Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank3 |
T |
C |
10: 69,837,848 (GRCm39) |
S1601P |
probably damaging |
Het |
Arnt |
A |
G |
3: 95,359,924 (GRCm39) |
N56D |
probably damaging |
Het |
Atad5 |
A |
G |
11: 79,986,715 (GRCm39) |
T601A |
probably benign |
Het |
Calr4 |
A |
G |
4: 109,103,379 (GRCm39) |
N163S |
probably damaging |
Het |
Cenpc1 |
C |
A |
5: 86,195,491 (GRCm39) |
A93S |
probably damaging |
Het |
Cep135 |
C |
T |
5: 76,786,040 (GRCm39) |
H1048Y |
possibly damaging |
Het |
Ctnna2 |
A |
G |
6: 77,613,696 (GRCm39) |
|
probably null |
Het |
Ddx60 |
T |
C |
8: 62,395,495 (GRCm39) |
L144P |
probably damaging |
Het |
Dera |
A |
T |
6: 137,757,736 (GRCm39) |
T96S |
possibly damaging |
Het |
Dock9 |
T |
A |
14: 121,796,419 (GRCm39) |
M1853L |
probably benign |
Het |
Erbb4 |
G |
A |
1: 68,383,080 (GRCm39) |
R306* |
probably null |
Het |
Glyat |
G |
T |
19: 12,628,644 (GRCm39) |
L146F |
possibly damaging |
Het |
Grk4 |
C |
A |
5: 34,852,157 (GRCm39) |
Q134K |
probably benign |
Het |
Hkdc1 |
T |
C |
10: 62,245,618 (GRCm39) |
Q181R |
probably benign |
Het |
Huwe1 |
A |
T |
X: 150,646,955 (GRCm39) |
I682F |
probably damaging |
Het |
Ipo4 |
C |
T |
14: 55,867,546 (GRCm39) |
|
probably benign |
Het |
Ivl |
CCTGCTGCTGCT |
CCTGCTGCTGCTGCT |
3: 92,479,262 (GRCm39) |
|
probably benign |
Het |
Kcnd2 |
A |
G |
6: 21,216,395 (GRCm39) |
Q33R |
probably benign |
Het |
Kdm7a |
C |
T |
6: 39,129,757 (GRCm39) |
R473Q |
probably damaging |
Het |
Klhl30 |
A |
T |
1: 91,288,753 (GRCm39) |
H504L |
probably damaging |
Het |
Map4 |
A |
G |
9: 109,881,439 (GRCm39) |
Y101C |
possibly damaging |
Het |
Mfn2 |
C |
A |
4: 147,961,492 (GRCm39) |
R707L |
probably damaging |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Myof |
T |
C |
19: 37,911,438 (GRCm39) |
N1511D |
probably benign |
Het |
Neb |
A |
T |
2: 52,176,167 (GRCm39) |
Y1431N |
probably damaging |
Het |
Nlrc5 |
A |
G |
8: 95,203,774 (GRCm39) |
T625A |
probably damaging |
Het |
Or5g27 |
G |
T |
2: 85,409,964 (GRCm39) |
C127F |
probably damaging |
Het |
Pax2 |
A |
G |
19: 44,824,402 (GRCm39) |
Y374C |
unknown |
Het |
Pde8a |
T |
A |
7: 80,958,568 (GRCm39) |
Y315* |
probably null |
Het |
Pkhd1 |
A |
T |
1: 20,604,943 (GRCm39) |
L1124Q |
possibly damaging |
Het |
Ppp1r3a |
A |
G |
6: 14,754,681 (GRCm39) |
F189L |
probably damaging |
Het |
Prex2 |
G |
A |
1: 11,254,769 (GRCm39) |
|
probably null |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Slc22a22 |
T |
A |
15: 57,126,781 (GRCm39) |
Q77L |
probably damaging |
Het |
Slc24a2 |
A |
T |
4: 87,145,634 (GRCm39) |
V140D |
probably damaging |
Het |
Slc35g2 |
C |
A |
9: 100,435,287 (GRCm39) |
R128L |
probably damaging |
Het |
Slco1b2 |
A |
G |
6: 141,616,893 (GRCm39) |
T409A |
probably benign |
Het |
Spag7 |
T |
C |
11: 70,555,816 (GRCm39) |
I80M |
probably damaging |
Het |
Srgap3 |
A |
G |
6: 112,758,015 (GRCm39) |
M164T |
probably damaging |
Het |
Sspo |
A |
T |
6: 48,452,468 (GRCm39) |
|
probably null |
Het |
Tcte2 |
T |
C |
17: 13,942,864 (GRCm39) |
|
probably benign |
Het |
Tmem117 |
A |
T |
15: 94,992,677 (GRCm39) |
M446L |
