Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
4921536K21Rik |
A |
G |
11: 3,840,052 (GRCm39) |
I115T |
probably benign |
Het |
Acads |
A |
T |
5: 115,251,123 (GRCm39) |
N120K |
probably damaging |
Het |
Aco1 |
T |
A |
4: 40,167,139 (GRCm39) |
C118S |
probably benign |
Het |
Alpk2 |
T |
C |
18: 65,422,819 (GRCm39) |
T1493A |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,208,268 (GRCm39) |
Y480H |
possibly damaging |
Het |
Brd4 |
A |
T |
17: 32,417,896 (GRCm39) |
I86N |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,945,023 (GRCm39) |
E1477G |
probably damaging |
Het |
Ccne2 |
A |
G |
4: 11,202,986 (GRCm39) |
N368S |
probably benign |
Het |
Cenpp |
A |
T |
13: 49,794,710 (GRCm39) |
F152L |
probably benign |
Het |
Cfap46 |
T |
A |
7: 139,232,320 (GRCm39) |
D881V |
possibly damaging |
Het |
Chmp7 |
A |
G |
14: 69,958,678 (GRCm39) |
V212A |
probably damaging |
Het |
Col9a2 |
A |
T |
4: 120,902,352 (GRCm39) |
K196N |
probably benign |
Het |
Copg2 |
T |
C |
6: 30,749,449 (GRCm39) |
D814G |
probably damaging |
Het |
Dcaf13 |
G |
A |
15: 38,982,288 (GRCm39) |
G85R |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 66,058,978 (GRCm39) |
S106P |
probably benign |
Het |
Dpp8 |
A |
G |
9: 64,983,085 (GRCm39) |
D739G |
probably damaging |
Het |
Drd2 |
T |
A |
9: 49,316,089 (GRCm39) |
M283K |
probably benign |
Het |
Espl1 |
A |
G |
15: 102,207,159 (GRCm39) |
T208A |
probably benign |
Het |
Glul |
G |
A |
1: 153,778,796 (GRCm39) |
G35D |
possibly damaging |
Het |
Gm14412 |
T |
C |
2: 177,007,005 (GRCm39) |
K297E |
unknown |
Het |
Gm21976 |
A |
T |
13: 98,442,318 (GRCm39) |
R120W |
probably damaging |
Het |
Hipk3 |
T |
A |
2: 104,271,622 (GRCm39) |
T437S |
probably benign |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Lipn |
T |
G |
19: 34,058,750 (GRCm39) |
Y321D |
probably damaging |
Het |
Lrwd1 |
A |
G |
5: 136,152,810 (GRCm39) |
V484A |
probably benign |
Het |
Madd |
T |
C |
2: 90,998,009 (GRCm39) |
D673G |
possibly damaging |
Het |
Marveld1 |
T |
A |
19: 42,136,203 (GRCm39) |
L39Q |
probably damaging |
Het |
Mfsd2b |
T |
C |
12: 4,915,807 (GRCm39) |
T299A |
possibly damaging |
Het |
Mmp7 |
T |
C |
9: 7,697,667 (GRCm39) |
V234A |
probably damaging |
Het |
Nhsl1 |
T |
A |
10: 18,403,357 (GRCm39) |
D1329E |
probably benign |
Het |
Or4a15 |
C |
T |
2: 89,193,669 (GRCm39) |
V35M |
probably damaging |
Het |
Or4f14b |
T |
C |
2: 111,774,997 (GRCm39) |
D268G |
possibly damaging |
Het |
Or52a33 |
A |
G |
7: 103,289,308 (GRCm39) |
F13S |
probably damaging |
Het |
Pcdhb21 |
T |
A |
18: 37,647,568 (GRCm39) |
D232E |
probably damaging |
Het |
Pebp1 |
G |
T |
5: 117,421,475 (GRCm39) |
D156E |
probably benign |
Het |
Pik3cb |
A |
G |
9: 98,937,459 (GRCm39) |
Y745H |
possibly damaging |
Het |
Pld2 |
T |
C |
11: 70,432,846 (GRCm39) |
L170P |
probably damaging |
Het |
Ptch1 |
T |
C |
13: 63,691,422 (GRCm39) |
D277G |
possibly damaging |
Het |
Rab11fip1 |
A |
T |
8: 27,644,603 (GRCm39) |
M394K |
probably damaging |
Het |
Rhoq |
T |
C |
17: 87,271,754 (GRCm39) |
