Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018B08Rik |
G |
T |
8: 122,266,719 (GRCm39) |
Q56K |
possibly damaging |
Het |
Adam18 |
C |
A |
8: 25,119,726 (GRCm39) |
V518L |
probably benign |
Het |
Akap6 |
A |
T |
12: 53,188,236 (GRCm39) |
K1883N |
probably damaging |
Het |
Arhgef12 |
C |
A |
9: 42,916,847 (GRCm39) |
R432L |
probably damaging |
Het |
Armcx6 |
G |
T |
X: 133,650,505 (GRCm39) |
H109N |
possibly damaging |
Het |
Ctnnd2 |
C |
A |
15: 30,647,075 (GRCm39) |
A257E |
possibly damaging |
Het |
Depdc5 |
T |
A |
5: 33,101,459 (GRCm39) |
C322* |
probably null |
Het |
Enpp7 |
T |
C |
11: 118,881,827 (GRCm39) |
I324T |
probably damaging |
Het |
Gm14401 |
T |
C |
2: 176,778,789 (GRCm39) |
Y292H |
possibly damaging |
Het |
Gm6871 |
A |
T |
7: 41,196,148 (GRCm39) |
H196Q |
probably damaging |
Het |
Gm9964 |
T |
C |
11: 79,187,202 (GRCm39) |
T82A |
unknown |
Het |
Gria2 |
T |
A |
3: 80,618,084 (GRCm39) |
Q317L |
possibly damaging |
Het |
Grtp1 |
G |
A |
8: 13,239,705 (GRCm39) |
T134I |
probably benign |
Het |
Itpkb |
A |
T |
1: 180,155,363 (GRCm39) |
|
probably benign |
Het |
Kbtbd12 |
A |
G |
6: 88,595,488 (GRCm39) |
V114A |
probably benign |
Het |
Lama3 |
A |
T |
18: 12,713,398 (GRCm39) |
K3230M |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,158,217 (GRCm39) |
I1023V |
possibly damaging |
Het |
Myof |
C |
T |
19: 37,889,711 (GRCm39) |
V1287M |
probably damaging |
Het |
Myof |
T |
G |
19: 38,011,058 (GRCm39) |
D60A |
possibly damaging |
Het |
Narf |
A |
T |
11: 121,129,247 (GRCm39) |
E10D |
possibly damaging |
Het |
Nlrx1 |
A |
T |
9: 44,166,722 (GRCm39) |
|
probably benign |
Het |
Or10a3m |
A |
G |
7: 108,313,060 (GRCm39) |
M155V |
probably benign |
Het |
Or8b54 |
A |
G |
9: 38,686,664 (GRCm39) |
T38A |
probably benign |
Het |
Pabpc5 |
A |
G |
X: 118,838,321 (GRCm39) |
E212G |
probably benign |
Het |
Pidd1 |
A |
G |
7: 141,018,995 (GRCm39) |
F829L |
possibly damaging |
Het |
Pik3r2 |
G |
A |
8: 71,223,065 (GRCm39) |
R452C |
probably benign |
Het |
Pkn2 |
A |
G |
3: 142,515,438 (GRCm39) |
C658R |
probably damaging |
Het |
Psd |
C |
T |
19: 46,312,845 (GRCm39) |
R175H |
probably benign |
Het |
Rb1cc1 |
T |
A |
1: 6,318,494 (GRCm39) |
|
probably benign |
Het |
Rnf39 |
C |
A |
17: 37,254,035 (GRCm39) |
T19K |
probably damaging |
Het |
Slc16a3 |
C |
T |
11: 120,846,251 (GRCm39) |
T60M |
possibly damaging |
Het |
Slc26a4 |
G |
T |
12: 31,578,686 (GRCm39) |
H656N |
probably damaging |
Het |
Slc27a1 |
A |
G |
8: 72,032,431 (GRCm39) |
E184G |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,348,327 (GRCm39) |
V742A |
probably benign |
Het |
Thoc1 |
T |
A |
18: 9,968,787 (GRCm39) |
V186D |
probably damaging |
Het |
Uhrf2 |
T |
C |
19: 30,057,315 (GRCm39) |
V491A |
probably damaging |
Het |
Uri1 |
A |
G |
7: 37,664,927 (GRCm39) |
V253A |
possibly damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,327,154 (GRCm39) |
N587K |
probably benign |
Het |
Vmn2r88 |
A |
T |
14: 51,650,647 (GRCm39) |
Y120F |
probably benign |
Het |
Wwox |
G |
A |
8: 115,215,673 (GRCm39) |
A149T |
probably damaging |
Het |
Zfp536 |
T |
C |
7: 37,173,255 (GRCm39) |
*282W |
probably null |
Het |
|
Other mutations in Rab39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03131:Rab39
|
APN |
9 |
53,597,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Rab39
|
UTSW |
9 |
53,617,271 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0238:Rab39
|
UTSW |
9 |
53,617,330 (GRCm39) |
missense |
probably damaging |
0.98 |
R0238:Rab39
|
UTSW |
9 |
53,617,330 (GRCm39) |
missense |
probably damaging |
0.98 |
R0529:Rab39
|
UTSW |
9 |
53,598,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Rab39
|
UTSW |
9 |
53,617,231 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2020:Rab39
|
UTSW |
9 |
53,597,698 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3968:Rab39
|
UTSW |
9 |
53,597,932 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3969:Rab39
|
UTSW |
9 |
53,597,932 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4128:Rab39
|
UTSW |
9 |
53,597,804 (GRCm39) |
missense |
probably benign |
0.01 |
R4394:Rab39
|
UTSW |
9 |
53,597,950 (GRCm39) |
missense |
probably benign |
|
R5173:Rab39
|
UTSW |
9 |
53,597,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5839:Rab39
|
UTSW |
9 |
53,617,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Rab39
|
UTSW |
9 |
53,597,821 (GRCm39) |
missense |
probably benign |
|
R6521:Rab39
|
UTSW |
9 |
53,617,331 (GRCm39) |
missense |
probably benign |
0.28 |
R6908:Rab39
|
UTSW |
9 |
53,617,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Rab39
|
UTSW |
9 |
53,597,700 (GRCm39) |
missense |
probably benign |
|
R8078:Rab39
|
UTSW |
9 |
53,617,255 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8285:Rab39
|
UTSW |
9 |
53,617,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Rab39
|
UTSW |
9 |
53,597,665 (GRCm39) |
missense |
probably benign |
0.06 |
R9406:Rab39
|
UTSW |
9 |
53,597,915 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Rab39
|
UTSW |
9 |
53,598,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|