Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcor |
A |
G |
X: 11,905,498 (GRCm39) |
S1556P |
possibly damaging |
Het |
Brd10 |
A |
G |
19: 29,694,259 (GRCm39) |
S1745P |
possibly damaging |
Het |
Ccdc6 |
T |
A |
10: 70,004,978 (GRCm39) |
I241N |
probably benign |
Het |
Cd81 |
T |
C |
7: 142,619,986 (GRCm39) |
I48T |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,837,118 (GRCm39) |
|
probably null |
Het |
Cfap54 |
T |
C |
10: 92,897,347 (GRCm39) |
M264V |
probably damaging |
Het |
Cmya5 |
G |
A |
13: 93,221,043 (GRCm39) |
|
probably benign |
Het |
Csn2 |
A |
G |
5: 87,843,941 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
G |
A |
7: 55,548,101 (GRCm39) |
R567Q |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,235,486 (GRCm39) |
|
probably null |
Het |
Ermp1 |
G |
A |
19: 29,623,359 (GRCm39) |
|
probably benign |
Het |
Erv3 |
C |
T |
2: 131,697,934 (GRCm39) |
V142I |
possibly damaging |
Het |
Fzd2 |
A |
G |
11: 102,495,730 (GRCm39) |
N58S |
probably damaging |
Het |
Gcm2 |
G |
A |
13: 41,259,269 (GRCm39) |
R67C |
probably damaging |
Het |
Gpr45 |
T |
C |
1: 43,072,478 (GRCm39) |
*374Q |
probably null |
Het |
Haus8 |
T |
C |
8: 71,708,202 (GRCm39) |
N165S |
probably damaging |
Het |
Hoxd4 |
T |
A |
2: 74,558,750 (GRCm39) |
L191Q |
probably damaging |
Het |
I830077J02Rik |
A |
G |
3: 105,834,565 (GRCm39) |
|
probably benign |
Het |
Lpl |
T |
C |
8: 69,333,424 (GRCm39) |
L7P |
possibly damaging |
Het |
Lrp1b |
T |
A |
2: 41,158,382 (GRCm39) |
K1612* |
probably null |
Het |
Myh14 |
G |
T |
7: 44,265,717 (GRCm39) |
A1546D |
possibly damaging |
Het |
Nbea |
A |
G |
3: 55,875,577 (GRCm39) |
S1698P |
probably damaging |
Het |
Or10p22 |
A |
T |
10: 128,826,570 (GRCm39) |
Q263L |
probably benign |
Het |
Or4c112 |
C |
T |
2: 88,854,015 (GRCm39) |
V111M |
probably benign |
Het |
Or52e7 |
C |
A |
7: 104,684,597 (GRCm39) |
T64N |
probably benign |
Het |
Or5p51 |
G |
A |
7: 107,444,385 (GRCm39) |
T185I |
probably benign |
Het |
Otog |
A |
T |
7: 45,945,417 (GRCm39) |
K40* |
probably null |
Het |
Rgma |
C |
A |
7: 73,067,181 (GRCm39) |
H145Q |
probably damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,977,776 (GRCm39) |
|
probably null |
Het |
Ssxb2 |
T |
A |
X: 8,324,743 (GRCm39) |
|
probably benign |
Het |
Tmem175 |
C |
T |
5: 108,790,002 (GRCm39) |
T118I |
probably damaging |
Het |
Wdhd1 |
A |
G |
14: 47,498,808 (GRCm39) |
V542A |
probably benign |
Het |
Zfp977 |
G |
A |
7: 42,230,136 (GRCm39) |
P130S |
probably damaging |
Het |
|
Other mutations in Gm17019 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R3617:Gm17019
|
UTSW |
5 |
15,081,081 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5175:Gm17019
|
UTSW |
5 |
15,082,817 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5520:Gm17019
|
UTSW |
5 |
15,082,819 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7424:Gm17019
|
UTSW |
5 |
15,079,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R7758:Gm17019
|
UTSW |
5 |
15,079,300 (GRCm39) |
makesense |
probably null |
|
R7762:Gm17019
|
UTSW |
5 |
15,081,006 (GRCm39) |
missense |
probably benign |
0.00 |
R7842:Gm17019
|
UTSW |
5 |
15,081,049 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8898:Gm17019
|
UTSW |
5 |
15,081,798 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9127:Gm17019
|
UTSW |
5 |
15,081,113 (GRCm39) |
nonsense |
probably null |
|
R9739:Gm17019
|
UTSW |
5 |
15,082,841 (GRCm39) |
nonsense |
probably null |
|
Z1176:Gm17019
|
UTSW |
5 |
15,083,011 (GRCm39) |
start gained |
probably benign |
|
Z1177:Gm17019
|
UTSW |
5 |
15,082,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|