Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,613,249 (GRCm39) |
M1K |
probably null |
Het |
Afap1l2 |
C |
A |
19: 56,904,238 (GRCm39) |
R683L |
probably damaging |
Het |
Ankfy1 |
C |
T |
11: 72,602,980 (GRCm39) |
|
probably benign |
Het |
Aoc1 |
A |
T |
6: 48,883,010 (GRCm39) |
E295D |
probably benign |
Het |
Asah1 |
C |
T |
8: 41,804,925 (GRCm39) |
|
probably benign |
Het |
B4galnt4 |
T |
C |
7: 140,650,752 (GRCm39) |
L842P |
probably damaging |
Het |
Bhmt |
T |
C |
13: 93,763,855 (GRCm39) |
E62G |
probably damaging |
Het |
Btbd10 |
T |
A |
7: 112,951,016 (GRCm39) |
R25* |
probably null |
Het |
Cdh5 |
T |
A |
8: 104,857,600 (GRCm39) |
I342N |
possibly damaging |
Het |
Clca3a2 |
T |
A |
3: 144,512,088 (GRCm39) |
E109D |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,035,112 (GRCm39) |
L913S |
probably damaging |
Het |
Col12a1 |
T |
A |
9: 79,587,593 (GRCm39) |
T1183S |
probably benign |
Het |
Col6a6 |
A |
T |
9: 105,655,166 (GRCm39) |
Y852N |
probably damaging |
Het |
Cpeb2 |
T |
C |
5: 43,438,573 (GRCm39) |
|
probably null |
Het |
Cyp2c66 |
T |
A |
19: 39,151,892 (GRCm39) |
N202K |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,405,711 (GRCm39) |
V2391A |
possibly damaging |
Het |
Dgat2 |
A |
G |
7: 98,806,300 (GRCm39) |
V299A |
probably benign |
Het |
Dnah6 |
G |
A |
6: 73,098,797 (GRCm39) |
S2034L |
possibly damaging |
Het |
Eps8l2 |
G |
A |
7: 140,937,832 (GRCm39) |
|
probably null |
Het |
Fgg |
T |
A |
3: 82,920,090 (GRCm39) |
F290I |
probably damaging |
Het |
Filip1 |
A |
T |
9: 79,760,952 (GRCm39) |
M194K |
probably damaging |
Het |
Foxl2 |
T |
C |
9: 98,838,035 (GRCm39) |
F108L |
probably damaging |
Het |
Fut1 |
T |
C |
7: 45,268,798 (GRCm39) |
F196L |
probably damaging |
Het |
Gm10323 |
A |
C |
13: 67,002,888 (GRCm39) |
W17G |
probably damaging |
Het |
Gstz1 |
T |
A |
12: 87,210,470 (GRCm39) |
|
probably null |
Het |
Hacd1 |
T |
C |
2: 14,049,586 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
T |
A |
2: 31,299,156 (GRCm39) |
L2834Q |
possibly damaging |
Het |
Hs3st3a1 |
C |
T |
11: 64,327,148 (GRCm39) |
R86W |
probably benign |
Het |
Krtap1-4 |
G |
C |
11: 99,474,020 (GRCm39) |
|
probably benign |
Het |
Lmntd2 |
A |
G |
7: 140,793,910 (GRCm39) |
V21A |
probably benign |
Het |
Lonp1 |
T |
A |
17: 56,925,337 (GRCm39) |
D485V |
probably damaging |
Het |
Mia2 |
A |
G |
12: 59,236,427 (GRCm39) |
T1346A |
possibly damaging |
Het |
Mpp2 |
T |
C |
11: 101,976,141 (GRCm39) |
T6A |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,466,866 (GRCm39) |
V1299E |
probably damaging |
Het |
Myo1d |
C |
T |
11: 80,573,236 (GRCm39) |
G197E |
probably damaging |
Het |
Nfib |
T |
C |
4: 82,416,532 (GRCm39) |
I168V |
possibly damaging |
Het |
Or2ak5 |
T |
A |
11: 58,611,097 (GRCm39) |
Y259F |
probably damaging |
Het |
Or2y1e |
C |
T |
11: 49,218,868 (GRCm39) |
A210V |
probably benign |
Het |
Or4c121 |
T |
A |
2: 89,023,617 (GRCm39) |
I254L |
probably benign |
Het |
Or4c29 |
C |
T |
2: 88,739,810 (GRCm39) |
R309Q |
probably benign |
Het |
Parp3 |
A |
T |
9: 106,351,922 (GRCm39) |
I150K |
probably damaging |
Het |
Pnp |
A |
G |
14: 51,185,443 (GRCm39) |
D49G |
probably benign |
Het |
Prkcq |
T |
C |
2: 11,251,781 (GRCm39) |
I206T |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rlf |
A |
G |
4: 121,007,729 (GRCm39) |
L417P |
probably benign |
Het |
Scn7a |
AT |
ATT |
2: 66,531,239 (GRCm39) |
|
