Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco2 |
G |
A |
15: 81,779,486 (GRCm39) |
A97T |
probably damaging |
Het |
Adat1 |
T |
C |
8: 112,705,994 (GRCm39) |
S371G |
probably benign |
Het |
Aoc3 |
T |
G |
11: 101,222,871 (GRCm39) |
I369R |
possibly damaging |
Het |
Apobr |
A |
T |
7: 126,186,694 (GRCm39) |
|
probably null |
Het |
Arhgap12 |
A |
T |
18: 6,111,774 (GRCm39) |
C69S |
probably damaging |
Het |
Astn2 |
A |
G |
4: 66,037,300 (GRCm39) |
|
probably benign |
Het |
Bcas1 |
T |
C |
2: 170,248,741 (GRCm39) |
D60G |
probably damaging |
Het |
Cacnb4 |
T |
A |
2: 52,367,783 (GRCm39) |
D62V |
probably damaging |
Het |
Cbx8 |
C |
A |
11: 118,931,618 (GRCm39) |
R20L |
probably damaging |
Het |
Ccdc92 |
G |
A |
5: 124,913,337 (GRCm39) |
T64M |
probably benign |
Het |
Cps1 |
G |
T |
1: 67,244,358 (GRCm39) |
S1135I |
probably null |
Het |
Eml2 |
G |
A |
7: 18,913,275 (GRCm39) |
R91H |
probably damaging |
Het |
Fbxl3 |
G |
A |
14: 103,320,313 (GRCm39) |
P426L |
probably damaging |
Het |
Fhod3 |
T |
A |
18: 25,243,296 (GRCm39) |
|
probably null |
Het |
Gabrb2 |
T |
C |
11: 42,488,521 (GRCm39) |
I329T |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,898,156 (GRCm39) |
D745E |
possibly damaging |
Het |
Itprid2 |
T |
A |
2: 79,488,164 (GRCm39) |
V749E |
probably damaging |
Het |
Lacc1 |
T |
A |
14: 77,271,470 (GRCm39) |
N239I |
probably damaging |
Het |
Lamb2 |
T |
A |
9: 108,363,997 (GRCm39) |
C1008S |
probably damaging |
Het |
Man2b1 |
G |
A |
8: 85,817,565 (GRCm39) |
V349I |
probably benign |
Het |
Mib1 |
A |
G |
18: 10,811,985 (GRCm39) |
T961A |
possibly damaging |
Het |
Mmp24 |
A |
G |
2: 155,655,908 (GRCm39) |
I449V |
possibly damaging |
Het |
Myo7b |
A |
G |
18: 32,147,282 (GRCm39) |
I87T |
probably benign |
Het |
Or13c7b |
A |
G |
4: 43,821,175 (GRCm39) |
F62S |
probably damaging |
Het |
Or5p72 |
T |
A |
7: 108,022,122 (GRCm39) |
C115S |
probably benign |
Het |
Pgr |
A |
G |
9: 8,958,420 (GRCm39) |
E809G |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,518,517 (GRCm39) |
S1091T |
probably benign |
Het |
Rab44 |
G |
A |
17: 29,358,871 (GRCm39) |
R353K |
probably benign |
Het |
Reck |
G |
A |
4: 43,891,001 (GRCm39) |
M46I |
probably benign |
Het |
Rorb |
G |
T |
19: 18,954,992 (GRCm39) |
S208Y |
possibly damaging |
Het |
Serinc2 |
G |
T |
4: 130,147,847 (GRCm39) |
T410N |
possibly damaging |
Het |
Slc23a2 |
G |
A |
2: 131,898,702 (GRCm39) |
R612* |
probably null |
Het |
Slx4 |
T |
C |
16: 3,812,773 (GRCm39) |
E145G |
probably damaging |
Het |
Spag16 |
A |
G |
1: 70,532,989 (GRCm39) |
D556G |
probably damaging |
Het |
Spopl |
C |
T |
2: 23,407,957 (GRCm39) |
V241M |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,149,293 (GRCm39) |
F485I |
probably benign |
Het |
Trmo |
C |
T |
4: 46,382,140 (GRCm39) |
V326M |
probably damaging |
Het |
Tssk5 |
T |
C |
15: 76,256,411 (GRCm39) |
D336G |
probably damaging |
Het |
Ttyh2 |
A |
T |
11: 114,601,789 (GRCm39) |
Q471L |
possibly damaging |
Het |
Wdr33 |
A |
C |
18: 32,026,132 (GRCm39) |
Q944H |
unknown |
Het |
Wdr55 |
G |
A |
18: 36,893,448 (GRCm39) |
V37M |
possibly damaging |
Het |
Zbtb18 |
A |
T |
1: 177,274,687 (GRCm39) |
S7C |
probably damaging |
Het |
Zfhx4 |
G |
A |
3: 5,464,680 (GRCm39) |
V1638M |
possibly damaging |
Het |
Zfp81 |
A |
T |
17: 33,553,677 (GRCm39) |
I379N |
possibly damaging |
Het |
|
Other mutations in Ppp1r3g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01946:Ppp1r3g
|
APN |
13 |
36,152,978 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02890:Ppp1r3g
|
APN |
13 |
36,153,314 (GRCm39) |
missense |
probably damaging |
0.98 |
R0413:Ppp1r3g
|
UTSW |
13 |
36,153,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1065:Ppp1r3g
|
UTSW |
13 |
36,153,418 (GRCm39) |
missense |
probably benign |
0.07 |
R5677:Ppp1r3g
|
UTSW |
13 |
36,153,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R6705:Ppp1r3g
|
UTSW |
13 |
36,152,880 (GRCm39) |
missense |
probably benign |
0.08 |
R8832:Ppp1r3g
|
UTSW |
13 |
36,153,143 (GRCm39) |
nonsense |
probably null |
|
R9127:Ppp1r3g
|
UTSW |
13 |
36,152,621 (GRCm39) |
missense |
probably benign |
|
R9287:Ppp1r3g
|
UTSW |
13 |
36,152,834 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9626:Ppp1r3g
|
UTSW |
13 |
36,153,612 (GRCm39) |
missense |
probably benign |
0.08 |
X0027:Ppp1r3g
|
UTSW |
13 |
36,153,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|