Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3 |
A |
T |
11: 95,726,625 (GRCm39) |
D150E |
probably damaging |
Het |
Akr1c14 |
T |
A |
13: 4,131,139 (GRCm39) |
I277N |
probably damaging |
Het |
Ap1b1 |
C |
T |
11: 4,969,433 (GRCm39) |
T263I |
probably damaging |
Het |
Atp6v0d2 |
C |
A |
4: 19,878,335 (GRCm39) |
V313L |
probably damaging |
Het |
Car2 |
G |
A |
3: 14,960,688 (GRCm39) |
|
probably null |
Het |
Cdh17 |
T |
A |
4: 11,771,262 (GRCm39) |
|
probably benign |
Het |
Cep295 |
A |
G |
9: 15,234,855 (GRCm39) |
|
probably null |
Het |
Cep97 |
T |
C |
16: 55,750,936 (GRCm39) |
K27E |
probably damaging |
Het |
Cops5 |
A |
T |
1: 10,097,474 (GRCm39) |
N258K |
probably damaging |
Het |
Dchs1 |
T |
A |
7: 105,404,509 (GRCm39) |
T2678S |
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,832,850 (GRCm39) |
F861Y |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,503,990 (GRCm39) |
E1777G |
probably damaging |
Het |
Dock5 |
G |
A |
14: 68,118,708 (GRCm39) |
Q23* |
probably null |
Het |
Ermp1 |
T |
C |
19: 29,593,236 (GRCm39) |
K752R |
probably benign |
Het |
Fhip1a |
A |
C |
3: 85,595,754 (GRCm39) |
I377S |
probably damaging |
Het |
Gjd2 |
T |
A |
2: 113,841,587 (GRCm39) |
I297L |
probably benign |
Het |
Gm28372 |
C |
T |
2: 130,248,818 (GRCm39) |
R59W |
probably damaging |
Het |
Gm9912 |
A |
C |
3: 148,891,074 (GRCm39) |
F20V |
unknown |
Het |
Gpat2 |
T |
C |
2: 127,272,816 (GRCm39) |
F176S |
possibly damaging |
Het |
Gpr150 |
T |
C |
13: 76,203,784 (GRCm39) |
H387R |
possibly damaging |
Het |
Gpr20 |
T |
A |
15: 73,568,269 (GRCm39) |
D40V |
probably damaging |
Het |
Hrob |
T |
C |
11: 102,146,422 (GRCm39) |
C233R |
probably benign |
Het |
Jakmip3 |
A |
T |
7: 138,622,633 (GRCm39) |
Q331L |
probably damaging |
Het |
Kif5b |
A |
G |
18: 6,225,647 (GRCm39) |
V179A |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,211,019 (GRCm39) |
|
probably benign |
Het |
Krt14 |
A |
T |
11: 100,095,242 (GRCm39) |
|
probably benign |
Het |
L3mbtl3 |
A |
G |
10: 26,207,798 (GRCm39) |
F307S |
unknown |
Het |
Laptm4a |
T |
C |
12: 8,984,687 (GRCm39) |
|
probably benign |
Het |
Marveld3 |
T |
C |
8: 110,674,719 (GRCm39) |
S366G |
possibly damaging |
Het |
Mga |
C |
A |
2: 119,781,676 (GRCm39) |
T2234K |
possibly damaging |
Het |
Mkrn2os |
T |
C |
6: 115,569,292 (GRCm39) |
N54S |
probably benign |
Het |
Mras |
T |
C |
9: 99,293,548 (GRCm39) |
I31V |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,110,732 (GRCm39) |
D1518G |
probably damaging |
Het |
Myoz2 |
A |
T |
3: 122,807,430 (GRCm39) |
Y127N |
possibly damaging |
Het |
Nhlrc1 |
C |
A |
13: 47,167,438 (GRCm39) |
W273L |
probably benign |
Het |
Nol9 |
C |
T |
4: 152,130,500 (GRCm39) |
|
probably benign |
Het |
Nrxn2 |
T |
C |
19: 6,559,959 (GRCm39) |
V1206A |
probably damaging |
Het |
Or2ag1b |
T |
C |
7: 106,288,540 (GRCm39) |
T133A |
probably benign |
Het |
Or5k16 |
A |
T |
16: 58,736,291 (GRCm39) |
F238I |
probably damaging |
Het |
Or6c5 |
T |
A |
