Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
A |
T |
6: 146,854,606 (GRCm39) |
F145L |
probably benign |
Het |
Abcc9 |
T |
C |
6: 142,551,645 (GRCm39) |
D1221G |
possibly damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,584,864 (GRCm39) |
K935E |
probably benign |
Het |
Ago4 |
A |
T |
4: 126,409,655 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,130,575 (GRCm39) |
D421G |
probably benign |
Het |
Armh4 |
T |
A |
14: 50,011,444 (GRCm39) |
M88L |
probably benign |
Het |
B4galt7 |
C |
A |
13: 55,756,152 (GRCm39) |
|
probably null |
Het |
Bltp3b |
A |
G |
10: 89,651,917 (GRCm39) |
N247S |
probably benign |
Het |
C8g |
A |
T |
2: 25,389,425 (GRCm39) |
S147T |
probably damaging |
Het |
Clstn3 |
A |
T |
6: 124,426,792 (GRCm39) |
Y510N |
possibly damaging |
Het |
Cnot2 |
A |
G |
10: 116,373,301 (GRCm39) |
V34A |
possibly damaging |
Het |
Cyb5d2 |
A |
T |
11: 72,686,606 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,421,144 (GRCm39) |
I3827T |
probably damaging |
Het |
Dnah7a |
G |
T |
1: 53,464,376 (GRCm39) |
Q3672K |
probably benign |
Het |
Dock1 |
A |
T |
7: 134,717,021 (GRCm39) |
Y1219F |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,478,518 (GRCm39) |
E2521D |
probably benign |
Het |
Gm10719 |
G |
T |
9: 3,019,043 (GRCm39) |
W96L |
probably damaging |
Het |
H2-M2 |
G |
A |
17: 37,792,399 (GRCm39) |
H291Y |
probably damaging |
Het |
Hmgcl |
T |
C |
4: 135,686,035 (GRCm39) |
Y167H |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,502,400 (GRCm39) |
D73V |
possibly damaging |
Het |
Incenp |
A |
T |
19: 9,861,142 (GRCm39) |
M480K |
unknown |
Het |
Irag1 |
G |
T |
7: 110,522,984 (GRCm39) |
A359D |
probably benign |
Het |
Kdm6a |
A |
G |
X: 18,117,114 (GRCm39) |
T266A |
probably benign |
Het |
Lipf |
A |
G |
19: 33,942,965 (GRCm39) |
N91S |
probably benign |
Het |
M1ap |
A |
T |
6: 82,980,756 (GRCm39) |
N214I |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,838 (GRCm39) |
V969A |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,057,005 (GRCm39) |
C826R |
probably damaging |
Het |
Msx1 |
C |
A |
5: 37,981,365 (GRCm39) |
A105S |
probably benign |
Het |
Or5ac23 |
A |
C |
16: 59,149,243 (GRCm39) |
S210A |
probably benign |
Het |
Otogl |
A |
T |
10: 107,626,510 (GRCm39) |
D1451E |
probably benign |
Het |
Otop2 |
G |
A |
11: 115,220,201 (GRCm39) |
G347D |
probably damaging |
Het |
Ppp1r13l |
A |
T |
7: 19,103,978 (GRCm39) |
H153L |
probably benign |
Het |
Pramel21 |
A |
G |
4: 143,342,559 (GRCm39) |
D222G |
possibly damaging |
Het |
Pramel29 |
T |
C |
4: 143,935,265 (GRCm39) |
K161E |
possibly damaging |
Het |
Proz |
A |
G |
8: 13,114,621 (GRCm39) |
Y85C |
probably damaging |
Het |
Prss50 |
A |
G |
9: 110,687,480 (GRCm39) |
D141G |
probably benign |
Het |
Rad54l2 |
T |
A |
9: 106,597,613 (GRCm39) |
Q131L |
probably benign |
Het |
Sdha |
A |
G |
13: 74,472,077 (GRCm39) |
|
probably benign |
Het |
Sema3d |
T |
A |
5: 12,635,091 (GRCm39) |
I719N |
probably benign |
Het |
Slc18b1 |
A |
T |
10: 23,681,879 (GRCm39) |
I148L |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,330,852 (GRCm39) |
D2086Y |
probably damaging |
Het |
Tchh |
T |
C |
3: 93,354,298 (GRCm39) |
L1246P |
unknown |
Het |
Tmprss11d |
T |
C |
5: 86,457,177 (GRCm39) |
I161V |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,725,172 (GRCm39) |
