Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
T |
C |
3: 89,969,021 (GRCm39) |
S215P |
probably benign |
Het |
Ano2 |
C |
T |
6: 126,016,460 (GRCm39) |
Q998* |
probably null |
Het |
Atg9a |
A |
T |
1: 75,164,736 (GRCm39) |
V76E |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 119,034,172 (GRCm39) |
I118M |
|
Het |
Cacna1g |
T |
A |
11: 94,323,383 (GRCm39) |
I1274F |
probably damaging |
Het |
Cd300lg |
C |
T |
11: 101,937,767 (GRCm39) |
A199V |
probably benign |
Het |
Cfap61 |
C |
T |
2: 145,887,390 (GRCm39) |
R612* |
probably null |
Het |
Cpeb4 |
A |
T |
11: 31,881,417 (GRCm39) |
Y692F |
probably damaging |
Het |
Dcun1d1 |
A |
G |
3: 35,951,940 (GRCm39) |
|
probably null |
Het |
Dennd2d |
T |
A |
3: 106,398,579 (GRCm39) |
M188K |
probably benign |
Het |
Dmgdh |
A |
G |
13: 93,845,354 (GRCm39) |
|
probably null |
Het |
Efl1 |
T |
A |
7: 82,330,652 (GRCm39) |
M275K |
probably benign |
Het |
Erp29 |
G |
T |
5: 121,583,392 (GRCm39) |
A178D |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,308,594 (GRCm39) |
N156S |
possibly damaging |
Het |
Frrs1 |
C |
T |
3: 116,675,426 (GRCm39) |
T118I |
probably damaging |
Het |
Frrs1l |
A |
G |
4: 56,968,230 (GRCm39) |
W181R |
probably benign |
Het |
Gprc5b |
C |
A |
7: 118,583,482 (GRCm39) |
W129L |
probably damaging |
Het |
Hoxc9 |
A |
G |
15: 102,890,593 (GRCm39) |
H170R |
probably benign |
Het |
Il12rb2 |
C |
T |
6: 67,333,617 (GRCm39) |
D221N |
probably benign |
Het |
Lmo1 |
T |
C |
7: 108,742,819 (GRCm39) |
N28S |
probably benign |
Het |
Lrrfip2 |
T |
A |
9: 111,006,525 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
T |
4: 123,400,130 (GRCm39) |
F722I |
probably damaging |
Het |
Mical1 |
T |
C |
10: 41,355,772 (GRCm39) |
|
probably null |
Het |
Mtcl3 |
A |
G |
10: 29,073,240 (GRCm39) |
Y844C |
probably damaging |
Het |
Mtmr11 |
C |
T |
3: 96,071,855 (GRCm39) |
T223M |
possibly damaging |
Het |
Mup21 |
A |
G |
4: 62,068,468 (GRCm39) |
V66A |
probably benign |
Het |
Nav2 |
C |
A |
7: 49,111,672 (GRCm39) |
A726D |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nudt21 |
A |
T |
8: 94,746,227 (GRCm39) |
V157D |
probably benign |
Het |
Numa1 |
T |
C |
7: 101,639,806 (GRCm39) |
I52T |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,946,442 (GRCm39) |
D4421G |
probably benign |
Het |
Oog3 |
T |
C |
4: 143,886,801 (GRCm39) |
I106M |
probably benign |
Het |
Or10g9 |
A |
T |
9: 39,912,106 (GRCm39) |
V139E |
probably benign |
Het |
Or2g25 |
T |
C |
17: 37,970,403 (GRCm39) |
T274A |
possibly damaging |
Het |
Or2z9 |
T |
C |
8: 72,853,793 (GRCm39) |
L63P |
probably damaging |
Het |
Or51f1 |
T |
A |
7: 102,505,706 (GRCm39) |
Y261F |
probably damaging |
Het |
Or5w20 |
T |
G |
2: 87,726,755 (GRCm39) |
C71G |
possibly damaging |
Het |
Orai2 |
T |
A |
5: 136,179,437 (GRCm39) |
I199F |
probably damaging |
Het |
P2rx5 |
C |
A |
11: 73,055,692 (GRCm39) |
L50M |
probably damaging |
Het |
Pdia2 |
T |
C |
17: 26,416,634 (GRCm39) |
E215G |
possibly damaging |
Het |
Pds5a |
A |
T |
5: 65,823,570 (GRCm39) |
S74T |
possibly damaging |
Het |
Phlpp2 |
A |
G |
8: 110,666,785 (GRCm39) |
S1105G |
probably damaging |
Het |
Pi4kb |
T |
A |
3: 94,891,888 (GRCm39) |
D189E |
probably benign |
Het |
Pigw |
G |
A |
11: 84,768,585 (GRCm39) |
T248M |
probably damaging |
Het |
Pnlip |
T |
A |
19: 58,670,134 (GRCm39) |
V458D |
probably damaging |
Het |
Ppm1l |
G |
A |
3: 69,225,044 (GRCm39) |
V49I |
probably benign |
Het |
Prl3b1 |
T |
A |
13: 27,426,473 (GRCm39) |
M1K |
probably null |
Het |
Rad1 |
T |
A |
15: 10,493,367 (GRCm39) |
C265S |
probably benign |
Het |
Rnaset2b |
C |
T |
17: 7,265,427 (GRCm39) |
