Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acer2 |
T |
A |
4: 86,792,805 (GRCm39) |
V27E |
possibly damaging |
Het |
Adam23 |
T |
C |
1: 63,605,787 (GRCm39) |
Y624H |
probably damaging |
Het |
Arhgef10 |
T |
A |
8: 14,980,157 (GRCm39) |
C132* |
probably null |
Het |
Boc |
A |
T |
16: 44,311,545 (GRCm39) |
L726H |
probably damaging |
Het |
Brip1 |
A |
T |
11: 86,039,255 (GRCm39) |
D426E |
possibly damaging |
Het |
Cadps2 |
T |
A |
6: 23,412,987 (GRCm39) |
Q654L |
probably benign |
Het |
Calr3 |
T |
A |
8: 73,182,008 (GRCm39) |
D120V |
probably damaging |
Het |
Cntnap3 |
A |
G |
13: 64,896,274 (GRCm39) |
Y1067H |
probably damaging |
Het |
Csnk1g1 |
T |
C |
9: 65,927,190 (GRCm39) |
V119A |
probably damaging |
Het |
Ddias |
G |
A |
7: 92,507,431 (GRCm39) |
T828I |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,729,687 (GRCm39) |
Y763C |
probably damaging |
Het |
Dscam |
T |
A |
16: 96,510,416 (GRCm39) |
I948F |
probably damaging |
Het |
E030018B13Rik |
A |
G |
7: 63,569,141 (GRCm39) |
|
probably benign |
Het |
E2f8 |
G |
A |
7: 48,516,847 (GRCm39) |
T844I |
possibly damaging |
Het |
Eps8 |
T |
A |
6: 137,476,590 (GRCm39) |
H603L |
probably benign |
Het |
Esrrg |
G |
A |
1: 187,775,908 (GRCm39) |
C122Y |
probably damaging |
Het |
Frmd4a |
C |
T |
2: 4,599,374 (GRCm39) |
R467* |
probably null |
Het |
Gad2 |
G |
A |
2: 22,575,422 (GRCm39) |
V509I |
probably benign |
Het |
Gpat4 |
A |
G |
8: 23,664,602 (GRCm39) |
I446T |
probably benign |
Het |
Klhl12 |
T |
G |
1: 134,415,392 (GRCm39) |
D435E |
probably damaging |
Het |
Luc7l |
T |
C |
17: 26,498,936 (GRCm39) |
|
probably benign |
Het |
Marchf2 |
C |
A |
17: 33,915,167 (GRCm39) |
M142I |
probably benign |
Het |
Marf1 |
T |
A |
16: 13,960,505 (GRCm39) |
Y513F |
possibly damaging |
Het |
Mdm2 |
T |
C |
10: 117,532,344 (GRCm39) |
D114G |
possibly damaging |
Het |
Med1 |
G |
A |
11: 98,043,688 (GRCm39) |
|
probably benign |
Het |
Myh9 |
A |
T |
15: 77,675,912 (GRCm39) |
|
probably benign |
Het |
Mylip |
T |
C |
13: 45,543,434 (GRCm39) |
M1T |
probably null |
Het |
Ncapg2 |
T |
C |
12: 116,403,497 (GRCm39) |
|
probably null |
Het |
Nmd3 |
T |
C |
3: 69,631,731 (GRCm39) |
|
probably benign |
Het |
Nwd2 |
T |
A |
5: 63,963,914 (GRCm39) |
L1166H |
probably damaging |
Het |
Or1j13 |
A |
G |
2: 36,370,010 (GRCm39) |
L44P |
probably damaging |
Het |
Or8b48 |
T |
C |
9: 38,493,349 (GRCm39) |
Y259H |
probably damaging |
Het |
Rubcn |
A |
G |
16: 32,677,272 (GRCm39) |
I71T |
probably damaging |
Het |
Rwdd3 |
T |
C |
3: 120,952,406 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,620,119 (GRCm39) |
E3826G |
probably damaging |
Het |
Sdad1 |
T |
C |
5: 92,446,116 (GRCm39) |
Q273R |
probably benign |
Het |
Sdha |
A |
T |
13: 74,475,104 (GRCm39) |
I579K |
possibly damaging |
Het |
Sema4d |
A |
G |
13: 51,856,919 (GRCm39) |
