Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210010C04Rik |
T |
G |
6: 41,031,688 (GRCm38) |
T231P |
possibly damaging |
Het |
Adgrg6 |
T |
C |
10: 14,467,334 (GRCm38) |
T290A |
probably benign |
Het |
Aff4 |
C |
T |
11: 53,400,267 (GRCm38) |
Q685* |
probably null |
Het |
Ankmy1 |
A |
G |
1: 92,896,094 (GRCm38) |
M150T |
probably damaging |
Het |
Armc1 |
T |
C |
3: 19,149,567 (GRCm38) |
Y65C |
probably damaging |
Het |
Armc8 |
A |
G |
9: 99,527,099 (GRCm38) |
V222A |
probably benign |
Het |
Bcar1 |
A |
T |
8: 111,715,738 (GRCm38) |
Y228* |
probably null |
Het |
Cct2 |
T |
C |
10: 117,060,824 (GRCm38) |
D158G |
possibly damaging |
Het |
Cul1 |
T |
A |
6: 47,515,063 (GRCm38) |
C426S |
possibly damaging |
Het |
Deup1 |
G |
T |
9: 15,592,375 (GRCm38) |
L297M |
possibly damaging |
Het |
Dpp10 |
A |
G |
1: 123,854,229 (GRCm38) |
S74P |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,507,079 (GRCm38) |
Y98H |
possibly damaging |
Het |
Epn3 |
T |
G |
11: 94,492,936 (GRCm38) |
D296A |
probably damaging |
Het |
Eri2 |
A |
C |
7: 119,772,597 (GRCm38) |
I252S |
probably benign |
Het |
Gm14025 |
T |
A |
2: 129,038,171 (GRCm38) |
I612F |
|
Het |
Gp9 |
C |
T |
6: 87,779,012 (GRCm38) |
T3I |
probably benign |
Het |
H2-Q5 |
T |
A |
17: 35,394,456 (GRCm38) |
V55E |
|
Het |
Kif3c |
G |
T |
12: 3,366,089 (GRCm38) |
V37L |
probably benign |
Het |
Lct |
A |
T |
1: 128,303,840 (GRCm38) |
N757K |
probably damaging |
Het |
Lhx8 |
A |
C |
3: 154,324,658 (GRCm38) |
N112K |
probably damaging |
Het |
Loxl3 |
T |
A |
6: 83,048,891 (GRCm38) |
S373R |
possibly damaging |
Het |
Mettl4 |
G |
A |
17: 94,733,649 (GRCm38) |
T359I |
probably damaging |
Het |
Mpp7 |
A |
G |
18: 7,444,096 (GRCm38) |
S109P |
probably damaging |
Het |
Nckap5 |
A |
G |
1: 126,026,295 (GRCm38) |
V840A |
probably benign |
Het |
Ncoa4 |
T |
A |
14: 32,176,936 (GRCm38) |
L571Q |
probably damaging |
Het |
Olfr453 |
T |
C |
6: 42,744,346 (GRCm38) |
F103S |
probably damaging |
Het |
Olfr46 |
A |
T |
7: 140,610,295 (GRCm38) |
Y35F |
possibly damaging |
Het |
Phgdh |
G |
A |
3: 98,321,245 (GRCm38) |
T204I |
probably damaging |
Het |
Pla2g4d |
C |
T |
2: 120,277,499 (GRCm38) |
V310M |
probably null |
Het |
Psmd12 |
C |
T |
11: 107,497,624 (GRCm38) |
P421L |
probably damaging |
Het |
Ptch1 |
A |
G |
13: 63,541,168 (GRCm38) |
Y432H |
probably damaging |
Het |
Rapgef1 |
G |
A |
2: 29,710,231 (GRCm38) |
G655S |
probably damaging |
Het |
Rilpl2 |
C |
A |
5: 124,478,034 (GRCm38) |
A18S |
probably damaging |
Het |
Srsf7 |
T |
C |
17: 80,205,386 (GRCm38) |
R88G |
probably benign |
Het |
St6galnac1 |
T |
C |
11: 116,769,233 (GRCm38) |
K85E |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,795,767 (GRCm38) |
S49R |
probably damaging |
Het |
Wdr48 |
A |
G |
9: 119,905,494 (GRCm38) |
T160A |
probably damaging |
Het |
|
Other mutations in Zfp704 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Zfp704
|
APN |
3 |
9,565,239 (GRCm38) |
missense |
possibly damaging |
0.61 |
IGL03288:Zfp704
|
APN |
3 |
9,439,891 (GRCm38) |
splice site |
probably benign |
|
R0265:Zfp704
|
UTSW |
3 |
9,565,157 (GRCm38) |
missense |
probably damaging |
1.00 |
R0524:Zfp704
|
UTSW |
3 |
9,609,364 (GRCm38) |
missense |
unknown |
|
R1466:Zfp704
|
UTSW |
3 |
9,447,348 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1466:Zfp704
|
UTSW |
3 |
9,447,348 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1647:Zfp704
|
UTSW |
3 |
9,471,039 (GRCm38) |
missense |
probably damaging |
1.00 |
R1648:Zfp704
|
UTSW |
3 |
9,471,039 (GRCm38) |
missense |
probably damaging |
1.00 |
R1865:Zfp704
|
UTSW |
3 |
9,474,491 (GRCm38) |
splice site |
probably benign |
|
R1912:Zfp704
|
UTSW |
3 |
9,609,358 (GRCm38) |
missense |
unknown |
|
R2109:Zfp704
|
UTSW |
3 |
9,474,525 (GRCm38) |
missense |
probably damaging |
1.00 |
R2566:Zfp704
|
UTSW |
3 |
9,609,493 (GRCm38) |
missense |
unknown |
|
R3551:Zfp704
|
UTSW |
3 |
9,474,525 (GRCm38) |
missense |
probably damaging |
1.00 |
R4495:Zfp704
|
UTSW |
3 |
9,471,077 (GRCm38) |
missense |
probably benign |
0.01 |
R6165:Zfp704
|
UTSW |
3 |
9,443,886 (GRCm38) |
missense |
probably benign |
0.00 |
R6682:Zfp704
|
UTSW |
3 |
9,565,193 (GRCm38) |
missense |
probably benign |
0.11 |
R7057:Zfp704
|
UTSW |
3 |
9,470,917 (GRCm38) |
missense |
probably damaging |
1.00 |
R7348:Zfp704
|
UTSW |
3 |
9,474,598 (GRCm38) |
missense |
probably damaging |
1.00 |
R7758:Zfp704
|
UTSW |
3 |
9,444,222 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7858:Zfp704
|
UTSW |
3 |
9,444,157 (GRCm38) |
critical splice donor site |
probably null |
|
R8104:Zfp704
|
UTSW |
3 |
9,565,241 (GRCm38) |
missense |
probably benign |
0.03 |
R8877:Zfp704
|
UTSW |
3 |
9,609,356 (GRCm38) |
missense |
unknown |
|
R9136:Zfp704
|
UTSW |
3 |
9,444,264 (GRCm38) |
missense |
probably benign |
0.03 |
Z1176:Zfp704
|
UTSW |
3 |
9,471,044 (GRCm38) |
missense |
probably damaging |
1.00 |
|