Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
C |
T |
13: 41,981,735 (GRCm39) |
V13I |
probably damaging |
Het |
Ak2 |
A |
G |
4: 128,902,013 (GRCm39) |
K229E |
probably benign |
Het |
Atp13a4 |
A |
T |
16: 29,241,502 (GRCm39) |
V741D |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,197,697 (GRCm39) |
M896K |
probably benign |
Het |
Ccser1 |
C |
T |
6: 61,288,547 (GRCm39) |
R237C |
probably benign |
Het |
Cdk7 |
A |
G |
13: 100,859,182 (GRCm39) |
|
probably benign |
Het |
CK137956 |
A |
G |
4: 127,845,180 (GRCm39) |
S188P |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dbndd2 |
A |
G |
2: 164,330,563 (GRCm39) |
D72G |
probably damaging |
Het |
Disp3 |
A |
T |
4: 148,344,423 (GRCm39) |
I493N |
probably damaging |
Het |
Dnaaf10 |
A |
T |
11: 17,179,832 (GRCm39) |
T278S |
probably benign |
Het |
Fbxw5 |
G |
T |
2: 25,394,810 (GRCm39) |
V235L |
probably damaging |
Het |
Fmo4 |
T |
A |
1: 162,621,741 (GRCm39) |
D490V |
probably damaging |
Het |
Fuca2 |
A |
G |
10: 13,382,518 (GRCm39) |
Y268C |
probably damaging |
Het |
Gm4787 |
C |
T |
12: 81,425,544 (GRCm39) |
V205I |
probably damaging |
Het |
Gpat3 |
G |
A |
5: 101,045,687 (GRCm39) |
R437K |
probably benign |
Het |
Herc2 |
A |
G |
7: 55,834,121 (GRCm39) |
S3109G |
probably damaging |
Het |
Hr |
G |
A |
14: 70,808,888 (GRCm39) |
R1117H |
probably damaging |
Het |
Htra4 |
T |
A |
8: 25,523,593 (GRCm39) |
D324V |
probably damaging |
Het |
Kcnd3 |
A |
G |
3: 105,366,853 (GRCm39) |
Y241C |
probably damaging |
Het |
Kcp |
G |
A |
6: 29,489,071 (GRCm39) |
L1072F |
probably damaging |
Het |
Lrrc52 |
T |
C |
1: 167,294,028 (GRCm39) |
N86D |
probably benign |
Het |
Mindy4 |
A |
G |
6: 55,188,247 (GRCm39) |
T26A |
probably damaging |
Het |
Mre11a |
A |
T |
9: 14,707,101 (GRCm39) |
N117Y |
probably damaging |
Het |
Mrgprb1 |
A |
T |
7: 48,097,076 (GRCm39) |
S279T |
possibly damaging |
Het |
Myh13 |
T |
G |
11: 67,241,064 (GRCm39) |
S814A |
probably benign |
Het |
Ncapd2 |
A |
G |
6: 125,153,678 (GRCm39) |
V679A |
possibly damaging |
Het |
Nipbl |
A |
T |
15: 8,379,771 (GRCm39) |
V1007D |
probably damaging |
Het |
Nlrp12 |
T |
A |
7: 3,277,049 (GRCm39) |
H960L |
probably damaging |
Het |
Or3a1c |
T |
A |
11: 74,046,769 (GRCm39) |
M263K |
possibly damaging |
Het |
Or4a72 |
C |
T |
2: 89,405,558 (GRCm39) |
V171I |
probably benign |
Het |
Or7e169 |
A |
G |
9: 19,757,709 (GRCm39) |
S69P |
probably benign |
Het |
Pklr |
A |
G |
3: 89,050,545 (GRCm39) |
Y402C |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,859,334 (GRCm39) |
T1319A |
possibly damaging |
Het |
Rif1 |
T |
A |
2: 51,982,358 (GRCm39) |
V541E |
probably damaging |
Het |
Ryk |
T |
A |
9: 102,758,855 (GRCm39) |
I248N |
possibly damaging |
Het |
Shisa2 |
A |
T |
14: 59,867,134 (GRCm39) |
I129F |
probably damaging |
Het |
Snap25 |
T |
G |
2: 136,611,973 (GRCm39) |
|
probably benign |
Het |
Snx31 |
G |
A |
15: 36,525,848 (GRCm39) |
P284S |
probably benign |
Het |
Spata31g1 |
C |
T |
4: 42,974,131 (GRCm39) |
Q1155* |
probably null |
Het |
Tas2r140 |
A |
G |
6: 40,469,154 (GRCm39) |
K328R |
possibly damaging |
Het |
Tas2r140 |
T |
C |
6: 133,032,213 (GRCm39) |
T182A |
probably benign |
Het |
Thumpd2 |
