Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad8 |
T |
A |
9: 26,890,544 (GRCm39) |
N255Y |
probably damaging |
Het |
Accsl |
A |
C |
2: 93,696,490 (GRCm39) |
L36R |
probably benign |
Het |
Acvr2a |
T |
A |
2: 48,763,469 (GRCm39) |
V171E |
probably benign |
Het |
Adgrl3 |
A |
G |
5: 81,794,451 (GRCm39) |
I491V |
probably benign |
Het |
Ak9 |
G |
A |
10: 41,193,842 (GRCm39) |
|
probably null |
Het |
Ak9 |
G |
T |
10: 41,258,869 (GRCm39) |
E789* |
probably null |
Het |
Akr1c19 |
T |
A |
13: 4,293,070 (GRCm39) |
N275K |
probably benign |
Het |
Alg1 |
A |
G |
16: 5,061,557 (GRCm39) |
H398R |
probably benign |
Het |
Apol11a |
T |
A |
15: 77,401,209 (GRCm39) |
I232N |
probably damaging |
Het |
Cacnb2 |
A |
G |
2: 14,989,080 (GRCm39) |
I437V |
probably benign |
Het |
Catsper4 |
A |
G |
4: 133,954,417 (GRCm39) |
|
probably null |
Het |
Cdhr17 |
G |
A |
5: 17,028,152 (GRCm39) |
G449D |
probably benign |
Het |
Crnn |
T |
C |
3: 93,055,609 (GRCm39) |
C132R |
probably benign |
Het |
Cyp4a14 |
T |
A |
4: 115,348,553 (GRCm39) |
H337L |
probably damaging |
Het |
Dcdc2a |
C |
T |
13: 25,386,266 (GRCm39) |
A380V |
probably benign |
Het |
Dclre1b |
T |
C |
3: 103,710,654 (GRCm39) |
N419S |
probably benign |
Het |
Dip2c |
A |
G |
13: 9,625,503 (GRCm39) |
D621G |
possibly damaging |
Het |
Dmwd |
T |
A |
7: 18,814,694 (GRCm39) |
L448Q |
probably damaging |
Het |
Dnajc13 |
G |
A |
9: 104,042,987 (GRCm39) |
H1922Y |
probably benign |
Het |
E2f3 |
A |
T |
13: 30,095,301 (GRCm39) |
I329N |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,927,988 (GRCm39) |
V266M |
probably benign |
Het |
Entpd2 |
A |
G |
2: 25,289,725 (GRCm39) |
T376A |
probably benign |
Het |
Flnb |
A |
G |
14: 7,908,671 (GRCm38) |
T1350A |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 53,016,077 (GRCm39) |
E999G |
unknown |
Het |
Hivep1 |
A |
G |
13: 42,312,407 (GRCm39) |
Q1549R |
possibly damaging |
Het |
Hps6 |
G |
A |
19: 45,992,446 (GRCm39) |
V128M |
possibly damaging |
Het |
Ifi27l2a |
T |
C |
12: 103,402,899 (GRCm39) |
S66P |
possibly damaging |
Het |
Ikbip |
T |
C |
10: 90,932,187 (GRCm39) |
V277A |
possibly damaging |
Het |
Ints8 |
T |
C |
4: 11,230,488 (GRCm39) |
E451G |
probably benign |
Het |
Itih2 |
A |
T |
2: 10,132,600 (GRCm39) |
S64T |
probably benign |
Het |
Kcnc4 |
T |
A |
3: 107,355,452 (GRCm39) |
E332V |
probably damaging |
Het |
Krt23 |
T |
C |
11: 99,374,567 (GRCm39) |
|
probably benign |
Het |
Lrpprc |
C |
A |
17: 85,078,920 (GRCm39) |
G265C |
probably damaging |
Het |
Nav1 |
G |
T |
1: 135,512,943 (GRCm39) |
A39E |
probably benign |
Het |
Ogfod1 |
G |
T |
8: 94,773,906 (GRCm39) |
D103Y |
probably damaging |
Het |
Or8b55 |
G |
A |
9: 38,727,285 (GRCm39) |
C162Y |
probably damaging |
Het |
Or8g37 |
A |
G |
9: 39,731,252 (GRCm39) |
T106A |
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,755,014 (GRCm39) |
S78T |
probably damaging |
Het |
Rnf148 |
A |
T |
6: 23,654,540 (GRCm39) |
V152E |
probably damaging |
Het |
Sdf2 |
A |
T |
11: 78,136,970 (GRCm39) |
H50L |
probably damaging |
Het |
Sec1 |
T |
A |
7: 45,328,700 (GRCm39) |
M116L |
probably benign |
Het |
Sema6d |
T |
C |
2: 124,496,114 (GRCm39) |
S53P |
probably damaging |
Het |
Siae |
A |
G |
9: 37,528,132 (GRCm39) |
Y35C |
probably damaging |
Het |
Slc18b1 |
A |
T |
10: 23,686,751 (GRCm39) |
