Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atf7ip |
T |
A |
6: 136,540,747 (GRCm39) |
|
probably null |
Het |
Cacna1b |
T |
C |
2: 24,542,950 (GRCm39) |
T1301A |
probably damaging |
Het |
Calcr |
A |
T |
6: 3,708,484 (GRCm39) |
|
probably null |
Het |
Camsap1 |
T |
C |
2: 25,842,770 (GRCm39) |
D262G |
probably damaging |
Het |
Ccdc141 |
A |
G |
2: 76,962,641 (GRCm39) |
V101A |
probably damaging |
Het |
Ccdc170 |
T |
C |
10: 4,464,128 (GRCm39) |
Y36H |
probably damaging |
Het |
Cd177 |
A |
T |
7: 24,451,428 (GRCm39) |
S492T |
probably benign |
Het |
Chrna4 |
T |
A |
2: 180,670,281 (GRCm39) |
I492F |
probably damaging |
Het |
Cit |
T |
C |
5: 116,012,043 (GRCm39) |
Y217H |
probably damaging |
Het |
Cnbd1 |
T |
A |
4: 19,098,150 (GRCm39) |
D90V |
probably benign |
Het |
Cryba2 |
A |
G |
1: 74,929,789 (GRCm39) |
F116S |
probably damaging |
Het |
Ctbp1 |
T |
C |
5: 33,408,213 (GRCm39) |
T240A |
possibly damaging |
Het |
D130043K22Rik |
C |
T |
13: 25,055,339 (GRCm39) |
S501L |
probably benign |
Het |
Ddhd2 |
A |
G |
8: 26,228,261 (GRCm39) |
F553S |
probably benign |
Het |
Ddr2 |
C |
A |
1: 169,815,983 (GRCm39) |
G575W |
probably damaging |
Het |
Dip2c |
T |
C |
13: 9,621,098 (GRCm39) |
V537A |
possibly damaging |
Het |
Dnah12 |
C |
T |
14: 26,593,812 (GRCm39) |
A752V |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,488,197 (GRCm39) |
D3260G |
probably benign |
Het |
Efemp2 |
T |
A |
19: 5,530,339 (GRCm39) |
C309S |
probably damaging |
Het |
Gse1 |
G |
A |
8: 121,297,553 (GRCm39) |
|
probably benign |
Het |
Hspa4l |
T |
C |
3: 40,707,636 (GRCm39) |
S53P |
possibly damaging |
Het |
Ighv5-4 |
T |
C |
12: 113,561,204 (GRCm39) |
D72G |
probably benign |
Het |
Igkv15-103 |
A |
G |
6: 68,414,780 (GRCm39) |
N73S |
probably benign |
Het |
Igsf11 |
T |
G |
16: 38,831,703 (GRCm39) |
N183K |
possibly damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Kcnk18 |
T |
C |
19: 59,223,263 (GRCm39) |
V136A |
probably damaging |
Het |
Krt75 |
A |
T |
15: 101,480,136 (GRCm39) |
Y240* |
probably null |
Het |
Lyst |
G |
A |
13: 13,809,968 (GRCm39) |
R546H |
probably damaging |
Het |
Man2a2 |
C |
T |
7: 80,009,023 (GRCm39) |
|
probably null |
Het |
Mme |
A |
G |
3: 63,254,613 (GRCm39) |
N491S |
probably benign |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Msi2 |
T |
C |
11: 88,608,185 (GRCm39) |
D39G |
possibly damaging |
Het |
Naa60 |
T |
A |
16: 3,718,585 (GRCm39) |
C122* |
probably null |
Het |
Nes |
A |
G |
3: 87,884,120 (GRCm39) |
E793G |
probably damaging |
Het |
Nfkb2 |
A |
G |
19: 46,296,878 (GRCm39) |
D316G |
probably damaging |
Het |
Nme6 |
C |
T |
9: 109,671,122 (GRCm39) |
L121F |
probably damaging |
Het |
Or4k47 |
T |
A |
2: 111,451,493 (GRCm39) |
K309* |
probably null |
Het |
Otud1 |
C |
T |
2: 19,664,146 (GRCm39) |
T425I |
probably damaging |
Het |
Pimreg |
T |
C |
11: 71,935,964 (GRCm39) |
V149A |
