Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,236,356 (GRCm39) |
T1236A |
possibly damaging |
Het |
9930111J21Rik1 |
A |
T |
11: 48,838,829 (GRCm39) |
M586K |
probably damaging |
Het |
Adamts4 |
T |
C |
1: 171,080,314 (GRCm39) |
V289A |
possibly damaging |
Het |
Ankrd44 |
A |
T |
1: 54,762,257 (GRCm39) |
D522E |
probably benign |
Het |
Asb14 |
A |
G |
14: 26,637,067 (GRCm39) |
Y603C |
probably damaging |
Het |
Bcl7b |
A |
G |
5: 135,197,308 (GRCm39) |
|
probably benign |
Het |
Cd5 |
T |
C |
19: 10,700,469 (GRCm39) |
K345R |
possibly damaging |
Het |
Celsr3 |
T |
C |
9: 108,708,988 (GRCm39) |
F1278S |
probably damaging |
Het |
Cndp1 |
T |
A |
18: 84,650,049 (GRCm39) |
T215S |
possibly damaging |
Het |
Crygb |
T |
G |
1: 65,119,709 (GRCm39) |
R90S |
probably damaging |
Het |
Dlg4 |
T |
A |
11: 69,933,078 (GRCm39) |
F555I |
possibly damaging |
Het |
Dnah3 |
C |
T |
7: 119,551,728 (GRCm39) |
V2864M |
probably damaging |
Het |
Dnttip2 |
A |
G |
3: 122,070,351 (GRCm39) |
E522G |
probably damaging |
Het |
Ercc4 |
G |
C |
16: 12,948,001 (GRCm39) |
R406P |
probably benign |
Het |
Foxp1 |
G |
A |
6: 98,922,543 (GRCm39) |
P430S |
unknown |
Het |
Galnt1 |
A |
G |
18: 24,400,628 (GRCm39) |
T245A |
probably benign |
Het |
Gnl2 |
T |
A |
4: 124,938,082 (GRCm39) |
N287K |
probably damaging |
Het |
Jcad |
C |
A |
18: 4,649,402 (GRCm39) |
A91E |
possibly damaging |
Het |
Kat6a |
G |
A |
8: 23,352,275 (GRCm39) |
V20I |
probably damaging |
Het |
Kcnb2 |
A |
G |
1: 15,781,777 (GRCm39) |
N883S |
probably damaging |
Het |
Lrch3 |
A |
T |
16: 32,775,750 (GRCm39) |
R205S |
probably damaging |
Het |
Lrr1 |
A |
G |
12: 69,215,825 (GRCm39) |
T66A |
probably benign |
Het |
Lrrc37a |
T |
A |
11: 103,351,635 (GRCm39) |
I2569F |
unknown |
Het |
Maip1 |
A |
T |
1: 57,449,102 (GRCm39) |
Q161L |
probably damaging |
Het |
Neb |
T |
C |
2: 52,047,923 (GRCm39) |
E6699G |
probably benign |
Het |
Nup205 |
A |
G |
6: 35,202,182 (GRCm39) |
R1305G |
probably damaging |
Het |
Or1e19 |
T |
A |
11: 73,316,794 (GRCm39) |
N5I |
probably damaging |
Het |
Pate1 |
G |
A |
9: 35,596,418 (GRCm39) |
R116W |
probably damaging |
Het |
Pcsk5 |
T |
G |
19: 17,410,809 (GRCm39) |
E1861A |
probably benign |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Per1 |
A |
T |
11: 68,999,953 (GRCm39) |
D1215V |
possibly damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,570 (GRCm39) |
S233P |
probably damaging |
Het |
Pramel28 |
A |
G |
4: 143,692,212 (GRCm39) |
V263A |
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,701,435 (GRCm39) |
N340Y |
possibly damaging |
Het |
Rhot1 |
C |
T |
11: 80,114,786 (GRCm39) |
P65S |
probably damaging |
Het |
Scrn2 |
T |
C |
11: 96,921,869 (GRCm39) |
L113P |
probably damaging |
Het |
Sema6a |
T |
C |
18: 47,381,958 (GRCm39) |
K863R |
probably benign |
Het |
Slc15a1 |
A |
G |
14: 121,715,528 (GRCm39) |
V337A |
possibly damaging |
Het |
Slc25a1 |
T |
C |
16: 17,743,720 (GRCm39) |
D298G |
probably benign |
Het |
Slc25a22 |
G |
A |
7: 141,011,737 (GRCm39) |
P168S |
probably benign |
Het |
Slc29a4 |
A |
T |
5: 142,691,109 (GRCm39) |
|
probably null |
Het |
Slc35d1 |
T |
C |
4: 103,047,007 (GRCm39) |
T264A |
|
Het |
Spice1 |
T |
C |
16: 44,205,060 (GRCm39) |
S789P |
probably damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Tectb |
T |
C |
19: 55,178,099 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,544,810 (GRCm39) |
Y32764F |
probably damaging |
Het |
Utrn |
T |
G |
10: 12,545,887 (GRCm39) |
S1684R |
possibly damaging |
Het |
Zic1 |
G |
T |
9: 91,246,847 (GRCm39) |
A75E |
probably damaging |
Het |
Zswim4 |
A |
G |
8: 84,939,014 (GRCm39) |
V956A |
possibly damaging |
Het |
|
Other mutations in Or5ac21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02003:Or5ac21
|
APN |
16 |
59,123,996 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02294:Or5ac21
|
APN |
16 |
59,123,975 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02412:Or5ac21
|
APN |
16 |
59,123,555 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02899:Or5ac21
|
APN |
16 |
59,123,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Or5ac21
|
UTSW |
16 |
59,124,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R1551:Or5ac21
|
UTSW |
16 |
59,123,766 (GRCm39) |
missense |
probably benign |
0.03 |
R1701:Or5ac21
|
UTSW |
16 |
59,123,651 (GRCm39) |
missense |
probably benign |
0.23 |
R1975:Or5ac21
|
UTSW |
16 |
59,124,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R2272:Or5ac21
|
UTSW |
16 |
59,123,807 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5199:Or5ac21
|
UTSW |
16 |
59,124,103 (GRCm39) |
missense |
probably benign |
|
R5843:Or5ac21
|
UTSW |
16 |
59,123,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5928:Or5ac21
|
UTSW |
16 |
59,123,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Or5ac21
|
UTSW |
16 |
59,124,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Or5ac21
|
UTSW |
16 |
59,124,004 (GRCm39) |
missense |
probably benign |
0.03 |
R6894:Or5ac21
|
UTSW |
16 |
59,124,142 (GRCm39) |
missense |
probably damaging |
0.98 |
R7324:Or5ac21
|
UTSW |
16 |
59,123,611 (GRCm39) |
missense |
probably benign |
|
R7380:Or5ac21
|
UTSW |
16 |
59,124,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R7612:Or5ac21
|
UTSW |
16 |
59,123,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R7775:Or5ac21
|
UTSW |
16 |
59,123,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Or5ac21
|
UTSW |
16 |
59,123,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Or5ac21
|
UTSW |
16 |
59,123,772 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8746:Or5ac21
|
UTSW |
16 |
59,123,973 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Or5ac21
|
UTSW |
16 |
59,123,532 (GRCm39) |
missense |
probably benign |
0.01 |
|