S237F |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,561,672 (GRCm39) |
A56T |
unknown |
Het |
S1pr2 |
T |
C |
9: 20,879,238 (GRCm39) |
I197V |
probably benign |
Het |
Smyd4 |
A |
G |
11: 75,281,082 (GRCm39) |
Q185R |
probably benign |
Het |
Sox5 |
T |
A |
6: 144,100,759 (GRCm39) |
T77S |
probably benign |
Het |
Sox7 |
A |
G |
14: 64,185,291 (GRCm39) |
Y109C |
probably damaging |
Het |
Styxl2 |
C |
T |
1: 165,954,676 (GRCm39) |
V25I |
probably damaging |
Het |
Tln1 |
G |
A |
4: 43,545,922 (GRCm39) |
R898C |
probably damaging |
Het |
Tmprss11b |
T |
A |
5: 86,812,173 (GRCm39) |
E158V |
probably damaging |
Het |
Tnpo3 |
C |
A |
6: 29,562,875 (GRCm39) |
R614L |
possibly damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,742,296 (GRCm39) |
D223E |
probably benign |
Het |
Zfp28 |
G |
T |
7: 6,386,593 (GRCm39) |
|
probably benign |
Het |
Zfp963 |
A |
T |
8: 70,195,759 (GRCm39) |
H231Q |
probably damaging |
Het |
Zscan4b |
A |
G |
7: 10,634,867 (GRCm39) |
S459P |
probably benign |
Het |
|
Other mutations in Zc3h12d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Zc3h12d
|
APN |
10 |
7,738,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01013:Zc3h12d
|
APN |
10 |
7,715,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02090:Zc3h12d
|
APN |
10 |
7,743,096 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02876:Zc3h12d
|
APN |
10 |
7,738,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R0040:Zc3h12d
|
UTSW |
10 |
7,743,678 (GRCm39) |
missense |
probably benign |
0.02 |
R0040:Zc3h12d
|
UTSW |
10 |
7,743,678 (GRCm39) |
missense |
probably benign |
0.02 |
R0242:Zc3h12d
|
UTSW |
10 |
7,738,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Zc3h12d
|
UTSW |
10 |
7,738,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Zc3h12d
|
UTSW |
10 |
7,729,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Zc3h12d
|
UTSW |
10 |
7,743,223 (GRCm39) |
missense |
probably benign |
0.00 |
R2354:Zc3h12d
|
UTSW |
10 |
7,743,702 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Zc3h12d
|
UTSW |
10 |
7,743,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4932:Zc3h12d
|
UTSW |
10 |
7,729,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R5191:Zc3h12d
|
UTSW |
10 |
7,743,582 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5384:Zc3h12d
|
UTSW |
10 |
7,729,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R5396:Zc3h12d
|
UTSW |
10 |
7,742,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Zc3h12d
|
UTSW |
10 |
7,743,082 (GRCm39) |
missense |
probably benign |
0.04 |
R6877:Zc3h12d
|
UTSW |
10 |
7,715,735 (GRCm39) |
missense |
probably damaging |
0.99 |
R6903:Zc3h12d
|
UTSW |
10 |
7,743,425 (GRCm39) |
missense |
probably benign |
|
R6967:Zc3h12d
|
UTSW |
10 |
7,715,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Zc3h12d
|
UTSW |
10 |
7,738,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Zc3h12d
|
UTSW |
10 |
7,743,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7645:Zc3h12d
|
UTSW |
10 |
7,743,340 (GRCm39) |
missense |
probably benign |
|
R7769:Zc3h12d
|
UTSW |
10 |
7,743,390 (GRCm39) |
missense |
probably benign |
0.03 |
R7864:Zc3h12d
|
UTSW |
10 |
7,715,723 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8371:Zc3h12d
|
UTSW |
10 |
7,715,735 (GRCm39) |
frame shift |
probably null |
|
R8414:Zc3h12d
|
UTSW |
10 |
7,715,735 (GRCm39) |
frame shift |
probably null |
|
R9255:Zc3h12d
|
UTSW |
10 |
7,729,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R9470:Zc3h12d
|
UTSW |
10 |
7,743,321 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Zc3h12d
|
UTSW |
10 |
7,743,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|