probably null |
Het |
Sgce |
T |
A |
6: 4,730,008 (GRCm39) |
D72V |
probably benign |
Het |
Sh3d21 |
A |
G |
4: 126,056,625 (GRCm39) |
S66P |
probably benign |
Het |
Sost |
C |
G |
11: 101,854,865 (GRCm39) |
G148A |
probably damaging |
Het |
Sybu |
T |
C |
15: 44,609,854 (GRCm39) |
E138G |
probably damaging |
Het |
Tas1r2 |
A |
G |
4: 139,396,886 (GRCm39) |
T742A |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,380,401 (GRCm39) |
V589A |
probably damaging |
Het |
Tnxb |
C |
A |
17: 34,891,605 (GRCm39) |
C649* |
probably null |
Het |
Tnxb |
A |
G |
17: 34,922,561 (GRCm39) |
Y2458C |
probably damaging |
Het |
Tsku |
T |
C |
7: 98,001,746 (GRCm39) |
N195S |
probably damaging |
Het |
Vmn1r215 |
T |
A |
13: 23,260,378 (GRCm39) |
N139K |
probably damaging |
Het |
Zfp106 |
T |
C |
2: 120,357,544 (GRCm39) |
H1117R |
probably benign |
Het |
Zfp26 |
A |
G |
9: 20,352,756 (GRCm39) |
|
probably benign |
Het |
Zfp764l1 |
T |
C |
7: 126,990,914 (GRCm39) |
T358A |
possibly damaging |
Het |
Zfp804b |
T |
A |
5: 7,230,625 (GRCm39) |
|
probably benign |
Het |
Zfr |
T |
C |
15: 12,153,006 (GRCm39) |
S546P |
probably benign |
Het |
|
Other mutations in Or2b7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01593:Or2b7
|
APN |
13 |
21,739,389 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01866:Or2b7
|
APN |
13 |
21,739,343 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02289:Or2b7
|
APN |
13 |
21,739,758 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02350:Or2b7
|
APN |
13 |
21,739,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Or2b7
|
APN |
13 |
21,739,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02793:Or2b7
|
APN |
13 |
21,740,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02875:Or2b7
|
APN |
13 |
21,740,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Or2b7
|
UTSW |
13 |
21,739,958 (GRCm39) |
missense |
probably benign |
0.02 |
R1773:Or2b7
|
UTSW |
13 |
21,739,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Or2b7
|
UTSW |
13 |
21,739,975 (GRCm39) |
nonsense |
probably null |
|
R4232:Or2b7
|
UTSW |
13 |
21,739,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Or2b7
|
UTSW |
13 |
21,739,658 (GRCm39) |
missense |
probably benign |
0.22 |
R5586:Or2b7
|
UTSW |
13 |
21,739,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Or2b7
|
UTSW |
13 |
21,740,077 (GRCm39) |
missense |
probably benign |
0.01 |
R6032:Or2b7
|
UTSW |
13 |
21,740,077 (GRCm39) |
missense |
probably benign |
0.01 |
R6542:Or2b7
|
UTSW |
13 |
21,739,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R7014:Or2b7
|
UTSW |
13 |
21,740,108 (GRCm39) |
missense |
probably benign |
0.02 |
R7579:Or2b7
|
UTSW |
13 |
21,740,176 (GRCm39) |
missense |
probably benign |
0.08 |
R7598:Or2b7
|
UTSW |
13 |
21,739,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Or2b7
|
UTSW |
13 |
21,740,136 (GRCm39) |
missense |
probably benign |
|
R8239:Or2b7
|
UTSW |
13 |
21,739,788 (GRCm39) |
missense |
probably benign |
0.01 |
R8339:Or2b7
|
UTSW |
13 |
21,739,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R8698:Or2b7
|
UTSW |
13 |
21,739,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Or2b7
|
UTSW |
13 |
21,740,169 (GRCm39) |
missense |
probably benign |
0.00 |
R8977:Or2b7
|
UTSW |
13 |
21,740,016 (GRCm39) |
missense |
possibly damaging |
0.57 |
RF051:Or2b7
|
UTSW |
13 |
21,739,693 (GRCm39) |
frame shift |
probably null |
|
|