D268G |
probably damaging |
Het |
Trpm8 |
G |
A |
1: 88,289,727 (GRCm39) |
R895H |
probably damaging |
Het |
Txndc2 |
A |
G |
17: 65,945,079 (GRCm39) |
I366T |
possibly damaging |
Het |
Ugt2a3 |
T |
C |
5: 87,484,725 (GRCm39) |
I100V |
probably benign |
Het |
Upp1 |
C |
A |
11: 9,081,709 (GRCm39) |
P82Q |
probably damaging |
Het |
Vim |
A |
G |
2: 13,584,827 (GRCm39) |
|
probably null |
Het |
Vmn2r12 |
A |
T |
5: 109,240,058 (GRCm39) |
N168K |
possibly damaging |
Het |
Zdhhc14 |
G |
T |
17: 5,802,983 (GRCm39) |
C362F |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,863 (GRCm39) |
V727A |
probably damaging |
Het |
Zswim5 |
G |
A |
4: 116,735,177 (GRCm39) |
G174D |
unknown |
Het |
|
Other mutations in Atl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02135:Atl2
|
APN |
17 |
80,167,214 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02692:Atl2
|
APN |
17 |
80,172,482 (GRCm39) |
missense |
probably benign |
|
IGL03127:Atl2
|
APN |
17 |
80,160,283 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03377:Atl2
|
APN |
17 |
80,172,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Atl2
|
UTSW |
17 |
80,161,260 (GRCm39) |
unclassified |
probably benign |
|
R1203:Atl2
|
UTSW |
17 |
80,160,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R1489:Atl2
|
UTSW |
17 |
80,160,135 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Atl2
|
UTSW |
17 |
80,172,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R1977:Atl2
|
UTSW |
17 |
80,160,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2032:Atl2
|
UTSW |
17 |
80,203,373 (GRCm39) |
missense |
probably benign |
|
R5104:Atl2
|
UTSW |
17 |
80,160,046 (GRCm39) |
missense |
probably benign |
0.01 |
R5201:Atl2
|
UTSW |
17 |
80,172,580 (GRCm39) |
missense |
probably benign |
|
R5362:Atl2
|
UTSW |
17 |
80,168,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Atl2
|
UTSW |
17 |
80,160,229 (GRCm39) |
missense |
probably benign |
0.03 |
R6128:Atl2
|
UTSW |
17 |
80,172,470 (GRCm39) |
critical splice donor site |
probably null |
|
R6369:Atl2
|
UTSW |
17 |
80,161,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R6416:Atl2
|
UTSW |
17 |
80,157,652 (GRCm39) |
missense |
probably benign |
0.00 |
R6597:Atl2
|
UTSW |
17 |
80,160,195 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6885:Atl2
|
UTSW |
17 |
80,159,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Atl2
|
UTSW |
17 |
80,183,227 (GRCm39) |
splice site |
probably null |
|
R7587:Atl2
|
UTSW |
17 |
80,172,496 (GRCm39) |
missense |
probably benign |
0.25 |
R7646:Atl2
|
UTSW |
17 |
80,162,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Atl2
|
UTSW |
17 |
80,167,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Atl2
|
UTSW |
17 |
80,167,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R8170:Atl2
|
UTSW |
17 |
80,163,690 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8313:Atl2
|
UTSW |
17 |
80,160,033 (GRCm39) |
nonsense |
probably null |
|
R8878:Atl2
|
UTSW |
17 |
80,160,232 (GRCm39) |
missense |
probably benign |
0.05 |
R8899:Atl2
|
UTSW |
17 |
80,183,469 (GRCm39) |
missense |
probably benign |
0.01 |
R9335:Atl2
|
UTSW |
17 |
80,160,207 (GRCm39) |
missense |
probably benign |
0.00 |
X0052:Atl2
|
UTSW |
17 |
80,160,046 (GRCm39) |
missense |
possibly damaging |
0.94 |
|