Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810408A11Rik |
G |
T |
11: 69,791,198 (GRCm39) |
T127K |
possibly damaging |
Het |
A2m |
T |
G |
6: 121,653,918 (GRCm39) |
I1417S |
probably damaging |
Het |
Acad10 |
A |
G |
5: 121,787,523 (GRCm39) |
I142T |
possibly damaging |
Het |
Adprm |
T |
A |
11: 66,932,678 (GRCm39) |
D77V |
probably damaging |
Het |
Apob |
C |
T |
12: 8,062,240 (GRCm39) |
T3574I |
probably damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,908 (GRCm39) |
K2489R |
probably damaging |
Het |
Bub1b |
A |
G |
2: 118,452,676 (GRCm39) |
E443G |
possibly damaging |
Het |
Cd9 |
A |
T |
6: 125,440,734 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
G |
A |
9: 71,538,160 (GRCm39) |
T1194M |
probably damaging |
Het |
Clec9a |
T |
C |
6: 129,387,274 (GRCm39) |
V43A |
probably benign |
Het |
Col11a1 |
C |
T |
3: 113,951,791 (GRCm39) |
R1074C |
probably damaging |
Het |
Dpep3 |
A |
G |
8: 106,701,346 (GRCm39) |
V401A |
probably damaging |
Het |
Duox2 |
G |
T |
2: 122,111,448 (GRCm39) |
H1417N |
probably damaging |
Het |
Efhb |
C |
T |
17: 53,733,937 (GRCm39) |
|
probably null |
Het |
F2r |
T |
C |
13: 95,741,418 (GRCm39) |
N39S |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,739,335 (GRCm39) |
F212L |
probably damaging |
Het |
Galt |
G |
A |
4: 41,758,162 (GRCm39) |
R309Q |
probably damaging |
Het |
Gas2l2 |
C |
A |
11: 83,318,209 (GRCm39) |
A167S |
probably benign |
Het |
Hecw1 |
A |
T |
13: 14,438,672 (GRCm39) |
F904I |
possibly damaging |
Het |
Herc2 |
C |
A |
7: 55,862,713 (GRCm39) |
H4127Q |
possibly damaging |
Het |
Hipk1 |
T |
C |
3: 103,657,670 (GRCm39) |
T805A |
probably benign |
Het |
Hivep1 |
A |
G |
13: 42,337,226 (GRCm39) |
E2435G |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,015,273 (GRCm39) |
C1813* |
probably null |
Het |
Hyal4 |
C |
T |
6: 24,755,749 (GRCm39) |
|
probably benign |
Het |
Inpp4b |
A |
G |
8: 82,678,903 (GRCm39) |
Y311C |
probably damaging |
Het |
Itih4 |
A |
G |
14: 30,614,280 (GRCm39) |
Y410C |
possibly damaging |
Het |
Lama2 |
A |
T |
10: 27,080,837 (GRCm39) |
C995* |
probably null |
Het |
Lingo4 |
C |
A |
3: 94,309,552 (GRCm39) |
D163E |
probably damaging |
Het |
Malt1 |
A |
G |
18: 65,606,218 (GRCm39) |
D642G |
probably damaging |
Het |
Mbd4 |
T |
A |
6: 115,825,918 (GRCm39) |
M358L |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,169,323 (GRCm39) |
F1498Y |
possibly damaging |
Het |
Me1 |
T |
C |
9: 86,495,607 (GRCm39) |
Q280R |
probably damaging |
Het |
Megf9 |
T |
C |
4: 70,367,004 (GRCm39) |
H326R |
probably damaging |
Het |
Nid2 |
G |
A |
14: 19,828,111 (GRCm39) |
G516S |
probably benign |
Het |
Or13p10 |
T |
C |
4: 118,523,301 (GRCm39) |
S196P |
probably damaging |
Het |
Or1e1 |
T |
C |
11: 73,245,247 (GRCm39) |
S223P |
possibly damaging |
Het |
Or4k1 |
T |
A |
14: 50,377,580 (GRCm39) |
N172I |
probably damaging |
Het |
Or5h18 |
C |
T |
16: 58,848,232 (GRCm39) |
V13I |
probably benign |
Het |
Or8b1c |
A |
G |
9: 38,384,223 (GRCm39) |
Y60C |
probably damaging |
Het |
Polr2j |
T |
C |
5: 136,145,625 (GRCm39) |
F7L |
probably damaging |
Het |
Ppp1r16a |
T |
