Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
G |
1: 58,102,665 (GRCm39) |
L527R |
probably damaging |
Het |
Ccdc172 |
T |
A |
19: 58,525,723 (GRCm39) |
C194S |
possibly damaging |
Het |
Ccnb1ip1 |
G |
T |
14: 51,031,121 (GRCm39) |
T64K |
possibly damaging |
Het |
Ces1b |
T |
C |
8: 93,806,109 (GRCm39) |
E44G |
probably benign |
Het |
Coro2a |
A |
T |
4: 46,543,421 (GRCm39) |
Y317* |
probably null |
Het |
Csnk1a1 |
T |
C |
18: 61,711,829 (GRCm39) |
F281S |
probably damaging |
Het |
Ddx28 |
A |
T |
8: 106,737,248 (GRCm39) |
|
probably null |
Het |
Dtnbp1 |
A |
G |
13: 45,084,721 (GRCm39) |
|
probably null |
Het |
Eif2s1 |
T |
C |
12: 78,930,126 (GRCm39) |
I258T |
possibly damaging |
Het |
Elp3 |
T |
C |
14: 65,784,488 (GRCm39) |
*554W |
probably null |
Het |
Golga1 |
T |
C |
2: 38,910,118 (GRCm39) |
M610V |
probably damaging |
Het |
Hc |
T |
A |
2: 34,935,906 (GRCm39) |
K156N |
probably benign |
Het |
Hcls1 |
G |
A |
16: 36,782,748 (GRCm39) |
G428D |
probably benign |
Het |
Il16 |
T |
C |
7: 83,371,677 (GRCm39) |
D43G |
probably damaging |
Het |
Klhl3 |
C |
A |
13: 58,242,930 (GRCm39) |
K91N |
probably damaging |
Het |
L3mbtl1 |
C |
T |
2: 162,790,095 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
T |
C |
2: 31,810,544 (GRCm39) |
F805L |
possibly damaging |
Het |
Lipg |
T |
C |
18: 75,081,275 (GRCm39) |
M269V |
probably benign |
Het |
Ly75 |
G |
A |
2: 60,148,720 (GRCm39) |
T1203I |
probably benign |
Het |
Mat1a |
T |
A |
14: 40,827,561 (GRCm39) |
V5E |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,548,866 (GRCm39) |
L5809Q |
probably benign |
Het |
Naip6 |
G |
A |
13: 100,420,266 (GRCm39) |
R1335C |
probably benign |
Het |
Ndufaf3 |
T |
C |
9: 108,443,416 (GRCm39) |
H128R |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,587,464 (GRCm39) |
|
probably null |
Het |
Or8u8 |
T |
A |
2: 86,012,309 (GRCm39) |
I49F |
probably damaging |
Het |
Otop3 |
T |
C |
11: 115,230,673 (GRCm39) |
V148A |
probably damaging |
Het |
Ovgp1 |
T |
C |
3: 105,893,747 (GRCm39) |
|
probably benign |
Het |
Pcsk5 |
T |
G |
19: 17,488,744 (GRCm39) |
R1025S |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,767,405 (GRCm39) |
D1295G |
probably benign |
Het |
Polr1d |
T |
A |
5: 147,015,359 (GRCm39) |
L14* |
probably null |
Het |
Rab26 |
T |
A |
17: 24,748,595 (GRCm39) |
K270* |
probably null |
Het |
Rasgef1c |
T |
A |
11: 49,862,246 (GRCm39) |
N378K |
probably damaging |
Het |
Rpl7a |
T |
C |
2: 26,801,536 (GRCm39) |
V76A |
probably benign |
Het |
Samd9l |
T |
A |
6: 3,377,229 (GRCm39) |
I11F |
possibly damaging |
Het |
Smarca2 |
C |
A |
19: 26,631,777 (GRCm39) |
Q531K |
probably benign |
Het |
Styxl1 |
C |
G |
5: 135,784,350 (GRCm39) |
G211A |
probably benign |
Het |
Tmem198 |
T |
A |
1: 75,457,017 (GRCm39) |
F48I |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,595,073 (GRCm39) |
N12032I |
probably damaging |
Het |
Ubr7 |
T |
A |
12: 102,727,723 (GRCm39) |
C82S |
probably damaging |
Het |
Wwtr1 |
T |
C |
3: 57,483,159 (GRCm39) |
E48G |
possibly damaging |
Het |
Zfp108 |
T |
C |
7: 23,960,819 (GRCm39) |
V470A |
probably damaging |
Het |
Zfp612 |
C |
A |
8: 110,816,181 (GRCm39) |
Q424K |
possibly damaging |
Het |
Zscan4-ps1 |
T |
C |
7: 10,802,761 (GRCm39) |
T13A |
probably benign |
Het |
|
Other mutations in Taar9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00955:Taar9
|
APN |
10 |
23,985,429 (GRCm39) |
missense |
probably benign |
|
IGL02011:Taar9
|
APN |
10 |
23,984,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02883:Taar9
|
APN |
10 |
23,985,378 (GRCm39) |
missense |
probably benign |
0.08 |
R1468:Taar9
|
UTSW |
10 |
23,985,382 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1468:Taar9
|
UTSW |
10 |
23,985,382 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1598:Taar9
|
UTSW |
10 |
23,985,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2072:Taar9
|
UTSW |
10 |
23,984,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R2471:Taar9
|
UTSW |
10 |
23,985,289 (GRCm39) |
missense |
probably benign |
0.00 |
R2519:Taar9
|
UTSW |
10 |
23,985,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Taar9
|
UTSW |
10 |
23,984,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4793:Taar9
|
UTSW |
10 |
23,985,408 (GRCm39) |
missense |
probably benign |
|
R4801:Taar9
|
UTSW |
10 |
23,984,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R4802:Taar9
|
UTSW |
10 |
23,984,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R5457:Taar9
|
UTSW |
10 |
23,985,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R6450:Taar9
|
UTSW |
10 |
23,985,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Taar9
|
UTSW |
10 |
23,984,910 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7179:Taar9
|
UTSW |
10 |
23,984,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7480:Taar9
|
UTSW |
10 |
23,984,843 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8200:Taar9
|
UTSW |
10 |
23,985,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R9311:Taar9
|
UTSW |
10 |
23,985,152 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Taar9
|
UTSW |
10 |
23,984,863 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Taar9
|
UTSW |
10 |
23,985,039 (GRCm39) |
missense |
probably benign |
0.01 |
|