probably benign |
Het |
Tmtc4 |
T |
C |
14: 123,200,710 (GRCm39) |
T194A |
probably benign |
Het |
Ttc21b |
T |
C |
2: 66,016,562 (GRCm39) |
Y1269C |
probably damaging |
Het |
Zfp236 |
A |
T |
18: 82,638,531 (GRCm39) |
I1363N |
probably damaging |
Het |
Zfp760 |
T |
A |
17: 21,942,648 (GRCm39) |
S608T |
probably benign |
Het |
|
Other mutations in Zfp947 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02092:Zfp947
|
APN |
17 |
22,366,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02592:Zfp947
|
APN |
17 |
22,365,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
deformity
|
UTSW |
17 |
22,364,594 (GRCm39) |
missense |
probably damaging |
1.00 |
Gnarled
|
UTSW |
17 |
22,365,165 (GRCm39) |
missense |
probably benign |
0.00 |
R0070:Zfp947
|
UTSW |
17 |
22,365,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1519:Zfp947
|
UTSW |
17 |
22,365,273 (GRCm39) |
missense |
probably benign |
0.02 |
R1521:Zfp947
|
UTSW |
17 |
22,364,813 (GRCm39) |
missense |
probably benign |
0.00 |
R1639:Zfp947
|
UTSW |
17 |
22,365,074 (GRCm39) |
missense |
probably benign |
|
R1721:Zfp947
|
UTSW |
17 |
22,365,184 (GRCm39) |
missense |
probably benign |
|
R1801:Zfp947
|
UTSW |
17 |
22,365,443 (GRCm39) |
missense |
probably benign |
|
R2264:Zfp947
|
UTSW |
17 |
22,364,919 (GRCm39) |
missense |
probably benign |
|
R3943:Zfp947
|
UTSW |
17 |
22,364,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Zfp947
|
UTSW |
17 |
22,365,124 (GRCm39) |
nonsense |
probably null |
|
R4943:Zfp947
|
UTSW |
17 |
22,364,813 (GRCm39) |
missense |
probably benign |
|
R5688:Zfp947
|
UTSW |
17 |
22,365,066 (GRCm39) |
missense |
probably benign |
0.00 |
R6037:Zfp947
|
UTSW |
17 |
22,366,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R6037:Zfp947
|
UTSW |
17 |
22,366,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R6414:Zfp947
|
UTSW |
17 |
22,365,395 (GRCm39) |
missense |
probably damaging |
0.98 |
R6786:Zfp947
|
UTSW |
17 |
22,364,750 (GRCm39) |
missense |
probably benign |
0.01 |
R6993:Zfp947
|
UTSW |
17 |
22,364,961 (GRCm39) |
missense |
probably benign |
0.11 |
R7556:Zfp947
|
UTSW |
17 |
22,364,597 (GRCm39) |
missense |
probably benign |
|
R8224:Zfp947
|
UTSW |
17 |
22,364,363 (GRCm39) |
missense |
probably benign |
|
R8398:Zfp947
|
UTSW |
17 |
22,365,102 (GRCm39) |
missense |
probably benign |
0.03 |
R8670:Zfp947
|
UTSW |
17 |
22,364,687 (GRCm39) |
missense |
probably benign |
0.09 |
R8871:Zfp947
|
UTSW |
17 |
22,364,695 (GRCm39) |
missense |
probably benign |
0.13 |
R9000:Zfp947
|
UTSW |
17 |
22,365,161 (GRCm39) |
missense |
probably benign |
0.12 |
R9099:Zfp947
|
UTSW |
17 |
22,364,855 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Zfp947
|
UTSW |
17 |
22,364,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Zfp947
|
UTSW |
17 |
22,364,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Zfp947
|
UTSW |
17 |
22,364,384 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9507:Zfp947
|
UTSW |
17 |
22,364,582 (GRCm39) |
missense |
probably benign |
0.00 |
R9738:Zfp947
|
UTSW |
17 |
22,365,341 (GRCm39) |
missense |
probably benign |
0.01 |
|