Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230112D13Rik |
A |
G |
14: 34,234,099 (GRCm39) |
M64T |
unknown |
Het |
Adamts15 |
C |
T |
9: 30,813,493 (GRCm39) |
G891R |
probably damaging |
Het |
Adck5 |
G |
A |
15: 76,477,486 (GRCm39) |
V107I |
possibly damaging |
Het |
Aoc3 |
G |
A |
11: 101,223,131 (GRCm39) |
V456M |
possibly damaging |
Het |
Apbb1 |
A |
T |
7: 105,223,062 (GRCm39) |
L183Q |
probably benign |
Het |
Camsap3 |
A |
G |
8: 3,654,442 (GRCm39) |
H693R |
probably benign |
Het |
Ccdc88a |
A |
G |
11: 29,406,509 (GRCm39) |
T414A |
probably benign |
Het |
Cdh17 |
T |
C |
4: 11,795,581 (GRCm39) |
V387A |
probably benign |
Het |
Coasy |
G |
T |
11: 100,976,696 (GRCm39) |
V489F |
probably damaging |
Het |
Ercc6 |
A |
T |
14: 32,274,578 (GRCm39) |
M574L |
probably benign |
Het |
Esrrb |
T |
C |
12: 86,552,598 (GRCm39) |
L180P |
probably damaging |
Het |
Fam83b |
A |
T |
9: 76,398,679 (GRCm39) |
V808D |
probably damaging |
Het |
Fat3 |
C |
T |
9: 15,909,100 (GRCm39) |
V2301I |
possibly damaging |
Het |
Ftdc1 |
C |
A |
16: 58,435,075 (GRCm39) |
R83S |
probably damaging |
Het |
Hyal4 |
T |
A |
6: 24,755,912 (GRCm39) |
Y43* |
probably null |
Het |
Hydin |
C |
A |
8: 111,257,685 (GRCm39) |
L2372M |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,459,809 (GRCm39) |
V145A |
probably benign |
Het |
Lypd10 |
A |
G |
7: 24,413,167 (GRCm39) |
K162R |
probably benign |
Het |
Muc21 |
A |
C |
17: 35,929,105 (GRCm39) |
S1581A |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,142,577 (GRCm39) |
I913V |
possibly damaging |
Het |
Nat10 |
C |
T |
2: 103,561,719 (GRCm39) |
G654D |
probably damaging |
Het |
Nbn |
A |
T |
4: 15,970,719 (GRCm39) |
|
probably null |
Het |
Nup50l |
A |
T |
6: 96,142,677 (GRCm39) |
N122K |
possibly damaging |
Het |
Oas3 |
T |
C |
5: 120,907,128 (GRCm39) |
Y503C |
unknown |
Het |
Pappa |
G |
T |
4: 65,233,029 (GRCm39) |
|
probably null |
Het |
Pfas |
A |
G |
11: 68,884,121 (GRCm39) |
|
probably null |
Het |
Pfas |
G |
T |
11: 68,881,573 (GRCm39) |
|
probably null |
Het |
Pign |
A |
T |
1: 105,519,422 (GRCm39) |
M500K |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,269,605 (GRCm39) |
K3313R |
probably benign |
Het |
Ptk2b |
A |
G |
14: 66,396,047 (GRCm39) |
V807A |
probably benign |
Het |
Ptpdc1 |
C |
T |
13: 48,740,286 (GRCm39) |
E382K |
probably damaging |
Het |
Rfpl4b |
A |
T |
10: 38,696,833 (GRCm39) |
I256N |
probably benign |
Het |
Skap1 |
C |
G |
11: 96,432,295 (GRCm39) |
S88* |
probably null |
Het |
Slc4a2 |
T |
C |
5: 24,640,884 (GRCm39) |
S742P |
probably damaging |
Het |
Supv3l1 |
T |
C |
10: 62,265,599 (GRCm39) |
D647G |
probably damaging |
Het |
Tmem184c |
A |
C |
8: 78,331,386 (GRCm39) |
V121G |
probably damaging |
Het |
Tonsl |
T |
C |
15: 76,507,421 (GRCm39) |
I118V |
probably benign |
Het |
Top1 |
T |
A |
2: 160,554,588 (GRCm39) |
Y446* |
probably null |
Het |
Trim37 |
A |
G |
11: 87,037,781 (GRCm39) |
R172G |
probably damaging |
Het |
Vgll4 |
C |
A |
6: 114,867,768 (GRCm39) |
|
probably null |
Het |
Vgll4 |
T |
A |
6: 114,867,769 (GRCm39) |
|
probably null |
Het |
Vmn1r5 |
T |
G |
6: 56,963,150 (GRCm39) |
I275S |
possibly damaging |
Het |
Vwde |
A |
T |
6: 13,187,874 (GRCm39) |
H584Q |
probably damaging |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp282 |
T |
A |
6: 47,856,943 (GRCm39) |
W59R |
probably damaging |
Het |
Zfp329 |
T |
A |
7: 12,545,395 (GRCm39) |
N43I |
probably benign |
Het |
Zswim2 |
T |
A |
2: 83,754,103 (GRCm39) |
T186S |
probably benign |
Het |
|
Other mutations in Or11g7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01663:Or11g7
|
APN |
14 |
50,690,607 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02117:Or11g7
|
APN |
14 |
50,691,399 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02663:Or11g7
|
APN |
14 |
50,691,309 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02858:Or11g7
|
APN |
14 |
50,690,507 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02955:Or11g7
|
APN |
14 |
50,691,442 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03210:Or11g7
|
APN |
14 |
50,691,440 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03249:Or11g7
|
APN |
14 |
50,690,668 (GRCm39) |
missense |
probably damaging |
0.98 |
G1Funyon:Or11g7
|
UTSW |
14 |
50,691,021 (GRCm39) |
missense |
probably benign |
0.08 |
R1449:Or11g7
|
UTSW |
14 |
50,691,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Or11g7
|
UTSW |
14 |
50,690,634 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1465:Or11g7
|
UTSW |
14 |
50,690,634 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1513:Or11g7
|
UTSW |
14 |
50,691,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1908:Or11g7
|
UTSW |
14 |
50,691,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R2422:Or11g7
|
UTSW |
14 |
50,690,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Or11g7
|
UTSW |
14 |
50,690,653 (GRCm39) |
missense |
probably benign |
0.14 |
R4184:Or11g7
|
UTSW |
14 |
50,690,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Or11g7
|
UTSW |
14 |
50,690,874 (GRCm39) |
missense |
probably damaging |
0.96 |
R5028:Or11g7
|
UTSW |
14 |
50,691,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Or11g7
|
UTSW |
14 |
50,691,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R6057:Or11g7
|
UTSW |
14 |
50,691,201 (GRCm39) |
nonsense |
probably null |
|
R6455:Or11g7
|
UTSW |
14 |
50,691,042 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6903:Or11g7
|
UTSW |
14 |
50,691,412 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6998:Or11g7
|
UTSW |
14 |
50,690,890 (GRCm39) |
missense |
probably benign |
0.29 |
R7671:Or11g7
|
UTSW |
14 |
50,691,342 (GRCm39) |
missense |
probably benign |
0.04 |
R8048:Or11g7
|
UTSW |
14 |
50,691,373 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8301:Or11g7
|
UTSW |
14 |
50,691,021 (GRCm39) |
missense |
probably benign |
0.08 |
X0066:Or11g7
|
UTSW |
14 |
50,691,115 (GRCm39) |
missense |
probably benign |
0.00 |
|