Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap3 |
G |
A |
4: 155,986,676 (GRCm39) |
V335M |
probably damaging |
Het |
Apex1 |
C |
T |
14: 51,163,711 (GRCm39) |
L113F |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 37,100,429 (GRCm39) |
H1218Q |
possibly damaging |
Het |
Cd33 |
C |
T |
7: 43,182,329 (GRCm39) |
V39M |
probably damaging |
Het |
Chek2 |
A |
G |
5: 110,996,536 (GRCm39) |
D166G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,054 (GRCm39) |
K1376R |
unknown |
Het |
Cpd |
C |
T |
11: 76,686,439 (GRCm39) |
R963H |
probably damaging |
Het |
Cracd |
A |
G |
5: 76,805,921 (GRCm39) |
|
probably benign |
Het |
Cyp2c67 |
A |
C |
19: 39,628,376 (GRCm39) |
Y189* |
probably null |
Het |
Dock6 |
T |
C |
9: 21,723,103 (GRCm39) |
E1606G |
possibly damaging |
Het |
Dusp4 |
A |
T |
8: 35,285,666 (GRCm39) |
E309V |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,162,789 (GRCm39) |
I600T |
probably damaging |
Het |
Fer1l4 |
A |
G |
2: 155,894,105 (GRCm39) |
V66A |
probably benign |
Het |
Fktn |
T |
C |
4: 53,737,568 (GRCm39) |
L269P |
possibly damaging |
Het |
Ftsj3 |
A |
G |
11: 106,141,185 (GRCm39) |
I645T |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,534,713 (GRCm39) |
H198R |
probably damaging |
Het |
Gm10295 |
T |
A |
7: 71,000,406 (GRCm39) |
D58V |
unknown |
Het |
Hdlbp |
T |
C |
1: 93,357,891 (GRCm39) |
I337V |
probably benign |
Het |
Hydin |
T |
C |
8: 111,053,033 (GRCm39) |
V235A |
probably benign |
Het |
Igfbp4 |
C |
T |
11: 98,939,069 (GRCm39) |
H30Y |
probably damaging |
Het |
Kcna4 |
T |
C |
2: 107,126,736 (GRCm39) |
V490A |
probably damaging |
Het |
Kcnj13 |
T |
G |
1: 87,314,700 (GRCm39) |
D174A |
probably benign |
Het |
Krt7 |
T |
A |
15: 101,321,302 (GRCm39) |
L373Q |
probably benign |
Het |
Lama3 |
G |
A |
18: 12,614,094 (GRCm39) |
V1288I |
probably benign |
Het |
Mroh9 |
T |
C |
1: 162,875,435 (GRCm39) |
D488G |
possibly damaging |
Het |
Myh7 |
T |
C |
14: 55,216,994 (GRCm39) |
E1121G |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,384,912 (GRCm39) |
N768D |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,622,196 (GRCm39) |
T48A |
probably damaging |
Het |
Naglu |
C |
T |
11: 100,964,773 (GRCm39) |
P287S |
probably benign |
Het |
Nipbl |
A |
G |
15: 8,379,939 (GRCm39) |
V951A |
possibly damaging |
Het |
Nlrp3 |
T |
A |
11: 59,442,713 (GRCm39) |
M755K |
probably benign |
Het |
Nlrp4e |
T |
C |
7: 23,052,586 (GRCm39) |
|
probably benign |
Het |
Nt5dc1 |
C |
T |
10: 34,283,553 (GRCm39) |
A79T |
possibly damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,251 (GRCm39) |
F104S |
probably damaging |
Het |
Or6c205 |
A |
T |
10: 129,086,609 (GRCm39) |
I69F |
possibly damaging |
Het |
Or8b47 |
A |
G |
9: 38,435,029 (GRCm39) |
|
probably benign |
Het |
Otof |
A |
G |
5: 30,541,597 (GRCm39) |
L774P |
possibly damaging |
Het |
Phf20l1 |
C |
T |
15: 66,484,981 (GRCm39) |
R322C |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,279,400 (GRCm39) |
G2973R |
probably benign |
Het |
Plekhg5 |
G |
T |
4: 152,192,983 (GRCm39) |
D613Y |
probably damaging |
Het |
Ppm1h |
T |
A |
10: 122,714,534 (GRCm39) |
|
probably null |
Het |
Pramel31 |
T |
A |
4: 144,089,947 (GRCm39) |
L329Q |
probably damaging |
Het |
Prpf39 |
T |
C |
12: 65,089,255 (GRCm39) |
|
