Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610528J11Rik |
A |
G |
4: 118,386,490 (GRCm39) |
M1V |
probably null |
Het |
Acss3 |
T |
C |
10: 106,773,124 (GRCm39) |
S621G |
probably benign |
Het |
Adam1a |
C |
T |
5: 121,657,145 (GRCm39) |
R716Q |
probably benign |
Het |
Ankrd26 |
G |
T |
6: 118,535,902 (GRCm39) |
N177K |
probably damaging |
Het |
Ankrd31 |
G |
A |
13: 96,969,212 (GRCm39) |
V950I |
probably damaging |
Het |
Ano4 |
A |
G |
10: 88,788,160 (GRCm39) |
Y922H |
probably damaging |
Het |
Axin2 |
A |
T |
11: 108,822,341 (GRCm39) |
N298Y |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,303,882 (GRCm39) |
M2392K |
probably benign |
Het |
Coasy |
A |
G |
11: 100,974,202 (GRCm39) |
S123G |
probably benign |
Het |
Cracdl |
A |
G |
1: 37,676,993 (GRCm39) |
V63A |
probably damaging |
Het |
Ctla2a |
A |
T |
13: 61,083,854 (GRCm39) |
M26K |
probably benign |
Het |
Cts8 |
A |
T |
13: 61,396,882 (GRCm39) |
|
probably benign |
Het |
Eif2ak4 |
A |
G |
2: 118,287,617 (GRCm39) |
Y1195C |
probably damaging |
Het |
Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
Exoc6 |
A |
G |
19: 37,578,360 (GRCm39) |
D401G |
probably benign |
Het |
Fmo1 |
A |
G |
1: 162,663,773 (GRCm39) |
V252A |
probably benign |
Het |
Furin |
T |
C |
7: 80,048,437 (GRCm39) |
K28E |
probably benign |
Het |
Gmip |
T |
A |
8: 70,270,428 (GRCm39) |
F713I |
probably damaging |
Het |
Hyal6 |
T |
C |
6: 24,734,103 (GRCm39) |
L12P |
possibly damaging |
Het |
Ido1 |
T |
C |
8: 25,081,523 (GRCm39) |
N144D |
probably benign |
Het |
Igsf10 |
T |
A |
3: 59,226,888 (GRCm39) |
T2262S |
possibly damaging |
Het |
Insrr |
T |
C |
3: 87,718,276 (GRCm39) |
F923S |
probably benign |
Het |
Kank1 |
G |
T |
19: 25,386,928 (GRCm39) |
M200I |
probably damaging |
Het |
Kctd15 |
A |
G |
7: 34,341,508 (GRCm39) |
Y140H |
probably damaging |
Het |
Kif3c |
T |
A |
12: 3,416,690 (GRCm39) |
I237N |
probably damaging |
Het |
Klhl26 |
T |
C |
8: 70,905,455 (GRCm39) |
S152G |
possibly damaging |
Het |
Lce1k |
C |
A |
3: 92,714,097 (GRCm39) |
C29F |
unknown |
Het |
Map1a |
A |
G |
2: 121,131,791 (GRCm39) |
E869G |
possibly damaging |
Het |
Mcmbp |
T |
C |
7: 128,300,281 (GRCm39) |
E576G |
probably benign |
Het |
Mrps22 |
A |
G |
9: 98,476,163 (GRCm39) |
V231A |
probably benign |
Het |
Myo1a |
C |
T |
10: 127,551,534 (GRCm39) |
L697F |
possibly damaging |
Het |
Ncapd3 |
T |
C |
9: 26,999,297 (GRCm39) |
V1291A |
probably benign |
Het |
Nherf4 |
T |
A |
9: 44,160,141 (GRCm39) |
|
probably benign |
Het |
Or9m1 |
A |
T |
2: 87,733,307 (GRCm39) |
S238T |
possibly damaging |
Het |
Pcdhb6 |
A |
G |
18: 37,468,431 (GRCm39) |
T451A |
possibly damaging |
Het |
Pi4ka |
C |
A |
16: 17,130,310 (GRCm39) |
W1032L |
|
Het |
Pkhd1l1 |
T |
A |
15: 44,396,403 (GRCm39) |
I1975N |
probably benign |
Het |
Pnpla6 |
T |
C |
8: 3,567,637 (GRCm39) |
M115T |
possibly damaging |
Het |
Poldip2 |
G |
A |
11: 78,412,667 (GRCm39) |
R347Q |
probably damaging |
Het |
Pramel18 |
G |
A |
4: 101,768,935 (GRCm39) |
V429M |
probably benign |
Het |
Rapgef6 |
C |
T |
11: 54,582,392 (GRCm39) |
Q1440* |
probably null |
Het |
Rtn3 |
A |
T |
19: 7,434,105 (GRCm39) |
I629K |
possibly damaging |
Het |
Selenov |
A |
G |
7: 27,987,728 (GRCm39) |
F278L |
probably damaging |
Het |
Skor2 |
G |
A |
18: 76,948,504 (GRCm39) |
G742D |
probably damaging |
Het |
Spata31d1c |
C |
T |
13: 65,183,429 (GRCm39) |
P324S |
probably benign |
Het |
Tbc1d14 |
A |
T |
5: 36,676,682 (GRCm39) |
I403N |
probably damaging |
Het |
Tekt3 |
A |
T |
11: 62,978,052 (GRCm39) |
Q374L |
probably damaging |
Het |
Tg |
T |
C |
