Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atm |
C |
A |
9: 53,366,068 (GRCm39) |
R2533L |
probably damaging |
Het |
Caprin1 |
T |
A |
2: 103,603,022 (GRCm39) |
M514L |
possibly damaging |
Het |
Ccdc78 |
A |
G |
17: 26,006,126 (GRCm39) |
E98G |
probably damaging |
Het |
Cmya5 |
A |
T |
13: 93,226,865 (GRCm39) |
M2741K |
possibly damaging |
Het |
Cnot1 |
T |
G |
8: 96,478,447 (GRCm39) |
R959S |
probably damaging |
Het |
Col12a1 |
G |
T |
9: 79,553,076 (GRCm39) |
|
probably null |
Het |
Col4a3 |
A |
G |
1: 82,696,605 (GRCm39) |
T177A |
probably benign |
Het |
Cpa3 |
T |
C |
3: 20,279,307 (GRCm39) |
N211D |
possibly damaging |
Het |
Cripto |
C |
T |
9: 110,775,017 (GRCm39) |
|
probably benign |
Het |
Cryba1 |
T |
C |
11: 77,613,543 (GRCm39) |
Y36C |
probably damaging |
Het |
Ctnna1 |
T |
A |
18: 35,377,897 (GRCm39) |
I632N |
probably benign |
Het |
D630045J12Rik |
T |
C |
6: 38,126,498 (GRCm39) |
N1504S |
probably damaging |
Het |
Dgkz |
C |
A |
2: 91,773,019 (GRCm39) |
R346L |
probably damaging |
Het |
Dnajc21 |
G |
A |
15: 10,461,318 (GRCm39) |
R211C |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,461,320 (GRCm39) |
I210N |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,411,524 (GRCm39) |
D1784G |
probably damaging |
Het |
Eya3 |
A |
G |
4: 132,400,262 (GRCm39) |
T94A |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,871,165 (GRCm39) |
D3742G |
possibly damaging |
Het |
Ficd |
T |
C |
5: 113,876,751 (GRCm39) |
F309L |
probably benign |
Het |
Gfra1 |
A |
T |
19: 58,226,878 (GRCm39) |
M451K |
probably benign |
Het |
Gm43517 |
T |
A |
12: 49,437,961 (GRCm39) |
L318Q |
|
Het |
Gsc |
A |
T |
12: 104,439,310 (GRCm39) |
V22E |
possibly damaging |
Het |
Il4ra |
T |
C |
7: 125,168,280 (GRCm39) |
Y100H |
probably damaging |
Het |
Ilf3 |
T |
C |
9: 21,309,340 (GRCm39) |
S486P |
probably benign |
Het |
Itga10 |
T |
A |
3: 96,560,269 (GRCm39) |
H594Q |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,226,137 (GRCm39) |
D28G |
probably benign |
Het |
Kiss1 |
A |
G |
1: 133,257,160 (GRCm39) |
K53R |
possibly damaging |
Het |
Lcn5 |
A |
G |
2: 25,551,426 (GRCm39) |
I182V |
probably benign |
Het |
Lcorl |
T |
C |
5: 45,859,307 (GRCm39) |
D269G |
probably benign |
Het |
Letm2 |
A |
T |
8: 26,082,553 (GRCm39) |
C174* |
probably null |
Het |
Met |
T |
G |
6: 17,558,834 (GRCm39) |
V1154G |
probably damaging |
Het |
Mindy3 |
A |
G |
2: 12,424,000 (GRCm39) |
S22P |
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,946,613 (GRCm39) |
R471Q |
probably damaging |
Het |
Nfe2l3 |
T |
C |
6: 51,435,252 (GRCm39) |
L604P |
probably damaging |
Het |
Or12e10 |
A |
G |
2: 87,640,683 (GRCm39) |
Q173R |
probably damaging |
Het |
Or14a256 |
A |
G |
7: 86,265,769 (GRCm39) |
F28S |
possibly damaging |
Het |
Or5h18 |
T |
A |
16: 58,847,382 (GRCm39) |
Q296L |
possibly damaging |
Het |
Or8b3b |
C |
T |
9: 38,583,919 (GRCm39) |
V274I |
probably benign |
Het |
Or8u9 |
A |
T |
2: 86,001,564 (GRCm39) |
I199N |
possibly damaging |
Het |
Or9r7 |
A |
C |
10: 129,962,455 (GRCm39) |
I157S |
probably damaging |
Het |
Pcdha9 |
T |
A |
18: 37,132,849 (GRCm39) |
Y639* |
probably null |
Het |
Prr14l |
T |
A |
5: 32,986,967 (GRCm39) |
