Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,055,976 (GRCm39) |
H316L |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,509,090 (GRCm38) |
|
probably benign |
Het |
Cluh |
A |
G |
11: 74,547,279 (GRCm39) |
D44G |
probably benign |
Het |
Copb1 |
A |
G |
7: 113,822,551 (GRCm39) |
V726A |
probably damaging |
Het |
Dsg4 |
T |
C |
18: 20,582,291 (GRCm39) |
V79A |
probably benign |
Het |
Exo1 |
A |
T |
1: 175,720,554 (GRCm39) |
I291F |
probably benign |
Het |
Eya4 |
C |
T |
10: 22,992,574 (GRCm39) |
A460T |
probably damaging |
Het |
Gjd3 |
G |
T |
11: 102,690,952 (GRCm39) |
D350E |
probably benign |
Het |
Hcar2 |
T |
C |
5: 124,002,475 (GRCm39) |
M343V |
probably benign |
Het |
Ifna15 |
T |
C |
4: 88,476,046 (GRCm39) |
Y146C |
probably damaging |
Het |
Lce3e |
C |
T |
3: 92,875,139 (GRCm39) |
Q32* |
probably null |
Het |
Llgl1 |
T |
C |
11: 60,598,075 (GRCm39) |
L373P |
probably damaging |
Het |
Mark2 |
A |
G |
19: 7,254,655 (GRCm39) |
C642R |
probably damaging |
Het |
Mbd3l2 |
A |
G |
9: 18,356,092 (GRCm39) |
Q139R |
probably benign |
Het |
Mki67 |
A |
C |
7: 135,297,859 (GRCm39) |
S2392A |
probably benign |
Het |
Nynrin |
T |
A |
14: 56,101,562 (GRCm39) |
N410K |
probably benign |
Het |
Or10g7 |
A |
T |
9: 39,905,450 (GRCm39) |
T115S |
probably damaging |
Het |
Or4a71 |
A |
T |
2: 89,357,917 (GRCm39) |
M279K |
possibly damaging |
Het |
Or5b112 |
A |
G |
19: 13,319,862 (GRCm39) |
T247A |
possibly damaging |
Het |
Or7a38 |
T |
A |
10: 78,752,781 (GRCm39) |
Y36N |
probably damaging |
Het |
Or8b1 |
G |
T |
9: 38,400,247 (GRCm39) |
R307S |
probably benign |
Het |
Padi3 |
T |
C |
4: 140,518,580 (GRCm39) |
|
probably benign |
Het |
Prkce |
A |
G |
17: 86,476,277 (GRCm39) |
D86G |
probably damaging |
Het |
Pwwp3b |
C |
T |
X: 138,137,403 (GRCm39) |
|
probably null |
Het |
Rad21 |
T |
G |
15: 51,835,712 (GRCm39) |
I234L |
probably benign |
Het |
Scn4a |
A |
T |
11: 106,210,932 (GRCm39) |
M1695K |
possibly damaging |
Het |
Sdccag8 |
T |
C |
1: 176,681,361 (GRCm39) |
S325P |
probably damaging |
Het |
Sebox |
G |
A |
11: 78,394,975 (GRCm39) |
G106R |
probably benign |
Het |
Serpinb9 |
A |
G |
13: 33,199,503 (GRCm39) |
E266G |
possibly damaging |
Het |
Shoc1 |
T |
C |
4: 59,047,390 (GRCm39) |
N1410D |
possibly damaging |
Het |
Snx14 |
T |
C |
9: 88,289,372 (GRCm39) |
|
probably benign |
Het |
Tmc6 |
A |
T |
11: 117,663,884 (GRCm39) |
L474* |
probably null |
Het |
Tmem132c |
T |
C |
5: 127,436,933 (GRCm39) |
Y141H |
probably benign |
Het |
Trap1 |
G |
A |
16: 3,872,686 (GRCm39) |
R328C |
possibly damaging |
Het |
Trim36 |
C |
A |
18: 46,305,439 (GRCm39) |
|
probably benign |
Het |
Trmt2a |
A |
T |
16: 18,069,055 (GRCm39) |
Y299F |
possibly damaging |
Het |
Trrap |
A |
G |
5: 144,728,975 (GRCm39) |
K630E |
probably damaging |
Het |
Tsnaxip1 |
A |
T |
8: 106,567,333 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
G |
T |
12: 57,775,335 (GRCm39) |
C1677F |
possibly damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,485,018 (GRCm39) |
V2D |
|
Het |
Usp9x |
A |
G |
X: 12,964,822 (GRCm39) |
D77G |
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,125,968 (GRCm39) |
V308L |
probably benign |
Het |
Zan |
A |
C |
5: 137,472,326 (GRCm39) |
L140R |
probably damaging |
Het |
Zswim3 |
A |
G |
2: 164,662,777 (GRCm39) |
Y419C |
possibly damaging |
Het |
|
Other mutations in Zc3h3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Zc3h3
|
APN |
15 |
75,651,162 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Zc3h3
|
UTSW |
15 |
75,712,414 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0477:Zc3h3
|
UTSW |
15 |
75,648,932 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0843:Zc3h3
|
UTSW |
15 |
75,709,328 (GRCm39) |
missense |
probably benign |
0.00 |
R1891:Zc3h3
|
UTSW |
15 |
75,628,780 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1918:Zc3h3
|
UTSW |
15 |
75,648,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Zc3h3
|
UTSW |
15 |
75,651,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Zc3h3
|
UTSW |
15 |
75,711,415 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5130:Zc3h3
|
UTSW |
15 |
75,651,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Zc3h3
|
UTSW |
15 |
75,681,512 (GRCm39) |
missense |
probably benign |
0.02 |
R5164:Zc3h3
|
UTSW |
15 |
75,648,875 (GRCm39) |
missense |
probably benign |
0.02 |
R5279:Zc3h3
|
UTSW |
15 |
75,711,439 (GRCm39) |
missense |
probably benign |
0.08 |
R5622:Zc3h3
|
UTSW |
15 |
75,648,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Zc3h3
|
UTSW |
15 |
75,651,380 (GRCm39) |
nonsense |
probably null |
|
R5923:Zc3h3
|
UTSW |
15 |
75,657,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R6294:Zc3h3
|
UTSW |
15 |
75,681,417 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6377:Zc3h3
|
UTSW |
15 |
75,711,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R6735:Zc3h3
|
UTSW |
15 |
75,628,483 (GRCm39) |
missense |
probably benign |
0.00 |
R7043:Zc3h3
|
UTSW |
15 |
75,681,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R7231:Zc3h3
|
UTSW |
15 |
75,712,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Zc3h3
|
UTSW |
15 |
75,657,452 (GRCm39) |
missense |
probably benign |
0.00 |
R9038:Zc3h3
|
UTSW |
15 |
75,711,237 (GRCm39) |
missense |
probably benign |
0.01 |
R9068:Zc3h3
|
UTSW |
15 |
75,711,499 (GRCm39) |
missense |
probably benign |
|
R9557:Zc3h3
|
UTSW |
15 |
75,711,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Zc3h3
|
UTSW |
15 |
75,651,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:Zc3h3
|
UTSW |
15 |
75,681,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Zc3h3
|
UTSW |
15 |
75,709,459 (GRCm39) |
missense |
probably benign |
0.04 |
R9782:Zc3h3
|
UTSW |
15 |
75,681,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|