Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
G |
A |
2: 19,498,995 (GRCm39) |
Q333* |
probably null |
Het |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Acvrl1 |
G |
A |
15: 101,033,741 (GRCm39) |
R141H |
probably benign |
Het |
Adprm |
A |
G |
11: 66,932,436 (GRCm39) |
F158L |
possibly damaging |
Het |
Aldoart2 |
C |
T |
12: 55,613,038 (GRCm39) |
T321M |
probably benign |
Het |
Ap3m2 |
A |
G |
8: 23,293,792 (GRCm39) |
V86A |
probably benign |
Het |
Arhgef19 |
T |
A |
4: 140,974,826 (GRCm39) |
|
probably null |
Het |
Bcl2l12 |
T |
G |
7: 44,643,615 (GRCm39) |
|
probably null |
Het |
Bptf |
T |
C |
11: 106,945,391 (GRCm39) |
Q2501R |
probably damaging |
Het |
C230029F24Rik |
A |
T |
1: 49,377,295 (GRCm39) |
|
noncoding transcript |
Het |
C7 |
C |
T |
15: 5,079,074 (GRCm39) |
G78D |
probably damaging |
Het |
Caly |
T |
C |
7: 139,650,538 (GRCm39) |
T135A |
probably benign |
Het |
Cbl |
A |
G |
9: 44,065,108 (GRCm39) |
M740T |
possibly damaging |
Het |
Cbx4 |
A |
G |
11: 118,972,037 (GRCm39) |
V446A |
probably benign |
Het |
Celsr1 |
C |
A |
15: 85,822,112 (GRCm39) |
R1735L |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,830,236 (GRCm39) |
D135G |
probably damaging |
Het |
Cgn |
T |
C |
3: 94,687,246 (GRCm39) |
T19A |
probably damaging |
Het |
Chic2 |
A |
T |
5: 75,204,865 (GRCm39) |
V32D |
probably damaging |
Het |
Cntln |
A |
G |
4: 84,968,120 (GRCm39) |
K780E |
probably benign |
Het |
Col8a2 |
A |
T |
4: 126,204,581 (GRCm39) |
D197V |
probably damaging |
Het |
Crot |
A |
T |
5: 9,024,000 (GRCm39) |
V372E |
probably damaging |
Het |
Cyb561d2 |
C |
T |
9: 107,418,747 (GRCm39) |
V26M |
probably damaging |
Het |
Ddx5 |
G |
A |
11: 106,676,062 (GRCm39) |
T237I |
probably damaging |
Het |
Dmxl2 |
G |
T |
9: 54,408,725 (GRCm39) |
|
probably benign |
Het |
Dock8 |
T |
A |
19: 25,135,747 (GRCm39) |
S1188R |
probably benign |
Het |
Ehbp1 |
T |
A |
11: 22,051,073 (GRCm39) |
H493L |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,090,792 (GRCm39) |
*1217K |
probably null |
Het |
Eprs1 |
A |
G |
1: 185,142,336 (GRCm39) |
|
probably benign |
Het |
Etfdh |
T |
C |
3: 79,513,095 (GRCm39) |
D376G |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,842,980 (GRCm39) |
Q1088R |
probably benign |
Het |
Fbxw16 |
G |
T |
9: 109,270,318 (GRCm39) |
T141N |
probably damaging |
Het |
Fgf11 |
G |
A |
11: 69,689,585 (GRCm39) |
H138Y |
probably damaging |
Het |
Htra3 |
T |
C |
5: 35,828,418 (GRCm39) |
E154G |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,296,274 (GRCm39) |
V3601D |
probably damaging |
Het |
Jup |
G |
T |
11: 100,270,367 (GRCm39) |
S380* |
probably null |
Het |
Klrg1 |
T |
A |
6: 122,255,234 (GRCm39) |
D66V |
probably benign |
Het |
Llgl1 |
C |
T |
11: 60,600,550 (GRCm39) |
A633V |
probably benign |
Het |
Lmln |
T |
A |
16: 32,894,467 (GRCm39) |
Y203* |
probably null |
Het |
Lrrc58 |
T |
G |
16: 37,697,418 (GRCm39) |
C165G |
probably benign |
Het |
Lss |
T |
C |
10: 76,383,371 (GRCm39) |
V557A |
probably benign |
Het |
Mast4 |
T |
C |
13: 103,042,262 (GRCm39) |
|
probably benign |
Het |
Med13l |
C |
A |
5: 118,869,014 (GRCm39) |
P754Q |
possibly damaging |
Het |
Mga |
C |
T |
2: 119,763,063 (GRCm39) |
R1240* |
probably null |
Het |
Mgat5b |
T |
A |
11: 116,865,025 (GRCm39) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,610,209 (GRCm39) |
D1572G |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,754,214 (GRCm38) |
S1363T |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,575,332 (GRCm39) |
S1306T |
probably benign |
Het |
Myo18b |
A |
G |
5: 112,908,258 (GRCm39) |
V2005A |
probably damaging |
Het |
Myo1e |
G |
A |
9: 70,260,554 (GRCm39) |
D571N |
probably benign |
Het |
Mypn |
T |
C |
10: 62,955,747 (GRCm39) |
|
probably null |
Het |
Ndufb10 |
T |
C |
17: 24,941,731 (GRCm39) |
|
probably null |
Het |
Nelfb |
G |
T |
2: 25,096,208 (GRCm39) |
D300E |
probably benign |
Het |
Nicol1 |
G |
A |
5: 34,142,270 (GRCm39) |
