Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
G |
T |
11: 94,357,318 |
T1152K |
possibly damaging |
Het |
Acpp |
T |
A |
9: 104,324,174 |
T82S |
probably damaging |
Het |
Adam23 |
C |
T |
1: 63,547,814 |
P445S |
probably benign |
Het |
Ap3b1 |
T |
A |
13: 94,446,143 |
|
probably benign |
Het |
Artn |
A |
G |
4: 117,926,861 |
V136A |
probably damaging |
Het |
Ash1l |
A |
G |
3: 89,058,499 |
T2403A |
probably damaging |
Het |
Bbof1 |
G |
T |
12: 84,423,499 |
V120L |
probably damaging |
Het |
Boc |
A |
G |
16: 44,503,565 |
Y158H |
probably damaging |
Het |
Casp8 |
A |
G |
1: 58,824,196 |
E105G |
probably damaging |
Het |
Cers4 |
T |
C |
8: 4,520,557 |
F206L |
probably benign |
Het |
Chrna9 |
A |
G |
5: 65,969,136 |
T78A |
probably benign |
Het |
Creb3 |
A |
T |
4: 43,566,193 |
T263S |
possibly damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,777,999 |
V384A |
probably damaging |
Het |
Dip2b |
G |
A |
15: 100,183,113 |
V879M |
probably damaging |
Het |
Dnah17 |
C |
A |
11: 118,125,387 |
V14F |
possibly damaging |
Het |
Epb41l4b |
T |
A |
4: 57,088,824 |
K144N |
probably damaging |
Het |
Ercc6 |
A |
T |
14: 32,569,864 |
I1062F |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,312,387 |
T57I |
probably benign |
Het |
Fam160b1 |
A |
G |
19: 57,368,575 |
I33V |
probably benign |
Het |
Fat2 |
C |
A |
11: 55,284,264 |
E1874D |
probably benign |
Het |
Fbxw21 |
T |
A |
9: 109,148,189 |
I151F |
probably damaging |
Het |
Foxn1 |
A |
G |
11: 78,365,935 |
|
probably benign |
Het |
Gm1966 |
C |
T |
7: 106,601,581 |
D819N |
probably benign |
Het |
Gpr63 |
G |
A |
4: 25,008,227 |
R317H |
probably damaging |
Het |
Grip1 |
C |
A |
10: 119,978,451 |
H296N |
probably damaging |
Het |
Gtdc1 |
A |
T |
2: 44,575,494 |
M288K |
possibly damaging |
Het |
Guf1 |
T |
A |
5: 69,567,166 |
D488E |
possibly damaging |
Het |
Heatr5b |
C |
A |
17: 78,753,147 |
R2033L |
probably damaging |
Het |
Hsd17b2 |
T |
A |
8: 117,702,265 |
|
probably null |
Het |
Ino80 |
A |
T |
2: 119,425,265 |
L913* |
probably null |
Het |
Inppl1 |
A |
C |
7: 101,823,967 |
S1159A |
probably benign |
Het |
Kcnk7 |
G |
A |
19: 5,706,112 |
C122Y |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,536,505 |
|
probably benign |
Het |
Muc4 |
A |
T |
16: 32,752,233 |
S704C |
possibly damaging |
Het |
Nckap5 |
A |
T |
1: 126,025,913 |
C967* |
probably null |
Het |
Nek10 |
T |
C |
14: 14,999,078 |
|
probably benign |
Het |
Oas1h |
A |
T |
5: 120,871,888 |
D342V |
possibly damaging |
Het |
Olfr134 |
A |
T |
17: 38,175,200 |
M39L |
probably benign |
Het |
Olfr320 |
T |
A |
11: 58,684,188 |
L105Q |
probably benign |
Het |
Olfr418 |
A |
G |
1: 173,270,769 |
N198S |
probably benign |
Het |
Olfr734 |
A |
G |
14: 50,320,484 |
V117A |
probably benign |
Het |
Olfr904 |
T |
C |
9: 38,464,143 |
M34T |
probably benign |
Het |
Prex1 |
A |
T |
2: 166,587,081 |
V694E |
probably damaging |
Het |
Rad50 |
G |
A |
11: 53,679,485 |
A810V |
probably damaging |
Het |
Rcor1 |
T |
C |
12: 111,109,837 |
S410P |
probably damaging |
Het |
Rps14 |
A |
T |
18: 60,776,479 |
N26I |
probably benign |
Het |
Slc38a1 |
T |
C |
15: 96,585,550 |
D299G |
probably benign |
Het |
Slc5a1 |
T |
A |
5: 33,154,708 |
N481K |
possibly damaging |
Het |
Slco3a1 |
A |
T |
7: 74,359,935 |
|
probably null |
Het |
Speg |
A |
G |
1: 75,417,663 |
T1701A |
probably benign |
Het |
Spg20 |
T |
C |
3: 55,117,571 |
S196P |
probably damaging |
Het |
Sugt1 |
A |
G |
14: 79,624,925 |
N271S |
probably benign |
Het |
Tbx15 |
A |
T |
3: 99,351,912 |
L366F |
possibly damaging |
Het |
Tnc |
G |
A |
4: 64,007,684 |
T953I |
possibly damaging |
Het |
Uqcc1 |
A |
G |
2: 155,911,818 |
S46P |
probably damaging |
Het |
Vmn2r18 |
T |
C |
5: 151,575,634 |
|
probably null |
Het |
Vmn2r7 |
T |
A |
3: 64,707,079 |
Y438F |
probably benign |
Het |
Vps52 |
T |
C |
17: 33,957,894 |
L74P |
probably damaging |
Het |
Xpo5 |
G |
T |
17: 46,227,888 |
M673I |
probably benign |
Het |
Zscan18 |
A |
G |
7: 12,774,202 |
V457A |
probably damaging |
Het |
|