A |
15: 76,577,796 (GRCm39) |
D303E |
probably damaging |
Het |
Prickle2 |
T |
C |
6: 92,353,345 (GRCm39) |
E763G |
probably damaging |
Het |
Rdh11 |
T |
C |
12: 79,229,556 (GRCm39) |
Y239C |
possibly damaging |
Het |
Sdhaf3 |
A |
G |
6: 6,956,048 (GRCm39) |
R8G |
probably benign |
Het |
Sgk2 |
T |
C |
2: 162,854,890 (GRCm39) |
S305P |
probably damaging |
Het |
Sptbn2 |
A |
G |
19: 4,788,587 (GRCm39) |
S1189G |
probably benign |
Het |
Stab2 |
A |
G |
10: 86,790,023 (GRCm39) |
L581P |
probably damaging |
Het |
Tifab |
T |
C |
13: 56,324,110 (GRCm39) |
Q111R |
probably damaging |
Het |
Ubr3 |
C |
T |
2: 69,784,108 (GRCm39) |
R775C |
probably damaging |
Het |
Usp17lb |
T |
A |
7: 104,489,622 (GRCm39) |
Q434L |
possibly damaging |
Het |
Wdr46 |
G |
T |
17: 34,160,425 (GRCm39) |
E135* |
probably null |
Het |
Zfp318 |
T |
A |
17: 46,720,590 (GRCm39) |
|
probably null |
Het |
Zscan29 |
A |
T |
2: 121,000,427 (GRCm39) |
L60* |
probably null |
Het |
|
Other mutations in Zfp874a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02490:Zfp874a
|
APN |
13 |
67,590,819 (GRCm39) |
nonsense |
probably null |
|
R1052:Zfp874a
|
UTSW |
13 |
67,590,539 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1991:Zfp874a
|
UTSW |
13 |
67,590,623 (GRCm39) |
missense |
probably benign |
0.03 |
R2103:Zfp874a
|
UTSW |
13 |
67,590,623 (GRCm39) |
missense |
probably benign |
0.03 |
R5129:Zfp874a
|
UTSW |
13 |
67,591,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Zfp874a
|
UTSW |
13 |
67,590,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Zfp874a
|
UTSW |
13 |
67,590,473 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5713:Zfp874a
|
UTSW |
13 |
67,597,476 (GRCm39) |
missense |
probably benign |
0.16 |
R5855:Zfp874a
|
UTSW |
13 |
67,590,812 (GRCm39) |
missense |
probably benign |
0.03 |
R6496:Zfp874a
|
UTSW |
13 |
67,590,694 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7046:Zfp874a
|
UTSW |
13 |
67,590,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Zfp874a
|
UTSW |
13 |
67,590,401 (GRCm39) |
missense |
probably damaging |
0.97 |
R7233:Zfp874a
|
UTSW |
13 |
67,590,776 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7271:Zfp874a
|
UTSW |
13 |
67,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R7465:Zfp874a
|
UTSW |
13 |
67,590,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R7468:Zfp874a
|
UTSW |
13 |
67,573,723 (GRCm39) |
splice site |
probably null |
|
R8108:Zfp874a
|
UTSW |
13 |
67,591,353 (GRCm39) |
nonsense |
probably null |
|
R8109:Zfp874a
|
UTSW |
13 |
67,597,563 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8843:Zfp874a
|
UTSW |
13 |
67,590,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R8859:Zfp874a
|
UTSW |
13 |
67,590,647 (GRCm39) |
missense |
probably benign |
0.17 |
R9137:Zfp874a
|
UTSW |
13 |
67,590,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R9673:Zfp874a
|
UTSW |
13 |
67,591,156 (GRCm39) |
missense |
probably benign |
0.03 |
X0063:Zfp874a
|
UTSW |
13 |
67,591,106 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zfp874a
|
UTSW |
13 |
67,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|