Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap13 |
A |
G |
7: 75,378,617 (GRCm39) |
N2090S |
possibly damaging |
Het |
Asxl3 |
T |
C |
18: 22,650,800 (GRCm39) |
S930P |
probably benign |
Het |
Cachd1 |
T |
A |
4: 100,823,466 (GRCm39) |
I506N |
probably damaging |
Het |
Calm1 |
G |
T |
12: 100,171,967 (GRCm39) |
V140L |
probably benign |
Het |
Cdsn |
A |
T |
17: 35,866,529 (GRCm39) |
K353* |
probably null |
Het |
Cldn11 |
T |
C |
3: 31,208,210 (GRCm39) |
V125A |
probably benign |
Het |
Ddx60 |
G |
A |
8: 62,470,284 (GRCm39) |
|
probably null |
Het |
Dlg2 |
A |
G |
7: 91,589,248 (GRCm39) |
I216V |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,311,279 (GRCm39) |
|
probably null |
Het |
Dnajc28 |
G |
A |
16: 91,413,795 (GRCm39) |
R150* |
probably null |
Het |
Erap1 |
A |
T |
13: 74,794,683 (GRCm39) |
Y114F |
probably benign |
Het |
Gm14443 |
G |
A |
2: 175,011,468 (GRCm39) |
P326L |
probably damaging |
Het |
Gm2042 |
T |
A |
12: 87,926,928 (GRCm39) |
L415Q |
probably damaging |
Het |
Gm8797 |
T |
C |
3: 5,816,094 (GRCm39) |
I44T |
probably benign |
Het |
Matn2 |
C |
A |
15: 34,422,555 (GRCm39) |
F547L |
probably benign |
Het |
Mpc2 |
T |
A |
1: 165,308,458 (GRCm39) |
|
probably null |
Het |
Or5b12b |
A |
G |
19: 12,861,268 (GRCm39) |
T8A |
probably benign |
Het |
Or7d10 |
A |
C |
9: 19,832,020 (GRCm39) |
T172P |
probably damaging |
Het |
Pcnx4 |
T |
A |
12: 72,603,687 (GRCm39) |
L536Q |
probably damaging |
Het |
Phlpp2 |
G |
A |
8: 110,595,321 (GRCm39) |
R24H |
unknown |
Het |
Pkmyt1 |
A |
T |
17: 23,952,813 (GRCm39) |
D123V |
probably damaging |
Het |
Polg |
A |
T |
7: 79,106,466 (GRCm39) |
M668K |
probably benign |
Het |
Ppp1r12a |
G |
T |
10: 108,107,598 (GRCm39) |
A974S |
probably benign |
Het |
Rabl3 |
T |
C |
16: 37,377,225 (GRCm39) |
Y61H |
probably damaging |
Het |
Rap2a |
T |
A |
14: 120,716,269 (GRCm39) |
I44N |
probably damaging |
Het |
Rev3l |
T |
C |
10: 39,735,111 (GRCm39) |
V2779A |
probably damaging |
Het |
Rnf43 |
G |
T |
11: 87,622,057 (GRCm39) |
R259L |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,376,450 (GRCm39) |
L448Q |
probably damaging |
Het |
Slc43a2 |
T |
G |
11: 75,434,193 (GRCm39) |
|
probably null |
Het |
Slc6a5 |
A |
G |
7: 49,598,057 (GRCm39) |
I640M |
probably benign |
Het |
Sp140l1 |
T |
G |
1: 85,077,261 (GRCm39) |
S102R |
probably damaging |
Het |
Srrm2 |
C |
T |
17: 24,034,297 (GRCm39) |
P314S |
unknown |
Het |
Strn4 |
C |
T |
7: 16,562,733 (GRCm39) |
R291C |
probably damaging |
Het |
Syt4 |
T |
A |
18: 31,577,230 (GRCm39) |
R41S |
probably benign |
Het |
Tfb1m |
T |
C |
17: 3,569,855 (GRCm39) |
D337G |
probably benign |
Het |
Togaram1 |
G |
T |
12: 65,029,465 (GRCm39) |
D963Y |
possibly damaging |
Het |
Tpsg1 |
T |
C |
17: 25,591,564 (GRCm39) |
C55R |
probably damaging |
Het |
Tram1l1 |
A |
G |
3: 124,115,911 (GRCm39) |
K357R |
probably benign |
Het |
Veph1 |
A |
G |
3: 66,171,316 (GRCm39) |
I42T |
probably damaging |
Het |
Vps13b |
C |
G |
15: 35,709,456 (GRCm39) |
S1801* |
probably null |
Het |
Zcwpw1 |
G |
A |
5: 137,817,839 (GRCm39) |
|
probably null |
Het |
Zfp266 |
G |
A |
9: 20,418,110 (GRCm39) |
|
probably benign |
Het |
Zmym5 |
T |
A |
14: 57,031,918 (GRCm39) |