probably benign |
Het |
Plbd1 |
T |
C |
6: 136,590,856 (GRCm39) |
I437V |
probably damaging |
Het |
Prlhr |
A |
T |
19: 60,455,519 (GRCm39) |
M349K |
probably benign |
Het |
Slc1a3 |
G |
A |
15: 8,668,579 (GRCm39) |
T462I |
probably damaging |
Het |
Slc25a26 |
A |
G |
6: 94,575,384 (GRCm39) |
T198A |
probably damaging |
Het |
Stkld1 |
A |
G |
2: 26,836,638 (GRCm39) |
N268S |
probably benign |
Het |
Syt6 |
A |
G |
3: 103,492,946 (GRCm39) |
E66G |
probably damaging |
Het |
Tas2r129 |
A |
G |
6: 132,928,317 (GRCm39) |
I85V |
probably benign |
Het |
Tent5a |
A |
G |
9: 85,207,100 (GRCm39) |
S233P |
probably damaging |
Het |
Tprn |
T |
C |
2: 25,158,904 (GRCm39) |
S643P |
probably damaging |
Het |
Ush2a |
C |
T |
1: 188,285,473 (GRCm39) |
T2003I |
possibly damaging |
Het |
Vmn2r17 |
T |
A |
5: 109,576,335 (GRCm39) |
V402E |
probably damaging |
Het |
Vmn2r3 |
C |
G |
3: 64,182,692 (GRCm39) |
G336R |
probably damaging |
Het |
Wdr89 |
A |
T |
12: 75,679,521 (GRCm39) |
D244E |
probably damaging |
Het |
|
Other mutations in Svop |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02220:Svop
|
APN |
5 |
114,203,589 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02612:Svop
|
APN |
5 |
114,166,321 (GRCm39) |
makesense |
probably null |
|
R0254:Svop
|
UTSW |
5 |
114,176,600 (GRCm39) |
missense |
probably benign |
|
R1705:Svop
|
UTSW |
5 |
114,180,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Svop
|
UTSW |
5 |
114,198,117 (GRCm39) |
critical splice donor site |
probably null |
|
R3084:Svop
|
UTSW |
5 |
114,180,299 (GRCm39) |
missense |
probably benign |
|
R4575:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Svop
|
UTSW |
5 |
114,203,546 (GRCm39) |
unclassified |
probably benign |
|
R5433:Svop
|
UTSW |
5 |
114,198,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R5731:Svop
|
UTSW |
5 |
114,198,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R5783:Svop
|
UTSW |
5 |
114,202,996 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5889:Svop
|
UTSW |
5 |
114,203,692 (GRCm39) |
missense |
probably benign |
0.37 |
R8134:Svop
|
UTSW |
5 |
114,180,992 (GRCm39) |
missense |
probably benign |
0.01 |
R8433:Svop
|
UTSW |
5 |
114,170,822 (GRCm39) |
missense |
probably benign |
0.21 |
R8848:Svop
|
UTSW |
5 |
114,183,687 (GRCm39) |
missense |
|
|
R8851:Svop
|
UTSW |
5 |
114,192,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Svop
|
UTSW |
5 |
114,170,854 (GRCm39) |
missense |
probably damaging |
0.98 |
R8965:Svop
|
UTSW |
5 |
114,173,271 (GRCm39) |
missense |
probably benign |
0.01 |
R9109:Svop
|
UTSW |
5 |
114,168,231 (GRCm39) |
missense |
probably benign |
0.16 |
R9298:Svop
|
UTSW |
5 |
114,168,231 (GRCm39) |
missense |
probably benign |
0.16 |
R9715:Svop
|
UTSW |
5 |
114,198,169 (GRCm39) |
missense |
probably benign |
0.39 |
R9732:Svop
|
UTSW |
5 |
114,201,142 (GRCm39) |
missense |
probably damaging |
1.00 |
|