Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,256,619 |
|
probably null |
Het |
Abca2 |
A |
G |
2: 25,447,879 |
|
probably benign |
Het |
Abcb11 |
A |
T |
2: 69,299,925 |
S262R |
probably damaging |
Het |
Abhd12 |
T |
A |
2: 150,848,421 |
Q118L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,518,971 |
L753* |
probably null |
Het |
Ahctf1 |
A |
T |
1: 179,779,652 |
I699N |
possibly damaging |
Het |
Arl11 |
C |
A |
14: 61,311,038 |
A99E |
probably damaging |
Het |
Atp5o |
G |
A |
16: 91,930,401 |
R16W |
probably damaging |
Het |
AW551984 |
T |
C |
9: 39,599,325 |
H238R |
probably null |
Het |
Bpifb9a |
C |
A |
2: 154,266,813 |
|
probably benign |
Het |
Carhsp1 |
A |
G |
16: 8,663,713 |
|
probably benign |
Het |
Ccdc33 |
T |
C |
9: 58,030,419 |
D623G |
probably damaging |
Het |
Chd6 |
C |
A |
2: 161,026,292 |
R378L |
possibly damaging |
Het |
Chn2 |
T |
C |
6: 54,300,245 |
|
probably benign |
Het |
Clgn |
T |
G |
8: 83,423,136 |
I422S |
probably damaging |
Het |
Col15a1 |
T |
A |
4: 47,300,606 |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,401,492 |
G219V |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,568,130 |
I470T |
probably benign |
Het |
Dcaf11 |
T |
A |
14: 55,564,523 |
|
probably null |
Het |
Dnah1 |
G |
T |
14: 31,300,967 |
T1071K |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,458,123 |
M2513L |
probably benign |
Het |
Dqx1 |
A |
G |
6: 83,058,910 |
|
probably benign |
Het |
Gm1587 |
T |
C |
14: 77,798,842 |
E8G |
unknown |
Het |
Hydin |
T |
C |
8: 110,609,966 |
I5125T |
possibly damaging |
Het |
Ighv5-9 |
G |
T |
12: 113,661,943 |
P60Q |
probably damaging |
Het |
Itga7 |
T |
G |
10: 128,953,782 |
L993R |
possibly damaging |
Het |
Itpr3 |
A |
G |
17: 27,098,442 |
N857S |
probably damaging |
Het |
Krt23 |
C |
T |
11: 99,492,664 |
|
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,554,271 |
N3093S |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,505,349 |
F203S |
probably damaging |
Het |
Morn5 |
A |
G |
2: 36,057,076 |
D122G |
probably damaging |
Het |
Mpp2 |
G |
T |
11: 102,063,262 |
L220I |
probably benign |
Het |
Mtmr12 |
T |
C |
15: 12,237,930 |
I165T |
probably damaging |
Het |
Mylk2 |
C |
A |
2: 152,919,157 |
N428K |
probably damaging |
Het |
Nfil3 |
A |
G |
13: 52,968,152 |
Y239H |
probably damaging |
Het |
Notch1 |
A |
G |
2: 26,460,339 |
L2263P |
probably damaging |
Het |
Olfr130 |
T |
A |
17: 38,067,267 |
I32N |
probably damaging |
Het |
Olfr888 |
A |
G |
9: 38,109,129 |
M148V |
probably benign |
Het |
P3h3 |
A |
T |
6: 124,853,092 |
Y387N |
probably damaging |
Het |
Pdcd6ip |
A |
T |
9: 113,680,053 |
Y324* |
probably null |
Het |
Plcb2 |
C |
A |
2: 118,711,363 |
R922L |
probably benign |
Het |
Pml |
T |
C |
9: 58,247,003 |
T196A |
probably benign |
Het |
Ppp2r1b |
C |
A |
9: 50,861,609 |
Q65K |
probably benign |
Het |
Ric8a |
A |
G |
7: 140,862,357 |
T507A |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,416,632 |
|
probably null |
Het |
Slc46a3 |
G |
T |
5: 147,886,234 |
T266N |
probably damaging |
Het |
Smg1 |
A |
G |
7: 118,212,946 |
S41P |
possibly damaging |
Het |
Snrnp200 |
T |
A |
2: 127,237,483 |
N1837K |
probably benign |
Het |
Sptan1 |
A |
G |
2: 30,030,324 |
T2318A |
probably damaging |
Het |
St7l |
C |
T |
3: 104,874,832 |
T175I |
possibly damaging |
Het |
Tmc7 |
G |
A |
7: 118,538,211 |
R703C |
probably damaging |
Het |
Urah |
A |
G |
7: 140,836,886 |
|
probably benign |
Het |
Vmn1r42 |
A |
T |
6: 89,845,314 |
I91N |
probably damaging |
Het |
Yy1 |
T |
A |
12: 108,814,599 |
|
probably benign |
Het |
|