Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn4 |
A |
T |
7: 28,904,684 (GRCm38) |
I384N |
probably damaging |
Het |
Adsl |
G |
T |
15: 80,948,700 (GRCm38) |
Q51H |
probably null |
Het |
Apcdd1 |
A |
G |
18: 62,937,286 (GRCm38) |
E208G |
probably damaging |
Het |
Arrdc4 |
G |
A |
7: 68,744,832 (GRCm38) |
R155* |
probably null |
Het |
Atp9b |
T |
C |
18: 80,756,455 (GRCm38) |
E823G |
probably benign |
Het |
Bmp1 |
A |
G |
14: 70,492,461 (GRCm38) |
W468R |
probably damaging |
Het |
C6 |
A |
G |
15: 4,759,917 (GRCm38) |
I281M |
possibly damaging |
Het |
Ccdc88b |
T |
C |
19: 6,846,710 (GRCm38) |
T1392A |
probably benign |
Het |
Dhx34 |
G |
T |
7: 16,205,473 (GRCm38) |
S665Y |
probably damaging |
Het |
Dock1 |
A |
T |
7: 135,137,813 (GRCm38) |
|
probably null |
Het |
Dpp7 |
T |
C |
2: 25,354,613 (GRCm38) |
N252S |
probably benign |
Het |
Dyrk2 |
A |
G |
10: 118,860,507 (GRCm38) |
V282A |
probably damaging |
Het |
Edrf1 |
T |
C |
7: 133,650,525 (GRCm38) |
L401P |
probably damaging |
Het |
Epc1 |
A |
G |
18: 6,439,724 (GRCm38) |
V150A |
probably benign |
Het |
Fam170a |
A |
T |
18: 50,281,667 (GRCm38) |
M127L |
possibly damaging |
Het |
Gabrg1 |
T |
A |
5: 70,777,205 (GRCm38) |
T277S |
probably damaging |
Het |
Galntl5 |
T |
C |
5: 25,189,825 (GRCm38) |
|
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,598,312 (GRCm38) |
N56S |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,150,409 (GRCm38) |
V172E |
probably damaging |
Het |
Gm10419 |
T |
C |
5: 108,372,358 (GRCm38) |
|
probably benign |
Het |
Gm7293 |
A |
G |
9: 51,623,606 (GRCm38) |
|
noncoding transcript |
Het |
Gstm3 |
T |
C |
3: 107,967,633 (GRCm38) |
E101G |
probably damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,686,545 (GRCm38) |
W2R |
possibly damaging |
Het |
Ighv13-1 |
A |
T |
12: 114,267,733 (GRCm38) |
|
probably benign |
Het |
Ighv7-1 |
T |
A |
12: 113,896,503 (GRCm38) |
I90F |
possibly damaging |
Het |
Itga2b |
A |
G |
11: 102,455,583 (GRCm38) |
L1009P |
probably damaging |
Het |
Kif1a |
A |
G |
1: 93,039,853 (GRCm38) |
V1112A |
possibly damaging |
Het |
Kif5a |
A |
T |
10: 127,245,368 (GRCm38) |
D232E |
possibly damaging |
Het |
Klb |
G |
A |
5: 65,375,679 (GRCm38) |
|
probably null |
Het |
Lrriq1 |
G |
A |
10: 103,215,628 (GRCm38) |
A421V |
probably benign |
Het |
Mdga1 |
G |
A |
17: 29,839,871 (GRCm38) |
R721C |
probably damaging |
Het |
Mrpl48 |
G |
T |
7: 100,550,532 (GRCm38) |
|
probably benign |
Het |
Myo18b |
T |
A |
5: 112,840,629 (GRCm38) |
R1030S |
possibly damaging |
Het |
Nf1 |
T |
A |
11: 79,547,120 (GRCm38) |
H2101Q |
probably damaging |
Het |
Nlrp3 |
C |
A |
11: 59,549,378 (GRCm38) |
L594I |
probably damaging |
Het |
Notch2 |
C |
T |
3: 98,146,060 (GRCm38) |
T2013I |
probably damaging |
Het |
Or2ah1 |
A |
T |
2: 85,822,988 (GRCm38) |
T6S |
probably benign |
Het |
Or2y3 |
G |
A |
17: 38,082,103 (GRCm38) |
L292F |
possibly damaging |
Het |
Or52s1 |
C |
A |
7: 103,212,177 (GRCm38) |
R95S |
probably benign |
Het |
Or6c216 |
A |
G |
10: 129,842,610 (GRCm38) |
L144P |
probably benign |
Het |
Panx3 |
T |
C |
9: 37,664,056 (GRCm38) |
D170G |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,540,034 (GRCm38) |
S783G |
unknown |
Het |
Pde3b |
T |
A |
7: 114,526,901 (GRCm38) |
L790* |
probably null |
Het |
Pik3r2 |
T |
C |
8: 70,772,348 (GRCm38) |
|
probably benign |
Het |
Rassf4 |
A |
G |
6: 116,641,690 (GRCm38) |
F211L |
probably damaging |
Het |
Rbl2 |
C |
T |
8: 91,106,438 (GRCm38) |
P666S |
probably benign |
Het |
Rnf123 |
