Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
A |
17: 24,519,294 (GRCm39) |
I664F |
probably damaging |
Het |
Abcg4 |
A |
T |
9: 44,192,920 (GRCm39) |
M142K |
probably benign |
Het |
Afdn |
A |
G |
17: 14,104,890 (GRCm39) |
T1198A |
probably damaging |
Het |
Angptl2 |
T |
C |
2: 33,136,239 (GRCm39) |
S475P |
probably damaging |
Het |
Ap3s2 |
T |
C |
7: 79,565,824 (GRCm39) |
E34G |
probably benign |
Het |
C1qtnf9 |
T |
C |
14: 61,017,442 (GRCm39) |
F324S |
probably damaging |
Het |
Cacng7 |
A |
G |
7: 3,414,547 (GRCm39) |
Y170C |
probably damaging |
Het |
Ceacam18 |
G |
A |
7: 43,286,435 (GRCm39) |
V103M |
possibly damaging |
Het |
Chrnb1 |
G |
A |
11: 69,684,742 (GRCm39) |
P144S |
probably damaging |
Het |
Chuk |
T |
C |
19: 44,066,751 (GRCm39) |
H652R |
probably damaging |
Het |
Ckap5 |
C |
T |
2: 91,450,170 (GRCm39) |
L1948F |
probably damaging |
Het |
Clstn1 |
A |
T |
4: 149,722,769 (GRCm39) |
H469L |
probably benign |
Het |
Csf2rb2 |
C |
T |
15: 78,169,047 (GRCm39) |
G594S |
possibly damaging |
Het |
Ctsq |
A |
T |
13: 61,184,941 (GRCm39) |
D248E |
probably benign |
Het |
Ep400 |
A |
T |
5: 110,903,771 (GRCm39) |
I276K |
possibly damaging |
Het |
Gbf1 |
G |
A |
19: 46,272,688 (GRCm39) |
|
probably null |
Het |
Gldn |
T |
A |
9: 54,245,748 (GRCm39) |
I433N |
probably damaging |
Het |
Gm136 |
T |
A |
4: 34,752,322 (GRCm39) |
E69V |
probably damaging |
Het |
Gm28177 |
T |
C |
1: 52,121,738 (GRCm39) |
|
probably null |
Het |
Gtf2h2 |
A |
G |
13: 100,617,506 (GRCm39) |
|
probably benign |
Het |
Ints12 |
T |
C |
3: 132,806,570 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
T |
C |
7: 27,026,158 (GRCm39) |
D615G |
probably damaging |
Het |
Mgme1 |
C |
T |
2: 144,113,909 (GRCm39) |
P4S |
probably benign |
Het |
Nae1 |
A |
G |
8: 105,252,910 (GRCm39) |
|
probably null |
Het |
Nup133 |
G |
A |
8: 124,636,733 (GRCm39) |
A956V |
probably damaging |
Het |
Oacyl |
T |
A |
18: 65,882,711 (GRCm39) |
M529K |
possibly damaging |
Het |
Osbpl1a |
T |
A |
18: 12,890,683 (GRCm39) |
E519V |
possibly damaging |
Het |
Pacs1 |
A |
T |
19: 5,203,726 (GRCm39) |
V333E |
probably damaging |
Het |
Pik3c3 |
T |
G |
18: 30,436,131 (GRCm39) |
|
probably benign |
Het |
Polh |
C |
T |
17: 46,483,169 (GRCm39) |
|
probably benign |
Het |
Ppp6r3 |
A |
G |
19: 3,540,826 (GRCm39) |
C431R |
probably damaging |
Het |
Pprc1 |
T |
C |
19: 46,051,087 (GRCm39) |
S206P |
possibly damaging |
Het |
Rab20 |
A |
G |
8: 11,504,212 (GRCm39) |
Y163H |
probably benign |
Het |
Sde2 |
T |
A |
1: 180,683,383 (GRCm39) |
C46S |
possibly damaging |
Het |
Serpinb1c |
T |
C |
13: 33,067,958 (GRCm39) |
K213E |
probably damaging |
Het |
Tnnt1 |
A |
C |
7: 4,510,549 (GRCm39) |
M224R |
possibly damaging |
Het |
Trank1 |
T |
C |
9: 111,178,358 (GRCm39) |
F349L |
possibly damaging |
Het |
Ttf1 |
T |
C |
2: 28,963,895 (GRCm39) |
|
probably benign |
Het |
Usp54 |
T |
A |
