Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
A |
11: 48,838,703 (GRCm39) |
H628L |
probably benign |
Het |
Adam6a |
T |
A |
12: 113,507,660 (GRCm39) |
V11E |
possibly damaging |
Het |
Amotl1 |
T |
G |
9: 14,467,059 (GRCm39) |
K660T |
possibly damaging |
Het |
Ap4m1 |
T |
C |
5: 138,171,077 (GRCm39) |
I59T |
probably damaging |
Het |
Brd3 |
T |
C |
2: 27,346,967 (GRCm39) |
Y389C |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Card11 |
C |
A |
5: 140,871,751 (GRCm39) |
R650L |
probably damaging |
Het |
Cercam |
G |
A |
2: 29,762,574 (GRCm39) |
|
probably null |
Het |
Cnst |
T |
C |
1: 179,452,650 (GRCm39) |
C673R |
probably damaging |
Het |
Dld |
G |
T |
12: 31,390,864 (GRCm39) |
T194K |
probably benign |
Het |
Dnah12 |
T |
A |
14: 26,507,890 (GRCm39) |
W1714R |
probably damaging |
Het |
Dsg1a |
T |
G |
18: 20,464,768 (GRCm39) |
V421G |
possibly damaging |
Het |
Fer1l4 |
G |
T |
2: 155,890,854 (GRCm39) |
P188Q |
probably benign |
Het |
Gpr158 |
T |
C |
2: 21,831,158 (GRCm39) |
S753P |
probably damaging |
Het |
Hdc |
A |
T |
2: 126,436,002 (GRCm39) |
M623K |
possibly damaging |
Het |
Herc1 |
CAACCCTGGTAAC |
CAAC |
9: 66,400,472 (GRCm39) |
|
probably benign |
Het |
Igf2r |
A |
T |
17: 12,954,878 (GRCm39) |
F203I |
probably damaging |
Het |
Jag2 |
A |
T |
12: 112,885,661 (GRCm39) |
I145N |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,446,686 (GRCm39) |
F694I |
probably benign |
Het |
Lpl |
A |
T |
8: 69,340,100 (GRCm39) |
R32* |
probably null |
Het |
Mcpt4 |
T |
A |
14: 56,297,428 (GRCm39) |
I243L |
probably benign |
Het |
Mtf1 |
C |
A |
4: 124,732,412 (GRCm39) |
A490E |
possibly damaging |
Het |
Mycbp2 |
A |
T |
14: 103,360,791 (GRCm39) |
M4497K |
probably damaging |
Het |
Myog |
T |
C |
1: 134,218,914 (GRCm39) |
|
probably null |
Het |
Nav2 |
T |
C |
7: 49,222,145 (GRCm39) |
S1757P |
probably damaging |
Het |
Or7g18 |
T |
G |
9: 18,786,709 (GRCm39) |
F26V |
probably benign |
Het |
Osmr |
T |
A |
15: 6,853,963 (GRCm39) |
I583F |
probably damaging |
Het |
Phf19 |
T |
A |
2: 34,785,816 (GRCm39) |
E551V |
probably damaging |
Het |
Plxnb2 |
A |
G |
15: 89,046,533 (GRCm39) |
M870T |
probably benign |
Het |
Psat1 |
A |
G |
19: 15,895,720 (GRCm39) |
F83L |
probably damaging |
Het |
Reep1 |
T |
A |
6: 71,757,725 (GRCm39) |
V108D |
possibly damaging |
Het |
Rorc |
A |
G |
3: 94,300,421 (GRCm39) |
T455A |
probably benign |
Het |
Serinc5 |
T |
G |
13: 92,821,698 (GRCm39) |
I169S |
probably damaging |
Het |
Serpinb6c |
T |
C |
13: 34,083,292 (GRCm39) |
M41V |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,892,927 (GRCm39) |
N335Y |
probably damaging |
Het |
Slamf7 |
C |
T |
1: 171,468,589 (GRCm39) |
R101H |
possibly damaging |
Het |
Slc17a4 |
A |
T |
13: 24,084,503 (GRCm39) |
L427* |
probably null |
Het |
Slc35a5 |
T |
C |
16: 44,964,246 (GRCm39) |
Q329R |
probably damaging |
Het |
Slc45a1 |
C |
T |
4: 150,715,397 (GRCm39) |
C656Y |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,773,643 (GRCm39) |
I18T |
probably damaging |
Het |
Syn3 |
T |
G |
10: 86,284,773 (GRCm39) |
H109P |
probably benign |
Het |
Synj2 |
T |
C |
17: 6,066,562 (GRCm39) |
V580A |
probably benign |
Het |
Tbc1d9b |
T |
C |
11: 50,026,742 (GRCm39) |
V70A |
possibly damaging |
Het |
Tc2n |
A |
G |
12: 101,617,406 (GRCm39) |
Y402H |
