Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
T |
A |
7: 40,642,950 (GRCm39) |
S297R |
possibly damaging |
Het |
5530400C23Rik |
A |
G |
6: 133,271,289 (GRCm39) |
E111G |
possibly damaging |
Het |
8030423J24Rik |
T |
A |
13: 71,032,029 (GRCm39) |
S34T |
unknown |
Het |
Ace3 |
T |
A |
11: 105,885,558 (GRCm39) |
W20R |
possibly damaging |
Het |
Adgrf1 |
A |
G |
17: 43,621,578 (GRCm39) |
E605G |
probably damaging |
Het |
Arhgap44 |
G |
A |
11: 65,053,375 (GRCm39) |
|
probably benign |
Het |
Atm |
A |
C |
9: 53,402,259 (GRCm39) |
H1404Q |
probably benign |
Het |
AW209491 |
A |
G |
13: 14,811,306 (GRCm39) |
E53G |
probably damaging |
Het |
Bhmt1b |
G |
A |
18: 87,775,245 (GRCm39) |
C256Y |
probably damaging |
Het |
Cdt1 |
C |
T |
8: 123,298,107 (GRCm39) |
T366I |
probably benign |
Het |
Cerk |
A |
T |
15: 86,026,974 (GRCm39) |
C179S |
probably benign |
Het |
Cldn10 |
T |
C |
14: 119,099,255 (GRCm39) |
V123A |
possibly damaging |
Het |
Clip1 |
T |
C |
5: 123,751,604 (GRCm39) |
K726E |
possibly damaging |
Het |
Dcaf12 |
A |
T |
4: 41,294,043 (GRCm39) |
Y365N |
probably damaging |
Het |
Dennd6b |
A |
G |
15: 89,073,024 (GRCm39) |
L171P |
probably damaging |
Het |
Dip2c |
G |
A |
13: 9,583,290 (GRCm39) |
V91I |
probably benign |
Het |
Dlec1 |
A |
G |
9: 118,972,387 (GRCm39) |
I1431V |
probably benign |
Het |
Egln1 |
T |
C |
8: 125,675,231 (GRCm39) |
D188G |
probably damaging |
Het |
Enpp5 |
T |
A |
17: 44,392,259 (GRCm39) |
N229K |
possibly damaging |
Het |
Fmo1 |
T |
G |
1: 162,663,867 (GRCm39) |
I221L |
probably benign |
Het |
Fsip2 |
G |
A |
2: 82,818,289 (GRCm39) |
W4674* |
probably null |
Het |
Gm12185 |
G |
A |
11: 48,799,255 (GRCm39) |
Q413* |
probably null |
Het |
Gm7298 |
A |
T |
6: 121,741,886 (GRCm39) |
H436L |
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,717,684 (GRCm39) |
Q430* |
probably null |
Het |
Hgd |
A |
G |
16: 37,433,660 (GRCm39) |
H134R |
probably damaging |
Het |
Hoxd8 |
A |
G |
2: 74,536,343 (GRCm39) |
E151G |
probably damaging |
Het |
Il15ra |
A |
G |
2: 11,724,827 (GRCm39) |
D99G |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,158,790 (GRCm39) |
|
probably null |
Het |
Itgb1 |
T |
A |
8: 129,446,764 (GRCm39) |
F426L |
possibly damaging |
Het |
Itpr1 |
A |
C |
6: 108,495,716 (GRCm39) |
I2534L |
probably benign |
Het |
Kcnq4 |
T |
A |
4: 120,573,756 (GRCm39) |
H235L |
probably damaging |
Het |
Kcnt1 |
T |
A |
2: 25,782,395 (GRCm39) |
I178N |
probably damaging |
Het |
Kidins220 |
A |
G |
12: 25,047,310 (GRCm39) |
D252G |
probably damaging |
Het |
Krt23 |
A |
G |
11: 99,376,544 (GRCm39) |
I204T |
probably damaging |
Het |
Lrp3 |
T |
C |
7: 34,903,548 (GRCm39) |
D245G |
possibly damaging |
Het |
Mmp16 |
A |
G |
4: 18,051,857 (GRCm39) |
D282G |
probably damaging |
Het |
Myo1c |
A |
T |
11: 75,541,568 (GRCm39) |
H18L |
probably benign |
Het |
Myo1f |
C |
A |
17: 33,823,318 (GRCm39) |
P981Q |
probably benign |
Het |
Nle1 |
A |
T |
11: 82,798,983 (GRCm39) |
F33I |
probably benign |
Het |
Nlrp4e |
T |
G |
7: 23,020,731 (GRCm39) |
M406R |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,942,611 (GRCm39) |
V4857E |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,727,643 (GRCm39) |
|
probably null |
Het |
Phospho1 |
A |
T |
11: 95,721,450 (GRCm39) |
E22V |
probably damaging |
Het |
Pom121l2 |
C |
T |
13: 22,167,838 (GRCm39) |
S703L |
possibly damaging |
Het |
Prex2 |
T |
C |
1: 11,064,075 (GRCm39) |
L20P |
probably damaging |
Het |
Psmb7 |
T |
C |
2: 38,533,393 (GRCm39) |
T45A |
probably damaging |
Het |
R3hdm2 |
T |
C |
10: 127,320,376 (GRCm39) |
I532T |
probably damaging |
Het |
Rcn1 |
T |
C |
2: 105,222,362 (GRCm39) |
D208G |
probably damaging |
Het |
Recql5 |
A |
G |
11: 115,823,613 (GRCm39) |
|
probably null |
Het |
Resf1 |
G |
A |
6: 149,233,005 (GRCm39) |
|
probably null |
Het |
