Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
C |
2: 25,333,742 (GRCm39) |
L1730P |
possibly damaging |
Het |
Adam9 |
T |
C |
8: 25,460,753 (GRCm39) |
N577S |
probably damaging |
Het |
Add1 |
T |
C |
5: 34,770,923 (GRCm39) |
Y316H |
probably benign |
Het |
Agpat3 |
T |
C |
10: 78,113,890 (GRCm39) |
D266G |
probably null |
Het |
Aldh3a2 |
C |
A |
11: 61,115,384 (GRCm39) |
Q524H |
probably benign |
Het |
Ano4 |
T |
A |
10: 88,788,154 (GRCm39) |
I753F |
possibly damaging |
Het |
AW011738 |
T |
A |
4: 156,288,104 (GRCm39) |
|
probably benign |
Het |
B4galt3 |
C |
T |
1: 171,103,738 (GRCm39) |
T103M |
probably damaging |
Het |
Cabs1 |
C |
T |
5: 88,128,054 (GRCm39) |
T235I |
probably damaging |
Het |
Casq2 |
A |
G |
3: 102,040,715 (GRCm39) |
H272R |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,912,866 (GRCm39) |
|
probably null |
Het |
Cdh12 |
A |
T |
15: 21,584,031 (GRCm39) |
M624L |
probably benign |
Het |
Cdh5 |
A |
C |
8: 104,867,314 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,798,651 (GRCm39) |
|
probably benign |
Het |
Cpne2 |
A |
T |
8: 95,281,561 (GRCm39) |
I199F |
probably damaging |
Het |
Crebbp |
A |
T |
16: 3,901,927 (GRCm39) |
F2399L |
possibly damaging |
Het |
Defb36 |
T |
C |
2: 152,454,499 (GRCm39) |
C53R |
probably damaging |
Het |
Degs1 |
T |
C |
1: 182,107,257 (GRCm39) |
M1V |
probably null |
Het |
Disp2 |
T |
A |
2: 118,620,819 (GRCm39) |
F517Y |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,246,465 (GRCm39) |
D601G |
probably benign |
Het |
Dnpep |
G |
A |
1: 75,289,182 (GRCm39) |
Q310* |
probably null |
Het |
Dsg1a |
A |
G |
18: 20,473,935 (GRCm39) |
T1003A |
probably benign |
Het |
Fbrsl1 |
C |
G |
5: 110,543,906 (GRCm39) |
|
probably benign |
Het |
Foxh1 |
A |
T |
15: 76,553,454 (GRCm39) |
L116H |
probably damaging |
Het |
Gigyf2 |
G |
A |
1: 87,339,597 (GRCm39) |
|
probably benign |
Het |
Golm2 |
T |
C |
2: 121,736,565 (GRCm39) |
|
probably benign |
Het |
Gp1ba |
A |
T |
11: 70,531,859 (GRCm39) |
|
probably benign |
Het |
Gucy1b1 |
A |
G |
3: 81,945,218 (GRCm39) |
|
probably benign |
Het |
Gucy2g |
T |
G |
19: 55,229,598 (GRCm39) |
D24A |
probably benign |
Het |
Hirip3 |
A |
G |
7: 126,462,614 (GRCm39) |
K190R |
probably damaging |
Het |
Hmmr |
T |
C |
11: 40,596,781 (GRCm39) |
N717D |
probably damaging |
Het |
Il12b |
A |
T |
11: 44,301,045 (GRCm39) |
Y187F |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,388,070 (GRCm39) |
I859T |
probably benign |
Het |
Jmjd1c |
T |
C |
10: 67,055,105 (GRCm39) |
L175P |
probably damaging |
Het |
Klc2 |
T |
C |
19: 5,162,774 (GRCm39) |
M242V |
possibly damaging |
Het |
Klf3 |
T |
C |
5: 64,979,446 (GRCm39) |
M96T |
probably benign |
Het |
Lrrc66 |
G |
T |
5: 73,764,431 (GRCm39) |
H871N |
probably benign |
Het |
Ltn1 |
A |
T |
16: 87,222,528 (GRCm39) |
D168E |
probably benign |
Het |
Mak |
T |
C |
13: 41,186,072 (GRCm39) |
D532G |
probably damaging |
Het |
Marchf6 |
A |
G |
15: 31,462,151 (GRCm39) |
M859T |
probably benign |
Het |
Meak7 |
T |
C |
8: 120,489,089 (GRCm39) |
D398G |
possibly damaging |
Het |
Mlxipl |
C |
A |
5: 135,161,177 (GRCm39) |
N365K |
probably damaging |
Het |
Mplkip |
T |
C |
13: 17,870,337 (GRCm39) |
S90P |
possibly damaging |
Het |
Myo5c |
A |
T |
