Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
T |
1: 71,247,184 (GRCm38) |
M2497K |
probably benign |
Het |
Abtb2 |
C |
T |
2: 103,567,376 (GRCm38) |
T217I |
probably damaging |
Het |
Adam29 |
T |
A |
8: 55,871,508 (GRCm38) |
N637I |
probably damaging |
Het |
Adgb |
T |
A |
10: 10,450,028 (GRCm38) |
E59V |
probably damaging |
Het |
Adh7 |
C |
T |
3: 138,228,017 (GRCm38) |
R312C |
probably benign |
Het |
Adprh |
A |
G |
16: 38,447,452 (GRCm38) |
I157T |
probably damaging |
Het |
Ap2b1 |
T |
C |
11: 83,346,825 (GRCm38) |
S572P |
probably damaging |
Het |
Asic1 |
T |
C |
15: 99,698,880 (GRCm38) |
L519P |
probably damaging |
Het |
Atp2a2 |
G |
C |
5: 122,501,649 (GRCm38) |
L13V |
probably benign |
Het |
Bst2 |
A |
T |
8: 71,537,288 (GRCm38) |
I47N |
possibly damaging |
Het |
Cacng6 |
G |
A |
7: 3,424,993 (GRCm38) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 135,251,528 (GRCm38) |
E1849G |
probably damaging |
Het |
Cep295 |
T |
A |
9: 15,332,754 (GRCm38) |
T213S |
probably damaging |
Het |
Chia1 |
A |
G |
3: 106,131,811 (GRCm38) |
T406A |
probably benign |
Het |
Chmp4c |
G |
T |
3: 10,367,217 (GRCm38) |
K62N |
probably damaging |
Het |
Cldn15 |
A |
G |
5: 136,968,125 (GRCm38) |
T7A |
probably benign |
Het |
Cmpk2 |
T |
A |
12: 26,478,020 (GRCm38) |
M412K |
probably benign |
Het |
Cnnm1 |
T |
C |
19: 43,465,266 (GRCm38) |
|
probably null |
Het |
Cubn |
A |
C |
2: 13,427,835 (GRCm38) |
|
probably null |
Het |
Dopey2 |
T |
C |
16: 93,782,248 (GRCm38) |
V1668A |
possibly damaging |
Het |
Erg28 |
T |
A |
12: 85,816,429 (GRCm38) |
Y77F |
probably damaging |
Het |
F830045P16Rik |
C |
T |
2: 129,536,438 (GRCm38) |
A9T |
probably benign |
Het |
Gli3 |
A |
G |
13: 15,723,555 (GRCm38) |
D740G |
probably damaging |
Het |
Gm13128 |
A |
T |
4: 144,333,147 (GRCm38) |
*476L |
probably null |
Het |
Gm14085 |
T |
C |
2: 122,524,807 (GRCm38) |
I555T |
probably benign |
Het |
Gpat2 |
G |
C |
2: 127,431,918 (GRCm38) |
G294R |
possibly damaging |
Het |
Gpat3 |
A |
T |
5: 100,893,144 (GRCm38) |
M357L |
probably benign |
Het |
Gpr179 |
A |
G |
11: 97,337,147 (GRCm38) |
V1394A |
possibly damaging |
Het |
Grn |
T |
A |
11: 102,436,795 (GRCm38) |
|
probably benign |
Het |
H2-Q6 |
G |
A |
17: 35,428,383 (GRCm38) |
|
probably null |
Het |
Igsf3 |
A |
G |
3: 101,435,648 (GRCm38) |
T514A |
probably benign |
Het |
Il1r1 |
A |
G |
1: 40,313,335 (GRCm38) |
D558G |
possibly damaging |
Het |
Irx4 |
T |
C |
13: 73,267,713 (GRCm38) |
M207T |
possibly damaging |
Het |
Kap |
T |
C |
6: 133,851,957 (GRCm38) |
I54V |
probably benign |
Het |
Kdm2b |
G |
A |
5: 122,934,778 (GRCm38) |
R340C |
probably damaging |
Het |
Lipo3 |
T |
A |
19: 33,556,431 (GRCm38) |
M334L |
probably benign |
Het |
Lmbrd1 |
C |
T |
1: 24,706,034 (GRCm38) |
L152F |
probably damaging |
Het |
Ltbp1 |
G |
A |
17: 75,359,457 (GRCm38) |
V1382I |
probably damaging |
Het |
Map3k4 |
C |
T |
17: 12,249,583 (GRCm38) |
D1008N |
possibly damaging |
Het |
Mcf2l |
T |
C |
8: 12,879,912 (GRCm38) |
|
probably benign |
Het |
Mecom |
T |
G |
3: 29,997,726 (GRCm38) |
D180A |
probably damaging |
Het |
Meis1 |
T |
C |
11: 18,941,741 (GRCm38) |
D269G |
probably benign |
Het |
Myh7 |
A |
C |
14: 54,988,894 (GRCm38) |
S430A |
probably benign |
Het |
Myo1h |
A |
G |
5: 114,336,264 (GRCm38) |
I439V |
probably damaging |
Het |
Nat1 |
T |
C |
8: 67,491,482 (GRCm38) |
V170A |
possibly damaging |
Het |
Nlrp12 |
A |
G |
7: 3,234,043 (GRCm38) |
L742P |
probably damaging |
Het |
Nlrp4c |
A |
G |
7: 6,066,053 (GRCm38) |
T318A |
probably benign |
Het |
Olfr1297 |
T |
A |
2: 111,621,186 (GRCm38) |
N296I |
probably benign |
Het |
Olfr1425 |
T |
A |
19: 12,074,363 (GRCm38) |
I90F |
probably damaging |
Het |
Olfr632 |
A |
G |
7: 103,937,823 (GRCm38) |
I148V |
probably benign |
Het |
Olfr952 |
G |
T |
