Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl2 |
A |
G |
2: 26,974,905 (GRCm39) |
R177G |
probably damaging |
Het |
Ap3b1 |
T |
C |
13: 94,531,303 (GRCm39) |
|
probably null |
Het |
Ascc3 |
A |
C |
10: 50,526,686 (GRCm39) |
K595T |
probably damaging |
Het |
Cnpy4 |
A |
G |
5: 138,191,125 (GRCm39) |
T234A |
probably benign |
Het |
Col13a1 |
T |
C |
10: 61,797,124 (GRCm39) |
Y101C |
probably damaging |
Het |
Crybg3 |
A |
G |
16: 59,323,513 (GRCm39) |
I2809T |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dgkz |
T |
C |
2: 91,767,805 (GRCm39) |
S824G |
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,397,373 (GRCm39) |
I27N |
probably damaging |
Het |
Efhb |
C |
T |
17: 53,708,652 (GRCm39) |
V673I |
probably benign |
Het |
Egr1 |
T |
C |
18: 34,995,916 (GRCm39) |
Y233H |
possibly damaging |
Het |
Fam184a |
T |
C |
10: 53,551,256 (GRCm39) |
E237G |
probably damaging |
Het |
Galt |
A |
G |
4: 41,755,623 (GRCm39) |
|
probably benign |
Het |
Gm4795 |
T |
C |
10: 44,883,211 (GRCm39) |
|
noncoding transcript |
Het |
Gm6563 |
G |
A |
19: 23,653,392 (GRCm39) |
E61K |
possibly damaging |
Het |
Igkv1-133 |
G |
A |
6: 67,702,590 (GRCm39) |
V103M |
probably damaging |
Het |
Iqcb1 |
T |
A |
16: 36,660,258 (GRCm39) |
H140Q |
probably benign |
Het |
Itpk1 |
G |
T |
12: 102,589,668 (GRCm39) |
P74Q |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,317,153 (GRCm39) |
W803R |
probably damaging |
Het |
Lgr4 |
A |
T |
2: 109,832,846 (GRCm39) |
D312V |
probably benign |
Het |
Lgr4 |
C |
T |
2: 109,838,420 (GRCm39) |
|
probably benign |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Mllt6 |
C |
A |
11: 97,561,158 (GRCm39) |
A282E |
probably benign |
Het |
Mtif2 |
T |
C |
11: 29,490,642 (GRCm39) |
S449P |
possibly damaging |
Het |
Nrg3 |
T |
C |
14: 38,093,269 (GRCm39) |
I533M |
probably damaging |
Het |
Nynrin |
C |
T |
14: 56,109,167 (GRCm39) |
Q1425* |
probably null |
Het |
Or12e13 |
A |
G |
2: 87,663,873 (GRCm39) |
I163M |
probably damaging |
Het |
Or1e1f |
A |
T |
11: 73,855,688 (GRCm39) |
M85L |
probably benign |
Het |
Or4n4b |
T |
A |
14: 50,536,571 (GRCm39) |
N65I |
probably damaging |
Het |
Or4p22 |
C |
T |
2: 88,317,771 (GRCm39) |
H232Y |
probably benign |
Het |
Or5b3 |
T |
A |
19: 13,388,831 (GRCm39) |
S299R |
probably benign |
Het |
Or7e175 |
G |
A |
9: 20,048,516 (GRCm39) |
V35I |
probably benign |
Het |
Plcb4 |
C |
T |
2: 135,836,245 (GRCm39) |
T20I |
possibly damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,763,721 (GRCm39) |
T771K |
probably benign |
Het |
Prss22 |
T |
C |
17: 24,215,363 (GRCm39) |
T138A |
probably benign |
Het |
Ros1 |
A |
T |
10: 52,005,677 (GRCm39) |
S907T |
probably damaging |
Het |
Rtel1 |
T |
A |
2: 180,993,134 (GRCm39) |
Y521* |
probably null |
Het |
Sacs |
T |
C |
14: 61,429,984 (GRCm39) |
F678S |
probably damaging |
Het |
Smtnl1 |
A |
T |
2: 84,647,372 (GRCm39) |
|
probably benign |
Het |
Sumf2 |
T |
C |
5: 129,888,986 (GRCm39) |
V258A |
probably damaging |
Het |
Tas1r2 |
A |
T |
4: 139,396,827 (GRCm39) |
Y722F |
probably damaging |
Het |
Tecpr1 |
A |
G |
5: 144,143,372 (GRCm39) |
F668L |
possibly damaging |
Het |
Timd4 |
T |
C |
11: 46,706,558 (GRCm39) |
F120S |
probably damaging |
Het |
Tnnt3 |
T |
C |
7: 142,062,062 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
G |
A |
2: 121,067,070 (GRCm39) |
S552F |
probably damaging |
Het |
Txlnb |
G |
A |
10: 17,706,090 (GRCm39) |
R333Q |
possibly damaging |
Het |
Txlnb |
A |
G |
10: 17,717,276 (GRCm39) |
|
probably benign |
Het |
Uroc1 |
A |
G |
6: 90,324,910 (GRCm39) |
E461G |
probably benign |
Het |
Vps45 |
G |
A |
3: 95,950,236 (GRCm39) |
T231I |
probably damaging |
Het |
Zfp648 |
T |
A |
1: 154,079,923 (GRCm39) |
S27R |
probably benign |
Het |
|
Other mutations in Or56a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02505:Or56a3
|
APN |
7 |
104,735,540 (GRCm39) |
missense |
probably benign |
|
IGL03160:Or56a3
|
APN |
7 |
104,735,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0079:Or56a3
|
UTSW |
7 |
104,735,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Or56a3
|
UTSW |
7 |
104,735,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Or56a3
|
UTSW |
7 |
104,735,509 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3122:Or56a3
|
UTSW |
7 |
104,735,385 (GRCm39) |
missense |
probably benign |
0.00 |
R3828:Or56a3
|
UTSW |
7 |
104,735,504 (GRCm39) |
missense |
probably benign |
0.00 |
R4235:Or56a3
|
UTSW |
7 |
104,734,994 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4360:Or56a3
|
UTSW |
7 |
104,735,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R4485:Or56a3
|
UTSW |
7 |
104,735,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Or56a3
|
UTSW |
7 |
104,735,844 (GRCm39) |
unclassified |
probably benign |
|
R5542:Or56a3
|
UTSW |
7 |
104,735,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Or56a3
|
UTSW |
7 |
104,735,757 (GRCm39) |
splice site |
probably null |
|
R5723:Or56a3
|
UTSW |
7 |
104,740,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R5770:Or56a3
|
UTSW |
7 |
104,740,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R5871:Or56a3
|
UTSW |
7 |
104,735,511 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7231:Or56a3
|
UTSW |
7 |
104,734,994 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7593:Or56a3
|
UTSW |
7 |
104,735,372 (GRCm39) |
missense |
probably benign |
|
R7881:Or56a3
|
UTSW |
7 |
104,735,780 (GRCm39) |
missense |
probably damaging |
0.98 |
R8878:Or56a3
|
UTSW |
7 |
104,735,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Or56a3
|
UTSW |
7 |
104,735,329 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9576:Or56a3
|
UTSW |
7 |
104,735,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R9684:Or56a3
|
UTSW |
7 |
104,735,589 (GRCm39) |
missense |
|
|
|