Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
G |
T |
11: 109,945,473 (GRCm39) |
Q1050K |
probably benign |
Het |
B4galt5 |
A |
G |
2: 167,151,145 (GRCm39) |
M121T |
probably damaging |
Het |
Birc2 |
A |
G |
9: 7,849,427 (GRCm39) |
L549P |
probably damaging |
Het |
Cacna1b |
T |
C |
2: 24,610,036 (GRCm39) |
N368S |
possibly damaging |
Het |
Cbr1 |
A |
G |
16: 93,406,779 (GRCm39) |
E165G |
probably damaging |
Het |
Ccdc178 |
T |
C |
18: 21,944,561 (GRCm39) |
D866G |
possibly damaging |
Het |
Cd40 |
G |
A |
2: 164,908,458 (GRCm39) |
G178E |
probably damaging |
Het |
Cers1 |
T |
A |
8: 70,782,223 (GRCm39) |
L349H |
probably benign |
Het |
Chd8 |
T |
C |
14: 52,470,275 (GRCm39) |
K445R |
probably benign |
Het |
Clca3a2 |
G |
T |
3: 144,513,114 (GRCm39) |
S477* |
probably null |
Het |
Clec4a1 |
T |
A |
6: 122,910,882 (GRCm39) |
*246R |
probably null |
Het |
CN725425 |
T |
C |
15: 91,124,973 (GRCm39) |
I171T |
probably benign |
Het |
Crybg3 |
A |
G |
16: 59,377,414 (GRCm39) |
M1280T |
probably benign |
Het |
Csf1r |
A |
T |
18: 61,250,663 (GRCm39) |
Q458L |
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,805,438 (GRCm39) |
V193E |
possibly damaging |
Het |
Cys1 |
A |
G |
12: 24,718,694 (GRCm39) |
I53T |
probably benign |
Het |
Dhrs3 |
A |
C |
4: 144,645,953 (GRCm39) |
|
probably null |
Het |
Dhx57 |
T |
C |
17: 80,582,919 (GRCm39) |
R229G |
probably benign |
Het |
Dhx9 |
T |
C |
1: 153,331,961 (GRCm39) |
N1336D |
unknown |
Het |
Dmgdh |
T |
A |
13: 93,845,238 (GRCm39) |
H410Q |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,031,781 (GRCm39) |
M2225K |
probably benign |
Het |
Eif4g3 |
T |
G |
4: 137,824,156 (GRCm39) |
Y80D |
probably damaging |
Het |
Ephx4 |
A |
T |
5: 107,561,384 (GRCm39) |
I164F |
possibly damaging |
Het |
Eppk1 |
C |
T |
15: 75,994,319 (GRCm39) |
R854Q |
probably benign |
Het |
Fhl4 |
G |
A |
10: 84,934,637 (GRCm39) |
A48V |
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,437,173 (GRCm39) |
L1048S |
unknown |
Het |
Gemin5 |
T |
C |
11: 58,017,384 (GRCm39) |
M1212V |
probably benign |
Het |
Gm9195 |
C |
T |
14: 72,697,899 (GRCm39) |
V1294I |
probably benign |
Het |
Gpr55 |
A |
T |
1: 85,868,849 (GRCm39) |
V244E |
probably damaging |
Het |
Hgfac |
T |
A |
5: 35,202,787 (GRCm39) |
F429Y |
probably damaging |
Het |
Jade2 |
T |
A |
11: 51,715,959 (GRCm39) |
E415D |
probably benign |
Het |
Kcnj4 |
T |
A |
15: 79,369,342 (GRCm39) |
I213F |
probably damaging |
Het |
Kcnq5 |
G |
A |
1: 21,549,648 (GRCm39) |
R360C |
probably damaging |
Het |
Klhl33 |
C |
T |
14: 51,129,689 (GRCm39) |
R312Q |
probably damaging |
Het |
Krt82 |
T |
C |
15: 101,453,546 (GRCm39) |
E280G |
probably benign |
Het |
Lemd1 |
C |
A |
1: 132,156,687 (GRCm39) |
Q40K |
probably damaging |
Het |
Lmo7 |
T |
C |
14: 102,124,444 (GRCm39) |
L423P |
possibly damaging |
Het |
Lrp8 |
A |
G |
4: 107,726,268 (GRCm39) |
Y773C |
probably damaging |
Het |
Miga2 |
AAGAG |
AAG |
2: 30,265,755 (GRCm39) |
|
probably null |
Het |
Mroh8 |
A |
T |
2: 157,094,896 (GRCm39) |
Y363* |
probably null |
Het |
Or2n1c |
G |
A |
17: 38,519,189 (GRCm39) |
A18T |
probably benign |
Het |
Or51a25 |
C |
A |
7: 102,372,790 (GRCm39) |
K302N |
probably damaging |
Het |
Or5p61 |
G |
A |
7: 107,758,435 (GRCm39) |
T215I |
probably benign |
Het |
Pcdha2 |
T |
C |
18: 37,073,316 (GRCm39) |
Y316H |
possibly damaging |
Het |
Pcdha6 |
T |
A |
18: 37,102,920 (GRCm39) |
C704* |
probably null |
Het |
Pik3c2g |
G |
A |
6: 139,881,782 (GRCm39) |
V923M |
unknown |
Het |
Rhd |
A |
G |
4: 134,603,694 (GRCm39) |
S72G |
probably benign |
Het |
Rhot1 |
T |
C |
11: 80,134,292 (GRCm39) |
L295P |
probably damaging |
