Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox3 |
T |
A |
5: 35,762,543 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
A |
T |
12: 112,742,100 (GRCm39) |
Y657* |
probably null |
Het |
Anxa3 |
T |
A |
5: 96,968,331 (GRCm39) |
I128N |
probably damaging |
Het |
Bsnd |
T |
C |
4: 106,345,198 (GRCm39) |
T83A |
probably benign |
Het |
Capn10 |
A |
G |
1: 92,871,635 (GRCm39) |
Y411C |
probably benign |
Het |
Capn3 |
G |
A |
2: 120,315,075 (GRCm39) |
W201* |
probably null |
Het |
Crtap |
T |
C |
9: 114,207,164 (GRCm39) |
T365A |
probably benign |
Het |
Daam1 |
A |
G |
12: 71,992,272 (GRCm39) |
D329G |
unknown |
Het |
Dmxl2 |
A |
T |
9: 54,283,550 (GRCm39) |
L2761Q |
possibly damaging |
Het |
Fcho2 |
A |
C |
13: 98,926,310 (GRCm39) |
V91G |
probably damaging |
Het |
Fen1 |
A |
T |
19: 10,178,022 (GRCm39) |
C141S |
possibly damaging |
Het |
Fkbp15 |
G |
C |
4: 62,225,166 (GRCm39) |
A831G |
probably benign |
Het |
Frmd4a |
A |
T |
2: 4,305,768 (GRCm39) |
R14S |
possibly damaging |
Het |
Fzr1 |
A |
G |
10: 81,206,160 (GRCm39) |
F176L |
possibly damaging |
Het |
Garre1 |
A |
T |
7: 33,944,505 (GRCm39) |
S76T |
probably damaging |
Het |
Iqca1 |
G |
T |
1: 89,998,257 (GRCm39) |
T549K |
probably damaging |
Het |
Itgax |
T |
A |
7: 127,739,647 (GRCm39) |
S686R |
probably damaging |
Het |
Knop1 |
C |
A |
7: 118,445,305 (GRCm39) |
G220C |
probably damaging |
Het |
Lyzl1 |
T |
A |
18: 4,169,142 (GRCm39) |
C49S |
probably damaging |
Het |
Mpzl1 |
A |
T |
1: 165,433,180 (GRCm39) |
I157K |
probably benign |
Het |
Mrgprb2 |
T |
C |
7: 48,202,261 (GRCm39) |
I155V |
probably benign |
Het |
Mucl3 |
T |
C |
17: 35,949,102 (GRCm39) |
M166V |
probably benign |
Het |
Mvb12b |
T |
C |
2: 33,717,728 (GRCm39) |
T167A |
probably benign |
Het |
Myh3 |
A |
G |
11: 66,979,445 (GRCm39) |
N491S |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,787,128 (GRCm39) |
D511G |
possibly damaging |
Het |
Or10ak8 |
C |
T |
4: 118,774,035 (GRCm39) |
V210I |
probably benign |
Het |
Or11h4 |
T |
C |
14: 50,974,509 (GRCm39) |
T37A |
probably benign |
Het |
Or6b1 |
C |
T |
6: 42,815,180 (GRCm39) |
R122C |
probably damaging |
Het |
Or8k21 |
T |
G |
2: 86,145,558 (GRCm39) |
Q24P |
probably damaging |
Het |
Ptcd1 |
A |
G |
5: 145,091,671 (GRCm39) |
M476T |
probably damaging |
Het |
Pum3 |
A |
G |
19: 27,398,695 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
G |
A |
10: 58,321,658 (GRCm39) |
D2652N |
probably damaging |
Het |
Rassf1 |
T |
C |
9: 107,435,213 (GRCm39) |
V166A |
probably damaging |
Het |
Rictor |
A |
G |
15: 6,812,585 (GRCm39) |
H907R |
probably benign |
Het |
Rorb |
T |
C |
19: 18,965,471 (GRCm39) |
E6G |
probably damaging |
Het |
Serpina3f |
A |
T |
12: 104,183,182 (GRCm39) |
T15S |
possibly damaging |
Het |
Sorbs2 |
T |
C |
8: 46,212,226 (GRCm39) |
L100P |
probably damaging |
Het |
Sprr2k |
T |
C |
3: 92,340,655 (GRCm39) |
|
probably benign |
Het |
Srrm2 |
T |
A |
17: 24,040,360 (GRCm39) |
S2431T |
probably damaging |
Het |
Stox2 |
T |
A |
8: 47,866,172 (GRCm39) |
K57* |
probably null |
Het |
Ttc21a |
G |
A |
9: 119,770,327 (GRCm39) |
V133I |
probably benign |
Het |
Vasn |
T |
C |
16: 4,468,026 (GRCm39) |
Y658H |
possibly damaging |
Het |
Zfp251 |
A |
G |
15: 76,754,527 (GRCm39) |
Y35H |
probably damaging |
Het |
|
Other mutations in Garem2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0194:Garem2
|
UTSW |
5 |
30,318,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0458:Garem2
|
UTSW |
5 |
30,319,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R1933:Garem2
|
UTSW |
5 |
30,319,860 (GRCm39) |
nonsense |
probably null |
|
R1955:Garem2
|
UTSW |
5 |
30,313,268 (GRCm39) |
missense |
probably benign |
0.36 |
R1970:Garem2
|
UTSW |
5 |
30,322,172 (GRCm39) |
nonsense |
probably null |
|
R2152:Garem2
|
UTSW |
5 |
30,313,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R2153:Garem2
|
UTSW |
5 |
30,313,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R2154:Garem2
|
UTSW |
5 |
30,313,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R2202:Garem2
|
UTSW |
5 |
30,319,762 (GRCm39) |
missense |
probably benign |
0.43 |
R2270:Garem2
|
UTSW |
5 |
30,321,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Garem2
|
UTSW |
5 |
30,321,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Garem2
|
UTSW |
5 |
30,310,366 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4439:Garem2
|
UTSW |
5 |
30,318,344 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4665:Garem2
|
UTSW |
5 |
30,319,665 (GRCm39) |
missense |
probably damaging |
0.98 |
R4666:Garem2
|
UTSW |
5 |
30,319,665 (GRCm39) |
missense |
probably damaging |
0.98 |
R5851:Garem2
|
UTSW |
5 |
30,319,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Garem2
|
UTSW |
5 |
30,321,735 (GRCm39) |
nonsense |
probably null |
|
R6998:Garem2
|
UTSW |
5 |
30,319,168 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8080:Garem2
|
UTSW |
5 |
30,313,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Garem2
|
UTSW |
5 |
30,313,262 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9199:Garem2
|
UTSW |
5 |
30,319,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R9327:Garem2
|
UTSW |
5 |
30,321,989 (GRCm39) |
missense |
probably benign |
|
R9502:Garem2
|
UTSW |
5 |
30,321,750 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9787:Garem2
|
UTSW |
5 |
30,319,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Garem2
|
UTSW |
5 |
30,319,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Garem2
|
UTSW |
5 |
30,319,747 (GRCm39) |
missense |
probably benign |
0.00 |
|