T843S |
possibly damaging |
Het |
Rln1 |
A |
T |
19: 29,309,499 (GRCm39) |
N93K |
probably damaging |
Het |
Rpl3l |
A |
T |
17: 24,951,401 (GRCm39) |
M101L |
probably benign |
Het |
Rtkn |
A |
G |
6: 83,129,158 (GRCm39) |
Y551C |
probably benign |
Het |
Rundc1 |
G |
C |
11: 101,324,305 (GRCm39) |
R337P |
possibly damaging |
Het |
Scarf1 |
T |
A |
11: 75,405,242 (GRCm39) |
|
probably null |
Het |
Serpinb1b |
T |
A |
13: 33,275,622 (GRCm39) |
|
probably null |
Het |
Sgsm1 |
A |
T |
5: 113,422,201 (GRCm39) |
C484* |
probably null |
Het |
Slc22a19 |
T |
A |
19: 7,650,668 (GRCm39) |
K547* |
probably null |
Het |
Slc22a19 |
T |
C |
19: 7,671,183 (GRCm39) |
T177A |
probably benign |
Het |
Slc6a5 |
A |
C |
7: 49,591,614 (GRCm39) |
K526N |
probably benign |
Het |
Sqle |
G |
A |
15: 59,202,603 (GRCm39) |
R519Q |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,518,627 (GRCm39) |
I517T |
probably benign |
Het |
Taf15 |
A |
T |
11: 83,395,849 (GRCm39) |
D518V |
unknown |
Het |
Tenm4 |
A |
G |
7: 96,545,192 (GRCm39) |
M2440V |
possibly damaging |
Het |
Tm6sf1 |
A |
G |
7: 81,518,458 (GRCm39) |
M122V |
possibly damaging |
Het |
Tmprss9 |
T |
A |
10: 80,728,053 (GRCm39) |
S548T |
possibly damaging |
Het |
Trim62 |
A |
T |
4: 128,777,471 (GRCm39) |
|
probably benign |
Het |
Ugt2b34 |
C |
T |
5: 87,039,141 (GRCm39) |
V507M |
possibly damaging |
Het |
Usp16 |
T |
A |
16: 87,273,693 (GRCm39) |
M423K |
probably benign |
Het |
Vmn1r199 |
T |
A |
13: 22,566,906 (GRCm39) |
S67T |
probably benign |
Het |
Vmn1r62 |
A |
T |
7: 5,678,600 (GRCm39) |
M94L |
probably benign |
Het |
Wnk4 |
G |
T |
11: 101,155,180 (GRCm39) |
E364* |
probably null |
Het |
Xpo1 |
T |
A |
11: 23,232,584 (GRCm39) |
I368N |
probably damaging |
Het |
Zfp366 |
A |
G |
13: 99,382,804 (GRCm39) |
T656A |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,666,338 (GRCm39) |
M113V |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,097,994 (GRCm39) |
V134A |
probably damaging |
Het |
|
Other mutations in Pom121l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02104:Pom121l2
|
APN |
13 |
22,166,445 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02223:Pom121l2
|
APN |
13 |
22,166,265 (GRCm39) |
missense |
probably benign |
0.01 |
R0401:Pom121l2
|
UTSW |
13 |
22,166,395 (GRCm39) |
missense |
probably benign |
0.01 |
R0402:Pom121l2
|
UTSW |
13 |
22,172,649 (GRCm39) |
splice site |
probably benign |
|
R0437:Pom121l2
|
UTSW |
13 |
22,167,375 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0575:Pom121l2
|
UTSW |
13 |
22,168,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R0605:Pom121l2
|
UTSW |
13 |
22,166,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Pom121l2
|
UTSW |
13 |
22,166,644 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0992:Pom121l2
|
UTSW |
13 |
22,166,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1259:Pom121l2
|
UTSW |
13 |
22,166,297 (GRCm39) |
nonsense |
probably null |
|
R1564:Pom121l2
|
UTSW |
13 |
22,167,523 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1603:Pom121l2
|
UTSW |
13 |
22,167,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Pom121l2
|
UTSW |
13 |
22,167,954 (GRCm39) |
missense |
