Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Abi2 |
C |
A |
1: 60,503,738 (GRCm39) |
P212T |
probably damaging |
Het |
Ano4 |
A |
G |
10: 89,153,108 (GRCm39) |
F68S |
possibly damaging |
Het |
Art5 |
C |
A |
7: 101,747,591 (GRCm39) |
A63S |
probably benign |
Het |
Asgr1 |
T |
A |
11: 69,947,247 (GRCm39) |
S96R |
probably benign |
Het |
Bdp1 |
A |
T |
13: 100,163,957 (GRCm39) |
V2248D |
possibly damaging |
Het |
Cacna1s |
C |
T |
1: 135,998,705 (GRCm39) |
A200V |
possibly damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,390,738 (GRCm39) |
K357E |
probably damaging |
Het |
Cdhr18 |
T |
C |
14: 13,864,282 (GRCm38) |
N348S |
probably damaging |
Het |
Cfap52 |
C |
T |
11: 67,837,126 (GRCm39) |
G212R |
probably benign |
Het |
Dcun1d3 |
A |
G |
7: 119,456,965 (GRCm39) |
F249S |
probably damaging |
Het |
Ece2 |
A |
G |
16: 20,449,112 (GRCm39) |
Y17C |
probably damaging |
Het |
Efemp1 |
C |
T |
11: 28,871,760 (GRCm39) |
T425I |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,128,306 (GRCm39) |
E562G |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,177,295 (GRCm39) |
T2001A |
probably benign |
Het |
Flt4 |
G |
A |
11: 49,527,867 (GRCm39) |
R940H |
probably damaging |
Het |
Fry |
T |
A |
5: 150,351,644 (GRCm39) |
M1716K |
probably benign |
Het |
Gm10684 |
T |
A |
9: 45,019,039 (GRCm39) |
|
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,311,416 (GRCm39) |
V1219I |
probably damaging |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Il23r |
C |
T |
6: 67,455,938 (GRCm39) |
V177M |
probably damaging |
Het |
Klf12 |
T |
C |
14: 100,137,650 (GRCm39) |
S299G |
probably benign |
Het |
Lama5 |
G |
A |
2: 179,848,806 (GRCm39) |
R265C |
probably damaging |
Het |
Lifr |
A |
G |
15: 7,216,424 (GRCm39) |
T800A |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,063,831 (GRCm39) |
L2729P |
probably damaging |
Het |
Mki67 |
A |
C |
7: 135,298,532 (GRCm39) |
S2167R |
possibly damaging |
Het |
Mus81 |
T |
C |
19: 5,534,032 (GRCm39) |
K400E |
probably damaging |
Het |
Nomo1 |
T |
A |
7: 45,712,423 (GRCm39) |
I656N |
possibly damaging |
Het |
Oas3 |
T |
C |
5: 120,907,384 (GRCm39) |
T418A |
probably benign |
Het |
Olr1 |
A |
G |
6: 129,470,504 (GRCm39) |
L221P |
probably damaging |
Het |
Or14c44 |
C |
T |
7: 86,062,478 (GRCm39) |
L303F |
probably benign |
Het |
Or5m9 |
T |
C |
2: 85,876,928 (GRCm39) |
M34T |
probably benign |
Het |
Or8b3 |
T |
A |
9: 38,314,601 (GRCm39) |
C144S |
probably benign |
Het |
Or8k28 |
T |
A |
2: 86,286,133 (GRCm39) |
I161L |
probably benign |
Het |
Pih1d1 |
C |
T |
7: 44,805,738 (GRCm39) |
A69V |
probably damaging |
Het |
Pkdrej |
A |
C |
15: 85,703,967 (GRCm39) |
S656R |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,377,943 (GRCm39) |
D171G |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,787,566 (GRCm39) |
V11A |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
A |
7: 27,063,595 (GRCm39) |
Y2277F |
probably damaging |
Het |
St6galnac6 |
A |
G |
2: 32,502,240 (GRCm39) |
Q7R |
probably damaging |
Het |
Thrsp |
T |
G |
7: 97,066,499 (GRCm39) |
D71A |
possibly damaging |
Het |
Vmn2r1 |
C |
A |
3: 63,989,150 (GRCm39) |
Q30K |
probably benign |
Het |
Vmn2r125 |
C |
A |
4: 156,703,396 (GRCm39) |
A258D |
probably benign |
Het |
Wipf2 |
C |
T |
11: 98,787,005 (GRCm39) |
P345S |
probably benign |
Het |
Zeb2 |
G |
T |
2: 44,878,652 (GRCm39) |
S1170* |
probably null |
Het |
Zfp947 |
A |
G |
17: 22,366,415 (GRCm39) |
Y38H |
probably damaging |
Het |
|
Other mutations in Or8g22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01928:Or8g22
|
APN |
9 |
38,958,709 (GRCm39) |
missense |
unknown |
|
R0086:Or8g22
|
UTSW |
9 |
38,958,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0561:Or8g22
|
UTSW |
9 |
38,958,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R0650:Or8g22
|
UTSW |
9 |
38,957,996 (GRCm39) |
missense |
probably benign |
0.01 |
R1221:Or8g22
|
UTSW |
9 |
38,958,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Or8g22
|
UTSW |
9 |
38,958,200 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1680:Or8g22
|
UTSW |
9 |
38,958,296 (GRCm39) |
missense |
probably benign |
0.43 |
R1733:Or8g22
|
UTSW |
9 |
38,958,678 (GRCm39) |
missense |
unknown |
|
R3767:Or8g22
|
UTSW |
9 |
38,958,707 (GRCm39) |
missense |
unknown |
|
R4786:Or8g22
|
UTSW |
9 |
38,958,783 (GRCm39) |
nonsense |
probably null |
|
R4944:Or8g22
|
UTSW |
9 |
38,958,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Or8g22
|
UTSW |
9 |
38,958,265 (GRCm39) |
nonsense |
probably null |
|
R5403:Or8g22
|
UTSW |
9 |
38,957,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Or8g22
|
UTSW |
9 |
38,958,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Or8g22
|
UTSW |
9 |
38,958,671 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6217:Or8g22
|
UTSW |
9 |
38,958,039 (GRCm39) |
makesense |
probably null |
|
R6711:Or8g22
|
UTSW |
9 |
38,958,162 (GRCm39) |
makesense |
probably null |
|
R6919:Or8g22
|
UTSW |
9 |
38,958,827 (GRCm39) |
utr 5 prime |
probably benign |
|
R7022:Or8g22
|
UTSW |
9 |
38,958,379 (GRCm39) |
nonsense |
probably null |
|
R7275:Or8g22
|
UTSW |
9 |
38,958,815 (GRCm39) |
utr 5 prime |
probably benign |
|
R7290:Or8g22
|
UTSW |
9 |
38,958,694 (GRCm39) |
missense |
unknown |
|
R7644:Or8g22
|
UTSW |
9 |
38,958,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Or8g22
|
UTSW |
9 |
38,958,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9099:Or8g22
|
UTSW |
9 |
38,958,026 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Or8g22
|
UTSW |
9 |
38,958,215 (GRCm39) |
missense |
probably damaging |
0.98 |
|