9: 75,176,807 (GRCm39) |
H584L |
probably benign |
Het |
Myt1l |
A |
G |
12: 29,901,719 (GRCm39) |
T228A |
possibly damaging |
Het |
Nxpe3 |
A |
T |
16: 55,686,592 (GRCm39) |
Y139N |
possibly damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or51f2 |
A |
G |
7: 102,526,347 (GRCm39) |
T7A |
probably benign |
Het |
Or8k40 |
T |
A |
2: 86,584,981 (GRCm39) |
I34L |
probably damaging |
Het |
Pak6 |
C |
T |
2: 118,520,813 (GRCm39) |
S268F |
possibly damaging |
Het |
Parp10 |
G |
A |
15: 76,127,266 (GRCm39) |
A57V |
probably damaging |
Het |
Pik3r3 |
T |
A |
4: 116,113,465 (GRCm39) |
D69E |
probably damaging |
Het |
Polr2a |
T |
G |
11: 69,638,251 (GRCm39) |
K105T |
probably damaging |
Het |
Prdm16 |
A |
T |
4: 154,413,295 (GRCm39) |
|
probably benign |
Het |
Prepl |
G |
A |
17: 85,390,670 (GRCm39) |
T96I |
probably benign |
Het |
Ret |
C |
T |
6: 118,142,956 (GRCm39) |
|
probably benign |
Het |
Rgl3 |
A |
T |
9: 21,887,108 (GRCm39) |
D541E |
probably benign |
Het |
Rpa1 |
A |
C |
11: 75,209,355 (GRCm39) |
Y143D |
probably benign |
Het |
Rps16 |
T |
A |
7: 28,050,508 (GRCm39) |
L47Q |
probably damaging |
Het |
Sbno2 |
A |
T |
10: 79,904,687 (GRCm39) |
|
probably null |
Het |
Scube1 |
A |
T |
15: 83,505,264 (GRCm39) |
N385K |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,585,092 (GRCm39) |
E31G |
probably damaging |
Het |
Slc38a9 |
G |
T |
13: 112,865,791 (GRCm39) |
C496F |
possibly damaging |
Het |
Snap47 |
A |
G |
11: 59,328,813 (GRCm39) |
V163A |
probably damaging |
Het |
Sntg2 |
T |
C |
12: 30,251,260 (GRCm39) |
|
probably benign |
Het |
Sp7 |
C |
A |
15: 102,266,895 (GRCm39) |
V322F |
probably damaging |
Het |
Spic |
T |
C |
10: 88,511,924 (GRCm39) |
K111E |
probably damaging |
Het |
Sqor |
T |
C |
2: 122,639,947 (GRCm39) |
|
probably benign |
Het |
St6galnac1 |
T |
A |
11: 116,657,410 (GRCm39) |
M385L |
probably benign |
Het |
Synpo2 |
A |
T |
3: 122,873,511 (GRCm39) |
S1211T |
possibly damaging |
Het |
Sytl2 |
T |
A |
7: 90,045,797 (GRCm39) |
V638E |
probably damaging |
Het |
Taar1 |
T |
A |
10: 23,796,445 (GRCm39) |
S48T |
probably benign |
Het |
Tbx18 |
T |
A |
9: 87,611,706 (GRCm39) |
D108V |
possibly damaging |
Het |
Tdh |
C |
T |
14: 63,735,042 (GRCm39) |
|
probably benign |
Het |
Tlr9 |
T |
A |
9: 106,102,881 (GRCm39) |
L724Q |
probably benign |
Het |
Tmem270 |
T |
A |
5: 134,931,642 (GRCm39) |
Y100F |
probably benign |
Het |
Trim65 |
G |
C |
11: 116,015,430 (GRCm39) |
|
probably benign |
Het |
Trrap |
A |
T |
5: 144,742,560 (GRCm39) |
K1393* |
probably null |
Het |
Ttc13 |
A |
G |
8: 125,410,030 (GRCm39) |
V523A |
probably damaging |
Het |
Utrn |
T |
A |
10: 12,587,219 (GRCm39) |
D939V |
probably benign |
Het |
Vmn1r46 |
G |
T |
6: 89,953,935 (GRCm39) |
M261I |
probably benign |
Het |
Vwa5a |
A |
G |
9: 38,649,103 (GRCm39) |
|
probably null |
Het |
Zfp108 |
A |
T |
7: 23,960,149 (GRCm39) |
T247S |
probably benign |
Het |
Zfp366 |
A |
T |
13: 99,365,129 (GRCm39) |
I97F |
probably benign |
Het |
Zfp986 |
C |
T |
4: 145,625,513 (GRCm39) |
R58C |
probably benign |
Het |
|
Other mutations in Alox12b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00959:Alox12b
|
APN |
11 |
69,057,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02990:Alox12b
|
