Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,471,840 (GRCm39) |
N1082Y |
possibly damaging |
Het |
4930444P10Rik |
G |
A |
1: 16,136,451 (GRCm39) |
Q122* |
probably null |
Het |
Afg2a |
A |
G |
3: 37,502,661 (GRCm39) |
N607D |
probably benign |
Het |
Ak8 |
C |
T |
2: 28,625,602 (GRCm39) |
T215M |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,614,074 (GRCm39) |
I210F |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,592,032 (GRCm39) |
F656L |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,824,793 (GRCm39) |
M292T |
probably benign |
Het |
Cachd1 |
G |
T |
4: 100,754,978 (GRCm39) |
C143F |
probably damaging |
Het |
Calcoco2 |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,808 (GRCm39) |
|
probably benign |
Het |
Ccnb1ip1 |
C |
T |
14: 51,029,450 (GRCm39) |
G204E |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,764,022 (GRCm39) |
L169F |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,364,550 (GRCm39) |
N593D |
possibly damaging |
Het |
Cdh20 |
T |
C |
1: 104,873,048 (GRCm39) |
S265P |
probably damaging |
Het |
Cenpk |
A |
G |
13: 104,367,365 (GRCm39) |
E67G |
probably damaging |
Het |
Cep76 |
A |
T |
18: 67,773,190 (GRCm39) |
I36K |
probably benign |
Het |
Clock |
A |
T |
5: 76,383,632 (GRCm39) |
I507N |
probably benign |
Het |
Cpne1 |
T |
C |
2: 155,920,873 (GRCm39) |
T110A |
probably benign |
Het |
Crybg2 |
A |
T |
4: 133,818,525 (GRCm39) |
E1427V |
possibly damaging |
Het |
Ctu1 |
A |
C |
7: 43,324,746 (GRCm39) |
K62Q |
probably damaging |
Het |
Dnai4 |
C |
T |
4: 102,944,529 (GRCm39) |
|
probably null |
Het |
Drd5 |
C |
A |
5: 38,477,747 (GRCm39) |
Q247K |
possibly damaging |
Het |
Ect2l |
A |
T |
10: 18,014,608 (GRCm39) |
L808* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,791,500 (GRCm39) |
T2905A |
probably benign |
Het |
Ficd |
A |
T |
5: 113,876,248 (GRCm39) |
D141V |
probably damaging |
Het |
Fnbp1 |
A |
G |
2: 30,938,222 (GRCm39) |
Y148H |
|
Het |
Gm49368 |
A |
G |
7: 127,700,685 (GRCm39) |
K485R |
probably benign |
Het |
Gpr75 |
C |
A |
11: 30,841,860 (GRCm39) |
A255D |
probably benign |
Het |
Hcrtr2 |
G |
T |
9: 76,153,666 (GRCm39) |
A242D |
probably damaging |
Het |
Iapp |
G |
T |
6: 142,244,602 (GRCm39) |
V10F |
probably benign |
Het |
Ikzf2 |
A |
G |
1: 69,722,417 (GRCm39) |
S31P |
possibly damaging |
Het |
Il18rap |
G |
A |
1: 40,564,280 (GRCm39) |
|
probably benign |
Het |
Irak2 |
A |
T |
6: 113,663,902 (GRCm39) |
N423Y |
probably damaging |
Het |
Itpkb |
A |
G |
1: 180,159,744 (GRCm39) |
|
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,365,172 (GRCm39) |
I874M |
probably damaging |
Het |
Kif26b |
G |
T |
1: 178,692,594 (GRCm39) |
V512F |
probably damaging |
Het |
Lhx6 |
G |
A |
2: 35,995,232 (GRCm39) |
|
probably benign |
Het |
Lrfn1 |
A |
G |
7: 28,158,918 (GRCm39) |
E279G |
possibly damaging |
Het |
Masp1 |
A |
C |
16: 23,314,882 (GRCm39) |
D126E |
probably damaging |
Het |
Mef2a |
T |
C |
7: 66,890,176 (GRCm39) |
I299V |
probably benign |
Het |
Midn |
A |
G |
10: 79,985,939 (GRCm39) |
S10G |
probably damaging |
Het |
Mrps12 |
A |
T |
7: 28,439,361 (GRCm39) |
L118Q |
probably damaging |
Het |
Mxi1 |
G |
A |
19: 53,360,126 (GRCm39) |
G283S |
probably damaging |
Het |
Mzf1 |
A |
G |
7: 12,786,836 (GRCm39) |
V78A |
probably benign |
Het |
Ncoa6 |
A |
G |
2: 155,263,078 (GRCm39) |
V452A |
probably damaging |
Het |
Neb |
A |
G |
2: 52,051,481 (GRCm39) |
Y6600H |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,297 (GRCm39) |
L748P |
possibly damaging |
Het |
Nnmt |
A |
T |
9: 48,514,801 (GRCm39) |
L72H |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,560 (GRCm39) |
T964A |
probably benign |
Het |
Or12k7 |
A |
G |
2: 36,958,982 (GRCm39) |
I222V |
probably benign |
Het |
Or1e35 |
T |
G |
11: 73,797,725 (GRCm39) |
M198L |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,335,350 (GRCm39) |
V224E |
probably damaging |
Het |
Or4k35 |
T |
A |
2: 111,100,464 (GRCm39) |
I83F |
possibly damaging |
Het |
Or5h27 |
G |
A |
16: 59,006,130 (GRCm39) |
P239S |
unknown |
Het |
Or8c11 |
A |
G |
9: 38,289,720 (GRCm39) |
N175S |
probably benign |
Het |
Osbpl11 |
A |
G |
16: 33,034,850 (GRCm39) |
N280D |
probably benign |
Het |
Peg10 |
A |
T |
6: 4,754,825 (GRCm39) |
Y202F |
probably damaging |
Het |
Pick1 |
A |
G |
15: 79,140,107 (GRCm39) |
R469G |
unknown |
Het |
Rev3l |
A |
G |
10: 39,738,786 (GRCm39) |
I2847V |
probably damaging |
