Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambp |
T |
C |
4: 63,067,721 (GRCm39) |
E163G |
probably benign |
Het |
Angptl3 |
A |
T |
4: 98,921,540 (GRCm39) |
K219N |
probably benign |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,255 (GRCm39) |
N86S |
probably benign |
Het |
Cadps |
A |
T |
14: 12,616,158 (GRCm38) |
|
probably null |
Het |
Ccdc146 |
A |
G |
5: 21,502,003 (GRCm39) |
S804P |
possibly damaging |
Het |
Cdc20b |
T |
C |
13: 113,215,233 (GRCm39) |
I267T |
probably damaging |
Het |
Cdh8 |
A |
G |
8: 100,127,350 (GRCm39) |
|
probably benign |
Het |
Dse |
G |
T |
10: 34,028,470 (GRCm39) |
N873K |
probably benign |
Het |
Ehd1 |
G |
T |
19: 6,327,044 (GRCm39) |
E14* |
probably null |
Het |
F8 |
A |
G |
X: 74,311,030 (GRCm39) |
|
probably benign |
Het |
Flnb |
T |
C |
14: 7,942,057 (GRCm38) |
V2345A |
probably damaging |
Het |
Fndc1 |
T |
C |
17: 7,969,189 (GRCm39) |
K1559E |
probably damaging |
Het |
Ighg1 |
T |
C |
12: 113,293,180 (GRCm39) |
E170G |
probably damaging |
Het |
Kmt2b |
G |
T |
7: 30,276,117 (GRCm39) |
P1794Q |
probably damaging |
Het |
Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
Med25 |
C |
A |
7: 44,535,314 (GRCm39) |
R37L |
possibly damaging |
Het |
Optc |
T |
C |
1: 133,825,617 (GRCm39) |
D303G |
probably damaging |
Het |
Or2n1d |
A |
G |
17: 38,646,323 (GRCm39) |
I92V |
probably damaging |
Het |
Or2n1e |
G |
A |
17: 38,586,421 (GRCm39) |
G253D |
probably damaging |
Het |
Or4c102 |
T |
A |
2: 88,422,448 (GRCm39) |
F100Y |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,767,478 (GRCm39) |
N1271D |
probably benign |
Het |
Plpp2 |
A |
T |
10: 79,363,647 (GRCm39) |
|
probably null |
Het |
Polq |
A |
T |
16: 36,882,699 (GRCm39) |
N1342I |
probably damaging |
Het |
Prr16 |
A |
G |
18: 51,436,195 (GRCm39) |
N225D |
probably benign |
Het |
Pwwp2a |
C |
T |
11: 43,597,015 (GRCm39) |
Q452* |
probably null |
Het |
Slfn2 |
A |
T |
11: 82,960,390 (GRCm39) |
H123L |
probably benign |
Het |
Sort1 |
T |
A |
3: 108,245,123 (GRCm39) |
I325N |
probably damaging |
Het |
Tmem132e |
A |
G |
11: 82,335,156 (GRCm39) |
Y654C |
probably damaging |
Het |
Tmprss11b |
A |
T |
5: 86,815,443 (GRCm39) |
Y48* |
probably null |
Het |
Tpp2 |
T |
C |
1: 43,979,304 (GRCm39) |
I67T |
probably damaging |
Het |
Trdn |
G |
A |
10: 33,344,191 (GRCm39) |
|
probably null |
Het |
Trim14 |
C |
T |
4: 46,523,739 (GRCm39) |
V100I |
possibly damaging |
Het |
Trim17 |
T |
C |
11: 58,856,059 (GRCm39) |
C39R |
probably damaging |
Het |
Unc13b |
T |
C |
4: 43,097,028 (GRCm39) |
|
probably benign |
Het |
Vmn2r94 |
G |
A |
17: 18,478,650 (GRCm39) |
|
probably benign |
Het |
Vsig4 |
A |
G |
X: 95,334,422 (GRCm39) |
V29A |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,405,866 (GRCm39) |
I454N |
probably benign |
Het |
Wnk3 |
T |
A |
X: 150,069,300 (GRCm39) |
F886I |
probably benign |
Het |
Ylpm1 |
T |
C |
12: 85,096,644 (GRCm39) |
|
probably null |
Het |
Zfp507 |
A |
T |
7: 35,487,195 (GRCm39) |
Y234N |
probably damaging |
Het |
|
Other mutations in Trim52 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01754:Trim52
|
APN |
14 |
106,344,623 (GRCm39) |
nonsense |
probably null |
|
IGL02285:Trim52
|
APN |
14 |
106,344,702 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Trim52
|
UTSW |
14 |
106,344,732 (GRCm39) |
missense |
probably benign |
0.36 |
R0453:Trim52
|
UTSW |
14 |
106,344,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Trim52
|
UTSW |
14 |
106,344,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R0963:Trim52
|
UTSW |
14 |
106,344,973 (GRCm39) |
missense |
probably benign |
0.01 |
R1823:Trim52
|
UTSW |
14 |
106,344,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Trim52
|
UTSW |
14 |
106,344,932 (GRCm39) |
missense |
probably benign |
0.13 |
R5878:Trim52
|
UTSW |
14 |
106,344,375 (GRCm39) |
missense |
probably damaging |
0.98 |
R6565:Trim52
|
UTSW |
14 |
106,344,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6603:Trim52
|
UTSW |
14 |
106,344,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Trim52
|
UTSW |
14 |
106,344,986 (GRCm39) |
missense |
possibly damaging |
0.68 |
|