R397* |
probably null |
Het |
|
Other mutations in Ppp2r3d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00792:Ppp2r3d
|
APN |
9 |
101,088,500 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01122:Ppp2r3d
|
APN |
9 |
101,088,844 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02332:Ppp2r3d
|
APN |
9 |
101,057,602 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02653:Ppp2r3d
|
APN |
9 |
101,088,892 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03329:Ppp2r3d
|
APN |
9 |
101,003,630 (GRCm39) |
splice site |
probably benign |
|
IGL03351:Ppp2r3d
|
APN |
9 |
101,088,391 (GRCm39) |
missense |
probably benign |
0.00 |
lank
|
UTSW |
9 |
101,075,829 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4480001:Ppp2r3d
|
UTSW |
9 |
101,003,576 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4687001:Ppp2r3d
|
UTSW |
9 |
101,021,579 (GRCm39) |
missense |
probably benign |
0.00 |
R0243:Ppp2r3d
|
UTSW |
9 |
101,089,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Ppp2r3d
|
UTSW |
9 |
101,075,829 (GRCm39) |
critical splice donor site |
probably null |
|
R1086:Ppp2r3d
|
UTSW |
9 |
101,031,021 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1215:Ppp2r3d
|
UTSW |
9 |
101,089,883 (GRCm39) |
missense |
probably benign |
0.02 |
R1245:Ppp2r3d
|
UTSW |
9 |
101,071,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R1458:Ppp2r3d
|
UTSW |
9 |
101,088,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Ppp2r3d
|
UTSW |
9 |
101,089,505 (GRCm39) |
missense |
probably benign |
0.00 |
R1857:Ppp2r3d
|
UTSW |
9 |
101,090,092 (GRCm39) |
missense |
probably damaging |
0.96 |
R1972:Ppp2r3d
|
UTSW |
9 |
101,088,976 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Ppp2r3d
|
UTSW |
9 |
101,022,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Ppp2r3d
|
UTSW |
9 |
101,021,570 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2135:Ppp2r3d
|
UTSW |
9 |
101,088,757 (GRCm39) |
missense |
probably damaging |
0.99 |
R2180:Ppp2r3d
|
UTSW |
9 |
101,004,214 (GRCm39) |
nonsense |
probably null |
|
R3155:Ppp2r3d
|
UTSW |
9 |
101,089,559 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4190:Ppp2r3d
|
UTSW |
9 |
124,424,123 (GRCm38) |
unclassified |
probably benign |
|
R4657:Ppp2r3d
|
UTSW |
9 |
124,476,821 (GRCm38) |
missense |
unknown |
|
R4797:Ppp2r3d
|
UTSW |
9 |
101,089,179 (GRCm39) |
missense |
probably benign |
0.01 |
R4829:Ppp2r3d
|
UTSW |
9 |
101,089,709 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5269:Ppp2r3d
|
UTSW |
9 |
101,031,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R5498:Ppp2r3d
|
UTSW |
9 |
124,439,123 (GRCm38) |
unclassified |
probably benign |
|
R5820:Ppp2r3d
|
UTSW |
9 |
124,422,765 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5917:Ppp2r3d
|
UTSW |
9 |
101,089,183 (GRCm39) |
missense |
probably benign |
0.10 |
R5939:Ppp2r3d
|
UTSW |
9 |
101,089,824 (GRCm39) |
missense |
probably benign |
0.37 |
R6089:Ppp2r3d
|
UTSW |
9 |
101,088,835 (GRCm39) |
missense |
probably benign |
0.00 |
R6254:Ppp2r3d
|
UTSW |
9 |
101,025,786 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6574:Ppp2r3d
|
UTSW |
9 |
101,071,584 (GRCm39) |
missense |
probably benign |
0.03 |
R6776:Ppp2r3d
|
UTSW |
9 |
