Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
C |
8: 60,996,566 (GRCm39) |
V389A |
possibly damaging |
Het |
Adgrl1 |
T |
C |
8: 84,660,519 (GRCm39) |
F792S |
probably benign |
Het |
Angptl2 |
A |
T |
2: 33,118,342 (GRCm39) |
I39F |
probably benign |
Het |
Aprt |
A |
G |
8: 123,303,355 (GRCm39) |
I29T |
probably damaging |
Het |
Arhgap21 |
A |
T |
2: 20,885,816 (GRCm39) |
S464T |
probably damaging |
Het |
Atic |
T |
C |
1: 71,603,636 (GRCm39) |
Y151H |
probably damaging |
Het |
BB014433 |
T |
C |
8: 15,092,623 (GRCm39) |
T77A |
unknown |
Het |
Boc |
C |
A |
16: 44,308,077 (GRCm39) |
C926F |
|
Het |
Brd10 |
A |
G |
19: 29,696,938 (GRCm39) |
S852P |
possibly damaging |
Het |
Cabin1 |
C |
T |
10: 75,530,550 (GRCm39) |
R1544Q |
probably benign |
Het |
Ccdc33 |
A |
G |
9: 57,938,388 (GRCm39) |
V861A |
probably benign |
Het |
Ccdc88c |
T |
C |
12: 100,904,322 (GRCm39) |
T230A |
unknown |
Het |
Cdc42bpa |
T |
A |
1: 179,939,460 (GRCm39) |
|
probably null |
Het |
Chrnb2 |
T |
C |
3: 89,668,128 (GRCm39) |
M396V |
probably benign |
Het |
Chst2 |
A |
G |
9: 95,287,155 (GRCm39) |
V397A |
probably damaging |
Het |
Cit |
T |
A |
5: 116,126,498 (GRCm39) |
N1643K |
probably damaging |
Het |
Ckb |
T |
A |
12: 111,637,869 (GRCm39) |
D113V |
probably benign |
Het |
Cyp2c68 |
A |
T |
19: 39,727,571 (GRCm39) |
M136K |
probably damaging |
Het |
Epas1 |
G |
T |
17: 87,116,873 (GRCm39) |
R181L |
probably damaging |
Het |
Flnc |
A |
C |
6: 29,452,353 (GRCm39) |
I1726L |
possibly damaging |
Het |
Fras1 |
G |
A |
5: 96,883,022 (GRCm39) |
R2518H |
probably damaging |
Het |
Gid4 |
T |
C |
11: 60,308,654 (GRCm39) |
V58A |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,610,262 (GRCm39) |
N1469I |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,278,377 (GRCm39) |
E1693G |
probably damaging |
Het |
Irx4 |
C |
G |
13: 73,416,649 (GRCm39) |
C348W |
probably damaging |
Het |
Lrig2 |
A |
G |
3: 104,387,438 (GRCm39) |
S410P |
possibly damaging |
Het |
Lsm11 |
A |
G |
11: 45,824,789 (GRCm39) |
V246A |
probably benign |
Het |
Ltbp1 |
G |
T |
17: 75,670,425 (GRCm39) |
V1489F |
probably damaging |
Het |
Mc2r |
T |
C |
18: 68,540,667 (GRCm39) |
T209A |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,581,153 (GRCm39) |
L821P |
probably damaging |
Het |
Mtus2 |
A |
T |
5: 148,238,293 (GRCm39) |
E1206V |
probably damaging |
Het |
Muc5b |
T |
A |
7: 141,410,129 (GRCm39) |
H1234Q |
unknown |
Het |
Naip5 |
A |
T |
13: 100,359,008 (GRCm39) |
F743I |
probably damaging |
Het |
Nphp3 |
G |
A |
9: 103,919,305 (GRCm39) |
V1318I |
probably benign |
Het |
Or4c10b |
T |
G |
2: 89,711,482 (GRCm39) |
L104W |
probably damaging |
Het |
Or5p60 |
A |
T |
7: 107,723,935 (GRCm39) |
N178K |
possibly damaging |
Het |
Or7g26 |
T |
C |
9: 19,229,995 (GRCm39) |
L61P |
probably damaging |
Het |
Or8b4 |
C |
A |
9: 37,830,670 (GRCm39) |
T239K |
probably damaging |
Het |
Or9k2b |
G |
C |
10: 130,016,566 (GRCm39) |
P61R |
probably damaging |
Het |
Paqr5 |
G |
A |