15: 66,645,332 (GRCm39) |
|
probably null |
Het |
Thnsl2 |
T |
C |
6: 71,116,927 (GRCm39) |
D75G |
probably benign |
Het |
Tnr |
A |
T |
1: 159,701,692 (GRCm39) |
K598* |
probably null |
Het |
Tshr |
T |
A |
12: 91,468,829 (GRCm39) |
|
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,185,735 (GRCm39) |
S1483P |
|
Het |
Usp42 |
T |
C |
5: 143,701,695 (GRCm39) |
E776G |
|
Het |
Vmn2r118 |
T |
C |
17: 55,917,216 (GRCm39) |
E432G |
possibly damaging |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,697,433 (GRCm39) |
I830T |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,464,159 (GRCm39) |
E1464G |
probably damaging |
Het |
Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
possibly damaging |
Het |
Zxdc |
A |
G |
6: 90,359,305 (GRCm39) |
T646A |
probably benign |
Het |
|
Other mutations in Cyp4a30b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03184:Cyp4a30b
|
APN |
4 |
115,316,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03233:Cyp4a30b
|
APN |
4 |
115,316,167 (GRCm39) |
missense |
probably benign |
0.08 |
sly
|
UTSW |
4 |
115,315,493 (GRCm39) |
missense |
probably benign |
0.00 |
tricky
|
UTSW |
4 |
115,311,662 (GRCm39) |
nonsense |
probably null |
|
R1394:Cyp4a30b
|
UTSW |
4 |
115,328,089 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2870:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2870:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2871:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2871:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2872:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2872:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2873:Cyp4a30b
|
UTSW |
4 |
115,315,559 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3818:Cyp4a30b
|
UTSW |
4 |
115,316,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R4052:Cyp4a30b
|
UTSW |
4 |
115,311,539 (GRCm39) |
missense |
probably benign |
0.00 |
R4684:Cyp4a30b
|
UTSW |
4 |
115,312,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5558:Cyp4a30b
|
UTSW |
4 |
115,316,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:Cyp4a30b
|
UTSW |
4 |
115,316,588 (GRCm39) |
nonsense |
probably null |
|
R6242:Cyp4a30b
|
UTSW |
4 |
115,311,587 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6511:Cyp4a30b
|
UTSW |
4 |
115,313,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:Cyp4a30b
|
UTSW |
4 |
115,318,571 (GRCm39) |
missense |
probably benign |
0.02 |
R7285:Cyp4a30b
|
UTSW |
4 |
115,313,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Cyp4a30b
|
UTSW |
4 |
115,315,493 (GRCm39) |
missense |
probably benign |
0.00 |
R8314:Cyp4a30b
|
UTSW |
4 |
115,315,535 (GRCm39) |
missense |
probably benign |
0.00 |
R8439:Cyp4a30b
|
UTSW |
4 |
115,314,972 (GRCm39) |
missense |
probably benign |
0.44 |
R8681:Cyp4a30b
|
UTSW |
4 |
115,314,942 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8735:Cyp4a30b
|
UTSW |
4 |
115,309,976 (GRCm39) |
nonsense |
probably null |
|
R8816:Cyp4a30b
|
UTSW |
4 |
115,309,834 (GRCm39) |
missense |
probably benign |
0.23 |
R8845:Cyp4a30b
|
UTSW |
4 |
115,315,493 (GRCm39) |
missense |
probably benign |
0.04 |
R9622:Cyp4a30b
|
UTSW |
4 |
115,328,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R9672:Cyp4a30b
|
UTSW |
4 |
115,316,576 (GRCm39) |
missense |
probably benign |
0.16 |
R9792:Cyp4a30b
|
UTSW |
4 |
115,316,167 (GRCm39) |
missense |
probably benign |
0.01 |
R9793:Cyp4a30b
|
UTSW |
4 |
115,316,167 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cyp4a30b
|
UTSW |
4 |
115,328,156 (GRCm39) |
missense |
possibly damaging |
0.61 |
|