Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,163,902 (GRCm39) |
|
probably null |
Het |
Abca2 |
A |
G |
2: 25,337,891 (GRCm39) |
|
probably benign |
Het |
Abcb11 |
A |
T |
2: 69,130,269 (GRCm39) |
S262R |
probably damaging |
Het |
Abhd12 |
T |
A |
2: 150,690,341 (GRCm39) |
Q118L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,034 (GRCm39) |
L753* |
probably null |
Het |
Ahctf1 |
A |
T |
1: 179,607,217 (GRCm39) |
I699N |
possibly damaging |
Het |
Arl11 |
C |
A |
14: 61,548,487 (GRCm39) |
A99E |
probably damaging |
Het |
Atp5po |
G |
A |
16: 91,727,289 (GRCm39) |
R16W |
probably damaging |
Het |
AW551984 |
T |
C |
9: 39,510,621 (GRCm39) |
H238R |
probably null |
Het |
Bpifb9a |
C |
A |
2: 154,108,733 (GRCm39) |
|
probably benign |
Het |
Carhsp1 |
A |
G |
16: 8,481,577 (GRCm39) |
|
probably benign |
Het |
Ccdc33 |
T |
C |
9: 57,937,702 (GRCm39) |
D623G |
probably damaging |
Het |
Chd6 |
C |
A |
2: 160,868,212 (GRCm39) |
R378L |
possibly damaging |
Het |
Chn2 |
T |
C |
6: 54,277,230 (GRCm39) |
|
probably benign |
Het |
Clgn |
T |
G |
8: 84,149,765 (GRCm39) |
I422S |
probably damaging |
Het |
Col15a1 |
T |
A |
4: 47,300,606 (GRCm39) |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,556,574 (GRCm39) |
I470T |
probably benign |
Het |
Dcaf11 |
T |
A |
14: 55,801,980 (GRCm39) |
|
probably null |
Het |
Dnah1 |
G |
T |
14: 31,022,924 (GRCm39) |
T1071K |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,348,949 (GRCm39) |
M2513L |
probably benign |
Het |
Dqx1 |
A |
G |
6: 83,035,891 (GRCm39) |
|
probably benign |
Het |
Gm1587 |
T |
C |
14: 78,036,282 (GRCm39) |
E8G |
unknown |
Het |
Hydin |
T |
C |
8: 111,336,598 (GRCm39) |
I5125T |
possibly damaging |
Het |
Ighv5-9 |
G |
T |
12: 113,625,563 (GRCm39) |
P60Q |
probably damaging |
Het |
Itga7 |
T |
G |
10: 128,789,651 (GRCm39) |
L993R |
possibly damaging |
Het |
Itpr3 |
A |
G |
17: 27,317,416 (GRCm39) |
N857S |
probably damaging |
Het |
Krt23 |
C |
T |
11: 99,383,490 (GRCm39) |
|
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,390,140 (GRCm39) |
N3093S |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,505,349 (GRCm39) |
F203S |
probably damaging |
Het |
Morn5 |
A |
G |
2: 35,947,088 (GRCm39) |
D122G |
probably damaging |
Het |
Mpp2 |
G |
T |
11: 101,954,088 (GRCm39) |
L220I |
probably benign |
Het |
Mrgpra6 |
A |
T |
7: 46,835,700 (GRCm39) |
Y240* |
probably null |
Het |
Mtmr12 |
T |
C |
15: 12,238,016 (GRCm39) |
I165T |
probably damaging |
Het |
Mylk2 |
C |
A |
2: 152,761,077 (GRCm39) |
N428K |
probably damaging |
Het |
Nfil3 |
A |
G |
13: 53,122,188 (GRCm39) |
Y239H |
probably damaging |
Het |
Notch1 |
A |
G |
2: 26,350,351 (GRCm39) |
L2263P |
probably damaging |
Het |
Or8b101 |
A |
G |
9: 38,020,425 (GRCm39) |
M148V |
probably benign |
Het |
P3h3 |
A |
T |
6: 124,830,055 (GRCm39) |
Y387N |
probably damaging |
Het |
Pdcd6ip |
A |
T |
9: 113,509,121 (GRCm39) |
Y324* |
probably null |
Het |
Plcb2 |
C |
A |
2: 118,541,844 (GRCm39) |
R922L |
probably benign |
Het |
Pml |
T |
C |
9: 58,154,286 (GRCm39) |
