Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810064F22Rik |
C |
T |
9: 22,119,367 (GRCm39) |
|
noncoding transcript |
Het |
Aass |
C |
T |
6: 23,075,151 (GRCm39) |
|
probably benign |
Het |
Abcb5 |
C |
A |
12: 118,869,933 (GRCm39) |
V742F |
possibly damaging |
Het |
Abcd4 |
A |
G |
12: 84,659,602 (GRCm39) |
I165T |
probably damaging |
Het |
Acer3 |
T |
C |
7: 97,906,949 (GRCm39) |
Y119C |
probably damaging |
Het |
Ap3d1 |
A |
T |
10: 80,568,789 (GRCm39) |
|
probably benign |
Het |
Ascc2 |
T |
A |
11: 4,618,380 (GRCm39) |
I325N |
probably benign |
Het |
Atad2b |
T |
A |
12: 5,074,591 (GRCm39) |
I1050N |
probably damaging |
Het |
Brms1l |
T |
C |
12: 55,912,742 (GRCm39) |
V245A |
probably benign |
Het |
Cadps2 |
T |
A |
6: 23,263,561 (GRCm39) |
D1270V |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,246,639 (GRCm39) |
M936K |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,792,666 (GRCm39) |
|
probably benign |
Het |
Dner |
T |
C |
1: 84,563,030 (GRCm39) |
|
probably benign |
Het |
Dzip1 |
T |
A |
14: 119,124,609 (GRCm39) |
R555* |
probably null |
Het |
Erich3 |
T |
A |
3: 154,444,788 (GRCm39) |
D518E |
probably benign |
Het |
Gli2 |
G |
A |
1: 118,765,236 (GRCm39) |
R972C |
probably damaging |
Het |
Gpc1 |
G |
A |
1: 92,785,031 (GRCm39) |
R358H |
possibly damaging |
Het |
Grb7 |
T |
C |
11: 98,344,634 (GRCm39) |
Y346H |
probably damaging |
Het |
Heg1 |
T |
C |
16: 33,581,173 (GRCm39) |
L1192P |
probably damaging |
Het |
Il16 |
T |
A |
7: 83,312,349 (GRCm39) |
Q445L |
probably benign |
Het |
Il17d |
C |
T |
14: 57,779,777 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,520,301 (GRCm39) |
N1936K |
probably benign |
Het |
Lrrc45 |
T |
C |
11: 120,609,064 (GRCm39) |
|
probably benign |
Het |
Mib2 |
C |
T |
4: 155,743,917 (GRCm39) |
G42S |
probably damaging |
Het |
Mphosph9 |
T |
A |
5: 124,400,100 (GRCm39) |
R934* |
probably null |
Het |
Nek11 |
T |
A |
9: 105,172,570 (GRCm39) |
|
probably null |
Het |
Nf1 |
T |
C |
11: 79,329,537 (GRCm39) |
S634P |
probably benign |
Het |
Or14c40 |
T |
A |
7: 86,313,314 (GRCm39) |
M148K |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,396,355 (GRCm39) |
V1959A |
probably benign |
Het |
Pkp2 |
G |
T |
16: 16,043,894 (GRCm39) |
G216V |
probably benign |
Het |
Ppp1r16a |
T |
C |
15: 76,578,211 (GRCm39) |
L394P |
probably damaging |
Het |
Ptprc |
G |
A |
1: 137,996,139 (GRCm39) |
Q1070* |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rprd2 |
A |
T |
3: 95,672,730 (GRCm39) |
I891N |
probably damaging |
Het |
Speer1e |
A |
T |
5: 11,236,488 (GRCm39) |
T174S |
probably benign |
Het |
Taf15 |
T |
C |
11: 83,389,932 (GRCm39) |
I40T |
probably damaging |
Het |
Tshz1 |
A |
G |
18: 84,031,178 (GRCm39) |
Y1077H |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,693,833 (GRCm39) |
E223G |
possibly damaging |
Het |
|
Other mutations in Enpp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01536:Enpp4
|
APN |
17 |
44,410,494 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02150:Enpp4
|
APN |
17 |
44,413,049 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02451:Enpp4
|
APN |
17 |
44,412,315 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02879:Enpp4
|
APN |
17 |
44,412,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0005:Enpp4
|
UTSW |
17 |
44,413,066 (GRCm39) |
missense |
probably benign |
0.04 |
R0540:Enpp4
|
UTSW |
17 |
44,410,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Enpp4
|
UTSW |
17 |
44,410,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1334:Enpp4
|
UTSW |
17 |
44,413,259 (GRCm39) |
missense |
probably benign |
0.02 |
R1632:Enpp4
|
UTSW |
17 |
44,410,544 (GRCm39) |
missense |
probably damaging |
0.99 |
R2567:Enpp4
|
UTSW |
17 |
44,412,736 (GRCm39) |
missense |
probably damaging |
0.97 |
R4272:Enpp4
|
UTSW |
17 |
44,412,698 (GRCm39) |
missense |
probably benign |
0.01 |
R4273:Enpp4
|
UTSW |
17 |
44,412,698 (GRCm39) |
missense |
probably benign |
0.01 |
R4750:Enpp4
|
UTSW |
17 |
44,413,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Enpp4
|
UTSW |
17 |
44,413,371 (GRCm39) |
missense |
probably benign |
0.00 |
R6296:Enpp4
|
UTSW |
17 |
44,413,371 (GRCm39) |
missense |
probably benign |
0.00 |
R7180:Enpp4
|
UTSW |
17 |
44,412,928 (GRCm39) |
missense |
probably benign |
0.03 |
R8036:Enpp4
|
UTSW |
17 |
44,413,136 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8135:Enpp4
|
UTSW |
17 |
44,412,226 (GRCm39) |
missense |
probably benign |
0.00 |
R9168:Enpp4
|
UTSW |
17 |
44,413,141 (GRCm39) |
missense |
probably damaging |
0.99 |
R9209:Enpp4
|
UTSW |
17 |
44,412,252 (GRCm39) |
nonsense |
probably null |
|
|