Het |
Rmc1 |
A |
G |
18: 12,321,618 (GRCm39) |
E473G |
probably benign |
Het |
Rnaseh2b |
T |
A |
14: 62,569,617 (GRCm39) |
L18Q |
probably damaging |
Het |
Rpl19 |
A |
G |
11: 97,920,615 (GRCm39) |
Y122C |
probably benign |
Het |
Selp |
A |
G |
1: 163,964,787 (GRCm39) |
Y483C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,423,321 (GRCm39) |
F347L |
|
Het |
Snx14 |
A |
G |
9: 88,295,541 (GRCm39) |
I208T |
probably benign |
Het |
Spag16 |
T |
A |
1: 70,036,017 (GRCm39) |
F348L |
probably benign |
Het |
Spata22 |
A |
T |
11: 73,231,091 (GRCm39) |
N115I |
probably damaging |
Het |
Spata31 |
T |
C |
13: 65,068,818 (GRCm39) |
V322A |
probably benign |
Het |
Stc1 |
A |
T |
14: 69,275,825 (GRCm39) |
H206L |
probably benign |
Het |
Tas2r129 |
A |
G |
6: 132,928,522 (GRCm39) |
D153G |
probably damaging |
Het |
Tmem196 |
T |
A |
12: 119,982,268 (GRCm39) |
N167K |
possibly damaging |
Het |
Tmpo |
T |
C |
10: 90,987,581 (GRCm39) |
T356A |
probably damaging |
Het |
Tnks |
A |
G |
8: 35,314,433 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
C |
17: 46,781,661 (GRCm39) |
L364R |
probably damaging |
Het |
Vmn1r176 |
A |
T |
7: 23,534,480 (GRCm39) |
N224K |
probably damaging |
Het |
Vmn1r36 |
T |
A |
6: 66,693,720 (GRCm39) |
M52L |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,525,320 (GRCm39) |
H326L |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,819,220 (GRCm39) |
M244K |
probably benign |
Het |
Zcchc24 |
C |
T |
14: 25,757,578 (GRCm39) |
A102T |
probably benign |
Het |
Zfp1010 |
T |
A |
2: 176,957,312 (GRCm39) |
Q62L |
probably benign |
Het |
|
Other mutations in Or8g33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Or8g33
|
APN |
9 |
39,337,953 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01368:Or8g33
|
APN |
9 |
39,337,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Or8g33
|
APN |
9 |
39,338,025 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01939:Or8g33
|
APN |
9 |
39,337,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03048:Or8g33
|
UTSW |
9 |
39,338,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0069:Or8g33
|
UTSW |
9 |
39,338,188 (GRCm39) |
missense |
probably damaging |
0.98 |
R1460:Or8g33
|
UTSW |
9 |
39,337,503 (GRCm39) |
missense |
probably benign |
0.43 |
R1478:Or8g33
|
UTSW |
9 |
39,337,888 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1737:Or8g33
|
UTSW |
9 |
39,338,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Or8g33
|
UTSW |
9 |
39,337,966 (GRCm39) |
missense |
probably benign |
0.26 |
R2169:Or8g33
|
UTSW |
9 |
39,337,654 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2225:Or8g33
|
UTSW |
9 |
39,337,915 (GRCm39) |
missense |
probably benign |
0.00 |
R3731:Or8g33
|
UTSW |
9 |
39,338,365 (GRCm39) |
start codon destroyed |
probably benign |
0.23 |
R3777:Or8g33
|
UTSW |
9 |
39,337,901 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3802:Or8g33
|
UTSW |
9 |
39,337,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Or8g33
|
UTSW |
9 |
39,337,731 (GRCm39) |
missense |
probably benign |
0.27 |
R4887:Or8g33
|
UTSW |
9 |
39,337,531 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5215:Or8g33
|
UTSW |
9 |
39,337,919 (GRCm39) |
nonsense |
probably null |
|
R5813:Or8g33
|
UTSW |
9 |
39,338,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Or8g33
|
UTSW |
9 |
39,337,543 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6180:Or8g33
|
UTSW |
9 |
39,338,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Or8g33
|
UTSW |
9 |
39,337,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Or8g33
|
UTSW |
9 |
39,338,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R6808:Or8g33
|
UTSW |
9 |
39,337,836 (GRCm39) |
missense |
probably damaging |
0.99 |
R7099:Or8g33
|
UTSW |
9 |
39,337,599 (GRCm39) |
missense |
probably benign |
0.01 |
R7826:Or8g33
|
UTSW |
9 |
39,337,423 (GRCm39) |
makesense |
probably null |
|
R8309:Or8g33
|
UTSW |
9 |
39,337,966 (GRCm39) |
missense |
probably benign |
0.40 |
R8879:Or8g33
|
UTSW |
9 |
39,337,515 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9084:Or8g33
|
UTSW |
9 |
39,337,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Or8g33
|
UTSW |
9 |
39,337,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R9435:Or8g33
|
UTSW |
9 |
39,337,506 (GRCm39) |
missense |
probably benign |
|
R9583:Or8g33
|
UTSW |
9 |
39,337,851 (GRCm39) |
missense |
possibly damaging |
0.91 |
|