Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
G |
8: 87,266,653 (GRCm39) |
|
probably null |
Het |
Abcc9 |
T |
C |
6: 142,634,755 (GRCm39) |
T170A |
probably benign |
Het |
Agbl2 |
T |
C |
2: 90,636,245 (GRCm39) |
S594P |
possibly damaging |
Het |
Aoc1l3 |
A |
G |
6: 48,964,331 (GRCm39) |
Y113C |
probably damaging |
Het |
Atf7 |
C |
T |
15: 102,442,858 (GRCm39) |
S417N |
probably benign |
Het |
Cacng7 |
T |
C |
7: 3,387,450 (GRCm39) |
V111A |
probably benign |
Het |
Chrm4 |
A |
G |
2: 91,757,705 (GRCm39) |
T38A |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,470,906 (GRCm39) |
E1314G |
possibly damaging |
Het |
Dcx |
A |
G |
X: 142,706,105 (GRCm39) |
Y229H |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,231,639 (GRCm39) |
F1945Y |
possibly damaging |
Het |
Glul |
T |
C |
1: 153,783,038 (GRCm39) |
F204L |
possibly damaging |
Het |
Grm2 |
A |
G |
9: 106,524,822 (GRCm39) |
V631A |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 173,855,901 (GRCm39) |
Y43F |
possibly damaging |
Het |
Irs3 |
A |
G |
5: 137,642,118 (GRCm39) |
L440P |
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,383,070 (GRCm39) |
D1466G |
possibly damaging |
Het |
Jarid2 |
T |
C |
13: 45,049,942 (GRCm39) |
S257P |
probably damaging |
Het |
Knl1 |
C |
A |
2: 118,900,872 (GRCm39) |
L858M |
possibly damaging |
Het |
Krt24 |
T |
A |
11: 99,173,262 (GRCm39) |
T298S |
possibly damaging |
Het |
Lrriq1 |
C |
T |
10: 103,006,294 (GRCm39) |
R1277Q |
probably benign |
Het |
Mgp |
A |
C |
6: 136,849,683 (GRCm39) |
Y92D |
probably damaging |
Het |
Micu3 |
A |
G |
8: 40,835,208 (GRCm39) |
H521R |
probably benign |
Het |
Mier3 |
T |
A |
13: 111,843,182 (GRCm39) |
I178N |
probably damaging |
Het |
Moxd1 |
G |
T |
10: 24,177,429 (GRCm39) |
E582* |
probably null |
Het |
Mprip |
T |
A |
11: 59,656,229 (GRCm39) |
|
probably null |
Het |
Mybph |
A |
G |
1: 134,122,476 (GRCm39) |
I174V |
probably benign |
Het |
Mynn |
C |
T |
3: 30,661,959 (GRCm39) |
T347M |
probably damaging |
Het |
Nhsl1 |
A |
T |
10: 18,400,916 (GRCm39) |
Q714L |
probably damaging |
Het |
Nr1d2 |
A |
T |
14: 18,215,504 (GRCm38) |
|
probably null |
Het |
Or10g3 |
T |
C |
14: 52,610,397 (GRCm39) |
T38A |
probably damaging |
Het |
Or2a5 |
T |
C |
6: 42,873,784 (GRCm39) |
V133A |
probably benign |
Het |
Or52h9 |
C |
A |
7: 104,202,295 (GRCm39) |
H56Q |
probably benign |
Het |
Or5p61 |
T |
C |
7: 107,759,029 (GRCm39) |
E17G |
probably benign |
Het |
Pcdha4 |
T |
C |
18: 37,086,603 (GRCm39) |
V262A |
probably benign |
Het |
Pde4d |
T |
A |
13: 110,084,792 (GRCm39) |
M519K |
probably damaging |
Het |
Phactr2 |
C |
A |
10: 13,137,645 (GRCm39) |
E166* |
probably null |
Het |
Prdx4 |
C |
T |
X: 154,113,407 (GRCm39) |
R167Q |
probably damaging |
Het |
Prkdc |
C |
T |
16: 15,482,222 (GRCm39) |
L422F |
probably benign |
Het |
Prph |
T |
A |
15: 98,953,337 (GRCm39) |
F84I |
probably damaging |
Het |
Rnmt |
A |
G |
18: 68,447,079 (GRCm39) |
E321G |
probably benign |
Het |
Serpinb13 |
A |