probably benign |
0.03 |
R1970:Pom121l2
|
UTSW |
13 |
22,167,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R2018:Pom121l2
|
UTSW |
13 |
22,166,904 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2180:Pom121l2
|
UTSW |
13 |
22,166,145 (GRCm39) |
missense |
probably benign |
0.08 |
R2277:Pom121l2
|
UTSW |
13 |
22,168,417 (GRCm39) |
missense |
probably benign |
|
R2365:Pom121l2
|
UTSW |
13 |
22,167,954 (GRCm39) |
missense |
probably benign |
0.20 |
R3951:Pom121l2
|
UTSW |
13 |
22,166,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4371:Pom121l2
|
UTSW |
13 |
22,166,409 (GRCm39) |
missense |
probably benign |
0.01 |
R4574:Pom121l2
|
UTSW |
13 |
22,168,572 (GRCm39) |
missense |
probably benign |
0.02 |
R4593:Pom121l2
|
UTSW |
13 |
22,168,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Pom121l2
|
UTSW |
13 |
22,167,984 (GRCm39) |
missense |
probably benign |
0.02 |
R5320:Pom121l2
|
UTSW |
13 |
22,166,015 (GRCm39) |
nonsense |
probably null |
|
R5661:Pom121l2
|
UTSW |
13 |
22,168,425 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5662:Pom121l2
|
UTSW |
13 |
22,166,358 (GRCm39) |
missense |
probably benign |
0.01 |
R5908:Pom121l2
|
UTSW |
13 |
22,165,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R5980:Pom121l2
|
UTSW |
13 |
22,167,546 (GRCm39) |
missense |
probably damaging |
0.96 |
R6145:Pom121l2
|
UTSW |
13 |
22,166,472 (GRCm39) |
nonsense |
probably null |
|
R6160:Pom121l2
|
UTSW |
13 |
22,167,838 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6327:Pom121l2
|
UTSW |
13 |
22,166,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6504:Pom121l2
|
UTSW |
13 |
22,167,631 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6745:Pom121l2
|
UTSW |
13 |
22,167,868 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Pom121l2
|
UTSW |
13 |
22,166,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Pom121l2
|
UTSW |
13 |
22,165,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R6796:Pom121l2
|
UTSW |
13 |
22,167,694 (GRCm39) |
missense |
probably benign |
0.09 |
R6984:Pom121l2
|
UTSW |
13 |
22,166,191 (GRCm39) |
missense |
probably benign |
0.33 |
R7284:Pom121l2
|
UTSW |
13 |
22,166,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Pom121l2
|
UTSW |
13 |
22,168,502 (GRCm39) |
missense |
probably benign |
0.16 |
R7568:Pom121l2
|
UTSW |
13 |
22,166,796 (GRCm39) |
missense |
probably benign |
0.03 |
R7832:Pom121l2
|
UTSW |
13 |
22,168,048 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7956:Pom121l2
|
UTSW |
13 |
22,167,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Pom121l2
|
UTSW |
13 |
22,166,544 (GRCm39) |
missense |
probably benign |
0.00 |
R8506:Pom121l2
|
UTSW |
13 |
22,167,789 (GRCm39) |
missense |
probably benign |
0.04 |
R9167:Pom121l2
|
UTSW |
13 |
22,167,160 (GRCm39) |
missense |
probably damaging |
0.97 |
R9313:Pom121l2
|
UTSW |
13 |
22,168,506 (GRCm39) |
missense |
probably benign |
0.09 |
R9332:Pom121l2
|
UTSW |
13 |
22,165,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R9463:Pom121l2
|
UTSW |
13 |
22,168,402 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Pom121l2
|
UTSW |
13 |
22,172,656 (GRCm39) |
critical splice acceptor site |
probably null |
|
|