Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap1 |
C |
A |
7: 101,039,429 (GRCm39) |
A563D |
probably damaging |
Het |
Arhgap28 |
G |
A |
17: 68,203,253 (GRCm39) |
L67F |
probably damaging |
Het |
Atp7b |
G |
T |
8: 22,485,675 (GRCm39) |
|
probably null |
Het |
Auts2 |
A |
G |
5: 131,475,669 (GRCm39) |
F485L |
probably benign |
Het |
Ccdc68 |
A |
G |
18: 70,093,510 (GRCm39) |
E239G |
probably damaging |
Het |
Cdc42bpg |
T |
G |
19: 6,363,487 (GRCm39) |
L449R |
probably damaging |
Het |
Colgalt2 |
G |
T |
1: 152,384,312 (GRCm39) |
A551S |
possibly damaging |
Het |
Ddx41 |
G |
T |
13: 55,678,421 (GRCm39) |
S630Y |
probably damaging |
Het |
Dntt |
T |
C |
19: 41,031,372 (GRCm39) |
L274P |
probably damaging |
Het |
Fhl4 |
G |
T |
10: 84,934,680 (GRCm39) |
H34N |
possibly damaging |
Het |
Filip1 |
A |
T |
9: 79,727,571 (GRCm39) |
N349K |
possibly damaging |
Het |
Gm9894 |
C |
T |
13: 67,913,145 (GRCm39) |
|
noncoding transcript |
Het |
Gpr179 |
A |
G |
11: 97,229,633 (GRCm39) |
S841P |
probably damaging |
Het |
Gpr35 |
G |
T |
1: 92,910,506 (GRCm39) |
V73L |
probably benign |
Het |
Grik5 |
A |
G |
7: 24,713,099 (GRCm39) |
V809A |
possibly damaging |
Het |
H2-T13 |
T |
A |
17: 36,392,413 (GRCm39) |
|
probably benign |
Het |
Heatr5b |
T |
C |
17: 79,128,283 (GRCm39) |
T451A |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,278,259 (GRCm39) |
V1654M |
probably damaging |
Het |
Htra3 |
G |
T |
5: 35,828,409 (GRCm39) |
A157E |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,902,835 (GRCm39) |
V2405D |
probably damaging |
Het |
Irs3 |
C |
A |
5: 137,642,139 (GRCm39) |
R433L |
probably benign |
Het |
Kcmf1 |
G |
A |
6: 72,825,224 (GRCm39) |
Q239* |
probably null |
Het |
Kcnk9 |
A |
G |
15: 72,384,905 (GRCm39) |
|
probably benign |
Het |
Kif28 |
A |
G |
1: 179,530,091 (GRCm39) |
V622A |
probably benign |
Het |
Klrb1f |
A |
T |
6: 129,031,294 (GRCm39) |
I164F |
probably benign |
Het |
Lama2 |
A |
G |
10: 27,066,621 (GRCm39) |
S1087P |
possibly damaging |
Het |
Mchr1 |
A |
T |
15: 81,119,948 (GRCm39) |
|
probably benign |
Het |
Mcidas |
A |
G |
13: 113,135,677 (GRCm39) |
T367A |
probably damaging |
Het |
Mphosph8 |
A |
C |
14: 56,911,870 (GRCm39) |
K298Q |
probably damaging |
Het |
Mroh2a |
G |
T |
1: 88,162,938 (GRCm39) |
Q360H |
probably benign |
Het |
Mst1 |
A |
C |
9: 107,960,793 (GRCm39) |
D461A |
probably benign |
Het |
Nckap1l |
A |
T |
15: 103,373,079 (GRCm39) |
S311C |
probably benign |
Het |
Or2y1 |
T |
A |
11: 49,385,594 (GRCm39) |
V78E |
probably damaging |
Het |
Or4c125 |
T |
A |
2: 89,170,422 (GRCm39) |
M75L |
probably benign |
Het |
Or5m9b |
C |
T |
2: 85,905,435 (GRCm39) |
A117V |
probably benign |
Het |
Or8c11 |
A |
C |
9: 38,290,090 (GRCm39) |
K298N |
probably damaging |
Het |
Pde3a |
T |
G |
6: 141,444,410 (GRCm39) |
C1073G |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,188,012 (GRCm39) |
D3432G |
probably damaging |
Het |
Ppargc1b |
G |
T |
18: 61,448,932 (GRCm39) |
P130Q |
probably damaging |
Het |
Pram1 |
A |
G |
17: 33,860,480 (GRCm39) |
N349S |
probably benign |
Het |
Ranbp6 |
C |
T |
19: 29,789,483 (GRCm39) |
V290I |
possibly damaging |
Het |
Rcan3 |
A |
T |
4: 135,143,914 (GRCm39) |
|
probably null |
Het |
Scn8a |
G |
C |
15: 100,906,187 (GRCm39) |
|
probably benign |
Het |
Slc12a5 |
C |
T |
2: 164,835,982 (GRCm39) |
T900M |
probably benign |
Het |
Srsf10 |
A |
G |
4: 135,585,714 (GRCm39) |
Y55C |
probably damaging |
Het |
Syt7 |
G |
T |
19: 10,421,444 (GRCm39) |
E450* |
probably null |
Het |
Tbrg4 |
T |
C |
11: 6,573,832 (GRCm39) |
K130R |
probably benign |
Het |
Tgm7 |
C |
A |
2: 120,931,546 (GRCm39) |
V206F |
probably damaging |
Het |
Tmem131l |
T |
C |
3: 83,938,955 (GRCm39) |
D67G |