Y189F |
probably damaging |
Het |
Slc35d1 |
T |
C |
4: 103,065,351 (GRCm39) |
T177A |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,729,747 (GRCm39) |
T124A |
possibly damaging |
Het |
Strn4 |
G |
A |
7: 16,560,570 (GRCm39) |
E241K |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,135,578 (GRCm39) |
I510T |
possibly damaging |
Het |
Svop |
T |
C |
5: 114,170,854 (GRCm39) |
D395G |
probably damaging |
Het |
Tbc1d14 |
A |
C |
5: 36,728,888 (GRCm39) |
S159R |
probably damaging |
Het |
Tex50 |
T |
A |
1: 160,984,848 (GRCm39) |
I131F |
possibly damaging |
Het |
Tssk1 |
A |
G |
16: 17,712,884 (GRCm39) |
K223R |
probably benign |
Het |
Ttc3 |
A |
G |
16: 94,252,002 (GRCm39) |
I1565V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,541,938 (GRCm39) |
F33683I |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,783,470 (GRCm39) |
M887V |
unknown |
Het |
Usp45 |
G |
A |
4: 21,815,399 (GRCm39) |
|
probably null |
Het |
Wdr47 |
C |
T |
3: 108,498,841 (GRCm39) |
|
probably benign |
Het |
Xirp1 |
A |
G |
9: 119,846,871 (GRCm39) |
S671P |
probably benign |
Het |
Zbtb18 |
A |
G |
1: 177,274,682 (GRCm39) |
D5G |
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,656,681 (GRCm39) |
R166Q |
probably benign |
Het |
Zfp260 |
T |
G |
7: 29,804,914 (GRCm39) |
Y271* |
probably null |
Het |
Zfp369 |
T |
A |
13: 65,445,082 (GRCm39) |
S742T |
possibly damaging |
Het |
Zfp786 |
A |
T |
6: 47,802,015 (GRCm39) |
D87E |
probably damaging |
Het |
|
Other mutations in Or7g20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01718:Or7g20
|
APN |
9 |
18,946,584 (GRCm39) |
nonsense |
probably null |
|
IGL02546:Or7g20
|
APN |
9 |
18,946,650 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0010:Or7g20
|
UTSW |
9 |
18,946,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Or7g20
|
UTSW |
9 |
18,946,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Or7g20
|
UTSW |
9 |
18,946,562 (GRCm39) |
missense |
probably benign |
0.36 |
R1891:Or7g20
|
UTSW |
9 |
18,947,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R1941:Or7g20
|
UTSW |
9 |
18,947,162 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4152:Or7g20
|
UTSW |
9 |
18,946,816 (GRCm39) |
nonsense |
probably null |
|
R5451:Or7g20
|
UTSW |
9 |
18,946,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Or7g20
|
UTSW |
9 |
18,946,854 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5970:Or7g20
|
UTSW |
9 |
18,946,443 (GRCm39) |
missense |
probably benign |
|
R6187:Or7g20
|
UTSW |
9 |
18,946,689 (GRCm39) |
missense |
probably benign |
0.12 |
R6805:Or7g20
|
UTSW |
9 |
18,946,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7183:Or7g20
|
UTSW |
9 |
18,946,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8029:Or7g20
|
UTSW |
9 |
18,947,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8139:Or7g20
|
UTSW |
9 |
18,946,871 (GRCm39) |
missense |
probably benign |
0.07 |
R8736:Or7g20
|
UTSW |
9 |
18,946,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8909:Or7g20
|
UTSW |
9 |
18,946,888 (GRCm39) |
missense |
probably benign |
0.08 |
R9116:Or7g20
|
UTSW |
9 |
18,946,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Or7g20
|
UTSW |
9 |
18,946,730 (GRCm39) |
missense |
probably benign |
0.30 |
R9786:Or7g20
|
UTSW |
9 |
18,947,241 (GRCm39) |
missense |
possibly damaging |
0.87 |
|