Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
A |
G |
12: 113,454,530 (GRCm39) |
D449G |
possibly damaging |
Het |
Ampd1 |
T |
C |
3: 102,988,305 (GRCm39) |
S83P |
probably benign |
Het |
Bub1 |
G |
A |
2: 127,649,750 (GRCm39) |
L703F |
probably benign |
Het |
C1rb |
T |
A |
6: 124,551,617 (GRCm39) |
D242E |
probably damaging |
Het |
Carf |
T |
A |
1: 60,189,752 (GRCm39) |
L659Q |
possibly damaging |
Het |
Carmil3 |
A |
G |
14: 55,736,522 (GRCm39) |
N662S |
probably damaging |
Het |
Ccno |
A |
G |
13: 113,124,678 (GRCm39) |
S83G |
possibly damaging |
Het |
Chd3 |
A |
T |
11: 69,245,252 (GRCm39) |
Y1155* |
probably null |
Het |
Clec16a |
A |
G |
16: 10,394,527 (GRCm39) |
E295G |
probably benign |
Het |
Clnk |
A |
G |
5: 38,952,253 (GRCm39) |
|
probably null |
Het |
Clvs2 |
T |
C |
10: 33,498,855 (GRCm39) |
D25G |
possibly damaging |
Het |
Cnr2 |
C |
T |
4: 135,644,827 (GRCm39) |
R302W |
probably damaging |
Het |
Col20a1 |
A |
G |
2: 180,640,498 (GRCm39) |
T594A |
probably damaging |
Het |
Dclk3 |
C |
T |
9: 111,297,787 (GRCm39) |
R444W |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 49,998,183 (GRCm39) |
V761A |
probably damaging |
Het |
Dnah7a |
C |
A |
1: 53,512,063 (GRCm39) |
K2999N |
possibly damaging |
Het |
Dusp28 |
T |
C |
1: 92,834,906 (GRCm39) |
S44P |
probably damaging |
Het |
Enpep |
T |
G |
3: 129,102,774 (GRCm39) |
N394T |
probably damaging |
Het |
Fam135a |
A |
T |
1: 24,060,998 (GRCm39) |
F1343I |
probably damaging |
Het |
Fbxl12 |
C |
A |
9: 20,550,160 (GRCm39) |
R165L |
possibly damaging |
Het |
Fbxo40 |
A |
T |
16: 36,790,947 (GRCm39) |
H54Q |
probably damaging |
Het |
Galnt9 |
A |
G |
5: 110,744,111 (GRCm39) |
D315G |
probably benign |
Het |
Gbp4 |
T |
A |
5: 105,267,800 (GRCm39) |
D482V |
probably damaging |
Het |
Gm17175 |
T |
A |
14: 51,809,070 (GRCm39) |
I99F |
possibly damaging |
Het |
Heatr4 |
A |
G |
12: 84,027,104 (GRCm39) |
F51S |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,415,442 (GRCm39) |
S4806P |
probably damaging |
Het |
Hoxc11 |
G |
A |
15: 102,863,177 (GRCm39) |
V73I |
possibly damaging |
Het |
Knl1 |
T |
G |
2: 118,900,513 (GRCm39) |
I738S |
probably damaging |
Het |
Lcor |
T |
C |
19: 41,573,888 (GRCm39) |
I881T |
possibly damaging |
Het |
Lipt2 |
T |
C |
7: 99,809,450 (GRCm39) |
F179S |
probably damaging |
Het |
Lrrc8b |
G |
A |
5: 105,628,622 (GRCm39) |
V323M |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,599,852 (GRCm39) |
S665P |
probably benign |
Het |
Miga1 |
A |
T |
3: 152,028,045 (GRCm39) |
D161E |
probably benign |
Het |
Mynn |
A |
G |
3: 30,657,933 (GRCm39) |
T84A |
probably benign |
Het |
Or3a1b |
T |
C |
11: 74,012,492 (GRCm39) |
F126L |
probably benign |
Het |
Or4a75 |
A |
T |
2: 89,448,331 (GRCm39) |
D68E |
probably damaging |
Het |
Pik3r3 |
C |
T |
4: 116,079,572 (GRCm39) |
S23L |
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Ralgapa1 |
A |
G |
12: 55,705,847 (GRCm39) |
S1892P |
probably damaging |
Het |
Slc6a18 |
T |
A |
13: 73,813,693 (GRCm39) |
Q540L |
probably benign |
Het |
Tfap2a |
A |
T |
13: 40,872,706 (GRCm39) |
N323K |
possibly damaging |
Het |
Tgm1 |
A |
T |
14: 55,943,100 (GRCm39) |
M580K |
probably benign |
Het |
Tnrc6b |
G |
A |
15: 80,813,619 (GRCm39) |
G1792D |
unknown |
Het |
Trim66 |
T |
A |
7: 109,074,599 (GRCm39) |
Q554L |
possibly damaging |
Het |
Ttc28 |
G |
A |
5: 111,381,207 (GRCm39) |
D1240N |
probably benign |
Het |
Vmn1r238 |
G |
T |
18: 3,123,365 (GRCm39) |
C16* |
probably null |
Het |
Vmn1r6 |
G |
A |
6: 56,979,495 (GRCm39) |
M52I |
probably benign |
Het |
Zfp61 |
A |
G |
7: 23,991,459 (GRCm39) |
F231L |
probably benign |
Het |
|
Other mutations in Or13c7d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01401:Or13c7d
|
APN |
4 |
43,770,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02701:Or13c7d
|
APN |
4 |
43,770,366 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02839:Or13c7d
|
APN |
4 |
43,770,943 (GRCm39) |
nonsense |
probably null |
|
IGL02956:Or13c7d
|
APN |
4 |
43,770,399 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03058:Or13c7d
|
APN |
4 |
43,770,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Or13c7d
|
UTSW |
4 |
43,770,991 (GRCm39) |
missense |
probably benign |
0.03 |
R1796:Or13c7d
|
UTSW |
4 |
43,770,495 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1812:Or13c7d
|
UTSW |
4 |
43,770,230 (GRCm39) |
nonsense |
probably null |
|
R4906:Or13c7d
|
UTSW |
4 |
43,770,476 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5426:Or13c7d
|
UTSW |
4 |
43,770,168 (GRCm39) |
missense |
probably benign |
0.04 |
R5684:Or13c7d
|
UTSW |
4 |
43,770,624 (GRCm39) |
missense |
probably benign |
0.03 |
R6002:Or13c7d
|
UTSW |
4 |
43,770,063 (GRCm39) |
missense |
probably benign |
|
R7174:Or13c7d
|
UTSW |
4 |
43,770,691 (GRCm39) |
missense |
not run |
|
R7431:Or13c7d
|
UTSW |
4 |
43,770,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Or13c7d
|
UTSW |
4 |
43,770,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R8789:Or13c7d
|
UTSW |
4 |
43,770,793 (GRCm39) |
missense |
probably damaging |
0.96 |
R8989:Or13c7d
|
UTSW |
4 |
43,770,346 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9616:Or13c7d
|
UTSW |
4 |
43,770,193 (GRCm39) |
nonsense |
probably null |
|
Z1176:Or13c7d
|
UTSW |
4 |
43,770,267 (GRCm39) |
missense |
probably damaging |
1.00 |
|