R79H |
probably damaging |
Het |
Odad2 |
G |
A |
18: 7,223,663 (GRCm39) |
T460M |
probably damaging |
Het |
Or2y1d |
T |
A |
11: 49,321,482 (GRCm39) |
Y60N |
probably damaging |
Het |
Or4e5 |
A |
T |
14: 52,727,988 (GRCm39) |
C61* |
probably null |
Het |
Or52n2c |
T |
A |
7: 104,574,942 (GRCm39) |
T10S |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,144,080 (GRCm39) |
T57M |
probably benign |
Het |
Pkp1 |
A |
T |
1: 135,808,593 (GRCm39) |
I458N |
possibly damaging |
Het |
Prr12 |
T |
A |
7: 44,700,653 (GRCm39) |
|
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,532,879 (GRCm39) |
|
probably benign |
Het |
Psd4 |
T |
C |
2: 24,287,259 (GRCm39) |
F397S |
probably benign |
Het |
Pygm |
T |
C |
19: 6,448,169 (GRCm39) |
I737T |
probably damaging |
Het |
Rfx1 |
T |
A |
8: 84,806,743 (GRCm39) |
|
probably null |
Het |
Rsl1 |
A |
G |
13: 67,330,313 (GRCm39) |
T254A |
possibly damaging |
Het |
Sh3rf3 |
A |
G |
10: 58,922,646 (GRCm39) |
Q574R |
probably benign |
Het |
Spire1 |
T |
C |
18: 67,685,849 (GRCm39) |
|
probably null |
Het |
St6galnac4 |
G |
A |
2: 32,484,075 (GRCm39) |
G91D |
probably damaging |
Het |
Sytl2 |
T |
C |
7: 90,031,465 (GRCm39) |
|
probably benign |
Het |
Tbpl2 |
T |
A |
2: 23,983,872 (GRCm39) |
K188N |
possibly damaging |
Het |
Tenm3 |
A |
T |
8: 48,682,172 (GRCm39) |
M2486K |
possibly damaging |
Het |
Tgoln1 |
A |
C |
6: 72,593,123 (GRCm39) |
V119G |
possibly damaging |
Het |
Tpgs1 |
A |
T |
10: 79,505,325 (GRCm39) |
N28Y |
probably benign |
Het |
U2surp |
A |
C |
9: 95,344,847 (GRCm39) |
|
probably benign |
Het |
Vmn2r103 |
A |
G |
17: 19,993,773 (GRCm39) |
H50R |
probably benign |
Het |
Vmn2r19 |
A |
G |
6: 123,306,869 (GRCm39) |
N459S |
probably benign |
Het |
Vmn2r72 |
T |
C |
7: 85,387,693 (GRCm39) |
S624G |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,826,603 (GRCm39) |
T1415A |
probably benign |
Het |
Vwa5b1 |
G |
A |
4: 138,336,154 (GRCm39) |
P147S |
probably damaging |
Het |
|
Other mutations in Or52z15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02547:Or52z15
|
APN |
7 |
103,331,973 (GRCm39) |
missense |
probably benign |
0.01 |
R1160:Or52z15
|
UTSW |
7 |
103,332,068 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1508:Or52z15
|
UTSW |
7 |
103,332,678 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1766:Or52z15
|
UTSW |
7 |
103,332,068 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1901:Or52z15
|
UTSW |
7 |
103,332,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R2116:Or52z15
|
UTSW |
7 |
103,332,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Or52z15
|
UTSW |
7 |
103,332,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Or52z15
|
UTSW |
7 |
103,331,936 (GRCm39) |
missense |
probably benign |
0.40 |
R5750:Or52z15
|
UTSW |
7 |
103,332,362 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5776:Or52z15
|
UTSW |
7 |
103,332,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Or52z15
|
UTSW |
7 |
103,332,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Or52z15
|
UTSW |
7 |
103,332,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Or52z15
|
UTSW |
7 |
103,332,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R7846:Or52z15
|
UTSW |
7 |
103,332,407 (GRCm39) |
missense |
probably benign |
0.03 |
R7878:Or52z15
|
UTSW |
7 |
103,332,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Or52z15
|
UTSW |
7 |
103,332,404 (GRCm39) |
missense |
probably benign |
0.00 |
R9347:Or52z15
|
UTSW |
7 |
103,332,464 (GRCm39) |
missense |
probably damaging |
0.97 |
R9474:Or52z15
|
UTSW |
7 |
103,332,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Or52z15
|
UTSW |
7 |
103,332,246 (GRCm39) |
missense |
probably damaging |
1.00 |
RF040:Or52z15
|
UTSW |
7 |
103,332,145 (GRCm39) |
frame shift |
probably null |
|
Z1088:Or52z15
|
UTSW |
7 |
103,332,393 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Or52z15
|
UTSW |
7 |
103,332,312 (GRCm39) |
missense |
probably benign |
0.09 |
|