Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,303,926 (GRCm39) |
L2117P |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,262,391 (GRCm39) |
S386R |
probably benign |
Het |
Agxt |
T |
C |
1: 93,069,779 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
T |
1: 179,611,675 (GRCm39) |
I565N |
possibly damaging |
Het |
Ank1 |
C |
T |
8: 23,572,300 (GRCm39) |
T70I |
probably damaging |
Het |
Anxa1 |
A |
G |
19: 20,360,287 (GRCm39) |
V108A |
probably benign |
Het |
Aqp3 |
A |
G |
4: 41,093,819 (GRCm39) |
F225L |
probably damaging |
Het |
Atp11b |
T |
G |
3: 35,888,532 (GRCm39) |
I934R |
possibly damaging |
Het |
Atp13a5 |
A |
T |
16: 29,169,566 (GRCm39) |
L42Q |
probably damaging |
Het |
Bcr |
A |
G |
10: 74,960,898 (GRCm39) |
D443G |
probably benign |
Het |
Cbfa2t3 |
G |
T |
8: 123,365,598 (GRCm39) |
D211E |
possibly damaging |
Het |
Ccdc146 |
A |
T |
5: 21,538,036 (GRCm39) |
L96Q |
probably damaging |
Het |
Cdh16 |
A |
G |
8: 105,343,660 (GRCm39) |
I612T |
probably damaging |
Het |
Clcn2 |
G |
A |
16: 20,525,965 (GRCm39) |
P785S |
probably damaging |
Het |
Dennd5a |
A |
G |
7: 109,513,983 (GRCm39) |
I743T |
possibly damaging |
Het |
Dnah12 |
T |
A |
14: 26,431,326 (GRCm39) |
D381E |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dnajc2 |
G |
A |
5: 21,962,771 (GRCm39) |
R521* |
probably null |
Het |
Dst |
T |
C |
1: 34,289,728 (GRCm39) |
V5776A |
probably damaging |
Het |
Eddm13 |
G |
A |
7: 6,269,332 (GRCm39) |
|
probably benign |
Het |
Eif1ad19 |
T |
A |
12: 87,740,512 (GRCm39) |
K16* |
probably null |
Het |
Ercc4 |
G |
A |
16: 12,941,445 (GRCm39) |
|
probably benign |
Het |
Eya1 |
T |
A |
1: 14,254,582 (GRCm39) |
N417Y |
probably damaging |
Het |
Fam149b |
T |
A |
14: 20,413,439 (GRCm39) |
H219Q |
possibly damaging |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fbxw17 |
C |
T |
13: 50,586,506 (GRCm39) |
R403C |
probably benign |
Het |
Fer1l4 |
T |
C |
2: 155,873,135 (GRCm39) |
Y1315C |
probably damaging |
Het |
Gatd1 |
G |
T |
7: 140,988,861 (GRCm39) |
|
probably benign |
Het |
Gm10330 |
A |
T |
12: 23,829,961 (GRCm39) |
Y73* |
probably null |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gsn |
T |
A |
2: 35,188,933 (GRCm39) |
Y440N |
probably damaging |
Het |
Hdc |
C |
T |
2: 126,446,220 (GRCm39) |
E180K |
probably benign |
Het |
Ilk |
A |
G |
7: 105,391,456 (GRCm39) |
D374G |
probably damaging |
Het |
Invs |
G |
A |
4: 48,421,807 (GRCm39) |
R813Q |
probably damaging |
Het |
Itln1 |
T |
A |
1: 171,360,958 (GRCm39) |
K45* |
probably null |
Het |
Ivd |
A |
G |
2: 118,710,946 (GRCm39) |
Y385C |
probably damaging |
Het |
Klk1b4 |
A |
G |
7: 43,860,492 (GRCm39) |
N170S |
probably benign |
Het |
Klk1b9 |
A |
C |
7: 43,445,419 (GRCm39) |
D203A |
probably damaging |
Het |
Lamtor3 |
A |
T |
3: 137,630,909 (GRCm39) |
R27S |
probably damaging |
Het |
Lcn6 |
T |
A |
2: 25,567,082 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
C |
10: 103,025,784 (GRCm39) |
D946G |
probably damaging |
Het |
Morc1 |
A |
G |
16: 48,322,699 (GRCm39) |
D332G |
probably benign |
Het |
Myo15a |
T |
C |
11: 60,382,493 (GRCm39) |
I1523T |
probably damaging |
Het |
Nagpa |
A |
T |
16: 5,013,743 (GRCm39) |
M365K |
probably benign |
Het |
Nckap5l |
G |
T |
15: 99,324,457 (GRCm39) |
P682Q |
probably benign |
Het |
Nfix |
A |
G |
8: 85,498,713 (GRCm39) |
F87L |
possibly damaging |
Het |
Nup155 |
C |
A |
15: 8,153,722 (GRCm39) |
T421K |
probably benign |
Het |
Or5ac25 |
A |
T |
16: 59,182,067 (GRCm39) |
N171K |
probably damaging |
Het |
Or5ae2 |
T |
C |
7: 84,505,646 (GRCm39) |
V23A |
probably damaging |
Het |
Or7c74 |
A |
G |
2: 37,160,937 (GRCm39) |
|
noncoding transcript |
Het |
Pate14 |
T |
C |
9: 36,549,120 (GRCm39) |
N47D |
probably benign |
Het |
Pds5a |
A |
C |
5: 65,792,680 (GRCm39) |
V751G |
probably benign |
Het |
Podnl1 |
G |
T |
8: 84,852,965 (GRCm39) |
C45F |
probably damaging |
Het |
Psme2b |
C |
T |
11: 48,836,654 (GRCm39) |
E98K |
probably benign |
Het |
Ptprk |
T |
A |
10: 28,427,713 (GRCm39) |
I764N |
probably damaging |
Het |
Rbm33 |
A |
T |
5: 28,547,409 (GRCm39) |