L771P |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc6a11 |
A |
G |
6: 114,224,688 (GRCm39) |
E624G |
possibly damaging |
Het |
Tada3 |
G |
T |
6: 113,347,340 (GRCm39) |
R117S |
probably damaging |
Het |
Tm9sf3 |
T |
C |
19: 41,236,372 (GRCm39) |
M130V |
probably damaging |
Het |
Trpc1 |
C |
A |
9: 95,614,161 (GRCm39) |
M34I |
probably benign |
Het |
Trpc4ap |
A |
G |
2: 155,482,427 (GRCm39) |
V521A |
possibly damaging |
Het |
Trpm2 |
A |
G |
10: 77,753,559 (GRCm39) |
V1315A |
probably benign |
Het |
Tvp23a |
A |
G |
16: 10,246,546 (GRCm39) |
S80P |
probably benign |
Het |
Usp54 |
A |
T |
14: 20,600,153 (GRCm39) |
|
probably null |
Het |
Vmn2r27 |
A |
G |
6: 124,201,115 (GRCm39) |
Y281H |
probably benign |
Het |
Vwf |
T |
A |
6: 125,632,079 (GRCm39) |
I37N |
unknown |
Het |
Zfp329 |
G |
A |
7: 12,545,584 (GRCm39) |
|
probably benign |
Het |
Zfp616 |
G |
T |
11: 73,974,005 (GRCm39) |
L91F |
possibly damaging |
Het |
|
Other mutations in Meikin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Meikin
|
APN |
11 |
54,289,320 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02893:Meikin
|
APN |
11 |
54,308,584 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03224:Meikin
|
APN |
11 |
54,289,286 (GRCm39) |
missense |
probably benign |
0.01 |
R0153:Meikin
|
UTSW |
11 |
54,300,468 (GRCm39) |
splice site |
probably benign |
|
R0634:Meikin
|
UTSW |
11 |
54,281,309 (GRCm39) |
missense |
probably benign |
0.22 |
R1374:Meikin
|
UTSW |
11 |
54,289,270 (GRCm39) |
splice site |
probably benign |
|
R1457:Meikin
|
UTSW |
11 |
54,261,767 (GRCm39) |
nonsense |
probably null |
|
R1659:Meikin
|
UTSW |
11 |
54,281,392 (GRCm39) |
nonsense |
probably null |
|
R1799:Meikin
|
UTSW |
11 |
54,308,613 (GRCm39) |
missense |
probably benign |
0.27 |
R2869:Meikin
|
UTSW |
11 |
54,264,333 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2869:Meikin
|
UTSW |
11 |
54,264,333 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3801:Meikin
|
UTSW |
11 |
54,290,697 (GRCm39) |
splice site |
probably null |
|
R6343:Meikin
|
UTSW |
11 |
54,261,592 (GRCm39) |
missense |
probably damaging |
0.97 |
R6523:Meikin
|
UTSW |
11 |
54,289,327 (GRCm39) |
nonsense |
probably null |
|
R6878:Meikin
|
UTSW |
11 |
54,302,712 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7214:Meikin
|
UTSW |
11 |
54,302,738 (GRCm39) |
missense |
probably benign |
0.40 |
R7969:Meikin
|
UTSW |
11 |
54,300,536 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8462:Meikin
|
UTSW |
11 |
54,290,666 (GRCm39) |
missense |
probably benign |
0.01 |
R8680:Meikin
|
UTSW |
11 |
54,317,477 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9136:Meikin
|
UTSW |
11 |
54,285,464 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9169:Meikin
|
UTSW |
11 |
54,285,517 (GRCm39) |
missense |
possibly damaging |
0.66 |
|