Het |
Rrp1b |
A |
G |
17: 32,268,458 (GRCm39) |
E139G |
possibly damaging |
Het |
Scnn1a |
T |
G |
6: 125,320,806 (GRCm39) |
Y620D |
possibly damaging |
Het |
Serpinb12 |
A |
T |
1: 106,884,135 (GRCm39) |
I294L |
probably benign |
Het |
Serpinb3d |
T |
C |
1: 107,008,469 (GRCm39) |
D132G |
probably damaging |
Het |
Slc26a3 |
A |
T |
12: 31,502,541 (GRCm39) |
D254V |
probably damaging |
Het |
Srrm1 |
A |
T |
4: 135,052,532 (GRCm39) |
I614N |
unknown |
Het |
Stt3b |
A |
G |
9: 115,095,243 (GRCm39) |
Y263H |
probably damaging |
Het |
Taf7 |
T |
A |
18: 37,776,552 (GRCm39) |
K5I |
probably damaging |
Het |
Tbck |
C |
A |
3: 132,458,285 (GRCm39) |
H638Q |
possibly damaging |
Het |
Tnfsf9 |
A |
C |
17: 57,412,541 (GRCm39) |
D37A |
probably benign |
Het |
Trim71 |
C |
A |
9: 114,344,857 (GRCm39) |
V354F |
probably benign |
Het |
Tspoap1 |
T |
G |
11: 87,669,127 (GRCm39) |
C1467G |
probably benign |
Het |
Xirp1 |
C |
T |
9: 119,848,499 (GRCm39) |
R128Q |
possibly damaging |
Het |
Zc3h12d |
GCCC |
GCC |
10: 7,715,735 (GRCm39) |
|
probably null |
Het |
Zfhx2 |
T |
C |
14: 55,301,549 (GRCm39) |
D2145G |
probably damaging |
Het |
|
Other mutations in Zfy2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02850:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02850:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02851:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02851:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02852:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4515001:Zfy2
|
UTSW |
Y |
2,117,096 (GRCm39) |
missense |
probably benign |
0.09 |
R0426:Zfy2
|
UTSW |
Y |
2,107,348 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0490:Zfy2
|
UTSW |
Y |
2,106,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1080:Zfy2
|
UTSW |
Y |
2,121,645 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Zfy2
|
UTSW |
Y |
2,116,185 (GRCm39) |
missense |
probably benign |
0.00 |
R1935:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R1936:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R2358:Zfy2
|
UTSW |
Y |
2,107,272 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4484:Zfy2
|
UTSW |
Y |
2,107,351 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4754:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.02 |
R4777:Zfy2
|
UTSW |
Y |
2,116,194 (GRCm39) |
missense |
probably benign |
0.00 |
R4812:Zfy2
|
UTSW |
Y |
2,106,334 (GRCm39) |
missense |
probably benign |
0.08 |
R5045:Zfy2
|
UTSW |
Y |
2,107,159 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5363:Zfy2
|
UTSW |
Y |
2,106,555 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6256:Zfy2
|
UTSW |
Y |
2,116,267 (GRCm39) |
missense |
probably benign |
0.02 |
R6618:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.10 |
R6941:Zfy2
|
UTSW |
Y |
2,121,491 (GRCm39) |
missense |
probably benign |
0.02 |
R7011:Zfy2
|
UTSW |
Y |
2,107,127 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7712:Zfy2
|
UTSW |
Y |
2,121,420 (GRCm39) |
missense |
probably benign |
0.05 |
R7759:Zfy2
|
UTSW |
Y |
2,117,083 (GRCm39) |
missense |
probably benign |
0.02 |
R7985:Zfy2
|
UTSW |
Y |
2,116,263 (GRCm39) |
missense |
probably benign |
0.00 |
R8051:Zfy2
|
UTSW |
Y |
2,117,380 (GRCm39) |
intron |
probably benign |
|
R8218:Zfy2
|
UTSW |
Y |
2,133,421 (GRCm39) |
missense |
unknown |
|
R8345:Zfy2
|
UTSW |
Y |
2,107,096 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8830:Zfy2
|
UTSW |
Y |
2,106,600 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9448:Zfy2
|
UTSW |
Y |
2,109,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R9537:Zfy2
|
UTSW |
Y |
2,108,596 (GRCm39) |
missense |
|
|
|