9: 61,868,826 (GRCm39) |
R246C |
probably benign |
Het |
Pdgfb |
T |
C |
15: 79,885,956 (GRCm39) |
Q128R |
probably damaging |
Het |
Prr3 |
T |
A |
17: 36,285,619 (GRCm39) |
I88F |
possibly damaging |
Het |
Ptprd |
C |
G |
4: 75,872,315 (GRCm39) |
A1134P |
possibly damaging |
Het |
R3hcc1l |
G |
A |
19: 42,552,301 (GRCm39) |
D433N |
probably benign |
Het |
Scnn1b |
A |
T |
7: 121,498,522 (GRCm39) |
T21S |
probably benign |
Het |
Smcr8 |
A |
G |
11: 60,668,857 (GRCm39) |
I2V |
probably damaging |
Het |
Stk33 |
T |
C |
7: 108,940,686 (GRCm39) |
D8G |
probably benign |
Het |
Tbc1d22a |
T |
C |
15: 86,098,803 (GRCm39) |
F10L |
probably benign |
Het |
Tmem126a |
T |
A |
7: 90,102,026 (GRCm39) |
I58F |
possibly damaging |
Het |
Ttf2 |
T |
C |
3: 100,869,880 (GRCm39) |
K398E |
probably benign |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Usp53 |
G |
T |
3: 122,741,068 (GRCm39) |
N727K |
probably benign |
Het |
Vmn2r25 |
T |
G |
6: 123,830,092 (GRCm39) |
I20L |
probably benign |
Het |
Zfp747l1 |
T |
A |
7: 126,984,332 (GRCm39) |
I257L |
unknown |
Het |
|
Other mutations in Or52a24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01892:Or52a24
|
APN |
7 |
103,381,687 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02121:Or52a24
|
APN |
7 |
103,381,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R0140:Or52a24
|
UTSW |
7 |
103,381,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Or52a24
|
UTSW |
7 |
103,381,583 (GRCm39) |
missense |
probably benign |
0.09 |
R0582:Or52a24
|
UTSW |
7 |
103,381,880 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1585:Or52a24
|
UTSW |
7 |
103,381,585 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1907:Or52a24
|
UTSW |
7 |
103,381,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Or52a24
|
UTSW |
7 |
103,381,457 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4954:Or52a24
|
UTSW |
7 |
103,381,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5464:Or52a24
|
UTSW |
7 |
103,381,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Or52a24
|
UTSW |
7 |
103,381,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R6761:Or52a24
|
UTSW |
7 |
103,381,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6782:Or52a24
|
UTSW |
7 |
103,381,549 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7015:Or52a24
|
UTSW |
7 |
103,382,024 (GRCm39) |
missense |
probably null |
0.85 |
R7503:Or52a24
|
UTSW |
7 |
103,381,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7959:Or52a24
|
UTSW |
7 |
103,382,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8347:Or52a24
|
UTSW |
7 |
103,381,150 (GRCm39) |
missense |
probably benign |
|
R8984:Or52a24
|
UTSW |
7 |
103,381,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R9000:Or52a24
|
UTSW |
7 |
103,381,672 (GRCm39) |
missense |
probably damaging |
0.99 |
X0058:Or52a24
|
UTSW |
7 |
103,381,489 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or52a24
|
UTSW |
7 |
103,381,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|