Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930518I15Rik |
C |
T |
2: 156,699,074 (GRCm39) |
|
probably benign |
Het |
Abcb6 |
G |
A |
1: 75,156,521 (GRCm39) |
T81I |
probably benign |
Het |
Acp6 |
A |
G |
3: 97,083,075 (GRCm39) |
K362R |
probably benign |
Het |
Adam26a |
A |
G |
8: 44,023,088 (GRCm39) |
M134T |
probably benign |
Het |
Ankrd27 |
C |
T |
7: 35,327,915 (GRCm39) |
P812S |
probably damaging |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 117,721,122 (GRCm39) |
|
probably benign |
Het |
Atp2a1 |
G |
A |
7: 126,047,795 (GRCm39) |
R672C |
probably damaging |
Het |
Atxn2 |
G |
T |
5: 121,919,406 (GRCm39) |
W371C |
probably damaging |
Het |
B3gnt2 |
T |
TTCACAAA |
11: 22,786,426 (GRCm39) |
|
probably null |
Het |
Btnl6 |
T |
A |
17: 34,727,435 (GRCm39) |
D365V |
possibly damaging |
Het |
Ccdc80 |
T |
A |
16: 44,915,928 (GRCm39) |
L228Q |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,936,759 (GRCm39) |
H718R |
probably benign |
Het |
Cdh18 |
A |
G |
15: 23,474,454 (GRCm39) |
K775E |
probably benign |
Het |
Cdh23 |
T |
G |
10: 60,173,445 (GRCm39) |
N1679T |
possibly damaging |
Het |
Cep192 |
T |
A |
18: 67,948,993 (GRCm39) |
D271E |
possibly damaging |
Het |
Cfap70 |
G |
T |
14: 20,493,729 (GRCm39) |
T124K |
probably benign |
Het |
Ckap5 |
A |
T |
2: 91,408,476 (GRCm39) |
E890D |
probably benign |
Het |
Col22a1 |
G |
T |
15: 71,824,188 (GRCm39) |
P569T |
probably benign |
Het |
Colq |
A |
T |
14: 31,267,060 (GRCm39) |
L150Q |
possibly damaging |
Het |
Csf1 |
T |
C |
3: 107,664,278 (GRCm39) |
|
probably null |
Het |
Csmd3 |
A |
T |
15: 47,868,211 (GRCm39) |
S770T |
possibly damaging |
Het |
Cul9 |
C |
A |
17: 46,841,072 (GRCm39) |
V733L |
probably damaging |
Het |
Cyp2c55 |
A |
G |
19: 39,019,830 (GRCm39) |
D256G |
possibly damaging |
Het |
Dclk3 |
A |
T |
9: 111,298,253 (GRCm39) |
D599V |
probably damaging |
Het |
Defb26 |
T |
A |
2: 152,350,104 (GRCm39) |
I59F |
possibly damaging |
Het |
Dnah6 |
A |
G |
6: 73,106,643 (GRCm39) |
V1646A |
possibly damaging |
Het |
Dnm2 |
T |
C |
9: 21,415,960 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,713,836 (GRCm39) |
L1867P |
probably damaging |
Het |
Dock9 |
G |
T |
14: 121,905,871 (GRCm39) |
T93K |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,140,995 (GRCm39) |
H1344R |
probably benign |
Het |
Enam |
A |
C |
5: 88,652,142 (GRCm39) |
Q1217P |
possibly damaging |
Het |
Fbf1 |
A |
T |
11: 116,049,748 (GRCm39) |
D91E |
possibly damaging |
Het |
Fbxo7 |
T |
G |
10: 85,882,666 (GRCm39) |
W393G |
probably damaging |
Het |
Gab2 |
A |
G |
7: 96,953,420 (GRCm39) |
T599A |
probably damaging |
Het |
Gfy |
T |
A |
7: 44,826,612 (GRCm39) |
I409F |
possibly damaging |
Het |
Gm19345 |
T |
A |
7: 19,591,433 (GRCm39) |
|
probably null |
Het |
Gm4787 |
A |
G |
12: 81,425,987 (GRCm39) |
M57T |
probably benign |
Het |
Gper1 |
A |
G |
5: 139,412,480 (GRCm39) |
E275G |
probably damaging |
Het |
Grik4 |
T |
C |
9: 42,435,882 (GRCm39) |
E803G |
probably damaging |
Het |
Gstm3 |
G |
A |
3: 107,875,513 (GRCm39) |
P39L |
possibly damaging |
Het |
Hax1 |
A |
T |
3: 89,904,767 (GRCm39) |
V142D |
probably damaging |
Het |
Hcn3 |
A |
T |
3: 89,057,747 (GRCm39) |
I383N |
probably damaging |
Het |
Hdac10 |
C |
A |
15: 89,009,600 (GRCm39) |
|
probably null |
Het |
Hipk3 |
A |
C |
2: 104,269,674 (GRCm39) |
M505R |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,313,225 (GRCm39) |
P1822S |
probably benign |
Het |
Hsd17b13 |
G |
T |
5: 104,104,124 (GRCm39) |
H281N |
unknown |
Het |
Ilrun |
T |
C |
17: 28,039,289 (GRCm39) |
D7G |
probably damaging |
Het |
Irak2 |
T |
A |
6: 113,649,848 (GRCm39) |
I222N |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,334,296 (GRCm39) |
L7F |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,359,106 (GRCm39) |
