Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
A |
11: 3,844,933 (GRCm39) |
E52V |
probably benign |
Het |
4930516K23Rik |
G |
A |
7: 103,708,083 (GRCm39) |
T242M |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,990,253 (GRCm39) |
I17F |
probably benign |
Het |
Adam25 |
T |
A |
8: 41,207,710 (GRCm39) |
Y325* |
probably null |
Het |
Adamts16 |
C |
T |
13: 70,939,910 (GRCm39) |
|
probably benign |
Het |
Akr1b1 |
A |
T |
6: 34,289,639 (GRCm39) |
V57E |
probably benign |
Het |
Api5 |
A |
G |
2: 94,255,374 (GRCm39) |
L267P |
probably damaging |
Het |
Asap3 |
T |
C |
4: 135,963,726 (GRCm39) |
Y329H |
probably benign |
Het |
Atp13a4 |
C |
T |
16: 29,273,592 (GRCm39) |
R442K |
|
Het |
Cadps2 |
T |
C |
6: 23,302,300 (GRCm39) |
D1129G |
probably benign |
Het |
Cd79b |
T |
A |
11: 106,203,632 (GRCm39) |
Q145L |
probably benign |
Het |
Cdh23 |
C |
T |
10: 60,140,908 (GRCm39) |
E3147K |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,424,481 (GRCm39) |
D722G |
possibly damaging |
Het |
Col4a4 |
A |
G |
1: 82,431,533 (GRCm39) |
W1584R |
unknown |
Het |
Cops8 |
T |
C |
1: 90,532,155 (GRCm39) |
L46P |
probably damaging |
Het |
Cpne1 |
T |
C |
2: 155,913,965 (GRCm39) |
Y146C |
probably benign |
Het |
Ctdnep1 |
T |
A |
11: 69,875,311 (GRCm39) |
V80E |
probably damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,434,877 (GRCm39) |
I327T |
probably benign |
Het |
Dlgap3 |
C |
A |
4: 127,127,463 (GRCm39) |
H710Q |
probably damaging |
Het |
Dnah9 |
T |
C |
11: 65,802,747 (GRCm39) |
M3448V |
probably benign |
Het |
E030018B13Rik |
C |
A |
7: 63,569,727 (GRCm39) |
Q84K |
unknown |
Het |
Efna5 |
A |
G |
17: 63,188,053 (GRCm39) |
S25P |
possibly damaging |
Het |
Egfl8 |
T |
G |
17: 34,833,751 (GRCm39) |
T76P |
probably damaging |
Het |
Endod1 |
A |
G |
9: 14,268,942 (GRCm39) |
L181P |
probably damaging |
Het |
Epha3 |
A |
G |
16: 63,472,838 (GRCm39) |
L349P |
possibly damaging |
Het |
Fam161b |
T |
A |
12: 84,395,056 (GRCm39) |
T553S |
probably benign |
Het |
Fmnl1 |
T |
C |
11: 103,087,967 (GRCm39) |
F981L |
unknown |
Het |
Galr2 |
T |
A |
11: 116,173,973 (GRCm39) |
V201E |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Greb1l |
T |
C |
18: 10,541,825 (GRCm39) |
S1191P |
probably benign |
Het |
Hmg20b |
T |
C |
10: 81,184,821 (GRCm39) |
R84G |
probably damaging |
Het |
Inppl1 |
T |
C |
7: 101,472,593 (GRCm39) |
D1234G |
possibly damaging |
Het |
Insl5 |
A |
G |
4: 102,883,760 (GRCm39) |
S54P |
probably damaging |
Het |
Itpr1 |
T |
A |
6: 108,355,159 (GRCm39) |
F483L |
possibly damaging |
Het |
Kif21a |
T |
C |
15: 90,855,930 (GRCm39) |
E609G |
probably benign |
Het |
Kpna7 |
A |
T |
5: 144,941,840 (GRCm39) |
V150D |
probably damaging |
Het |
L1td1 |
T |
A |
4: 98,622,175 (GRCm39) |
C246S |
possibly damaging |
Het |
Laptm4a |
T |
A |
12: 8,988,139 (GRCm39) |
M292K |
possibly damaging |
Het |
Lefty2 |
C |
G |
1: 180,725,043 (GRCm39) |
P258A |
possibly damaging |
Het |
Map4k1 |
G |
A |
7: 28,701,052 (GRCm39) |
V719M |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,463,590 (GRCm39) |
H1292Q |
probably benign |
Het |
Nfkbia |
C |
T |
12: 55,537,340 (GRCm39) |
G250S |
probably damaging |
Het |
Nkain3 |
T |
C |
4: 20,245,902 (GRCm39) |
T163A |
unknown |
Het |
Npcd |
T |
C |
15: 79,713,163 (GRCm39) |
E88G |
probably benign |
Het |
Oas1f |
A |
T |
5: 120,989,556 (GRCm39) |
Y165F |
probably benign |
Het |
Or10d4 |
T |
A |
9: 39,580,737 (GRCm39) |
L128* |
probably null |
Het |
Or51aa5 |
A |
G |
7: 103,167,030 (GRCm39) |
I187T |
possibly damaging |
Het |
Or52e2 |
T |
C |
7: 102,804,660 (GRCm39) |
D98G |
probably benign |
Het |
Phtf2 |
T |
C |
5: 21,008,275 (GRCm39) |
I135M |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,125,604 (GRCm39) |
E1177G |
|
Het |
Polr3gl |
A |
T |
3: 96,485,833 (GRCm39) |
D214E |
probably damaging |
Het |
Pramel25 |
C |
T |
4: 143,519,322 (GRCm39) |
Q28* |
probably null |
Het |
Pramel51 |
T |
C |
12: 88,143,952 (GRCm39) |
E295G |
probably benign |
Het |
Prkar1a |
C |
A |
11: 109,556,744 (GRCm39) |
Q275K |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,054,039 (GRCm39) |
