Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
C |
5: 113,331,221 (GRCm39) |
T998A |
probably damaging |
Het |
Aadacl4fm2 |
A |
G |
4: 144,291,580 (GRCm39) |
F42S |
probably damaging |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Akt3 |
T |
A |
1: 176,847,673 (GRCm39) |
K465* |
probably null |
Het |
Ankar |
T |
C |
1: 72,727,800 (GRCm39) |
D371G |
probably benign |
Het |
Ankib1 |
T |
G |
5: 3,805,734 (GRCm39) |
N178H |
possibly damaging |
Het |
Arhgap10 |
A |
G |
8: 78,146,699 (GRCm39) |
|
probably null |
Het |
Arhgef4 |
A |
G |
1: 34,848,785 (GRCm39) |
D286G |
probably damaging |
Het |
Bsdc1 |
A |
T |
4: 129,355,477 (GRCm39) |
|
probably benign |
Het |
Camk4 |
T |
C |
18: 33,318,085 (GRCm39) |
V414A |
probably benign |
Het |
Cyp2d9 |
T |
A |
15: 82,338,293 (GRCm39) |
V139E |
possibly damaging |
Het |
Dhrs13 |
C |
A |
11: 77,923,260 (GRCm39) |
N21K |
unknown |
Het |
Dop1a |
C |
T |
9: 86,388,343 (GRCm39) |
A439V |
probably damaging |
Het |
Dpy19l4 |
G |
A |
4: 11,317,160 (GRCm39) |
Q13* |
probably null |
Het |
Ecpas |
A |
G |
4: 58,847,038 (GRCm39) |
I508T |
possibly damaging |
Het |
Eif2ak1 |
T |
C |
5: 143,823,716 (GRCm39) |
S388P |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,581,974 (GRCm39) |
S251G |
probably benign |
Het |
Eml4 |
T |
A |
17: 83,753,379 (GRCm39) |
L350Q |
probably damaging |
Het |
Fblim1 |
A |
T |
4: 141,317,391 (GRCm39) |
L98H |
probably damaging |
Het |
Fcrl6 |
T |
A |
1: 172,425,239 (GRCm39) |
N264I |
probably benign |
Het |
Gzme |
A |
C |
14: 56,356,790 (GRCm39) |
D57E |
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,484,909 (GRCm39) |
T257A |
probably damaging |
Het |
Hectd4 |
C |
A |
5: 121,481,728 (GRCm39) |
D3092E |
possibly damaging |
Het |
Hrc |
A |
G |
7: 44,985,803 (GRCm39) |
E318G |
probably benign |
Het |
Hspbp1 |
A |
G |
7: 4,666,435 (GRCm39) |
L315P |
probably damaging |
Het |
Insr |
A |
T |
8: 3,242,642 (GRCm39) |
Y591N |
probably damaging |
Het |
Lrch4 |
T |
A |
5: 137,637,727 (GRCm39) |
I582N |
probably damaging |
Het |
Lrit2 |
A |
G |
14: 36,794,450 (GRCm39) |
K505E |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,547,428 (GRCm39) |
N4251K |
|
Het |
Mfsd13a |
T |
C |
19: 46,357,716 (GRCm39) |
F290S |
probably damaging |
Het |
Mgam |
T |
G |
6: 40,742,954 (GRCm39) |
N1791K |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,566,899 (GRCm39) |
I450N |
probably benign |
Het |
Mylk |
G |
A |
16: 34,809,357 (GRCm39) |
M1771I |
probably benign |
Het |
Or10ak12 |
A |
T |
4: 118,666,691 (GRCm39) |
F123L |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,188,338 (GRCm39) |
C34* |
probably null |
Het |
Or8d1 |
A |
T |
9: 38,766,534 (GRCm39) |
M59L |
possibly damaging |
Het |
Or8g55 |
T |
A |
9: 39,785,435 (GRCm39) |
L288* |
probably null |
Het |
Parp14 |
A |
T |
16: 35,677,861 (GRCm39) |
H702Q |
probably benign |
Het |
Pcdhga1 |
T |
C |
18: 37,795,281 (GRCm39) |
L95P |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,619,954 (GRCm39) |
T373A |
probably damaging |
Het |
Pdzph1 |
A |
G |
17: 59,274,336 (GRCm39) |
V836A |
possibly damaging |
Het |
Pgap1 |
T |
A |
1: 54,570,081 (GRCm39) |
N322I |
probably benign |
Het |
Pikfyve |
C |
T |
1: 65,283,585 (GRCm39) |
R741* |
probably null |
Het |
Pip4k2c |
A |
G |
10: 127,044,773 (GRCm39) |
S80P |
probably damaging |
Het |
Plekhh3 |
A |
G |
11: 101,057,445 (GRCm39) |
F271L |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,490,191 (GRCm39) |
Y565F |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,374,701 (GRCm39) |
R612G |
probably benign |
Het |
Psap |
T |
C |
10: 60,135,253 (GRCm39) |
V303A |
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,659,528 (GRCm39) |
R1375H |
probably benign |
Het |
Slc24a3 |
A |
C |
2: 145,455,450 (GRCm39) |
K446N |
probably benign |
Het |