T |
1: 106,910,568 (GRCm39) |
E64V |
probably null |
Het |
Slc12a4 |
A |
T |
8: 106,686,091 (GRCm39) |
S81T |
probably damaging |
Het |
Slc47a1 |
A |
G |
11: 61,258,506 (GRCm39) |
L179P |
possibly damaging |
Het |
Sp140l2 |
C |
G |
1: 85,235,106 (GRCm39) |
|
probably benign |
Het |
Spata31e5 |
A |
C |
1: 28,815,410 (GRCm39) |
V874G |
possibly damaging |
Het |
Sycp2l |
C |
A |
13: 41,302,274 (GRCm39) |
T456K |
probably benign |
Het |
Tenm2 |
A |
G |
11: 35,914,193 (GRCm39) |
L2447P |
probably damaging |
Het |
Tll1 |
A |
G |
8: 64,506,900 (GRCm39) |
C614R |
probably damaging |
Het |
Usp5 |
T |
C |
6: 124,792,560 (GRCm39) |
Y826C |
probably damaging |
Het |
Vmn2r71 |
A |
C |
7: 85,272,866 (GRCm39) |
D560A |
probably damaging |
Het |
Wdr91 |
A |
G |
6: 34,882,522 (GRCm39) |
L209P |
probably damaging |
Het |
Zfp511 |
T |
A |
7: 139,616,504 (GRCm39) |
D46E |
probably benign |
Het |
Zscan22 |
T |
C |
7: 12,641,217 (GRCm39) |
I328T |
probably benign |
Het |
|
Other mutations in Zfp81 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
feuer
|
UTSW |
17 |
33,553,307 (GRCm39) |
nonsense |
probably null |
|
R0143:Zfp81
|
UTSW |
17 |
33,554,095 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0220:Zfp81
|
UTSW |
17 |
33,555,698 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0520:Zfp81
|
UTSW |
17 |
33,553,351 (GRCm39) |
missense |
probably damaging |
0.97 |
R0611:Zfp81
|
UTSW |
17 |
33,553,593 (GRCm39) |
missense |
probably benign |
0.02 |
R1171:Zfp81
|
UTSW |
17 |
33,554,254 (GRCm39) |
missense |
probably benign |
|
R1613:Zfp81
|
UTSW |
17 |
33,553,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R1779:Zfp81
|
UTSW |
17 |
33,554,080 (GRCm39) |
missense |
probably benign |
0.06 |
R1970:Zfp81
|
UTSW |
17 |
33,554,475 (GRCm39) |
missense |
probably benign |
|
R2063:Zfp81
|
UTSW |
17 |
33,554,278 (GRCm39) |
missense |
probably benign |
0.03 |
R2314:Zfp81
|
UTSW |
17 |
33,553,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R2898:Zfp81
|
UTSW |
17 |
33,553,274 (GRCm39) |
nonsense |
probably null |
|
R4207:Zfp81
|
UTSW |
17 |
33,553,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R4497:Zfp81
|
UTSW |
17 |
33,553,677 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4498:Zfp81
|
UTSW |
17 |
33,553,677 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5756:Zfp81
|
UTSW |
17 |
33,553,307 (GRCm39) |
nonsense |
probably null |
|
R5964:Zfp81
|
UTSW |
17 |
33,555,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R6671:Zfp81
|
UTSW |
17 |
33,554,413 (GRCm39) |
missense |
probably benign |
0.17 |
R7728:Zfp81
|
UTSW |
17 |
33,555,791 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9047:Zfp81
|
UTSW |
17 |
33,553,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Zfp81
|
UTSW |
17 |
33,553,774 (GRCm39) |
missense |
probably benign |
0.15 |
R9800:Zfp81
|
UTSW |
17 |
33,554,411 (GRCm39) |
nonsense |
probably null |
|
Z1176:Zfp81
|
UTSW |
17 |
33,553,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
|