Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
C |
17: 9,226,927 (GRCm39) |
V494A |
probably benign |
Het |
1700017B05Rik |
A |
T |
9: 57,166,041 (GRCm39) |
L111Q |
probably damaging |
Het |
Adgrf4 |
T |
G |
17: 42,977,424 (GRCm39) |
I640L |
possibly damaging |
Het |
Afdn |
T |
G |
17: 14,111,074 (GRCm39) |
|
probably null |
Het |
Ammecr1l |
A |
T |
18: 31,894,877 (GRCm39) |
|
probably benign |
Het |
Aox1 |
A |
T |
1: 58,375,808 (GRCm39) |
Y879F |
probably benign |
Het |
Arhgap45 |
G |
A |
10: 79,862,181 (GRCm39) |
|
probably null |
Het |
Arpp21 |
G |
T |
9: 111,955,514 (GRCm39) |
H542N |
probably benign |
Het |
Ccdc192 |
C |
T |
18: 57,725,059 (GRCm39) |
T96I |
probably benign |
Het |
Cdt1 |
G |
A |
8: 123,298,719 (GRCm39) |
R452Q |
probably damaging |
Het |
Clcn7 |
C |
T |
17: 25,372,667 (GRCm39) |
H149Y |
|
Het |
Clpp |
T |
G |
17: 57,297,421 (GRCm39) |
W32G |
probably benign |
Het |
Dnmt1 |
G |
T |
9: 20,819,785 (GRCm39) |
L1572M |
probably damaging |
Het |
Drd3 |
G |
T |
16: 43,627,741 (GRCm39) |
R128S |
probably damaging |
Het |
Elmo2 |
A |
T |
2: 165,146,849 (GRCm39) |
F243I |
possibly damaging |
Het |
Endou |
G |
A |
15: 97,618,126 (GRCm39) |
P128L |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,908,214 (GRCm39) |
M2596T |
probably benign |
Het |
Fbxl16 |
A |
G |
17: 26,035,703 (GRCm39) |
K100R |
probably benign |
Het |
Fbxo10 |
A |
G |
4: 45,062,230 (GRCm39) |
S99P |
possibly damaging |
Het |
Fez1 |
A |
T |
9: 36,778,999 (GRCm39) |
R225S |
probably benign |
Het |
Gm14326 |
A |
T |
2: 177,588,464 (GRCm39) |
H177Q |
probably damaging |
Het |
Gm32742 |
T |
A |
9: 51,054,546 (GRCm39) |
M1360L |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,271,677 (GRCm39) |
V2481A |
possibly damaging |
Het |
Ifnl3 |
A |
G |
7: 28,223,283 (GRCm39) |
K101E |
probably benign |
Het |
Il15 |
A |
T |
8: 83,064,204 (GRCm39) |
S77R |
probably damaging |
Het |
Ints13 |
T |
C |
6: 146,476,216 (GRCm39) |
D95G |
probably damaging |
Het |
Kcmf1 |
G |
A |
6: 72,819,929 (GRCm39) |
P357S |
probably benign |
Het |
Kcmf1 |
G |
T |
6: 72,825,289 (GRCm39) |
T268K |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,748,153 (GRCm39) |
I3057N |
unknown |
Het |
Lgi2 |
A |
G |
5: 52,695,832 (GRCm39) |
F376L |
probably damaging |
Het |
Lrig3 |
T |
G |
10: 125,832,993 (GRCm39) |
L289R |
probably damaging |
Het |
Mafk |
A |
G |
5: 139,785,876 (GRCm39) |
S25G |
probably benign |
Het |
Mpz |
T |
C |
1: 170,987,204 (GRCm39) |
|
probably null |
Het |
Nalcn |
A |
C |
14: 123,515,761 (GRCm39) |
I1680R |
probably benign |
Het |
Or13d1 |
C |
T |
4: 52,971,470 (GRCm39) |
P283L |
probably damaging |
Het |
Or5ak24 |
T |
A |
2: 85,260,902 (GRCm39) |
K90N |
probably benign |
Het |
Or5g26 |
C |
T |
2: 85,494,518 (GRCm39) |
V87M |
possibly damaging |
Het |
Or5p62 |
A |
T |
7: 107,771,701 (GRCm39) |
N83K |
probably benign |
Het |
Otof |
A |
C |
5: 30,528,912 (GRCm39) |
I1827S |
possibly damaging |
Het |
Oxgr1 |
A |
G |
14: 120,259,614 (GRCm39) |
Y198H |
probably damaging |
Het |
P3h2 |
T |
A |
16: 25,784,559 (GRCm39) |
N645I |
probably damaging |
Het |
Pbld2 |
A |
G |
10: 62,889,691 (GRCm39) |
T158A |
probably benign |
Het |
Pdgfrb |
C |
T |
18: 61,206,315 (GRCm39) |
R608C |
probably damaging |
Het |
Pdia5 |
T |
C |
16: 35,228,049 (GRCm39) |
T408A |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,226,845 (GRCm39) |
V1014A |
probably benign |
Het |
Prpf8 |
A |
G |
11: 75,399,374 (GRCm39) |
T2180A |
probably damaging |
Het |
Rabgap1l |
A |
T |
1: 160,551,742 (GRCm39) |
Y245* |
probably null |
Het |
Rerg |
T |
C |
6: 137,044,033 (GRCm39) |
T28A |
possibly damaging |
Het |
Rhcg |
A |
G |
7: 79,249,216 (GRCm39) |
I335T |
probably damaging |
Het |
Rmnd1 |
C |
T |
10: 4,353,873 (GRCm39) |
V78I |
probably damaging |
Het |
Ryr2 |
A |
C |
13: 11,664,662 (GRCm39) |
V3547G |
probably benign |
Het |
Scnn1a |
C |
A |
6: 125,314,770 (GRCm39) |
Q324K |
probably benign |
Het |
Serpinb6e |
G |
A |
13: 34,016,698 (GRCm39) |
T345I |
probably damaging |
Het |
Smchd1 |
T |
C |
17: 71,668,955 (GRCm39) |
T1687A |
probably benign |
Het |
Smim45 |
A |
T |
15: 82,136,774 (GRCm39) |
|
probably benign |
Het |
Speer4f2 |
A |
C |
5: 17,581,661 (GRCm39) |
H201P |
|
Het |
Spef2 |
G |
A |
15: 9,725,257 (GRCm39) |
R167C |
probably damaging |
Het |
Srp68 |
A |
G |
11: 116,162,733 (GRCm39) |
|
probably null |
Het |
Tbc1d14 |
A |
T |
5: 36,669,884 (GRCm39) |
F455I |
probably benign |
Het |
Tet3 |
A |
G |
6: 83,432,006 (GRCm39) |
V10A |
possibly damaging |
Het |
Tlr3 |
A |
T |
8: 45,850,810 (GRCm39) |
S696T |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,978,709 (GRCm39) |
N300S |
probably benign |
Het |
Tmprss11g |
T |
C |
5: 86,637,150 (GRCm39) |
I328M |
probably damaging |
Het |
Tpm3 |
C |
T |
3: 89,980,029 (GRCm39) |
|
probably benign |
Het |
Trim28 |
T |
A |
7: 12,758,833 (GRCm39) |
L63Q |
probably damaging |
Het |
Unc5b |
G |
A |
10: 60,613,265 (GRCm39) |
R324C |
probably damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,507,204 (GRCm39) |
N107K |
possibly damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,656,100 (GRCm39) |
T770A |
|
Het |
Zcchc2 |
C |
A |
1: 105,958,211 (GRCm39) |
P894Q |
probably damaging |
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 |
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 |
|
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 |
|