Rfc4 |
A |
T |
16: 22,933,433 (GRCm39) |
I242N |
probably damaging |
Het |
Rims1 |
T |
C |
1: 22,503,235 (GRCm39) |
Y650C |
probably damaging |
Het |
Shc2 |
C |
T |
10: 79,462,853 (GRCm39) |
|
probably null |
Het |
Slc14a2 |
A |
T |
18: 78,202,190 (GRCm39) |
|
probably null |
Het |
Slc6a6 |
A |
T |
6: 91,716,995 (GRCm39) |
|
probably null |
Het |
Synj2 |
C |
A |
17: 6,058,336 (GRCm39) |
H275N |
possibly damaging |
Het |
T |
A |
T |
17: 8,660,618 (GRCm39) |
T410S |
probably benign |
Het |
Tars3 |
A |
G |
7: 65,332,527 (GRCm39) |
I543V |
probably benign |
Het |
Tbc1d8 |
T |
A |
1: 39,411,484 (GRCm39) |
K1117N |
probably damaging |
Het |
Tm7sf3 |
A |
T |
6: 146,507,787 (GRCm39) |
L425* |
probably null |
Het |
Trav14-3 |
A |
G |
14: 54,000,978 (GRCm39) |
Y63C |
probably damaging |
Het |
Tyro3 |
A |
C |
2: 119,633,751 (GRCm39) |
D133A |
probably damaging |
Het |
Vmn1r119 |
T |
G |
7: 20,745,740 (GRCm39) |
H214P |
possibly damaging |
Het |
Vmn2r120 |
G |
A |
17: 57,816,418 (GRCm39) |
P646S |
probably benign |
Het |
Zbtb7c |
A |
T |
18: 76,278,904 (GRCm39) |
Y454F |
probably benign |
Het |
Zmym2 |
T |
C |
14: 57,187,766 (GRCm39) |
L1144P |
probably damaging |
Het |
|
Other mutations in Lipo4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00536:Lipo4
|
APN |
19 |
33,493,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Lipo4
|
APN |
19 |
33,476,654 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01731:Lipo4
|
APN |
19 |
33,490,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Lipo4
|
UTSW |
19 |
33,479,006 (GRCm39) |
missense |
probably benign |
0.02 |
R0225:Lipo4
|
UTSW |
19 |
33,479,006 (GRCm39) |
missense |
probably benign |
0.02 |
R1155:Lipo4
|
UTSW |
19 |
33,480,595 (GRCm39) |
missense |
probably benign |
|
R1381:Lipo4
|
UTSW |
19 |
33,476,741 (GRCm39) |
missense |
probably benign |
0.02 |
R1460:Lipo4
|
UTSW |
19 |
33,476,718 (GRCm39) |
missense |
probably benign |
|
R1607:Lipo4
|
UTSW |
19 |
33,490,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Lipo4
|
UTSW |
19 |
33,476,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Lipo4
|
UTSW |
19 |
33,476,671 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1998:Lipo4
|
UTSW |
19 |
33,491,701 (GRCm39) |
missense |
probably damaging |
0.98 |
R2088:Lipo4
|
UTSW |
19 |
33,477,469 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2112:Lipo4
|
UTSW |
19 |
33,488,926 (GRCm39) |
missense |
probably benign |
0.07 |
R3931:Lipo4
|
UTSW |
19 |
33,480,619 (GRCm39) |
missense |
probably benign |
|
R4588:Lipo4
|
UTSW |
19 |
33,476,647 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4869:Lipo4
|
UTSW |
19 |
33,478,953 (GRCm39) |
critical splice donor site |
probably null |
|
R5406:Lipo4
|
UTSW |
19 |
33,480,618 (GRCm39) |
missense |
probably benign |
0.00 |
R5640:Lipo4
|
UTSW |
19 |
33,478,986 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6957:Lipo4
|
UTSW |
19 |
33,476,767 (GRCm39) |
missense |
probably benign |
0.30 |
R7403:Lipo4
|
UTSW |
19 |
33,480,679 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7816:Lipo4
|
UTSW |
19 |
33,491,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:Lipo4
|
UTSW |
19 |
33,491,599 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7868:Lipo4
|
UTSW |
19 |
33,488,968 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7890:Lipo4
|
UTSW |
19 |
33,478,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R7975:Lipo4
|
UTSW |
19 |
33,490,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R8391:Lipo4
|
UTSW |
19 |
33,488,965 (GRCm39) |
missense |
probably benign |
0.02 |
R9428:Lipo4
|
UTSW |
19 |
33,495,074 (GRCm39) |
missense |
probably benign |
0.09 |
X0028:Lipo4
|
UTSW |
19 |
33,480,688 (GRCm39) |
frame shift |
probably null |
|
Z1176:Lipo4
|
UTSW |
19 |
33,480,584 (GRCm39) |
missense |
probably benign |
0.00 |
|