A |
G |
9: 108,058,238 (GRCm38) |
F979L |
probably damaging |
Het |
Rock2 |
T |
A |
12: 16,965,171 (GRCm38) |
D788E |
probably benign |
Het |
Serpina3b |
A |
G |
12: 104,132,957 (GRCm38) |
T244A |
probably benign |
Het |
Setd1b |
T |
C |
5: 123,148,513 (GRCm38) |
S541P |
unknown |
Het |
Slc12a4 |
T |
C |
8: 105,960,707 (GRCm38) |
D60G |
possibly damaging |
Het |
Stac2 |
T |
C |
11: 98,041,354 (GRCm38) |
E241G |
probably benign |
Het |
Tafa3 |
C |
T |
3: 104,773,079 (GRCm38) |
V75M |
probably damaging |
Het |
Tas2r115 |
A |
G |
6: 132,737,629 (GRCm38) |
Y120H |
probably damaging |
Het |
Tmtc2 |
A |
T |
10: 105,370,085 (GRCm38) |
F450I |
probably benign |
Het |
Txnl1 |
A |
T |
18: 63,674,191 (GRCm38) |
I198N |
probably damaging |
Het |
Ubr2 |
A |
T |
17: 46,956,654 (GRCm38) |
M1049K |
probably damaging |
Het |
Ugt2b5 |
T |
C |
5: 87,139,900 (GRCm38) |
E136G |
probably benign |
Het |
Unc13b |
C |
T |
4: 43,241,066 (GRCm38) |
T3623I |
probably damaging |
Het |
Usp13 |
T |
A |
3: 32,919,064 (GRCm38) |
S797T |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,702,948 (GRCm38) |
T203S |
probably damaging |
Het |
Vwf |
T |
A |
6: 125,645,736 (GRCm38) |
I1718N |
probably damaging |
Het |
Zfr |
A |
G |
15: 12,159,646 (GRCm38) |
H676R |
probably benign |
Het |
|
Other mutations in Or7g27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01546:Or7g27
|
APN |
9 |
19,338,772 (GRCm38) |
missense |
possibly damaging |
0.56 |
IGL01767:Or7g27
|
APN |
9 |
19,339,302 (GRCm38) |
missense |
possibly damaging |
0.54 |
IGL01945:Or7g27
|
APN |
9 |
19,339,332 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02202:Or7g27
|
APN |
9 |
19,339,249 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02877:Or7g27
|
APN |
9 |
19,339,201 (GRCm38) |
missense |
possibly damaging |
0.86 |
R0466:Or7g27
|
UTSW |
9 |
19,339,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R1521:Or7g27
|
UTSW |
9 |
19,338,652 (GRCm38) |
missense |
probably benign |
0.35 |
R1650:Or7g27
|
UTSW |
9 |
19,338,647 (GRCm38) |
missense |
possibly damaging |
0.49 |
R1766:Or7g27
|
UTSW |
9 |
19,338,858 (GRCm38) |
missense |
probably benign |
0.06 |
R2060:Or7g27
|
UTSW |
9 |
19,339,056 (GRCm38) |
missense |
probably benign |
0.01 |
R2082:Or7g27
|
UTSW |
9 |
19,339,278 (GRCm38) |
missense |
probably benign |
0.36 |
R2257:Or7g27
|
UTSW |
9 |
19,338,493 (GRCm38) |
missense |
probably benign |
0.01 |
R2892:Or7g27
|
UTSW |
9 |
19,338,738 (GRCm38) |
missense |
probably benign |
0.04 |
R3156:Or7g27
|
UTSW |
9 |
19,339,424 (GRCm38) |
splice site |
probably null |
|
R3943:Or7g27
|
UTSW |
9 |
19,339,075 (GRCm38) |
missense |
probably benign |
0.05 |
R4116:Or7g27
|
UTSW |
9 |
19,338,644 (GRCm38) |
missense |
probably benign |
0.39 |
R4518:Or7g27
|
UTSW |
9 |
19,339,260 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4814:Or7g27
|
UTSW |
9 |
19,339,180 (GRCm38) |
missense |
probably damaging |
1.00 |
R5339:Or7g27
|
UTSW |
9 |
19,339,159 (GRCm38) |
missense |
possibly damaging |
0.78 |
R6647:Or7g27
|
UTSW |
9 |
19,338,629 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7493:Or7g27
|
UTSW |
9 |
19,338,813 (GRCm38) |
missense |
probably damaging |
0.98 |
R7522:Or7g27
|
UTSW |
9 |
19,338,998 (GRCm38) |
nonsense |
probably null |
|
R7584:Or7g27
|
UTSW |
9 |
19,339,273 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9127:Or7g27
|
UTSW |
9 |
19,338,730 (GRCm38) |
missense |
probably benign |
|
R9463:Or7g27
|
UTSW |
9 |
19,339,024 (GRCm38) |
missense |
possibly damaging |
0.94 |
|