Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700092M07Rik |
A |
T |
19: 8,740,784 |
D6V |
probably damaging |
Het |
2310057M21Rik |
G |
T |
7: 131,357,613 |
H165Q |
probably damaging |
Het |
Akap13 |
T |
A |
7: 75,677,416 |
F721Y |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,140,354 |
D1517V |
probably damaging |
Het |
Amigo3 |
T |
A |
9: 108,053,728 |
S117T |
probably damaging |
Het |
Atf7ip2 |
T |
A |
16: 10,201,411 |
N34K |
probably damaging |
Het |
Cacnb1 |
A |
C |
11: 98,005,782 |
V351G |
probably damaging |
Het |
Casp9 |
T |
A |
4: 141,805,349 |
|
probably null |
Het |
Ccdc51 |
C |
T |
9: 109,089,415 |
T24I |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,434,512 |
Y618F |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,758,688 |
W1271R |
probably damaging |
Het |
Dars |
T |
C |
1: 128,368,439 |
T386A |
probably benign |
Het |
Dchs1 |
T |
A |
7: 105,765,106 |
D834V |
probably damaging |
Het |
Dgkd |
T |
A |
1: 87,936,381 |
V933E |
possibly damaging |
Het |
Dnah17 |
A |
G |
11: 118,025,654 |
F4203S |
probably damaging |
Het |
Fancm |
T |
C |
12: 65,130,382 |
L2000P |
probably damaging |
Het |
Fbxo11 |
A |
T |
17: 88,008,669 |
H444Q |
probably benign |
Het |
Fbxw14 |
T |
A |
9: 109,276,222 |
T292S |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,559,206 |
S237P |
probably damaging |
Het |
Frem3 |
T |
C |
8: 80,615,047 |
I1323T |
probably benign |
Het |
Grin2a |
A |
G |
16: 9,653,449 |
F652L |
probably benign |
Het |
Grin2b |
T |
A |
6: 135,923,458 |
M142L |
possibly damaging |
Het |
Helz |
A |
G |
11: 107,619,060 |
Q503R |
possibly damaging |
Het |
Ighv5-17 |
A |
G |
12: 113,859,295 |
Y69H |
probably benign |
Het |
Il17ra |
A |
G |
6: 120,475,582 |
N242S |
probably benign |
Het |
Immp1l |
G |
C |
2: 105,964,208 |
G117A |
probably damaging |
Het |
Itm2c |
T |
C |
1: 85,894,692 |
V10A |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,238,426 |
K679E |
possibly damaging |
Het |
Kng1 |
T |
C |
16: 23,074,645 |
V256A |
possibly damaging |
Het |
Lamc2 |
T |
G |
1: 153,166,153 |
R78S |
possibly damaging |
Het |
Loxl4 |
A |
G |
19: 42,598,793 |
F621S |
probably damaging |
Het |
Lpl |
T |
A |
8: 68,892,747 |
D134E |
probably damaging |
Het |
Lypd3 |
T |
C |
7: 24,640,494 |
Y329H |
probably benign |
Het |
Mettl13 |
T |
C |
1: 162,535,886 |
D225G |
probably benign |
Het |
Myo7b |
A |
G |
18: 31,999,974 |
F441L |
probably damaging |
Het |
Nnt |
T |
A |
13: 119,336,328 |
M699L |
possibly damaging |
Het |
Nr1h3 |
A |
T |
2: 91,191,851 |
M144K |
probably damaging |
Het |
Olfr1040 |
A |
G |
2: 86,145,969 |
V255A |
probably benign |
Het |
Olfr1347 |
T |
C |
7: 6,488,845 |
T3A |
probably benign |
Het |
Olfr325 |
A |
T |
11: 58,581,068 |
M75L |
probably benign |
Het |
Pappa2 |
A |
T |
1: 158,871,543 |
Y667N |
probably damaging |
Het |
Prps1l3 |
A |
G |
12: 57,238,888 |
I155V |
probably benign |
Het |
Ptgs2 |
T |
A |
1: 150,100,993 |
N24K |
probably benign |
Het |
Ralgds |
A |
T |
2: 28,547,588 |
M514L |
probably damaging |
Het |
Rbm47 |
G |
C |
5: 66,026,283 |
R326G |
probably damaging |
Het |
Sacm1l |
T |
A |
9: 123,569,005 |
V254D |
probably damaging |
Het |
Selenot |
A |
T |
3: 58,585,284 |
Q64L |
probably damaging |
Het |
Sgsm2 |
G |
A |
11: 74,850,851 |
R1037W |
probably damaging |
Het |
Slc22a12 |
A |
G |
19: 6,542,724 |
V10A |
probably benign |
Het |
Spem2 |
G |
T |
11: 69,816,696 |
S481* |
probably null |
Het |
Styk1 |
C |
T |
6: 131,311,016 |
G128D |
probably damaging |
Het |
Tmc6 |
A |
T |
11: 117,776,328 |
L148Q |
probably damaging |
Het |
Tmem138 |
A |
C |
19: 10,574,835 |
|
probably null |
Het |
Tnpo3 |
A |
G |
6: 29,555,268 |
V772A |
probably benign |
Het |
Topaz1 |
T |
C |
9: 122,797,756 |
F1483S |
possibly damaging |
Het |
Tuba4a |
C |
A |
1: 75,216,055 |
C305F |
probably damaging |
Het |
Ubap1 |
T |
G |
4: 41,379,262 |
F159V |
possibly damaging |
Het |
Wwc2 |
A |
T |
8: 47,856,263 |
M828K |
unknown |
Het |
Zfp236 |
A |
T |
18: 82,671,794 |
S187T |
possibly damaging |
Het |
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