Slc39a12 |
T |
A |
2: 14,499,272 (GRCm39) |
M661K |
probably benign |
Het |
Slc6a16 |
T |
C |
7: 44,908,537 (GRCm39) |
L39P |
probably benign |
Het |
Syne1 |
T |
G |
10: 5,135,559 (GRCm39) |
|
probably null |
Het |
Taar8c |
T |
C |
10: 23,977,764 (GRCm39) |
N16S |
probably benign |
Het |
Tmem98 |
A |
G |
11: 80,708,344 (GRCm39) |
T105A |
probably damaging |
Het |
Tmub1 |
T |
A |
5: 24,651,011 (GRCm39) |
Y216F |
probably damaging |
Het |
Trim16 |
T |
G |
11: 62,711,580 (GRCm39) |
C84G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,561,573 (GRCm39) |
K28978* |
probably null |
Het |
Usp38 |
A |
G |
8: 81,740,875 (GRCm39) |
V64A |
probably damaging |
Het |
Vmn2r63 |
A |
T |
7: 42,576,406 (GRCm39) |
F469Y |
possibly damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,610,510 (GRCm39) |
W61R |
probably benign |
Het |
Whamm |
G |
T |
7: 81,243,598 (GRCm39) |
G607C |
probably damaging |
Het |
Zfp398 |
A |
G |
6: 47,842,752 (GRCm39) |
D268G |
probably benign |
Het |
|
Other mutations in Xkr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Xkr6
|
APN |
14 |
64,056,664 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01419:Xkr6
|
APN |
14 |
64,056,325 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01450:Xkr6
|
APN |
14 |
64,035,664 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02010:Xkr6
|
APN |
14 |
64,056,653 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02352:Xkr6
|
APN |
14 |
64,057,156 (GRCm39) |
missense |
unknown |
|
IGL02359:Xkr6
|
APN |
14 |
64,057,156 (GRCm39) |
missense |
unknown |
|
R0148:Xkr6
|
UTSW |
14 |
64,056,998 (GRCm39) |
missense |
unknown |
|
R0521:Xkr6
|
UTSW |
14 |
64,056,871 (GRCm39) |
missense |
probably benign |
0.28 |
R1555:Xkr6
|
UTSW |
14 |
64,056,374 (GRCm39) |
missense |
unknown |
|
R1619:Xkr6
|
UTSW |
14 |
64,056,766 (GRCm39) |
missense |
probably benign |
0.39 |
R1874:Xkr6
|
UTSW |
14 |
64,035,745 (GRCm39) |
missense |
unknown |
|
R2864:Xkr6
|
UTSW |
14 |
64,057,205 (GRCm39) |
missense |
unknown |
|
R2960:Xkr6
|
UTSW |
14 |
63,844,586 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3014:Xkr6
|
UTSW |
14 |
64,056,793 (GRCm39) |
missense |
unknown |
|
R4888:Xkr6
|
UTSW |
14 |
64,056,953 (GRCm39) |
missense |
unknown |
|
R5019:Xkr6
|
UTSW |
14 |
64,056,515 (GRCm39) |
missense |
unknown |
|
R5193:Xkr6
|
UTSW |
14 |
64,056,356 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5354:Xkr6
|
UTSW |
14 |
64,056,353 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5485:Xkr6
|
UTSW |
14 |
64,056,833 (GRCm39) |
missense |
unknown |
|
R5825:Xkr6
|
UTSW |
14 |
64,056,481 (GRCm39) |
missense |
probably benign |
0.39 |
R5885:Xkr6
|
UTSW |
14 |
63,844,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R6074:Xkr6
|
UTSW |
14 |
63,844,519 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6861:Xkr6
|
UTSW |
14 |
64,057,093 (GRCm39) |
missense |
probably benign |
0.39 |
R7289:Xkr6
|
UTSW |
14 |
64,035,748 (GRCm39) |
missense |
unknown |
|
R7477:Xkr6
|
UTSW |
14 |
63,844,129 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7528:Xkr6
|
UTSW |
14 |
64,056,610 (GRCm39) |
missense |
probably benign |
0.39 |
R7529:Xkr6
|
UTSW |
14 |
64,056,610 (GRCm39) |
missense |
probably benign |
0.39 |
R7646:Xkr6
|
UTSW |
14 |
63,844,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R7686:Xkr6
|
UTSW |
14 |
63,844,295 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7697:Xkr6
|
UTSW |
14 |
63,844,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R8331:Xkr6
|
UTSW |
14 |
64,056,392 (GRCm39) |
missense |
unknown |
|
R8702:Xkr6
|
UTSW |
14 |
64,057,103 (GRCm39) |
missense |
unknown |
|
R9169:Xkr6
|
UTSW |
14 |
63,844,067 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1176:Xkr6
|
UTSW |
14 |
63,844,394 (GRCm39) |
missense |
probably benign |
0.08 |
|