|
probably null |
Het |
Pwwp2a |
C |
A |
11: 43,596,344 (GRCm39) |
P503Q |
probably damaging |
Het |
Rad17 |
T |
C |
13: 100,754,192 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
T |
C |
11: 54,570,065 (GRCm39) |
L1146S |
probably benign |
Het |
Rara |
C |
A |
11: 98,864,452 (GRCm39) |
Q460K |
unknown |
Het |
Rassf4 |
C |
T |
6: 116,638,897 (GRCm39) |
|
probably benign |
Het |
Rere |
A |
G |
4: 150,696,471 (GRCm39) |
D492G |
unknown |
Het |
Selenon |
T |
G |
4: 134,268,153 (GRCm39) |
K460T |
possibly damaging |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,241,988 (GRCm39) |
T245A |
probably benign |
Het |
Stat4 |
C |
T |
1: 52,144,892 (GRCm39) |
A726V |
probably benign |
Het |
Stim1 |
G |
T |
7: 102,070,597 (GRCm39) |
V277L |
probably damaging |
Het |
Strbp |
A |
G |
2: 37,514,503 (GRCm39) |
|
probably null |
Het |
Tln2 |
T |
C |
9: 67,174,105 (GRCm39) |
Y860C |
probably damaging |
Het |
Tmod4 |
T |
A |
3: 95,033,289 (GRCm39) |
|
probably null |
Het |
Tpm3-rs7 |
T |
C |
14: 113,552,493 (GRCm39) |
V129A |
probably benign |
Het |
Trp53bp2 |
C |
T |
1: 182,273,971 (GRCm39) |
P41S |
|
Het |
Tubal3 |
G |
A |
13: 3,983,428 (GRCm39) |
D403N |
probably damaging |
Het |
Zfp369 |
T |
C |
13: 65,444,044 (GRCm39) |
S396P |
possibly damaging |
Het |
Zfp976 |
G |
A |
7: 42,262,575 (GRCm39) |
H422Y |
possibly damaging |
Het |
|
Other mutations in Cyp4a32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02225:Cyp4a32
|
APN |
4 |
115,467,700 (GRCm39) |
missense |
probably benign |
|
IGL02546:Cyp4a32
|
APN |
4 |
115,468,520 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02578:Cyp4a32
|
APN |
4 |
115,466,939 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02663:Cyp4a32
|
APN |
4 |
115,467,787 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02832:Cyp4a32
|
APN |
4 |
115,471,818 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03283:Cyp4a32
|
APN |
4 |
115,468,280 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03357:Cyp4a32
|
APN |
4 |
115,468,798 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03406:Cyp4a32
|
APN |
4 |
115,459,500 (GRCm39) |
missense |
probably benign |
0.00 |
R0379:Cyp4a32
|
UTSW |
4 |
115,478,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R1339:Cyp4a32
|
UTSW |
4 |
115,468,760 (GRCm39) |
missense |
probably damaging |
0.98 |
R1435:Cyp4a32
|
UTSW |
4 |
115,463,863 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Cyp4a32
|
UTSW |
4 |
115,460,147 (GRCm39) |
nonsense |
probably null |
|
R1520:Cyp4a32
|
UTSW |
4 |
115,471,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R1587:Cyp4a32
|
UTSW |
4 |
115,467,731 (GRCm39) |
missense |
probably benign |
0.06 |
R1719:Cyp4a32
|
UTSW |
4 |
115,468,505 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1932:Cyp4a32
|
UTSW |
4 |
115,468,474 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4184:Cyp4a32
|
UTSW |
4 |
115,478,720 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4580:Cyp4a32
|
UTSW |
4 |
115,460,126 (GRCm39) |
splice site |
silent |
|
R5004:Cyp4a32
|
UTSW |
4 |
115,458,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R6345:Cyp4a32
|
UTSW |
4 |
115,459,560 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7231:Cyp4a32
|
UTSW |
4 |
115,466,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Cyp4a32
|
UTSW |
4 |
115,459,499 (GRCm39) |
missense |
probably benign |
|
R7419:Cyp4a32
|
UTSW |
4 |
115,468,234 (GRCm39) |
missense |
probably benign |
|
R7716:Cyp4a32
|
UTSW |
4 |
115,458,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R9009:Cyp4a32
|
UTSW |
4 |
115,467,802 (GRCm39) |
missense |
probably null |
1.00 |
R9266:Cyp4a32
|
UTSW |
4 |
115,468,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R9330:Cyp4a32
|
UTSW |
4 |
115,478,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9345:Cyp4a32
|
UTSW |
4 |
115,467,699 (GRCm39) |
missense |
probably benign |
|
R9442:Cyp4a32
|
UTSW |
4 |
115,468,422 (GRCm39) |
missense |
probably benign |
0.21 |
Z1177:Cyp4a32
|
UTSW |
4 |
115,468,542 (GRCm39) |
missense |
probably benign |
0.03 |
|