101,090,061 (GRCm39) |
missense |
probably benign |
0.00 |
R6823:Ppp2r3d
|
UTSW |
9 |
124,439,078 (GRCm38) |
unclassified |
probably benign |
|
R6927:Ppp2r3d
|
UTSW |
9 |
101,052,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Ppp2r3d
|
UTSW |
9 |
124,439,080 (GRCm38) |
nonsense |
probably null |
|
R7162:Ppp2r3d
|
UTSW |
9 |
124,439,673 (GRCm38) |
missense |
|
|
R7189:Ppp2r3d
|
UTSW |
9 |
101,003,621 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7190:Ppp2r3d
|
UTSW |
9 |
101,089,726 (GRCm39) |
missense |
probably benign |
0.11 |
R7288:Ppp2r3d
|
UTSW |
9 |
101,004,203 (GRCm39) |
missense |
probably damaging |
0.98 |
R7292:Ppp2r3d
|
UTSW |
9 |
101,089,871 (GRCm39) |
missense |
probably damaging |
0.96 |
R7512:Ppp2r3d
|
UTSW |
9 |
101,052,532 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7655:Ppp2r3d
|
UTSW |
9 |
101,088,911 (GRCm39) |
missense |
probably benign |
0.30 |
R7656:Ppp2r3d
|
UTSW |
9 |
101,088,911 (GRCm39) |
missense |
probably benign |
0.30 |
R7661:Ppp2r3d
|
UTSW |
9 |
124,442,696 (GRCm38) |
missense |
|
|
R7666:Ppp2r3d
|
UTSW |
9 |
124,440,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R7769:Ppp2r3d
|
UTSW |
9 |
124,439,087 (GRCm38) |
missense |
|
|
R8195:Ppp2r3d
|
UTSW |
9 |
101,090,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R8236:Ppp2r3d
|
UTSW |
9 |
124,440,067 (GRCm38) |
missense |
|
|
R8344:Ppp2r3d
|
UTSW |
9 |
101,088,985 (GRCm39) |
missense |
probably benign |
0.03 |
R8505:Ppp2r3d
|
UTSW |
9 |
124,439,084 (GRCm38) |
missense |
|
|
R8720:Ppp2r3d
|
UTSW |
9 |
101,089,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R8765:Ppp2r3d
|
UTSW |
9 |
124,439,649 (GRCm38) |
missense |
|
|
R8775:Ppp2r3d
|
UTSW |
9 |
101,004,204 (GRCm39) |
missense |
probably benign |
0.00 |
R8775-TAIL:Ppp2r3d
|
UTSW |
9 |
101,004,204 (GRCm39) |
missense |
probably benign |
0.00 |
R8853:Ppp2r3d
|
UTSW |
9 |
101,090,110 (GRCm39) |
missense |
probably benign |
0.05 |
R8958:Ppp2r3d
|
UTSW |
9 |
101,088,634 (GRCm39) |
missense |
probably benign |
|
R9069:Ppp2r3d
|
UTSW |
9 |
101,090,006 (GRCm39) |
missense |
probably benign |
0.02 |
R9210:Ppp2r3d
|
UTSW |
9 |
101,063,175 (GRCm39) |
missense |
probably benign |
0.09 |
R9212:Ppp2r3d
|
UTSW |
9 |
101,063,175 (GRCm39) |
missense |
probably benign |
0.09 |
R9300:Ppp2r3d
|
UTSW |
9 |
124,423,977 (GRCm38) |
missense |
unknown |
|
R9404:Ppp2r3d
|
UTSW |
9 |
101,025,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R9465:Ppp2r3d
|
UTSW |
9 |
124,442,222 (GRCm38) |
missense |
|
|
R9477:Ppp2r3d
|
UTSW |
9 |
124,476,857 (GRCm38) |
missense |
|
|
R9538:Ppp2r3d
|
UTSW |
9 |
124,424,007 (GRCm38) |
missense |
unknown |
|
R9545:Ppp2r3d
|
UTSW |
9 |
101,089,214 (GRCm39) |
missense |
probably benign |
|
R9639:Ppp2r3d
|
UTSW |
9 |
101,022,713 (GRCm39) |
missense |
probably benign |
|
R9649:Ppp2r3d
|
UTSW |
9 |
124,440,831 (GRCm38) |
missense |
|
|
X0020:Ppp2r3d
|
UTSW |
9 |
101,089,238 (GRCm39) |
missense |
probably benign |
0.19 |
Z1176:Ppp2r3d
|
UTSW |
9 |
101,003,588 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1177:Ppp2r3d
|
UTSW |
9 |
124,476,815 (GRCm38) |
missense |
unknown |
|
Z1177:Ppp2r3d
|
UTSW |
9 |
124,422,692 (GRCm38) |
missense |
probably benign |
0.03 |
|