probably damaging |
Het |
Tmbim4 |
T |
C |
10: 120,059,767 (GRCm39) |
C164R |
possibly damaging |
Het |
Tnfrsf11b |
T |
A |
15: 54,117,470 (GRCm39) |
R262* |
probably null |
Het |
Tnip1 |
T |
C |
11: 54,828,805 (GRCm39) |
K121E |
probably benign |
Het |
Tut1 |
T |
C |
19: 8,941,740 (GRCm39) |
|
probably null |
Het |
Uhrf2 |
T |
A |
19: 30,052,501 (GRCm39) |
C332S |
probably damaging |
Het |
Vmn2r101 |
A |
G |
17: 19,831,950 (GRCm39) |
I649V |
possibly damaging |
Het |
Vwa8 |
A |
G |
14: 79,232,589 (GRCm39) |
T644A |
probably benign |
Het |
Zfhx2 |
T |
C |
14: 55,304,357 (GRCm39) |
H1209R |
possibly damaging |
Het |
Zfp384 |
A |
G |
6: 125,008,635 (GRCm39) |
I306V |
probably benign |
Het |
Zmym2 |
A |
T |
14: 57,193,638 (GRCm39) |
Y1151F |
possibly damaging |
Het |
|
Other mutations in Zfp964 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Zfp964
|
APN |
8 |
70,112,043 (GRCm39) |
splice site |
probably null |
|
R0506:Zfp964
|
UTSW |
8 |
70,116,587 (GRCm39) |
missense |
unknown |
|
R0740:Zfp964
|
UTSW |
8 |
70,115,828 (GRCm39) |
missense |
probably damaging |
0.98 |
R0786:Zfp964
|
UTSW |
8 |
70,116,731 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1158:Zfp964
|
UTSW |
8 |
70,116,503 (GRCm39) |
missense |
unknown |
|
R1204:Zfp964
|
UTSW |
8 |
70,116,668 (GRCm39) |
missense |
probably benign |
0.08 |
R1413:Zfp964
|
UTSW |
8 |
70,115,720 (GRCm39) |
missense |
unknown |
|
R1562:Zfp964
|
UTSW |
8 |
70,115,654 (GRCm39) |
missense |
probably benign |
|
R1663:Zfp964
|
UTSW |
8 |
70,116,733 (GRCm39) |
splice site |
probably null |
|
R1693:Zfp964
|
UTSW |
8 |
70,116,800 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2029:Zfp964
|
UTSW |
8 |
70,116,567 (GRCm39) |
missense |
unknown |
|
R2847:Zfp964
|
UTSW |
8 |
70,116,504 (GRCm39) |
missense |
unknown |
|
R2849:Zfp964
|
UTSW |
8 |
70,116,504 (GRCm39) |
missense |
unknown |
|
R4111:Zfp964
|
UTSW |
8 |
70,116,754 (GRCm39) |
missense |
probably benign |
0.18 |
R4792:Zfp964
|
UTSW |
8 |
70,116,665 (GRCm39) |
missense |
probably benign |
0.18 |
R4907:Zfp964
|
UTSW |
8 |
70,115,972 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4938:Zfp964
|
UTSW |
8 |
70,116,758 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5688:Zfp964
|
UTSW |
8 |
70,116,766 (GRCm39) |
missense |
probably benign |
0.03 |
R5905:Zfp964
|
UTSW |
8 |
70,116,563 (GRCm39) |
missense |
unknown |
|
R6009:Zfp964
|
UTSW |
8 |
70,116,106 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6021:Zfp964
|
UTSW |
8 |
70,115,742 (GRCm39) |
missense |
unknown |
|
R6028:Zfp964
|
UTSW |
8 |
70,116,563 (GRCm39) |
missense |
unknown |
|
R6374:Zfp964
|
UTSW |
8 |
70,111,994 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6583:Zfp964
|
UTSW |
8 |
70,115,633 (GRCm39) |
missense |
probably damaging |
0.98 |
R8263:Zfp964
|
UTSW |
8 |
70,116,345 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8309:Zfp964
|
UTSW |
8 |
70,115,924 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8889:Zfp964
|
UTSW |
8 |
70,116,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Zfp964
|
UTSW |
8 |
70,116,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R9133:Zfp964
|
UTSW |
8 |
70,115,783 (GRCm39) |
missense |
probably benign |
0.00 |
R9185:Zfp964
|
UTSW |
8 |
70,115,873 (GRCm39) |
missense |
possibly damaging |
0.53 |
|