Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
A |
T |
5: 8,765,035 (GRCm39) |
D675V |
probably benign |
Het |
Adam21 |
T |
C |
12: 81,607,211 (GRCm39) |
R184G |
probably benign |
Het |
Adcy10 |
A |
G |
1: 165,379,593 (GRCm39) |
K952E |
probably damaging |
Het |
Allc |
A |
T |
12: 28,605,351 (GRCm39) |
I316N |
probably damaging |
Het |
Ano8 |
T |
C |
8: 71,934,812 (GRCm39) |
T432A |
probably benign |
Het |
Cadps2 |
C |
A |
6: 23,412,942 (GRCm39) |
|
probably benign |
Het |
Camsap2 |
T |
C |
1: 136,208,985 (GRCm39) |
S168G |
|
Het |
Ccl19 |
T |
C |
4: 42,756,297 (GRCm39) |
S12G |
probably damaging |
Het |
Cfap91 |
A |
G |
16: 38,140,733 (GRCm39) |
S407P |
possibly damaging |
Het |
Cltc |
A |
G |
11: 86,616,031 (GRCm39) |
S412P |
probably damaging |
Het |
Cwc25 |
A |
G |
11: 97,641,696 (GRCm39) |
|
probably null |
Het |
Cxcr4 |
A |
G |
1: 128,517,535 (GRCm39) |
F42S |
probably damaging |
Het |
Dnal4 |
T |
C |
15: 79,646,169 (GRCm39) |
T112A |
probably benign |
Het |
Dock9 |
C |
A |
14: 121,889,206 (GRCm39) |
G304C |
probably benign |
Het |
Evpl |
T |
C |
11: 116,113,758 (GRCm39) |
T1311A |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,035,815 (GRCm39) |
Y3156H |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,733,841 (GRCm39) |
I1070M |
possibly damaging |
Het |
Hcls1 |
A |
G |
16: 36,771,511 (GRCm39) |
D139G |
probably damaging |
Het |
Ighv1-7 |
A |
G |
12: 114,502,390 (GRCm39) |
S26P |
probably benign |
Het |
Il1r1 |
A |
T |
1: 40,352,509 (GRCm39) |
T563S |
probably benign |
Het |
Kcna1 |
C |
T |
6: 126,619,703 (GRCm39) |
D206N |
probably benign |
Het |
Kcnk4 |
A |
G |
19: 6,904,995 (GRCm39) |
Y219H |
probably damaging |
Het |
Kcnt2 |
G |
A |
1: 140,377,955 (GRCm39) |
A403T |
probably damaging |
Het |
Mdp1 |
T |
A |
14: 55,897,523 (GRCm39) |
N44I |
probably benign |
Het |
Nceh1 |
A |
G |
3: 27,295,374 (GRCm39) |
N212D |
probably benign |
Het |
Nynrin |
G |
A |
14: 56,108,982 (GRCm39) |
G1363D |
probably benign |
Het |
Or5d20-ps1 |
T |
A |
2: 87,931,703 (GRCm39) |
R209S |
unknown |
Het |
Or6n1 |
T |
C |
1: 173,916,723 (GRCm39) |
I39T |
possibly damaging |
Het |
Or6x1 |
A |
G |
9: 40,098,717 (GRCm39) |
H102R |
probably damaging |
Het |
Or8d1 |
T |
A |
9: 38,766,460 (GRCm39) |
I34N |
probably damaging |
Het |
Parp2 |
T |
A |
14: 51,047,630 (GRCm39) |
M47K |
probably benign |
Het |
Pfdn6 |
T |
C |
17: 34,158,951 (GRCm39) |
|
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Plb1 |
T |
A |
5: 32,430,413 (GRCm39) |
H123Q |
possibly damaging |
Het |
Pml |
C |
A |
9: 58,141,968 (GRCm39) |
R288L |
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,205,836 (GRCm39) |
D238G |
probably damaging |
Het |
Rad51ap2 |
T |
A |
12: 11,508,792 (GRCm39) |
S905T |
probably benign |
Het |
Sclt1 |
C |
T |
3: 41,611,811 (GRCm39) |
R487H |
probably damaging |
Het |
Serpina3b |
A |
G |
12: 104,097,335 (GRCm39) |
I205M |
probably benign |
Het |
Sowahb |
A |
G |
5: 93,191,292 (GRCm39) |
S476P |
possibly damaging |
Het |
Srgap3 |
C |
T |
6: 112,716,325 (GRCm39) |
R625H |
probably benign |
Het |
Tent4a |
A |
G |
13: 69,648,600 (GRCm39) |
Y719H |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,935,532 (GRCm39) |