10: 129,074,941 (GRCm39) |
F308I |
probably benign |
Het |
Or6f2 |
T |
C |
7: 139,756,447 (GRCm39) |
I138T |
probably benign |
Het |
Or8g2b |
T |
A |
9: 39,750,907 (GRCm39) |
M59K |
probably damaging |
Het |
Pappa |
T |
C |
4: 65,123,395 (GRCm39) |
|
probably null |
Het |
Pfkl |
A |
G |
10: 77,836,565 (GRCm39) |
S151P |
probably damaging |
Het |
Pgbd5 |
C |
T |
8: 125,111,118 (GRCm39) |
G191D |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,292,512 (GRCm39) |
V1276A |
probably benign |
Het |
Pla2g4c |
T |
A |
7: 13,082,241 (GRCm39) |
Y486N |
probably damaging |
Het |
Rasal2 |
C |
A |
1: 157,003,502 (GRCm39) |
V386L |
probably benign |
Het |
S1pr3 |
G |
A |
13: 51,573,548 (GRCm39) |
R243Q |
probably damaging |
Het |
Slc44a4 |
A |
G |
17: 35,140,219 (GRCm39) |
D208G |
probably benign |
Het |
Slc6a4 |
T |
C |
11: 76,904,114 (GRCm39) |
S190P |
probably damaging |
Het |
Snapc5 |
A |
T |
9: 64,087,779 (GRCm39) |
|
probably null |
Het |
Tbc1d14 |
C |
A |
5: 36,728,913 (GRCm39) |
R151L |
probably damaging |
Het |
Tecpr2 |
T |
A |
12: 110,897,826 (GRCm39) |
|
probably benign |
Het |
Tmem219 |
G |
A |
7: 126,496,310 (GRCm39) |
P44L |
probably damaging |
Het |
Ube2e1 |
T |
C |
14: 18,330,951 (GRCm38) |
R51G |
probably null |
Het |
Ugp2 |
T |
C |
11: 21,303,447 (GRCm39) |
K53E |
probably benign |
Het |
Vmn1r214 |
T |
C |
13: 23,218,662 (GRCm39) |
I52T |
probably benign |
Het |
Vmn2r124 |
C |
T |
17: 18,284,330 (GRCm39) |
T457I |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,878,935 (GRCm39) |
E2978G |
probably damaging |
Het |
Zfr |
A |
G |
15: 12,159,741 (GRCm39) |
D679G |
probably damaging |
Het |
Zhx3 |
T |
C |
2: 160,622,634 (GRCm39) |
N511S |
probably damaging |
Het |
|
Other mutations in Gm1123 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02502:Gm1123
|
APN |
9 |
98,891,443 (GRCm39) |
nonsense |
probably null |
|
R0091:Gm1123
|
UTSW |
9 |
98,905,405 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4628:Gm1123
|
UTSW |
9 |
98,896,289 (GRCm39) |
missense |
probably damaging |
0.98 |
R4668:Gm1123
|
UTSW |
9 |
98,891,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R4754:Gm1123
|
UTSW |
9 |
98,905,294 (GRCm39) |
critical splice donor site |
probably null |
|
R4754:Gm1123
|
UTSW |
9 |
98,905,293 (GRCm39) |
splice site |
probably null |
|
R4778:Gm1123
|
UTSW |
9 |
98,900,560 (GRCm39) |
missense |
probably benign |
|
R4840:Gm1123
|
UTSW |
9 |
98,900,622 (GRCm39) |
missense |
probably damaging |
0.98 |
R4905:Gm1123
|
UTSW |
9 |
98,891,369 (GRCm39) |
missense |
probably benign |
0.16 |
R5645:Gm1123
|
UTSW |
9 |
98,896,244 (GRCm39) |
missense |
probably benign |
0.41 |
R5685:Gm1123
|
UTSW |
9 |
98,891,486 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7390:Gm1123
|
UTSW |
9 |
98,893,033 (GRCm39) |
missense |
probably benign |
0.19 |
R7858:Gm1123
|
UTSW |
9 |
98,896,107 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8196:Gm1123
|
UTSW |
9 |
98,905,309 (GRCm39) |
missense |
probably benign |
|
|