTSW |
17 |
32,844,126 (GRCm39) |
missense |
probably benign |
|
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 |
|