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,460,406 (GRCm39) |
S15P |
unknown |
Het |
Slc22a28 |
G |
T |
19: 8,094,272 (GRCm39) |
|
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,239,515 (GRCm39) |
L143Q |
probably damaging |
Het |
Sox17 |
T |
C |
1: 4,562,426 (GRCm39) |
D130G |
possibly damaging |
Het |
Stag1 |
A |
G |
9: 100,833,710 (GRCm39) |
T1108A |
possibly damaging |
Het |
Sugp2 |
G |
A |
8: 70,695,185 (GRCm39) |
D53N |
probably damaging |
Het |
Trim33 |
G |
A |
3: 103,261,234 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,629,568 (GRCm39) |
I14291T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,619,869 (GRCm39) |
V15933A |
probably damaging |
Het |
Tulp3 |
A |
C |
6: 128,302,847 (GRCm39) |
I324S |
probably damaging |
Het |
Zfhx2 |
T |
C |
14: 55,301,717 (GRCm39) |
E2089G |
probably damaging |
Het |
Zhx1 |
T |
C |
15: 57,918,075 (GRCm39) |
D57G |
probably benign |
Het |
|
Other mutations in Fzd7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01505:Fzd7
|
APN |
1 |
59,523,062 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02647:Fzd7
|
APN |
1 |
59,523,554 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4495001:Fzd7
|
UTSW |
1 |
59,523,466 (GRCm39) |
missense |
probably benign |
0.44 |
R0479:Fzd7
|
UTSW |
1 |
59,522,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Fzd7
|
UTSW |
1 |
59,522,443 (GRCm39) |
missense |
probably damaging |
0.99 |
R0639:Fzd7
|
UTSW |
1 |
59,523,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1587:Fzd7
|
UTSW |
1 |
59,522,165 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2056:Fzd7
|
UTSW |
1 |
59,523,361 (GRCm39) |
missense |
probably benign |
0.00 |
R2566:Fzd7
|
UTSW |
1 |
59,523,695 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2890:Fzd7
|
UTSW |
1 |
59,523,593 (GRCm39) |
missense |
probably benign |
0.27 |
R4078:Fzd7
|
UTSW |
1 |
59,522,948 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4306:Fzd7
|
UTSW |
1 |
59,523,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4744:Fzd7
|
UTSW |
1 |
59,523,595 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5249:Fzd7
|
UTSW |
1 |
59,522,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R5740:Fzd7
|
UTSW |
1 |
59,522,839 (GRCm39) |
missense |
probably benign |
0.03 |
R5997:Fzd7
|
UTSW |
1 |
59,523,703 (GRCm39) |
missense |
probably benign |
0.01 |
R6136:Fzd7
|
UTSW |
1 |
59,522,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Fzd7
|
UTSW |
1 |
59,523,004 (GRCm39) |
missense |
probably benign |
0.01 |
R6476:Fzd7
|
UTSW |
1 |
59,523,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Fzd7
|
UTSW |
1 |
59,522,443 (GRCm39) |
missense |
probably damaging |
0.99 |
R7753:Fzd7
|
UTSW |
1 |
59,522,641 (GRCm39) |
missense |
probably benign |
|
R8322:Fzd7
|
UTSW |
1 |
59,522,242 (GRCm39) |
missense |
probably benign |
0.01 |
R9066:Fzd7
|
UTSW |
1 |
59,521,991 (GRCm39) |
start gained |
probably benign |
|
R9188:Fzd7
|
UTSW |
1 |
59,523,797 (GRCm39) |
missense |
probably benign |
|
R9255:Fzd7
|
UTSW |
1 |
59,522,495 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9326:Fzd7
|
UTSW |
1 |
59,522,837 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9458:Fzd7
|
UTSW |
1 |
59,523,554 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Fzd7
|
UTSW |
1 |
59,523,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|