Q193L |
probably benign |
Het |
Rnasel |
C |
A |
1: 153,629,677 (GRCm39) |
H64Q |
probably damaging |
Het |
Ryr1 |
G |
A |
7: 28,802,234 (GRCm39) |
|
probably null |
Het |
Scamp3 |
A |
G |
3: 89,088,216 (GRCm39) |
|
probably benign |
Het |
Sema6b |
C |
T |
17: 56,439,497 (GRCm39) |
|
probably null |
Het |
Six4 |
A |
C |
12: 73,150,400 (GRCm39) |
I715R |
probably benign |
Het |
Slc28a2 |
T |
C |
2: 122,288,371 (GRCm39) |
M554T |
possibly damaging |
Het |
Snhg11 |
T |
C |
2: 158,218,872 (GRCm39) |
|
probably benign |
Het |
Spdya |
A |
T |
17: 71,869,499 (GRCm39) |
Y98F |
possibly damaging |
Het |
Tert |
T |
C |
13: 73,794,428 (GRCm39) |
|
probably null |
Het |
Tex22 |
G |
A |
12: 113,052,104 (GRCm39) |
C54Y |
probably damaging |
Het |
Tmem198b |
C |
T |
10: 128,637,942 (GRCm39) |
R207H |
probably damaging |
Het |
Trbv13-1 |
C |
T |
6: 41,093,189 (GRCm39) |
Q42* |
probably null |
Het |
Trcg1 |
T |
C |
9: 57,149,562 (GRCm39) |
L378P |
probably damaging |
Het |
Trpv5 |
T |
G |
6: 41,636,647 (GRCm39) |
D433A |
probably damaging |
Het |
Ube3b |
A |
G |
5: 114,545,702 (GRCm39) |
N654D |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
Vwa7 |
A |
T |
17: 35,241,709 (GRCm39) |
Y448F |
probably damaging |
Het |
Zan |
A |
C |
5: 137,382,099 (GRCm39) |
D5149E |
unknown |
Het |
Zfp106 |
A |
G |
2: 120,341,015 (GRCm39) |
W1832R |
probably damaging |
Het |
Zfp189 |
G |
A |
4: 49,530,438 (GRCm39) |
G514S |
probably damaging |
Het |
Zhx1 |
G |
A |
15: 57,917,538 (GRCm39) |
T236I |
possibly damaging |
Het |
|
Other mutations in Or8k53 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01548:Or8k53
|
APN |
2 |
86,178,077 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02524:Or8k53
|
APN |
2 |
86,177,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0134:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0225:Or8k53
|
UTSW |
2 |
86,178,072 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1981:Or8k53
|
UTSW |
2 |
86,177,486 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4181:Or8k53
|
UTSW |
2 |
86,177,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Or8k53
|
UTSW |
2 |
86,177,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5077:Or8k53
|
UTSW |
2 |
86,177,683 (GRCm39) |
missense |
probably benign |
0.00 |
R6312:Or8k53
|
UTSW |
2 |
86,177,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:Or8k53
|
UTSW |
2 |
86,177,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R6591:Or8k53
|
UTSW |
2 |
86,177,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R6626:Or8k53
|
UTSW |
2 |
86,177,364 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6680:Or8k53
|
UTSW |
2 |
86,177,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6691:Or8k53
|
UTSW |
2 |
86,177,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Or8k53
|
UTSW |
2 |
86,177,150 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7622:Or8k53
|
UTSW |
2 |
86,178,006 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8114:Or8k53
|
UTSW |
2 |
86,177,530 (GRCm39) |
missense |
probably benign |
0.00 |
R8138:Or8k53
|
UTSW |
2 |
86,177,930 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8242:Or8k53
|
UTSW |
2 |
86,177,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R8260:Or8k53
|
UTSW |
2 |
86,177,276 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8360:Or8k53
|
UTSW |
2 |
86,177,668 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8433:Or8k53
|
UTSW |
2 |
86,177,144 (GRCm39) |
missense |
unknown |
|
R8927:Or8k53
|
UTSW |
2 |
86,178,090 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8928:Or8k53
|
UTSW |
2 |
86,178,090 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9150:Or8k53
|
UTSW |
2 |
86,177,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Or8k53
|
UTSW |
2 |
86,177,768 (GRCm39) |
missense |
probably benign |
0.14 |
R9487:Or8k53
|
UTSW |
2 |
86,177,846 (GRCm39) |
missense |
probably benign |
0.10 |
R9712:Or8k53
|
UTSW |
2 |
86,177,583 (GRCm39) |
missense |
probably benign |
0.22 |
Z1176:Or8k53
|
UTSW |
2 |
86,177,227 (GRCm39) |
missense |
possibly damaging |
0.95 |
|