|
probably null |
Het |
Kcnn3 |
G |
T |
3: 89,427,727 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
A |
C |
12: 31,328,775 (GRCm39) |
D218A |
probably damaging |
Het |
Lrrtm1 |
A |
T |
6: 77,221,127 (GRCm39) |
N195Y |
probably damaging |
Het |
Ltf |
A |
T |
9: 110,851,409 (GRCm39) |
N72I |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,447,527 (GRCm39) |
I479T |
probably damaging |
Het |
Mfhas1 |
T |
C |
8: 36,055,764 (GRCm39) |
S80P |
probably benign |
Het |
Mknk1 |
A |
G |
4: 115,735,224 (GRCm39) |
E364G |
probably damaging |
Het |
Msh4 |
C |
T |
3: 153,577,920 (GRCm39) |
C458Y |
probably damaging |
Het |
Mtrr |
A |
T |
13: 68,712,631 (GRCm39) |
|
probably null |
Het |
Myo1a |
T |
C |
10: 127,547,007 (GRCm39) |
W356R |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,631,069 (GRCm39) |
V2186A |
probably benign |
Het |
Nfe2l3 |
T |
C |
6: 51,427,992 (GRCm39) |
S185P |
probably damaging |
Het |
Nhsl1 |
A |
C |
10: 18,407,158 (GRCm39) |
K1397Q |
probably damaging |
Het |
Nmbr |
C |
T |
10: 14,645,908 (GRCm39) |
R261W |
probably damaging |
Het |
Npy2r |
A |
G |
3: 82,448,365 (GRCm39) |
S137P |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,971,031 (GRCm39) |
G2494D |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,013,572 (GRCm39) |
K1092E |
probably damaging |
Het |
Oosp2 |
A |
C |
19: 11,627,047 (GRCm39) |
I92S |
probably benign |
Het |
Or5ar1 |
C |
T |
2: 85,671,526 (GRCm39) |
C203Y |
probably damaging |
Het |
Pcdh9 |
T |
C |
14: 94,124,616 (GRCm39) |
D518G |
probably damaging |
Het |
Pde11a |
G |
T |
2: 76,168,137 (GRCm39) |
T272K |
possibly damaging |
Het |
Plekha2 |
T |
A |
8: 25,549,851 (GRCm39) |
Q162L |
probably null |
Het |
Prkag2 |
T |
A |
5: 25,083,732 (GRCm39) |
I84F |
probably damaging |
Het |
Prm2 |
G |
T |
16: 10,609,613 (GRCm39) |
|
probably benign |
Het |
Prpf40a |
A |
T |
2: 53,032,035 (GRCm39) |
C800S |
probably damaging |
Het |
Prr5l |
A |
T |
2: 101,559,793 (GRCm39) |
C158S |
probably benign |
Het |
Prrt3 |
C |
A |
6: 113,475,198 (GRCm39) |
C8F |
possibly damaging |
Het |
Ruvbl1 |
T |
C |
6: 88,462,887 (GRCm39) |
V337A |
probably benign |
Het |
Sall1 |
T |
A |
8: 89,756,969 (GRCm39) |
Q1045L |
probably damaging |
Het |
Sec22c |
T |
C |
9: 121,524,708 (GRCm39) |
Y25C |
probably damaging |
Het |
Serpina3i |
A |
T |
12: 104,234,036 (GRCm39) |
T335S |
possibly damaging |
Het |
Setd1b |
TCCACCACCACCACCACCACCACCA |
TCCACCACCACCACCACCACCA |
5: 123,290,137 (GRCm39) |
|
probably benign |
Het |
Slc12a8 |
T |
A |
16: 33,428,529 (GRCm39) |
I279N |
probably damaging |
Het |
Slc15a1 |
G |
A |
14: 121,727,319 (GRCm39) |
T83I |
probably damaging |
Het |
Slc22a3 |
A |
G |
17: 12,678,658 (GRCm39) |
F222S |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,682,353 (GRCm39) |
T463S |
probably benign |
Het |
Spsb4 |
C |
A |
9: 96,877,931 (GRCm39) |
A131S |
probably benign |
Het |
Sting1 |
T |
A |
18: 35,871,743 (GRCm39) |
I170F |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,014,484 (GRCm39) |
E3225G |
probably damaging |
Het |
Tchp |
G |
A |
5: 114,857,634 (GRCm39) |
|
probably null |
Het |
Tekt4 |
T |
A |
17: 25,690,749 (GRCm39) |
D18E |
probably benign |
Het |
Timm50 |
A |
G |
7: 28,010,443 (GRCm39) |
V37A |
probably benign |
Het |
Tlx2 |
A |
C |
6: 83,045,741 (GRCm39) |
*285G |
probably null |
Het |
Tshz1 |
C |
A |
18: 84,031,499 (GRCm39) |
D970Y |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,700,805 (GRCm39) |
V50E |
probably damaging |
Het |
Txndc17 |
T |
A |
11: 72,100,274 (GRCm39) |
S113T |
probably benign |
Het |
Tyk2 |
T |
C |
9: 21,019,305 (GRCm39) |
Y1039C |
probably damaging |
Het |
Ubqln3 |
A |
G |
7: 103,791,698 (GRCm39) |
S131P |
probably benign |
Het |
Uncx |
A |
T |
5: 139,529,837 (GRCm39) |