T196A |
probably benign |
Het |
Ppp2r1b |
C |
A |
9: 50,772,909 (GRCm39) |
Q65K |
probably benign |
Het |
Ric8a |
A |
G |
7: 140,442,270 (GRCm39) |
T507A |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,306,644 (GRCm39) |
|
probably null |
Het |
Slc46a3 |
G |
T |
5: 147,823,044 (GRCm39) |
T266N |
probably damaging |
Het |
Smg1 |
A |
G |
7: 117,812,169 (GRCm39) |
S41P |
possibly damaging |
Het |
Snrnp200 |
T |
A |
2: 127,079,403 (GRCm39) |
N1837K |
probably benign |
Het |
Sptan1 |
A |
G |
2: 29,920,336 (GRCm39) |
T2318A |
probably damaging |
Het |
St7l |
C |
T |
3: 104,782,148 (GRCm39) |
T175I |
possibly damaging |
Het |
Tmc7 |
G |
A |
7: 118,137,434 (GRCm39) |
R703C |
probably damaging |
Het |
Urah |
A |
G |
7: 140,416,799 (GRCm39) |
|
probably benign |
Het |
Vmn1r42 |
A |
T |
6: 89,822,296 (GRCm39) |
I91N |
probably damaging |
Het |
Yy1 |
T |
A |
12: 108,780,525 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or2g7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01527:Or2g7
|
APN |
17 |
38,378,986 (GRCm39) |
missense |
probably benign |
|
IGL03172:Or2g7
|
APN |
17 |
38,378,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R0389:Or2g7
|
UTSW |
17 |
38,378,562 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0448:Or2g7
|
UTSW |
17 |
38,378,563 (GRCm39) |
missense |
probably benign |
0.00 |
R0616:Or2g7
|
UTSW |
17 |
38,378,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:Or2g7
|
UTSW |
17 |
38,378,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Or2g7
|
UTSW |
17 |
38,378,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Or2g7
|
UTSW |
17 |
38,378,746 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4600:Or2g7
|
UTSW |
17 |
38,378,853 (GRCm39) |
missense |
probably damaging |
0.99 |
R4977:Or2g7
|
UTSW |
17 |
38,378,638 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5120:Or2g7
|
UTSW |
17 |
38,378,157 (GRCm39) |
missense |
probably damaging |
0.97 |
R5930:Or2g7
|
UTSW |
17 |
38,378,641 (GRCm39) |
missense |
probably benign |
0.11 |
R6273:Or2g7
|
UTSW |
17 |
38,378,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R6636:Or2g7
|
UTSW |
17 |
38,378,115 (GRCm39) |
missense |
probably damaging |
0.98 |
R6637:Or2g7
|
UTSW |
17 |
38,378,115 (GRCm39) |
missense |
probably damaging |
0.98 |
R7030:Or2g7
|
UTSW |
17 |
38,378,948 (GRCm39) |
missense |
probably benign |
0.13 |
R7045:Or2g7
|
UTSW |
17 |
38,378,862 (GRCm39) |
missense |
probably benign |
0.01 |
R7175:Or2g7
|
UTSW |
17 |
38,378,370 (GRCm39) |
missense |
probably damaging |
0.96 |
R7359:Or2g7
|
UTSW |
17 |
38,378,506 (GRCm39) |
nonsense |
probably null |
|
R7762:Or2g7
|
UTSW |
17 |
38,378,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R7980:Or2g7
|
UTSW |
17 |
38,378,412 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8050:Or2g7
|
UTSW |
17 |
38,378,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Or2g7
|
UTSW |
17 |
38,378,179 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Or2g7
|
UTSW |
17 |
38,378,613 (GRCm39) |
missense |
probably benign |
0.01 |
|