Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,220,148 (GRCm39) |
N299S |
probably damaging |
Het |
Abi3 |
A |
G |
11: 95,723,541 (GRCm39) |
*368R |
probably null |
Het |
Agbl1 |
T |
C |
7: 76,348,588 (GRCm39) |
|
probably null |
Het |
Ap3b2 |
T |
C |
7: 81,115,941 (GRCm39) |
D650G |
possibly damaging |
Het |
Arhgap30 |
A |
G |
1: 171,235,998 (GRCm39) |
S791G |
probably benign |
Het |
Arvcf |
T |
A |
16: 18,222,208 (GRCm39) |
L722Q |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,594,498 (GRCm39) |
R1198* |
probably null |
Het |
Atf2 |
G |
T |
2: 73,660,200 (GRCm39) |
T189N |
probably benign |
Het |
Atf7ip |
A |
G |
6: 136,536,814 (GRCm39) |
K16E |
probably damaging |
Het |
Atg9b |
G |
T |
5: 24,592,396 (GRCm39) |
Q621K |
probably damaging |
Het |
Atp12a |
G |
A |
14: 56,610,330 (GRCm39) |
E234K |
probably damaging |
Het |
C8a |
T |
C |
4: 104,684,012 (GRCm39) |
K368E |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,096,365 (GRCm39) |
K1578E |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,366,757 (GRCm39) |
Y241C |
probably damaging |
Het |
Cdon |
G |
A |
9: 35,398,103 (GRCm39) |
S940N |
probably benign |
Het |
Cds2 |
G |
T |
2: 132,147,075 (GRCm39) |
G402V |
possibly damaging |
Het |
Cog6 |
T |
C |
3: 52,900,171 (GRCm39) |
|
probably null |
Het |
Commd10 |
T |
C |
18: 47,100,903 (GRCm39) |
S114P |
possibly damaging |
Het |
Dram2 |
T |
C |
3: 106,478,133 (GRCm39) |
V155A |
possibly damaging |
Het |
Egr2 |
T |
A |
10: 67,376,310 (GRCm39) |
V252E |
probably benign |
Het |
Exoc3l |
C |
T |
8: 106,020,317 (GRCm39) |
V203M |
probably damaging |
Het |
Fsip1 |
C |
A |
2: 118,078,773 (GRCm39) |
|
probably null |
Het |
Gm10840 |
C |
A |
11: 106,051,926 (GRCm39) |
|
probably benign |
Het |
Gpr37l1 |
A |
G |
1: 135,088,883 (GRCm39) |
L394P |
probably damaging |
Het |
Gsap |
T |
C |
5: 21,431,830 (GRCm39) |
M243T |
possibly damaging |
Het |
Hsd3b5 |
T |
A |
3: 98,526,460 (GRCm39) |
I329F |
probably benign |
Het |
Htra1 |
T |
A |
7: 130,563,262 (GRCm39) |
S164R |
probably damaging |
Het |
Il17b |
G |
A |
18: 61,823,315 (GRCm39) |
V50M |
probably damaging |
Het |
Itga4 |
A |
T |
2: 79,131,375 (GRCm39) |
Y581F |
probably damaging |
Het |
Jmjd8 |
A |
G |
17: 26,048,255 (GRCm39) |
E92G |
probably damaging |
Het |
Kcnq4 |
T |
A |
4: 120,555,152 (GRCm39) |
D677V |
probably damaging |
Het |
Klhl42 |
A |
G |
6: 146,993,666 (GRCm39) |
T213A |
probably benign |
Het |
Lcn5 |
T |
C |
2: 25,550,710 (GRCm39) |
S133P |
probably damaging |
Het |
Liph |
T |
C |
16: 21,786,803 (GRCm39) |
Y271C |
probably damaging |
Het |
Lpcat3 |
T |
C |
6: 124,678,437 (GRCm39) |
I228T |
probably benign |
Het |
Lrrd1 |
A |
G |
5: 3,916,418 (GRCm39) |
K812E |
possibly damaging |
Het |
Ltbp2 |
T |
C |
12: 84,860,062 (GRCm39) |
T631A |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,856,361 (GRCm39) |
T701I |
probably damaging |
Het |
Mavs |
G |
A |
2: 131,080,751 (GRCm39) |
R13Q |
probably damaging |
Het |
Mtor |
C |
G |
4: 148,549,406 (GRCm39) |
H597D |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,410,555 (GRCm39) |
H1309Q |
unknown |
Het |
Myl3 |
A |
C |
9: 110,596,997 (GRCm39) |
D119A |
probably damaging |
Het |
Nnat |
A |
T |
2: 157,402,408 (GRCm39) |
|
probably benign |
Het |
Or14c40 |
T |
C |
7: 86,313,548 (GRCm39) |
L226S |
possibly damaging |
Het |
Or2ag19 |
T |
A |
7: 106,444,596 (GRCm39) |
Y259* |
probably null |
Het |
Or5h17 |
G |
A |
16: 58,820,854 (GRCm39) |
D269N |
probably benign |