9: 39,426,234 (GRCm38) |
T279N |
probably damaging |
Het |
Olfr955 |
A |
T |
9: 39,470,630 (GRCm38) |
L32Q |
probably damaging |
Het |
Otop3 |
A |
G |
11: 115,345,072 (GRCm38) |
E529G |
probably damaging |
Het |
Parp6 |
T |
C |
9: 59,623,939 (GRCm38) |
Y35H |
probably damaging |
Het |
Pcdhb4 |
A |
C |
18: 37,308,021 (GRCm38) |
D128A |
probably damaging |
Het |
Phldb2 |
C |
T |
16: 45,748,750 (GRCm38) |
D1249N |
probably damaging |
Het |
Ptpn12 |
T |
A |
5: 20,987,468 (GRCm38) |
K765* |
probably null |
Het |
Ptprb |
T |
A |
10: 116,347,007 (GRCm38) |
Y1529* |
probably null |
Het |
Ptprc |
A |
T |
1: 138,078,451 (GRCm38) |
Y798N |
possibly damaging |
Het |
Sdk2 |
G |
A |
11: 113,832,265 (GRCm38) |
T1300I |
probably damaging |
Het |
Sptbn2 |
G |
A |
19: 4,732,496 (GRCm38) |
V487I |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 120,046,269 (GRCm38) |
|
probably benign |
Het |
Srpk1 |
A |
G |
17: 28,590,062 (GRCm38) |
S648P |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,666,407 (GRCm38) |
|
probably null |
Het |
Tmem135 |
A |
T |
7: 89,144,670 (GRCm38) |
I388N |
probably damaging |
Het |
Top3a |
A |
T |
11: 60,749,459 (GRCm38) |
I446N |
probably benign |
Het |
Trpv1 |
T |
C |
11: 73,246,036 (GRCm38) |
S482P |
probably damaging |
Het |
Ugt3a1 |
C |
T |
15: 9,306,455 (GRCm38) |
A230V |
probably benign |
Het |
Vmn2r15 |
A |
C |
5: 109,293,226 (GRCm38) |
Y255* |
probably null |
Het |
Vmn2r60 |
A |
G |
7: 42,116,471 (GRCm38) |
M1V |
probably null |
Het |
Vmn2r87 |
A |
G |
10: 130,479,000 (GRCm38) |
V239A |
probably damaging |
Het |
Vwce |
T |
A |
19: 10,659,592 (GRCm38) |
C679* |
probably null |
Het |
Zfp385b |
C |
T |
2: 77,415,841 (GRCm38) |
A281T |
probably benign |
Het |
Zfp398 |
T |
G |
6: 47,866,595 (GRCm38) |
L395W |
probably damaging |
Het |
Zfp442 |
C |
T |
2: 150,451,401 (GRCm38) |
|
probably null |
Het |
Zfp606 |
A |
G |
7: 12,492,944 (GRCm38) |
S331G |
probably benign |
Het |
|
Other mutations in Zfp882 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00676:Zfp882
|
APN |
8 |
71,913,827 (GRCm38) |
missense |
probably benign |
|
R0244:Zfp882
|
UTSW |
8 |
71,913,523 (GRCm38) |
missense |
possibly damaging |
0.79 |
R0270:Zfp882
|
UTSW |
8 |
71,914,615 (GRCm38) |
missense |
probably benign |
0.05 |
R0636:Zfp882
|
UTSW |
8 |
71,914,337 (GRCm38) |
missense |
probably benign |
0.01 |
R0840:Zfp882
|
UTSW |
8 |
71,914,686 (GRCm38) |
nonsense |
probably null |
|
R1299:Zfp882
|
UTSW |
8 |
71,913,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R4439:Zfp882
|
UTSW |
8 |
71,913,609 (GRCm38) |
missense |
probably damaging |
0.97 |
R4829:Zfp882
|
UTSW |
8 |
71,914,389 (GRCm38) |
missense |
probably damaging |
1.00 |
R5028:Zfp882
|
UTSW |
8 |
71,914,654 (GRCm38) |
missense |
possibly damaging |
0.70 |
R5296:Zfp882
|
UTSW |
8 |
71,914,360 (GRCm38) |
missense |
probably damaging |
1.00 |
R5882:Zfp882
|
UTSW |
8 |
71,913,459 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5974:Zfp882
|
UTSW |
8 |
71,913,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R6052:Zfp882
|
UTSW |
8 |
71,914,505 (GRCm38) |
missense |
probably benign |
0.01 |
R6888:Zfp882
|
UTSW |
8 |
71,914,286 (GRCm38) |
missense |
probably benign |
0.01 |
R6987:Zfp882
|
UTSW |
8 |
71,914,673 (GRCm38) |
missense |
probably benign |
0.01 |
R7045:Zfp882
|
UTSW |
8 |
71,913,249 (GRCm38) |
critical splice donor site |
probably null |
|
R7780:Zfp882
|
UTSW |
8 |
71,914,229 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7793:Zfp882
|
UTSW |
8 |
71,913,141 (GRCm38) |
missense |
probably damaging |
1.00 |
R8386:Zfp882
|
UTSW |
8 |
71,914,118 (GRCm38) |
missense |
probably benign |
0.00 |
R9452:Zfp882
|
UTSW |
8 |
71,914,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R9694:Zfp882
|
UTSW |
8 |
71,914,071 (GRCm38) |
missense |
probably benign |
0.01 |
|