Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,414,921 (GRCm39) |
I3996T |
probably damaging |
Het |
Adgra1 |
A |
G |
7: 139,432,492 (GRCm39) |
N110S |
probably damaging |
Het |
Arhgap31 |
T |
C |
16: 38,427,017 (GRCm39) |
T612A |
probably benign |
Het |
Atp13a4 |
C |
T |
16: 29,290,706 (GRCm39) |
|
probably null |
Het |
C1rb |
T |
C |
6: 124,553,984 (GRCm39) |
S352P |
probably damaging |
Het |
Cc2d2b |
T |
C |
19: 40,784,216 (GRCm39) |
I671T |
unknown |
Het |
Cmas |
A |
G |
6: 142,710,105 (GRCm39) |
D116G |
probably damaging |
Het |
Col24a1 |
T |
C |
3: 145,021,009 (GRCm39) |
V460A |
probably damaging |
Het |
Cracdl |
G |
A |
1: 37,663,553 (GRCm39) |
R782C |
possibly damaging |
Het |
Cubn |
T |
G |
2: 13,461,466 (GRCm39) |
D687A |
probably damaging |
Het |
Cul9 |
A |
C |
17: 46,854,696 (GRCm39) |
V2G |
probably damaging |
Het |
Elp3 |
T |
C |
14: 65,797,582 (GRCm39) |
Y382C |
probably damaging |
Het |
Fbxo11 |
A |
T |
17: 88,310,249 (GRCm39) |
I443K |
|
Het |
Fdps |
G |
A |
3: 89,006,639 (GRCm39) |
R84W |
probably benign |
Het |
Helz |
C |
T |
11: 107,547,019 (GRCm39) |
A1112V |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,380,782 (GRCm39) |
M3553K |
probably benign |
Het |
Hspa12a |
T |
C |
19: 58,813,720 (GRCm39) |
Y135C |
probably damaging |
Het |
Hspa1l |
A |
G |
17: 35,196,849 (GRCm39) |
Y296C |
probably benign |
Het |
Ifna12 |
T |
G |
4: 88,521,079 (GRCm39) |
E156A |
possibly damaging |
Het |
Ilf3 |
C |
T |
9: 21,314,434 (GRCm39) |
Q689* |
probably null |
Het |
Ints1 |
A |
G |
5: 139,760,041 (GRCm39) |
|
probably null |
Het |
Itga8 |
T |
A |
2: 12,235,019 (GRCm39) |
D413V |
possibly damaging |
Het |
Kcnd3 |
C |
T |
3: 105,574,290 (GRCm39) |
L492F |
possibly damaging |
Het |
Kcnh5 |
T |
C |
12: 74,944,774 (GRCm39) |
K825R |
probably benign |
Het |
Kcnma1 |
A |
G |
14: 23,700,214 (GRCm39) |
I194T |
possibly damaging |
Het |
Kmo |
A |
G |
1: 175,465,108 (GRCm39) |
R30G |
probably damaging |
Het |
Krtap19-4 |
C |
A |
16: 88,681,801 (GRCm39) |
G52C |
unknown |
Het |
Ksr1 |
A |
G |
11: 78,918,465 (GRCm39) |
V563A |
possibly damaging |
Het |
Lyn |
A |
T |
4: 3,780,925 (GRCm39) |
M355L |
possibly damaging |
Het |
Med13 |
A |
T |
11: 86,189,660 (GRCm39) |
L1083* |
probably null |
Het |
Mfsd13a |
A |
G |
19: 46,354,900 (GRCm39) |
T26A |
probably benign |
Het |
Mup14 |
T |
C |
4: 61,259,430 (GRCm39) |
I41V |
probably benign |
Het |
Myo9b |
T |
A |
8: 71,804,906 (GRCm39) |
S1466T |
probably benign |
Het |
Nampt |
T |
C |
12: 32,888,458 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
T |
C |
1: 60,317,885 (GRCm39) |
Y1941H |
probably damaging |
Het |
Nyap2 |
C |
T |
1: 81,314,314 (GRCm39) |
A670V |
probably benign |
Het |
Or10h28 |
A |
G |
17: 33,487,794 (GRCm39) |
Y32C |
probably damaging |
Het |
Or2aj6 |
A |
G |
16: 19,443,791 (GRCm39) |
S20P |
probably benign |
Het |
Or4k44 |
T |
C |
2: 111,368,488 (GRCm39) |
I49V |
probably benign |
Het |
Or8g31-ps1 |
T |
C |
9: 39,276,416 (GRCm39) |
V187A |
unknown |
Het |
Pcdh15 |
A |
G |
10: 74,221,731 (GRCm39) |
D677G |
probably damaging |
Het |
Pogz |
T |
A |
3: 94,787,530 (GRCm39) |
S1373T |
probably benign |
Het |
Ptprj |
T |
C |
2: 90,288,613 (GRCm39) |
D691G |
probably benign |
Het |
Qpctl |
T |
A |
7: 18,880,961 (GRCm39) |
D157V |
probably damaging |
Het |
Rbbp8 |
T |
C |
18: 11,810,677 (GRCm39) |
F60L |
possibly damaging |
Het |
Ripor1 |
T |
A |
8: 106,344,072 (GRCm39) |
L402Q |
possibly damaging |
Het |
