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 |
Fzd7 |
T |
C |
1: 59,523,539 (GRCm39) |
V474A |
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 |
Zhx1 |
T |
C |
15: 57,918,075 (GRCm39) |
D57G |
probably benign |
Het |
|
Other mutations in Zfhx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Zfhx2
|
APN |
14 |
55,304,022 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00164:Zfhx2
|
APN |
14 |
55,302,483 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00235:Zfhx2
|
APN |
14 |
55,300,714 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00925:Zfhx2
|
APN |
14 |
55,310,518 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01061:Zfhx2
|
APN |
14 |
55,311,339 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01486:Zfhx2
|
APN |
14 |
55,304,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Zfhx2
|
APN |
14 |
55,301,372 (GRCm39) |
missense |
unknown |
|
IGL01990:Zfhx2
|
APN |
14 |
55,311,047 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02097:Zfhx2
|
APN |
14 |
55,300,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02269:Zfhx2
|
APN |
14 |
55,309,393 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02488:Zfhx2
|
APN |
14 |
55,302,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02624:Zfhx2
|
APN |
14 |
55,304,085 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03087:Zfhx2
|
APN |
14 |
55,310,302 (GRCm39) |
missense |
possibly damaging |
0.85 |
G1patch:Zfhx2
|
UTSW |
14 |
55,301,539 (GRCm39) |
nonsense |
probably null |
|
PIT4403001:Zfhx2
|
UTSW |
14 |
55,312,437 (GRCm39) |
missense |
probably benign |
|
R0148:Zfhx2
|
UTSW |
14 |
55,310,354 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0323:Zfhx2
|
UTSW |
14 |
55,303,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0328:Zfhx2
|
UTSW |
14 |
55,309,445 (GRCm39) |
missense |
probably benign |
|
R0348:Zfhx2
|
UTSW |
14 |
55,300,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R0442:Zfhx2
|
UTSW |
14 |
55,304,357 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0533:Zfhx2
|
UTSW |
14 |
55,301,547 (GRCm39) |
missense |
probably benign |
0.23 |
R0561:Zfhx2
|
UTSW |
14 |
55,303,346 (GRCm39) |
missense |
probably benign |
0.01 |
R0627:Zfhx2
|
UTSW |
14 |
55,302,784 (GRCm39) |
missense |
probably benign |
|
R0659:Zfhx2
|
UTSW |
14 |
55,311,258 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0675:Zfhx2
|
UTSW |
14 |
55,300,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R1301:Zfhx2
|
UTSW |
14 |
55,300,854 (GRCm39) |
missense |
probably benign |
0.32 |
R1563:Zfhx2
|
UTSW |
14 |
55,302,545 (GRCm39) |
missense |
probably benign |
0.33 |
R1607:Zfhx2
|
UTSW |
14 |
55,300,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Zfhx2
|
UTSW |
14 |
55,311,401 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1710:Zfhx2
|
UTSW |
14 |
55,303,455 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1773:Zfhx2
|
UTSW |
14 |
55,310,348 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1879:Zfhx2
|
UTSW |
14 |
55,310,206 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1879:Zfhx2
|
UTSW |
14 |
55,303,074 (GRCm39) |
missense |
probably benign |
0.32 |
R1933:Zfhx2
|
UTSW |
14 |
55,312,695 (GRCm39) |
start gained |
probably benign |
|
R1944:Zfhx2
|
UTSW |
14 |
55,312,189 (GRCm39) |
missense |
probably benign |
0.18 |
R2888:Zfhx2
|
UTSW |
14 |
55,302,260 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2889:Zfhx2
|
UTSW |
14 |
55,302,260 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2915:Zfhx2
|
UTSW |
14 |
55,302,014 (GRCm39) |
missense |
probably damaging |
0.98 |
R3971:Zfhx2
|
UTSW |
14 |
55,311,932 (GRCm39) |
missense |
probably benign |
0.33 |
R4082:Zfhx2
|
UTSW |
14 |
55,302,662 (GRCm39) |
missense |
probably benign |
|
R4134:Zfhx2
|
UTSW |
14 |
55,302,600 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4231:Zfhx2
|
UTSW |
14 |
55,310,991 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4675:Zfhx2
|
UTSW |
14 |
55,304,678 (GRCm39) |
missense |
probably benign |
0.03 |
R4764:Zfhx2
|
UTSW |
14 |
55,304,372 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4866:Zfhx2
|
UTSW |
14 |
55,302,993 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4940:Zfhx2
|
UTSW |
14 |
