Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,754,420 (GRCm39) |
T1338A |
probably benign |
Het |
Adcy3 |
G |
A |
12: 4,184,699 (GRCm39) |
C125Y |
probably damaging |
Het |
Aoc1 |
A |
T |
6: 48,882,896 (GRCm39) |
K257N |
probably damaging |
Het |
Apob |
T |
C |
12: 8,039,407 (GRCm39) |
V497A |
possibly damaging |
Het |
Atp8b5 |
T |
A |
4: 43,364,167 (GRCm39) |
V684D |
probably benign |
Het |
AW551984 |
A |
G |
9: 39,500,987 (GRCm39) |
W763R |
probably damaging |
Het |
Blm |
G |
A |
7: 80,119,504 (GRCm39) |
T1026M |
probably damaging |
Het |
Cd160 |
A |
G |
3: 96,712,886 (GRCm39) |
I126T |
possibly damaging |
Het |
Cdk14 |
T |
C |
5: 5,430,083 (GRCm39) |
K15E |
probably benign |
Het |
Cnot6l |
T |
C |
5: 96,239,518 (GRCm39) |
K261R |
probably damaging |
Het |
Cyp3a13 |
T |
G |
5: 137,909,865 (GRCm39) |
T153P |
probably benign |
Het |
Ddx24 |
A |
G |
12: 103,374,743 (GRCm39) |
|
probably benign |
Het |
Dido1 |
G |
A |
2: 180,304,040 (GRCm39) |
T1288I |
possibly damaging |
Het |
Dnajc13 |
A |
G |
9: 104,106,208 (GRCm39) |
V322A |
possibly damaging |
Het |
Dnajc25 |
T |
A |
4: 59,017,693 (GRCm39) |
Y117* |
probably null |
Het |
Dsg1a |
A |
G |
18: 20,465,089 (GRCm39) |
N427D |
probably benign |
Het |
Gabrq |
T |
G |
X: 71,871,151 (GRCm39) |
|
probably null |
Het |
Glce |
A |
G |
9: 61,977,883 (GRCm39) |
|
probably benign |
Het |
Gm10477 |
T |
C |
X: 55,570,761 (GRCm39) |
L45P |
probably damaging |
Het |
Htt |
T |
A |
5: 35,048,825 (GRCm39) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,252,104 (GRCm39) |
E317G |
probably benign |
Het |
Jak1 |
A |
G |
4: 101,016,283 (GRCm39) |
M827T |
probably benign |
Het |
Kalrn |
A |
G |
16: 34,040,592 (GRCm39) |
V932A |
probably damaging |
Het |
Mdm2 |
A |
C |
10: 117,528,622 (GRCm39) |
S227R |
possibly damaging |
Het |
Or14a259 |
T |
C |
7: 86,013,074 (GRCm39) |
Y157C |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,843,470 (GRCm39) |
|
probably benign |
Het |
Or5ak25 |
A |
G |
2: 85,268,611 (GRCm39) |
V297A |
probably damaging |
Het |
Or5g27 |
G |
A |
2: 85,410,017 (GRCm39) |
V145I |
probably damaging |
Het |
Pdilt |
T |
G |
7: 119,086,173 (GRCm39) |
E514A |
probably benign |
Het |
Pepd |
A |
G |
7: 34,645,028 (GRCm39) |
D153G |
probably damaging |
Het |
Ptgis |
A |
T |
2: 167,067,367 (GRCm39) |
V70E |
probably damaging |
Het |
Rnf112 |
T |
C |
11: 61,342,841 (GRCm39) |
K262E |
probably benign |
Het |
Setd5 |
G |
T |
6: 113,127,946 (GRCm39) |
G1300* |
probably null |
Het |
Snx15 |
A |
G |
19: 6,172,104 (GRCm39) |
L113P |
possibly damaging |
Het |
Sptbn1 |
T |
C |
11: 30,087,427 (GRCm39) |
D1004G |
probably damaging |
Het |
Ston2 |
A |
C |
12: 91,606,498 (GRCm39) |
*896G |
probably null |
Het |
Suco |
A |
G |
1: 161,655,274 (GRCm39) |
S1073P |
probably damaging |
Het |
Susd1 |
A |
C |
4: 59,369,636 (GRCm39) |
D344E |
possibly damaging |
Het |
Trnt1 |
G |
T |
6: 106,755,073 (GRCm39) |
|
probably null |
Het |
Ttll12 |
A |
G |
15: 83,466,264 (GRCm39) |
F399S |
probably damaging |
Het |
Vmn1r124 |
C |
T |
7: 20,994,467 (GRCm39) |
V26I |
probably benign |
Het |
Vmn1r52 |
T |
A |
6: 90,156,189 (GRCm39) |
N164K |
possibly damaging |
Het |
Vmn1r56 |
A |
T |
7: 5,199,335 (GRCm39) |
M94K |
possibly damaging |
Het |
Vmn1r80 |
T |
C |
7: 11,927,618 (GRCm39) |
F243L |
probably damaging |
Het |
Zdhhc8 |
G |
A |
16: 18,043,063 (GRCm39) |
S379F |
possibly damaging |
Het |
|
Other mutations in Or5w22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01320:Or5w22
|
APN |
2 |
87,362,629 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02604:Or5w22
|
APN |
2 |
87,362,949 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02695:Or5w22
|
APN |
2 |
87,362,461 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02961:Or5w22
|
APN |
2 |
87,363,028 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4696001:Or5w22
|
UTSW |
2 |
87,363,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R0727:Or5w22
|
UTSW |
2 |
87,363,245 (GRCm39) |
nonsense |
probably null |
|
R1534:Or5w22
|
UTSW |
2 |
87,363,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R1699:Or5w22
|
UTSW |
2 |
87,362,427 (GRCm39) |
missense |
probably benign |
0.07 |
R1885:Or5w22
|
UTSW |
2 |
87,363,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R3705:Or5w22
|
UTSW |
2 |
87,362,412 (GRCm39) |
missense |
probably benign |
0.01 |
R5664:Or5w22
|
UTSW |
2 |
87,363,178 (GRCm39) |
missense |
probably benign |
0.35 |
R6492:Or5w22
|
UTSW |
2 |
87,363,085 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6808:Or5w22
|
UTSW |
2 |
87,363,285 (GRCm39) |
missense |
probably benign |
|
R7432:Or5w22
|
UTSW |
2 |
87,362,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Or5w22
|
UTSW |
2 |
87,362,431 (GRCm39) |
missense |
probably benign |
0.00 |
R8014:Or5w22
|
UTSW |
2 |
87,362,508 (GRCm39) |
missense |
probably benign |
0.13 |
R8345:Or5w22
|
UTSW |
2 |
87,362,691 (GRCm39) |
missense |
probably benign |
0.01 |
R8887:Or5w22
|
UTSW |
2 |
87,363,187 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8971:Or5w22
|
UTSW |
2 |
87,362,580 (GRCm39) |
missense |
probably benign |
0.19 |
R9311:Or5w22
|
UTSW |
2 |
87,362,358 (GRCm39) |
start gained |
probably benign |
|
R9690:Or5w22
|
UTSW |
2 |
87,362,759 (GRCm39) |
missense |
probably benign |
0.03 |
X0028:Or5w22
|
UTSW |
2 |
87,362,383 (GRCm39) |
missense |
probably benign |
0.01 |
|