Y57H |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,900,731 (GRCm39) |
I979V |
probably benign |
Het |
Slc6a4 |
A |
G |
11: 76,910,689 (GRCm39) |
I447V |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,663,663 (GRCm39) |
K607R |
probably damaging |
Het |
Stt3a |
T |
C |
9: 36,646,808 (GRCm39) |
I602V |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,013,845 (GRCm39) |
Q3012L |
possibly damaging |
Het |
Taf1b |
T |
A |
12: 24,550,441 (GRCm39) |
F9I |
possibly damaging |
Het |
Tex35 |
T |
A |
1: 156,926,909 (GRCm39) |
Y195F |
probably benign |
Het |
Tnc |
T |
C |
4: 63,913,982 (GRCm39) |
T1277A |
probably damaging |
Het |
Tnfsf15 |
G |
T |
4: 63,648,180 (GRCm39) |
Y153* |
probably null |
Het |
Trim5 |
C |
A |
7: 103,914,639 (GRCm39) |
V477F |
probably damaging |
Het |
Trp73 |
A |
G |
4: 154,148,874 (GRCm39) |
I245T |
probably damaging |
Het |
Zbtb16 |
C |
T |
9: 48,743,380 (GRCm39) |
E311K |
possibly damaging |
Het |
Zmynd19 |
A |
G |
2: 24,849,000 (GRCm39) |
D165G |
probably damaging |
Het |
|
Other mutations in Micu3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02970:Micu3
|
APN |
8 |
40,835,171 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0491:Micu3
|
UTSW |
8 |
40,819,294 (GRCm39) |
splice site |
probably benign |
|
R1518:Micu3
|
UTSW |
8 |
40,788,893 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2089:Micu3
|
UTSW |
8 |
40,761,413 (GRCm39) |
missense |
probably benign |
0.01 |
R3115:Micu3
|
UTSW |
8 |
40,835,208 (GRCm39) |
missense |
probably benign |
0.21 |
R3893:Micu3
|
UTSW |
8 |
40,819,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R4026:Micu3
|
UTSW |
8 |
40,812,496 (GRCm39) |
intron |
probably benign |
|
R4094:Micu3
|
UTSW |
8 |
40,788,929 (GRCm39) |
missense |
probably null |
1.00 |
R4678:Micu3
|
UTSW |
8 |
40,833,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R5501:Micu3
|
UTSW |
8 |
40,807,341 (GRCm39) |
splice site |
probably null |
|
R6327:Micu3
|
UTSW |
8 |
40,819,238 (GRCm39) |
missense |
probably benign |
0.13 |
R6793:Micu3
|
UTSW |
8 |
40,833,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R7292:Micu3
|
UTSW |
8 |
40,835,166 (GRCm39) |
missense |
probably benign |
0.09 |
R7350:Micu3
|
UTSW |
8 |
40,801,999 (GRCm39) |
missense |
probably benign |
0.09 |
R7427:Micu3
|
UTSW |
8 |
40,831,955 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7453:Micu3
|
UTSW |
8 |
40,788,939 (GRCm39) |
missense |
probably benign |
|
R7635:Micu3
|
UTSW |
8 |
40,819,275 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8428:Micu3
|
UTSW |
8 |
40,761,205 (GRCm39) |
missense |
probably benign |
|
R9468:Micu3
|
UTSW |
8 |
40,807,422 (GRCm39) |
nonsense |
probably null |
|
R9561:Micu3
|
UTSW |
8 |
40,835,156 (GRCm39) |
nonsense |
probably null |
|
R9665:Micu3
|
UTSW |
8 |
40,828,666 (GRCm39) |
missense |
probably benign |
0.13 |
R9752:Micu3
|
UTSW |
8 |
40,833,751 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0003:Micu3
|
UTSW |
8 |
40,819,263 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Micu3
|
UTSW |
8 |
40,761,265 (GRCm39) |
missense |
probably damaging |
1.00 |
|