55,303,891 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5125:Zfhx2
|
UTSW |
14 |
55,312,232 (GRCm39) |
missense |
probably benign |
0.00 |
R5178:Zfhx2
|
UTSW |
14 |
55,312,232 (GRCm39) |
missense |
probably benign |
0.00 |
R5554:Zfhx2
|
UTSW |
14 |
55,301,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R5689:Zfhx2
|
UTSW |
14 |
55,311,360 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5768:Zfhx2
|
UTSW |
14 |
55,311,822 (GRCm39) |
missense |
probably benign |
|
R5792:Zfhx2
|
UTSW |
14 |
55,304,303 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5834:Zfhx2
|
UTSW |
14 |
55,310,787 (GRCm39) |
nonsense |
probably null |
|
R5895:Zfhx2
|
UTSW |
14 |
55,303,348 (GRCm39) |
missense |
probably benign |
|
R5999:Zfhx2
|
UTSW |
14 |
55,311,462 (GRCm39) |
missense |
probably benign |
|
R6025:Zfhx2
|
UTSW |
14 |
55,302,665 (GRCm39) |
missense |
probably benign |
0.00 |
R6106:Zfhx2
|
UTSW |
14 |
55,305,767 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6135:Zfhx2
|
UTSW |
14 |
55,311,653 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6186:Zfhx2
|
UTSW |
14 |
55,300,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R6379:Zfhx2
|
UTSW |
14 |
55,311,795 (GRCm39) |
missense |
probably benign |
|
R6725:Zfhx2
|
UTSW |
14 |
55,301,539 (GRCm39) |
nonsense |
probably null |
|
R7089:Zfhx2
|
UTSW |
14 |
55,303,229 (GRCm39) |
missense |
probably benign |
0.33 |
R7383:Zfhx2
|
UTSW |
14 |
55,305,710 (GRCm39) |
missense |
probably benign |
0.00 |
R7470:Zfhx2
|
UTSW |
14 |
55,304,207 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7606:Zfhx2
|
UTSW |
14 |
55,304,120 (GRCm39) |
missense |
probably benign |
0.12 |
R7607:Zfhx2
|
UTSW |
14 |
55,303,688 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7698:Zfhx2
|
UTSW |
14 |
55,300,306 (GRCm39) |
missense |
probably benign |
0.00 |
R7730:Zfhx2
|
UTSW |
14 |
55,304,357 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8142:Zfhx2
|
UTSW |
14 |
55,310,895 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8188:Zfhx2
|
UTSW |
14 |
55,301,898 (GRCm39) |
missense |
probably benign |
0.18 |
R8212:Zfhx2
|
UTSW |
14 |
55,310,373 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8264:Zfhx2
|
UTSW |
14 |
55,302,969 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8331:Zfhx2
|
UTSW |
14 |
55,309,444 (GRCm39) |
missense |
probably benign |
0.00 |
R8369:Zfhx2
|
UTSW |
14 |
55,304,201 (GRCm39) |
missense |
probably benign |
0.05 |
R8371:Zfhx2
|
UTSW |
14 |
55,301,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R8383:Zfhx2
|
UTSW |
14 |
55,311,528 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8415:Zfhx2
|
UTSW |
14 |
55,308,079 (GRCm39) |
missense |
probably benign |
|
R8441:Zfhx2
|
UTSW |
14 |
55,303,985 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8466:Zfhx2
|
UTSW |
14 |
55,310,353 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8504:Zfhx2
|
UTSW |
14 |
55,303,243 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Zfhx2
|
UTSW |
14 |
55,312,509 (GRCm39) |
missense |
probably benign |
|
R8804:Zfhx2
|
UTSW |
14 |
55,312,191 (GRCm39) |
missense |
probably benign |
0.18 |
R8913:Zfhx2
|
UTSW |
14 |
55,309,543 (GRCm39) |
missense |
probably benign |
0.02 |
R8952:Zfhx2
|
UTSW |
14 |
55,310,207 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9057:Zfhx2
|
UTSW |
14 |
55,310,027 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9060:Zfhx2
|
UTSW |
14 |
55,311,803 (GRCm39) |
missense |
probably benign |
0.00 |
R9197:Zfhx2
|
UTSW |
14 |
55,312,179 (GRCm39) |
nonsense |
probably null |
|
R9622:Zfhx2
|
UTSW |
14 |
55,303,483 (GRCm39) |
missense |
probably benign |
0.18 |
R9623:Zfhx2
|
UTSW |
14 |
55,302,191 (GRCm39) |
missense |
probably damaging |
0.98 |
R9775:Zfhx2
|
UTSW |
14 |
55,304,562 (GRCm39) |
missense |
probably benign |
0.01 |
R9780:Zfhx2
|
UTSW |
14 |
55,312,494 (GRCm39) |
missense |
probably benign |
0.02 |
X0065:Zfhx2
|
UTSW |
14 |
55,304,417 (GRCm39) |
missense |
probably benign |
0.33 |
Z1088:Zfhx2
|
UTSW |
14 |
55,311,637 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Zfhx2
|
UTSW |
14 |
55,304,439 (GRCm39) |
missense |
possibly damaging |
0.70 |
Z1177:Zfhx2
|
UTSW |
14 |
55,303,377 (GRCm39) |
missense |
probably benign |
0.40 |
|