Y2611H |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,250,554 (GRCm39) |
E237G |
possibly damaging |
Het |
Vmn1r87 |
T |
A |
7: 12,866,086 (GRCm39) |
Y67F |
possibly damaging |
Het |
Vmn2r107 |
G |
A |
17: 20,595,808 (GRCm39) |
C787Y |
probably damaging |
Het |
Zscan4-ps3 |
T |
A |
7: 11,346,600 (GRCm39) |
I212N |
probably damaging |
Het |
|
Other mutations in Cyp4a12a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00931:Cyp4a12a
|
APN |
4 |
115,159,153 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00948:Cyp4a12a
|
APN |
4 |
115,159,159 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03143:Cyp4a12a
|
APN |
4 |
115,159,200 (GRCm39) |
missense |
probably benign |
0.00 |
R0099:Cyp4a12a
|
UTSW |
4 |
115,183,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Cyp4a12a
|
UTSW |
4 |
115,183,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R1893:Cyp4a12a
|
UTSW |
4 |
115,183,864 (GRCm39) |
missense |
probably benign |
0.03 |
R2018:Cyp4a12a
|
UTSW |
4 |
115,184,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R3423:Cyp4a12a
|
UTSW |
4 |
115,184,471 (GRCm39) |
missense |
probably benign |
0.37 |
R4445:Cyp4a12a
|
UTSW |
4 |
115,183,980 (GRCm39) |
critical splice donor site |
probably null |
|
R4586:Cyp4a12a
|
UTSW |
4 |
115,184,509 (GRCm39) |
missense |
probably benign |
0.01 |
R4765:Cyp4a12a
|
UTSW |
4 |
115,183,388 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4823:Cyp4a12a
|
UTSW |
4 |
115,184,610 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5131:Cyp4a12a
|
UTSW |
4 |
115,185,017 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5841:Cyp4a12a
|
UTSW |
4 |
115,183,899 (GRCm39) |
missense |
probably benign |
0.03 |
R6017:Cyp4a12a
|
UTSW |
4 |
115,183,476 (GRCm39) |
nonsense |
probably null |
|
R6039:Cyp4a12a
|
UTSW |
4 |
115,184,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Cyp4a12a
|
UTSW |
4 |
115,184,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Cyp4a12a
|
UTSW |
4 |
115,184,643 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6883:Cyp4a12a
|
UTSW |
4 |
115,159,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7308:Cyp4a12a
|
UTSW |
4 |
115,184,955 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7327:Cyp4a12a
|
UTSW |
4 |
115,184,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Cyp4a12a
|
UTSW |
4 |
115,184,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R7595:Cyp4a12a
|
UTSW |
4 |
115,189,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R7638:Cyp4a12a
|
UTSW |
4 |
115,184,670 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8303:Cyp4a12a
|
UTSW |
4 |
115,186,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8491:Cyp4a12a
|
UTSW |
4 |
115,158,650 (GRCm39) |
splice site |
probably null |
|
R8954:Cyp4a12a
|
UTSW |
4 |
115,185,935 (GRCm39) |
nonsense |
probably null |
|
R9031:Cyp4a12a
|
UTSW |
4 |
115,189,199 (GRCm39) |
makesense |
probably null |
|
R9356:Cyp4a12a
|
UTSW |
4 |
115,185,915 (GRCm39) |
missense |
probably benign |
|
R9674:Cyp4a12a
|
UTSW |
4 |
115,186,156 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Cyp4a12a
|
UTSW |
4 |
115,185,009 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Cyp4a12a
|
UTSW |
4 |
115,186,200 (GRCm39) |
critical splice donor site |
probably null |
|
|