H30L |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,912,303 (GRCm39) |
D1007E |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,701,038 (GRCm39) |
V1083A |
probably damaging |
Het |
Wdr24 |
T |
A |
17: 26,047,479 (GRCm39) |
H765Q |
probably damaging |
Het |
Wrnip1 |
A |
G |
13: 32,986,330 (GRCm39) |
D37G |
probably damaging |
Het |
Xpo6 |
T |
C |
7: 125,712,924 (GRCm39) |
T686A |
possibly damaging |
Het |
Zfp941 |
G |
A |
7: 140,392,124 (GRCm39) |
R412C |
probably damaging |
Het |
Znrf2 |
T |
A |
6: 54,855,425 (GRCm39) |
C71* |
probably null |
Het |
|
Other mutations in Psg25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Psg25
|
APN |
7 |
18,260,106 (GRCm39) |
splice site |
probably benign |
|
IGL00508:Psg25
|
APN |
7 |
18,263,656 (GRCm39) |
missense |
probably benign |
|
IGL01154:Psg25
|
APN |
7 |
18,258,624 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01388:Psg25
|
APN |
7 |
18,263,590 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02222:Psg25
|
APN |
7 |
18,263,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02261:Psg25
|
APN |
7 |
18,255,268 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02309:Psg25
|
APN |
7 |
18,260,349 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02803:Psg25
|
APN |
7 |
18,260,212 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03334:Psg25
|
APN |
7 |
18,263,699 (GRCm39) |
missense |
probably benign |
0.01 |
R0711:Psg25
|
UTSW |
7 |
18,263,485 (GRCm39) |
nonsense |
probably null |
|
R1458:Psg25
|
UTSW |
7 |
18,263,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Psg25
|
UTSW |
7 |
18,265,928 (GRCm39) |
nonsense |
probably null |
|
R2064:Psg25
|
UTSW |
7 |
18,255,178 (GRCm39) |
missense |
probably damaging |
0.96 |
R2066:Psg25
|
UTSW |
7 |
18,263,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4485:Psg25
|
UTSW |
7 |
18,260,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Psg25
|
UTSW |
7 |
18,258,816 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4514:Psg25
|
UTSW |
7 |
18,263,533 (GRCm39) |
nonsense |
probably null |
|
R4547:Psg25
|
UTSW |
7 |
18,258,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Psg25
|
UTSW |
7 |
18,258,838 (GRCm39) |
missense |
probably benign |
0.00 |
R5121:Psg25
|
UTSW |
7 |
18,260,461 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5208:Psg25
|
UTSW |
7 |
18,260,460 (GRCm39) |
missense |
probably benign |
0.00 |
R5267:Psg25
|
UTSW |
7 |
18,258,711 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5376:Psg25
|
UTSW |
7 |
18,260,460 (GRCm39) |
missense |
probably benign |
0.00 |
R5425:Psg25
|
UTSW |
7 |
18,258,709 (GRCm39) |
nonsense |
probably null |
|
R5749:Psg25
|
UTSW |
7 |
18,258,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Psg25
|
UTSW |
7 |
18,260,403 (GRCm39) |
missense |
probably benign |
0.37 |
R6862:Psg25
|
UTSW |
7 |
18,255,323 (GRCm39) |
missense |
probably benign |
0.03 |
R6962:Psg25
|
UTSW |
7 |
18,263,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Psg25
|
UTSW |
7 |
18,266,127 (GRCm39) |
start gained |
probably benign |
|
R7782:Psg25
|
UTSW |
7 |
18,255,227 (GRCm39) |
missense |
probably benign |
0.15 |
R7812:Psg25
|
UTSW |
7 |
18,255,093 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8155:Psg25
|
UTSW |
7 |
18,260,445 (GRCm39) |
missense |
probably benign |
0.00 |
R8775:Psg25
|
UTSW |
7 |
18,255,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R8775-TAIL:Psg25
|
UTSW |
7 |
18,255,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Psg25
|
UTSW |
7 |
18,263,519 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9013:Psg25
|
UTSW |
7 |
18,258,690 (GRCm39) |
missense |
probably benign |
0.02 |
R9755:Psg25
|
UTSW |
7 |
18,260,460 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Psg25
|
UTSW |
7 |
18,263,516 (GRCm39) |
missense |
probably benign |
0.00 |
|