Het |
Or7e175 |
A |
T |
9: 20,048,487 (GRCm39) |
Q25L |
probably benign |
Het |
Pclo |
C |
T |
5: 14,589,485 (GRCm39) |
A595V |
unknown |
Het |
Pcsk6 |
T |
A |
7: 65,612,676 (GRCm39) |
C315S |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,603,671 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
A |
G |
2: 72,029,122 (GRCm39) |
H398R |
possibly damaging |
Het |
Ripor2 |
A |
G |
13: 24,878,209 (GRCm39) |
D328G |
probably damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,378,601 (GRCm39) |
T509S |
possibly damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,622 (GRCm39) |
I1032T |
probably damaging |
Het |
Slc25a13 |
A |
T |
6: 6,109,277 (GRCm39) |
S362T |
probably benign |
Het |
Stk35 |
A |
T |
2: 129,642,488 (GRCm39) |
R10* |
probably null |
Het |
Tal1 |
A |
G |
4: 114,925,762 (GRCm39) |
D277G |
probably damaging |
Het |
Tecta |
G |
A |
9: 42,286,487 (GRCm39) |
T723I |
probably damaging |
Het |
Trp53bp1 |
A |
C |
2: 121,034,978 (GRCm39) |
V103G |
probably benign |
Het |
Trpv4 |
A |
G |
5: 114,774,518 (GRCm39) |
S189P |
probably benign |
Het |
Ttll5 |
T |
G |
12: 85,926,133 (GRCm39) |
|
probably benign |
Het |
Usp8 |
A |
G |
2: 126,584,143 (GRCm39) |
T451A |
probably benign |
Het |
Vac14 |
G |
A |
8: 111,363,584 (GRCm39) |
D340N |
probably benign |
Het |
Vars1 |
C |
A |
17: 35,217,042 (GRCm39) |
A471S |
probably benign |
Het |
Vars1 |
A |
T |
17: 35,229,595 (GRCm39) |
H404L |
probably damaging |
Het |
Vmn2r70 |
T |
C |
7: 85,215,252 (GRCm39) |
N94S |
probably damaging |
Het |
Vpreb1b |
T |
C |
16: 17,798,631 (GRCm39) |
L39P |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,618,174 (GRCm39) |
L693* |
probably null |
Het |
Wapl |
A |
G |
14: 34,455,751 (GRCm39) |
I176V |
probably benign |
Het |
Wdr31 |
G |
T |
4: 62,382,270 (GRCm39) |
L4I |
possibly damaging |
Het |
|
Other mutations in Ppp2r3c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00928:Ppp2r3c
|
APN |
12 |
55,339,283 (GRCm39) |
splice site |
probably null |
|
IGL01122:Ppp2r3c
|
APN |
12 |
55,344,587 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01954:Ppp2r3c
|
APN |
12 |
55,339,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Ppp2r3c
|
APN |
12 |
55,345,192 (GRCm39) |
unclassified |
probably benign |
|
R0129:Ppp2r3c
|
UTSW |
12 |
55,345,207 (GRCm39) |
missense |
probably damaging |
0.96 |
R2411:Ppp2r3c
|
UTSW |
12 |
55,345,269 (GRCm39) |
missense |
probably benign |
0.19 |
R4468:Ppp2r3c
|
UTSW |
12 |
55,344,668 (GRCm39) |
nonsense |
probably null |
|
R4746:Ppp2r3c
|
UTSW |
12 |
55,349,420 (GRCm39) |
splice site |
probably null |
|
R5499:Ppp2r3c
|
UTSW |
12 |
55,335,411 (GRCm39) |
missense |
probably benign |
0.09 |
R5724:Ppp2r3c
|
UTSW |
12 |
55,344,617 (GRCm39) |
missense |
probably benign |
0.45 |
R6724:Ppp2r3c
|
UTSW |
12 |
55,335,281 (GRCm39) |
missense |
probably benign |
0.02 |
R6776:Ppp2r3c
|
UTSW |
12 |
55,345,252 (GRCm39) |
nonsense |
probably null |
|
R7706:Ppp2r3c
|
UTSW |
12 |
55,328,490 (GRCm39) |
missense |
probably benign |
0.23 |
R8111:Ppp2r3c
|
UTSW |
12 |
55,344,634 (GRCm39) |
missense |
probably benign |
|
R8698:Ppp2r3c
|
UTSW |
12 |
55,328,499 (GRCm39) |
missense |
probably benign |
0.10 |
R8892:Ppp2r3c
|
UTSW |
12 |
55,336,453 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9349:Ppp2r3c
|
UTSW |
12 |
55,345,268 (GRCm39) |
missense |
probably benign |
0.36 |
RF006:Ppp2r3c
|
UTSW |
12 |
55,340,600 (GRCm39) |
missense |
probably benign |
0.24 |
|