probably damaging |
Het |
Ttc7 |
A |
G |
17: 87,637,472 (GRCm39) |
K409R |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,590,096 (GRCm39) |
|
probably benign |
Het |
Vmn1r171 |
C |
T |
7: 23,332,080 (GRCm39) |
L102F |
possibly damaging |
Het |
Vmn2r59 |
A |
C |
7: 41,695,916 (GRCm39) |
|
probably benign |
Het |
Vsig2 |
A |
G |
9: 37,453,986 (GRCm39) |
R191G |
probably damaging |
Het |
Wdr86 |
T |
A |
5: 24,923,232 (GRCm39) |
Q153H |
probably benign |
Het |
Wdr87-ps |
C |
G |
7: 29,229,995 (GRCm39) |
|
noncoding transcript |
Het |
Xxylt1 |
T |
A |
16: 30,826,616 (GRCm39) |
N233I |
probably damaging |
Het |
Zfp160 |
A |
T |
17: 21,247,139 (GRCm39) |
E563V |
probably damaging |
Het |
Zfp345 |
T |
A |
2: 150,315,323 (GRCm39) |
E71D |
probably benign |
Het |
Zfp541 |
A |
G |
7: 15,816,099 (GRCm39) |
D862G |
possibly damaging |
Het |
Zfp639 |
A |
C |
3: 32,571,259 (GRCm39) |
Q47P |
possibly damaging |
Het |
|
Other mutations in Ppp6r1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01883:Ppp6r1
|
APN |
7 |
4,642,986 (GRCm39) |
splice site |
probably null |
|
IGL02232:Ppp6r1
|
APN |
7 |
4,636,341 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02674:Ppp6r1
|
APN |
7 |
4,649,812 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Ppp6r1
|
APN |
7 |
4,645,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02990:Ppp6r1
|
APN |
7 |
4,646,022 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03135:Ppp6r1
|
APN |
7 |
4,645,159 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03399:Ppp6r1
|
APN |
7 |
4,646,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Ppp6r1
|
UTSW |
7 |
4,636,286 (GRCm39) |
missense |
probably benign |
0.00 |
R0760:Ppp6r1
|
UTSW |
7 |
4,642,722 (GRCm39) |
missense |
probably benign |
0.00 |
R0883:Ppp6r1
|
UTSW |
7 |
4,642,709 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1478:Ppp6r1
|
UTSW |
7 |
4,643,377 (GRCm39) |
splice site |
probably null |
|
R1515:Ppp6r1
|
UTSW |
7 |
4,646,257 (GRCm39) |
missense |
probably damaging |
0.97 |
R1768:Ppp6r1
|
UTSW |
7 |
4,636,691 (GRCm39) |
critical splice donor site |
probably null |
|
R1772:Ppp6r1
|
UTSW |
7 |
4,645,030 (GRCm39) |
missense |
probably benign |
0.00 |
R4017:Ppp6r1
|
UTSW |
7 |
4,636,743 (GRCm39) |
missense |
probably benign |
0.07 |
R4519:Ppp6r1
|
UTSW |
7 |
4,644,045 (GRCm39) |
splice site |
probably null |
|
R4795:Ppp6r1
|
UTSW |
7 |
4,644,053 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4849:Ppp6r1
|
UTSW |
7 |
4,646,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Ppp6r1
|
UTSW |
7 |
4,646,176 (GRCm39) |
missense |
probably benign |
0.00 |
R5416:Ppp6r1
|
UTSW |
7 |
4,642,747 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5643:Ppp6r1
|
UTSW |
7 |
4,636,771 (GRCm39) |
missense |
probably benign |
0.30 |
R5765:Ppp6r1
|
UTSW |
7 |
4,645,207 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6126:Ppp6r1
|
UTSW |
7 |
4,646,376 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6854:Ppp6r1
|
UTSW |
7 |
4,635,395 (GRCm39) |
missense |
probably benign |
0.02 |
R6932:Ppp6r1
|
UTSW |
7 |
4,636,291 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7011:Ppp6r1
|
UTSW |
7 |
4,649,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Ppp6r1
|
UTSW |
7 |
4,642,899 (GRCm39) |
missense |
probably benign |
0.17 |
R7500:Ppp6r1
|
UTSW |
7 |
4,639,129 (GRCm39) |
missense |
probably benign |
0.04 |
R7982:Ppp6r1
|
UTSW |
7 |
4,646,157 (GRCm39) |
missense |
probably benign |
0.00 |
R8769:Ppp6r1
|
UTSW |
7 |
4,644,289 (GRCm39) |
missense |
probably benign |
|
R9628:Ppp6r1
|
UTSW |
7 |
4,636,112 (GRCm39) |
missense |
probably benign |
0.01 |
X0062:Ppp6r1
|
UTSW |
7 |
4,643,306 (GRCm39) |
critical splice donor site |
probably null |
|
|