Rptn |
C |
T |
3: 93,304,412 (GRCm39) |
H582Y |
probably benign |
Het |
Rusc1 |
T |
A |
3: 88,996,990 (GRCm39) |
Q611L |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,610,817 (GRCm39) |
V4003A |
possibly damaging |
Het |
Siglech |
T |
A |
7: 55,422,294 (GRCm39) |
W300R |
probably benign |
Het |
Slc25a51 |
T |
C |
4: 45,399,494 (GRCm39) |
D232G |
probably damaging |
Het |
Slc6a11 |
T |
A |
6: 114,220,905 (GRCm39) |
C479S |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,127,101 (GRCm39) |
T1970A |
probably benign |
Het |
Sspo |
G |
T |
6: 48,450,608 (GRCm39) |
G2599V |
probably damaging |
Het |
Tfpt |
T |
A |
7: 3,627,604 (GRCm39) |
E116V |
probably null |
Het |
Tmem260 |
T |
A |
14: 48,717,774 (GRCm39) |
V121E |
probably benign |
Het |
Tmem54 |
T |
C |
4: 129,002,120 (GRCm39) |
F45L |
probably benign |
Het |
Trim2 |
T |
A |
3: 84,080,128 (GRCm39) |
N631I |
probably damaging |
Het |
Tshr |
C |
T |
12: 91,474,563 (GRCm39) |
T179I |
probably damaging |
Het |
Vmn1r40 |
A |
G |
6: 89,691,198 (GRCm39) |
N5S |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,871,420 (GRCm39) |
V621A |
possibly damaging |
Het |
Zc2hc1c |
TTTATCC |
T |
12: 85,343,230 (GRCm39) |
|
probably benign |
Het |
Zfp644 |
G |
A |
5: 106,783,944 (GRCm39) |
Q837* |
probably null |
Het |
Zfp773 |
A |
T |
7: 7,135,989 (GRCm39) |
N202K |
probably damaging |
Het |
|
Other mutations in Or4m1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Or4m1
|
APN |
14 |
50,557,732 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01285:Or4m1
|
APN |
14 |
50,557,713 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02106:Or4m1
|
APN |
14 |
50,557,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02313:Or4m1
|
APN |
14 |
50,557,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03125:Or4m1
|
APN |
14 |
50,558,149 (GRCm39) |
missense |
probably benign |
0.01 |
R0276:Or4m1
|
UTSW |
14 |
50,557,636 (GRCm39) |
missense |
probably benign |
0.23 |
R0547:Or4m1
|
UTSW |
14 |
50,557,575 (GRCm39) |
missense |
probably benign |
0.06 |
R0567:Or4m1
|
UTSW |
14 |
50,558,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R0927:Or4m1
|
UTSW |
14 |
50,558,186 (GRCm39) |
nonsense |
probably null |
|
R1506:Or4m1
|
UTSW |
14 |
50,557,941 (GRCm39) |
missense |
probably benign |
0.00 |
R4032:Or4m1
|
UTSW |
14 |
50,557,767 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5179:Or4m1
|
UTSW |
14 |
50,557,993 (GRCm39) |
nonsense |
probably null |
|
R5401:Or4m1
|
UTSW |
14 |
50,557,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Or4m1
|
UTSW |
14 |
50,558,043 (GRCm39) |
missense |
probably benign |
0.00 |
R7752:Or4m1
|
UTSW |
14 |
50,557,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R7901:Or4m1
|
UTSW |
14 |
50,557,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8034:Or4m1
|
UTSW |
14 |
50,558,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Or4m1
|
UTSW |
14 |
50,557,615 (GRCm39) |
missense |
probably benign |
0.09 |
R8420:Or4m1
|
UTSW |
14 |
50,558,233 (GRCm39) |
missense |
probably benign |
|
R9128:Or4m1
|
UTSW |
14 |
50,558,214 (GRCm39) |
missense |
probably benign |
0.08 |
R9618:Or4m1
|
UTSW |
14 |
50,557,760 (GRCm39) |
nonsense |
probably null |
|
R9659:Or4m1
|
UTSW |
14 |
50,558,181 (GRCm39) |
missense |
probably benign |
0.10 |
R9788:Or4m1
|
UTSW |
14 |
50,558,181 (GRCm39) |
missense |
probably benign |
0.10 |
X0064:Or4m1
|
UTSW |
14 |
50,557,511 (GRCm39) |
nonsense |
probably null |
|
|