G |
A |
17: 81,372,387 (GRCm39) |
R35C |
probably damaging |
Het |
Tnxb |
A |
T |
17: 34,937,443 (GRCm39) |
N3811Y |
probably damaging |
Het |
Tpte |
A |
C |
8: 22,835,901 (GRCm39) |
N428T |
probably damaging |
Het |
Trpm6 |
A |
G |
19: 18,831,629 (GRCm39) |
D1498G |
probably benign |
Het |
Tsc2 |
C |
T |
17: 24,842,444 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,703,277 (GRCm39) |
|
probably benign |
Het |
Wdr24 |
A |
G |
17: 26,045,017 (GRCm39) |
I251V |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 128,848,006 (GRCm39) |
Y278H |
probably damaging |
Het |
Zfat |
A |
G |
15: 67,990,783 (GRCm39) |
|
probably null |
Het |
Zfp442 |
A |
T |
2: 150,250,042 (GRCm39) |
V620E |
possibly damaging |
Het |
Zfp788 |
A |
G |
7: 41,298,984 (GRCm39) |
H540R |
probably damaging |
Het |
|
Other mutations in Epx |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00543:Epx
|
APN |
11 |
87,760,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Epx
|
APN |
11 |
87,760,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02096:Epx
|
APN |
11 |
87,760,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02423:Epx
|
APN |
11 |
87,762,144 (GRCm39) |
missense |
possibly damaging |
0.85 |
K7371:Epx
|
UTSW |
11 |
87,755,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Epx
|
UTSW |
11 |
87,760,129 (GRCm39) |
missense |
probably benign |
0.05 |
R1607:Epx
|
UTSW |
11 |
87,759,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R2017:Epx
|
UTSW |
11 |
87,765,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R3838:Epx
|
UTSW |
11 |
87,765,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R4417:Epx
|
UTSW |
11 |
87,760,256 (GRCm39) |
nonsense |
probably null |
|
R5083:Epx
|
UTSW |
11 |
87,763,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R5712:Epx
|
UTSW |
11 |
87,765,679 (GRCm39) |
nonsense |
probably null |
|
R5935:Epx
|
UTSW |
11 |
87,756,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Epx
|
UTSW |
11 |
87,759,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Epx
|
UTSW |
11 |
87,760,781 (GRCm39) |
nonsense |
probably null |
|
R6984:Epx
|
UTSW |
11 |
87,759,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R7031:Epx
|
UTSW |
11 |
87,766,349 (GRCm39) |
start gained |
probably benign |
|
R7652:Epx
|
UTSW |
11 |
87,766,160 (GRCm39) |
critical splice donor site |
probably null |
|
R7667:Epx
|
UTSW |
11 |
87,765,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R7969:Epx
|
UTSW |
11 |
87,763,547 (GRCm39) |
missense |
probably benign |
0.01 |
R8313:Epx
|
UTSW |
11 |
87,763,557 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8559:Epx
|
UTSW |
11 |
87,755,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R9030:Epx
|
UTSW |
11 |
87,763,470 (GRCm39) |
missense |
probably benign |
|
R9629:Epx
|
UTSW |
11 |
87,755,651 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Epx
|
UTSW |
11 |
87,756,301 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Epx
|
UTSW |
11 |
87,763,593 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Epx
|
UTSW |
11 |
87,760,720 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1177:Epx
|
UTSW |
11 |
87,760,087 (GRCm39) |
missense |
probably damaging |
1.00 |
|