Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
G |
A |
5: 109,885,570 (GRCm39) |
T96I |
probably benign |
Het |
Add2 |
G |
T |
6: 86,084,457 (GRCm39) |
|
probably null |
Het |
Agbl1 |
C |
T |
7: 75,984,985 (GRCm39) |
T134M |
probably benign |
Het |
Agfg1 |
T |
A |
1: 82,848,445 (GRCm39) |
S32T |
probably benign |
Het |
Ankrd17 |
A |
C |
5: 90,391,083 (GRCm39) |
S2087A |
probably benign |
Het |
Apob |
A |
T |
12: 8,048,662 (GRCm39) |
E1012V |
probably damaging |
Het |
Baiap2 |
T |
A |
11: 119,887,737 (GRCm39) |
V297E |
probably benign |
Het |
BC034090 |
T |
G |
1: 155,117,214 (GRCm39) |
K301N |
probably benign |
Het |
Bhlha9 |
T |
C |
11: 76,563,595 (GRCm39) |
I74T |
probably damaging |
Het |
Btnl9 |
T |
C |
11: 49,069,712 (GRCm39) |
H189R |
probably benign |
Het |
Ccdc122 |
G |
A |
14: 77,329,317 (GRCm39) |
M123I |
probably benign |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,724,922 (GRCm39) |
|
probably null |
Het |
Dnaja2 |
A |
T |
8: 86,266,033 (GRCm39) |
L351I |
possibly damaging |
Het |
Efcab6 |
C |
A |
15: 83,834,201 (GRCm39) |
S469I |
probably benign |
Het |
Esp15 |
C |
A |
17: 39,953,564 (GRCm39) |
T17K |
probably damaging |
Het |
Fads1 |
A |
G |
19: 10,163,238 (GRCm39) |
T172A |
probably benign |
Het |
Fbp2 |
A |
T |
13: 62,985,005 (GRCm39) |
D305E |
probably benign |
Het |
Golga4 |
A |
G |
9: 118,382,602 (GRCm39) |
T541A |
probably benign |
Het |
Herc3 |
T |
C |
6: 58,865,710 (GRCm39) |
Y768H |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,753,931 (GRCm39) |
V514A |
possibly damaging |
Het |
Melk |
A |
G |
4: 44,312,255 (GRCm39) |
E141G |
probably null |
Het |
Nln |
A |
G |
13: 104,195,338 (GRCm39) |
Y245H |
probably damaging |
Het |
Nrap |
C |
T |
19: 56,310,414 (GRCm39) |
R1563H |
probably damaging |
Het |
Or7g34 |
T |
A |
9: 19,478,369 (GRCm39) |
M101L |
probably benign |
Het |
Or8b44 |
A |
C |
9: 38,410,204 (GRCm39) |
K80Q |
probably damaging |
Het |
Pde4b |
T |
A |
4: 102,287,359 (GRCm39) |
I34N |
probably damaging |
Het |
Pex11g |
A |
G |
8: 3,515,875 (GRCm39) |
S53P |
probably damaging |
Het |
Pole |
A |
T |
5: 110,459,931 (GRCm39) |
K1112* |
probably null |
Het |
Ppfia4 |
T |
G |
1: 134,250,788 (GRCm39) |
D184A |
possibly damaging |
Het |
Rpp30 |
T |
A |
19: 36,079,251 (GRCm39) |
D216E |
probably benign |
Het |
Sbno2 |
C |
T |
10: 79,903,171 (GRCm39) |
A398T |
probably damaging |
Het |
Sbp |
T |
A |
17: 24,164,552 (GRCm39) |
S94T |
probably benign |
Het |
Skp1 |
T |
G |
11: 52,133,415 (GRCm39) |
D33E |
possibly damaging |
Het |
Slc17a8 |
A |
G |
10: 89,433,364 (GRCm39) |
W220R |
probably damaging |
Het |
Slfn9 |
A |
T |
11: 82,872,258 (GRCm39) |
M826K |
probably benign |
Het |
Snx2 |
A |
G |
18: 53,343,822 (GRCm39) |
K322E |
probably benign |
Het |
Spata32 |
T |
A |
11: 103,100,653 (GRCm39) |
N38I |
possibly damaging |
Het |
Sycp1 |
T |
C |
3: 102,726,218 (GRCm39) |
R969G |
probably damaging |
Het |
Trgc2 |
T |
C |
13: 19,489,301 (GRCm39) |
I144V |
probably benign |
Het |
Trpc1 |
A |
G |
9: 95,603,377 (GRCm39) |
L385S |
probably damaging |
Het |
Vmn2r105 |
C |
T |
17: 20,444,836 (GRCm39) |
|
probably null |
Het |
Xrcc6 |
T |
A |
15: 81,906,693 (GRCm39) |
D79E |
probably damaging |
Het |
Zan |
A |
T |
5: 137,426,744 (GRCm39) |
C2467* |
probably null |
Het |
Zfp26 |
A |
G |
9: 20,348,803 (GRCm39) |
V587A |
possibly damaging |
Het |
|
Other mutations in Zfp553 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01501:Zfp553
|
APN |
7 |
126,835,387 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01528:Zfp553
|
APN |
7 |
126,835,387 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03228:Zfp553
|
APN |
7 |
126,835,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Zfp553
|
UTSW |
7 |
126,835,977 (GRCm39) |
nonsense |
probably null |
|
R1859:Zfp553
|
UTSW |
7 |
126,834,517 (GRCm39) |
missense |
probably benign |
0.04 |
R1899:Zfp553
|
UTSW |
7 |
126,834,826 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4997:Zfp553
|
UTSW |
7 |
126,834,683 (GRCm39) |
missense |
probably benign |
0.15 |
R5090:Zfp553
|
UTSW |
7 |
126,834,659 (GRCm39) |
missense |
probably damaging |
0.98 |
R5282:Zfp553
|
UTSW |
7 |
126,836,013 (GRCm39) |
missense |
probably benign |
0.12 |
R5468:Zfp553
|
UTSW |
7 |
126,836,202 (GRCm39) |
missense |
probably benign |
|
R6334:Zfp553
|
UTSW |
7 |
126,836,064 (GRCm39) |
splice site |
probably null |
|
R6828:Zfp553
|
UTSW |
7 |
126,835,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6974:Zfp553
|
UTSW |
7 |
126,835,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Zfp553
|
UTSW |
7 |
126,835,605 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7615:Zfp553
|
UTSW |
7 |
126,835,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Zfp553
|
UTSW |
7 |
126,835,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R8103:Zfp553
|
UTSW |
7 |
126,835,936 (GRCm39) |
missense |
probably benign |
|
R8111:Zfp553
|
UTSW |
7 |
126,836,093 (GRCm39) |
nonsense |
probably null |
|
R8199:Zfp553
|
UTSW |
7 |
126,835,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R8390:Zfp553
|
UTSW |
7 |
126,835,476 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Zfp553
|
UTSW |
7 |
126,834,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|