Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
A |
T |
5: 105,109,052 (GRCm39) |
V415D |
possibly damaging |
Het |
Adcy3 |
C |
T |
12: 4,262,118 (GRCm39) |
A1056V |
probably damaging |
Het |
Adcy5 |
G |
A |
16: 35,092,468 (GRCm39) |
A610T |
probably damaging |
Het |
Arhgap21 |
G |
A |
2: 20,884,813 (GRCm39) |
T788I |
probably benign |
Het |
Asic1 |
T |
C |
15: 99,592,567 (GRCm39) |
|
probably benign |
Het |
Cdhr4 |
T |
A |
9: 107,870,199 (GRCm39) |
M68K |
probably benign |
Het |
Cdhr5 |
G |
T |
7: 140,849,894 (GRCm39) |
T637K |
probably damaging |
Het |
Corin |
A |
T |
5: 72,529,489 (GRCm39) |
C289S |
probably damaging |
Het |
Cpne4 |
T |
C |
9: 104,563,701 (GRCm39) |
V26A |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,261,773 (GRCm39) |
D908G |
probably null |
Het |
Cyp2c29 |
A |
G |
19: 39,296,064 (GRCm39) |
D126G |
probably damaging |
Het |
Ddx42 |
G |
A |
11: 106,129,986 (GRCm39) |
S426N |
probably benign |
Het |
Dnah1 |
C |
T |
14: 31,026,958 (GRCm39) |
V689M |
possibly damaging |
Het |
Dtwd1 |
A |
G |
2: 126,006,715 (GRCm39) |
T246A |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,205,889 (GRCm39) |
M1036K |
probably damaging |
Het |
Fbxo10 |
T |
C |
4: 45,048,527 (GRCm39) |
N536S |
probably benign |
Het |
Gnal |
G |
A |
18: 67,350,279 (GRCm39) |
|
probably benign |
Het |
Gns |
A |
G |
10: 121,226,598 (GRCm39) |
T416A |
probably benign |
Het |
Heatr5b |
G |
A |
17: 79,124,943 (GRCm39) |
T603I |
probably damaging |
Het |
Hsp90b1 |
T |
A |
10: 86,527,548 (GRCm39) |
|
probably benign |
Het |
Krt23 |
C |
T |
11: 99,383,836 (GRCm39) |
G19R |
probably benign |
Het |
Lama2 |
C |
T |
10: 27,014,956 (GRCm39) |
R1584H |
probably benign |
Het |
Lmbr1l |
C |
T |
15: 98,815,772 (GRCm39) |
V11M |
probably damaging |
Het |
Man1a2 |
T |
C |
3: 100,489,447 (GRCm39) |
K511E |
possibly damaging |
Het |
Mrgpra3 |
C |
A |
7: 47,239,204 (GRCm39) |
V241F |
possibly damaging |
Het |
Myh3 |
A |
G |
11: 66,973,750 (GRCm39) |
D141G |
probably benign |
Het |
Mylk2 |
G |
A |
2: 152,757,056 (GRCm39) |
C277Y |
probably damaging |
Het |
Myo3b |
A |
T |
2: 70,069,173 (GRCm39) |
T471S |
probably damaging |
Het |
Naip1 |
A |
G |
13: 100,562,096 (GRCm39) |
V1023A |
probably benign |
Het |
Olfm5 |
T |
A |
7: 103,803,438 (GRCm39) |
T342S |
probably benign |
Het |
Or10g1 |
A |
G |
14: 52,647,511 (GRCm39) |
F273L |
probably benign |
Het |
Or2f1b |
T |
A |
6: 42,739,394 (GRCm39) |
M136K |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,642,910 (GRCm39) |
F263L |
probably benign |
Het |
Plekhh2 |
A |
T |
17: 84,906,608 (GRCm39) |
T1148S |
possibly damaging |
Het |
Prrc2b |
T |
C |
2: 32,081,513 (GRCm39) |
|
probably benign |
Het |
Rbm28 |
G |
T |
6: 29,138,617 (GRCm39) |
D398E |
possibly damaging |
Het |
Rnf220 |
A |
G |
4: 117,130,524 (GRCm39) |
F234L |
probably benign |
Het |
Sele |
T |
C |
1: 163,880,662 (GRCm39) |
S415P |
probably benign |
Het |
Shpk |
T |
C |
11: 73,094,821 (GRCm39) |
L79P |
probably damaging |
Het |
Slc35f4 |
C |
T |
14: 49,543,703 (GRCm39) |
A148T |
probably damaging |
Het |
Slc6a20a |
G |
A |
9: 123,489,684 (GRCm39) |
P120S |
possibly damaging |
Het |
Slc8a2 |
A |
G |
7: 15,891,081 (GRCm39) |
E701G |
possibly damaging |
Het |
Slco1a1 |
T |
A |
6: 141,885,765 (GRCm39) |
I87F |
possibly damaging |
Het |
Srebf1 |
T |
G |
11: 60,093,650 (GRCm39) |
D739A |
probably damaging |
Het |
Thg1l |
A |
G |
11: 45,841,055 (GRCm39) |
Y175H |
probably benign |
Het |
Traf3ip2 |
G |
A |
10: 39,530,475 (GRCm39) |
V540M |
probably damaging |
Het |
Wdr48 |
A |
G |
9: 119,753,329 (GRCm39) |
D644G |
probably damaging |
Het |
Zbtb1 |
A |
T |
12: 76,433,371 (GRCm39) |
K452N |
probably damaging |
Het |
Zfp334 |
A |
T |
2: 165,223,643 (GRCm39) |
Y133* |
probably null |
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 |
IGL01025:Zfhx2
|
APN |
14 |
55,301,717 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|