APN |
11 |
69,054,032 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03106:Alox12b
|
APN |
11 |
69,059,702 (GRCm39) |
nonsense |
probably null |
|
R0135:Alox12b
|
UTSW |
11 |
69,053,574 (GRCm39) |
missense |
probably benign |
0.06 |
R0305:Alox12b
|
UTSW |
11 |
69,058,205 (GRCm39) |
missense |
probably benign |
0.25 |
R0432:Alox12b
|
UTSW |
11 |
69,060,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0828:Alox12b
|
UTSW |
11 |
69,057,132 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0854:Alox12b
|
UTSW |
11 |
69,055,302 (GRCm39) |
critical splice donor site |
probably null |
|
R1139:Alox12b
|
UTSW |
11 |
69,055,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1558:Alox12b
|
UTSW |
11 |
69,056,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1870:Alox12b
|
UTSW |
11 |
69,049,199 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4088:Alox12b
|
UTSW |
11 |
69,049,211 (GRCm39) |
missense |
probably benign |
0.14 |
R4195:Alox12b
|
UTSW |
11 |
69,060,426 (GRCm39) |
missense |
probably benign |
0.02 |
R4248:Alox12b
|
UTSW |
11 |
69,054,431 (GRCm39) |
missense |
probably benign |
|
R4371:Alox12b
|
UTSW |
11 |
69,060,442 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4774:Alox12b
|
UTSW |
11 |
69,054,033 (GRCm39) |
missense |
probably benign |
0.00 |
R5108:Alox12b
|
UTSW |
11 |
69,048,208 (GRCm39) |
missense |
probably benign |
0.11 |
R5252:Alox12b
|
UTSW |
11 |
69,056,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Alox12b
|
UTSW |
11 |
69,053,758 (GRCm39) |
missense |
probably benign |
0.04 |
R6000:Alox12b
|
UTSW |
11 |
69,060,394 (GRCm39) |
missense |
probably damaging |
0.98 |
R6168:Alox12b
|
UTSW |
11 |
69,060,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6322:Alox12b
|
UTSW |
11 |
69,049,199 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6634:Alox12b
|
UTSW |
11 |
69,059,647 (GRCm39) |
nonsense |
probably null |
|
R7026:Alox12b
|
UTSW |
11 |
69,048,131 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7519:Alox12b
|
UTSW |
11 |
69,054,039 (GRCm39) |
missense |
probably benign |
0.37 |
R7669:Alox12b
|
UTSW |
11 |
69,060,167 (GRCm39) |
missense |
probably benign |
0.07 |
R7863:Alox12b
|
UTSW |
11 |
69,057,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7870:Alox12b
|
UTSW |
11 |
69,060,135 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7998:Alox12b
|
UTSW |
11 |
69,059,663 (GRCm39) |
missense |
probably damaging |
0.99 |
R8228:Alox12b
|
UTSW |
11 |
69,054,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R8674:Alox12b
|
UTSW |
11 |
69,054,801 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9055:Alox12b
|
UTSW |
11 |
69,054,884 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9306:Alox12b
|
UTSW |
11 |
69,060,396 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9544:Alox12b
|
UTSW |
11 |
69,054,812 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9568:Alox12b
|
UTSW |
11 |
69,054,836 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0018:Alox12b
|
UTSW |
11 |
69,048,125 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Alox12b
|
UTSW |
11 |
69,048,151 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Alox12b
|
UTSW |
11 |
69,048,149 (GRCm39) |
missense |
possibly damaging |
0.95 |
|