14: 20,623,905 (GRCm39) |
S651C |
probably damaging |
Het |
Vps45 |
A |
G |
3: 95,907,378 (GRCm39) |
*571R |
probably null |
Het |
Yod1 |
G |
A |
1: 130,646,870 (GRCm39) |
G249E |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,997,428 (GRCm39) |
Y340C |
probably damaging |
Het |
Zfp366 |
G |
A |
13: 99,383,080 (GRCm39) |
|
probably benign |
Het |
Zfp648 |
T |
A |
1: 154,079,935 (GRCm39) |
D31E |
possibly damaging |
Het |
|
Other mutations in Spata20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Spata20
|
APN |
11 |
94,374,221 (GRCm39) |
missense |
probably benign |
|
IGL02008:Spata20
|
APN |
11 |
94,374,289 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Spata20
|
UTSW |
11 |
94,375,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Spata20
|
UTSW |
11 |
94,371,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Spata20
|
UTSW |
11 |
94,372,472 (GRCm39) |
missense |
probably benign |
|
R0557:Spata20
|
UTSW |
11 |
94,376,048 (GRCm39) |
missense |
probably benign |
0.00 |
R0657:Spata20
|
UTSW |
11 |
94,371,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Spata20
|
UTSW |
11 |
94,371,340 (GRCm39) |
missense |
probably benign |
|
R2166:Spata20
|
UTSW |
11 |
94,369,930 (GRCm39) |
missense |
probably benign |
0.25 |
R4298:Spata20
|
UTSW |
11 |
94,373,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R4740:Spata20
|
UTSW |
11 |
94,375,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4791:Spata20
|
UTSW |
11 |
94,375,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R4980:Spata20
|
UTSW |
11 |
94,375,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Spata20
|
UTSW |
11 |
94,374,444 (GRCm39) |
missense |
probably damaging |
0.98 |
R6373:Spata20
|
UTSW |
11 |
94,374,226 (GRCm39) |
missense |
probably benign |
|
R7400:Spata20
|
UTSW |
11 |
94,374,226 (GRCm39) |
missense |
probably benign |
|
R7439:Spata20
|
UTSW |
11 |
94,374,867 (GRCm39) |
missense |
probably benign |
0.02 |
R7441:Spata20
|
UTSW |
11 |
94,374,867 (GRCm39) |
missense |
probably benign |
0.02 |
R7562:Spata20
|
UTSW |
11 |
94,373,379 (GRCm39) |
missense |
probably benign |
0.31 |
R7974:Spata20
|
UTSW |
11 |
94,374,966 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8036:Spata20
|
UTSW |
11 |
94,369,963 (GRCm39) |
missense |
probably benign |
0.17 |
R8060:Spata20
|
UTSW |
11 |
94,373,065 (GRCm39) |
missense |
probably benign |
|
R8335:Spata20
|
UTSW |
11 |
94,373,369 (GRCm39) |
missense |
probably benign |
0.05 |
R8447:Spata20
|
UTSW |
11 |
94,373,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Spata20
|
UTSW |
11 |
94,372,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Spata20
|
UTSW |
11 |
94,374,444 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Spata20
|
UTSW |
11 |
94,371,361 (GRCm39) |
missense |
probably benign |
0.45 |
Z1177:Spata20
|
UTSW |
11 |
94,373,965 (GRCm39) |
missense |
probably benign |
0.00 |
|