Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvrl1 |
A |
T |
15: 101,034,924 (GRCm39) |
K228* |
probably null |
Het |
Adrb2 |
T |
C |
18: 62,312,276 (GRCm39) |
D183G |
probably benign |
Het |
Ap1m2 |
A |
G |
9: 21,216,935 (GRCm39) |
Y134H |
probably damaging |
Het |
Arid5a |
A |
G |
1: 36,358,073 (GRCm39) |
T217A |
probably benign |
Het |
Cdnf |
C |
T |
2: 3,522,075 (GRCm39) |
T89I |
possibly damaging |
Het |
Cntnap3 |
G |
A |
13: 65,051,648 (GRCm39) |
R3W |
probably benign |
Het |
Col6a6 |
A |
G |
9: 105,651,825 (GRCm39) |
I1062T |
probably benign |
Het |
Ctss |
T |
C |
3: 95,454,258 (GRCm39) |
F270S |
possibly damaging |
Het |
Ddhd1 |
C |
T |
14: 45,895,117 (GRCm39) |
G118R |
possibly damaging |
Het |
Ddx11 |
A |
G |
17: 66,436,912 (GRCm39) |
K69E |
probably benign |
Het |
Dgkb |
G |
A |
12: 38,189,657 (GRCm39) |
G328D |
probably damaging |
Het |
Dock1 |
C |
T |
7: 134,774,228 (GRCm39) |
T1852M |
probably damaging |
Het |
Gm19410 |
T |
C |
8: 36,272,356 (GRCm39) |
Y1346H |
probably benign |
Het |
Gprin1 |
G |
T |
13: 54,887,383 (GRCm39) |
T297N |
probably damaging |
Het |
Gramd1c |
A |
G |
16: 43,833,381 (GRCm39) |
F187S |
probably damaging |
Het |
Gse1 |
A |
G |
8: 121,303,074 (GRCm39) |
N1072D |
unknown |
Het |
Gtf3c6 |
G |
A |
10: 40,133,520 (GRCm39) |
|
probably benign |
Het |
Hipk3 |
T |
A |
2: 104,263,562 (GRCm39) |
T897S |
probably benign |
Het |
Igsf21 |
T |
A |
4: 139,973,762 (GRCm39) |
|
probably benign |
Het |
Itgb1 |
A |
G |
8: 129,452,605 (GRCm39) |
I757V |
probably damaging |
Het |
Lamb2 |
C |
T |
9: 108,364,366 (GRCm39) |
R1102W |
possibly damaging |
Het |
Lzts2 |
T |
G |
19: 45,013,208 (GRCm39) |
C374W |
unknown |
Het |
Mapk10 |
A |
T |
5: 103,061,152 (GRCm39) |
S462T |
probably damaging |
Het |
Mtcl1 |
A |
T |
17: 66,755,462 (GRCm39) |
D293E |
possibly damaging |
Het |
Nf1 |
T |
G |
11: 79,438,018 (GRCm39) |
H109Q |
probably damaging |
Het |
Nlrp9b |
T |
C |
7: 19,783,435 (GRCm39) |
L926P |
probably damaging |
Het |
Notch2 |
G |
A |
3: 98,009,668 (GRCm39) |
D532N |
probably damaging |
Het |
Olfm4 |
A |
T |
14: 80,249,249 (GRCm39) |
Y122F |
probably benign |
Het |
Or52e19b |
T |
A |
7: 103,032,487 (GRCm39) |
T241S |
probably damaging |
Het |
Or52r1 |
A |
G |
7: 102,537,000 (GRCm39) |
M120T |
probably damaging |
Het |
Or56a4 |
A |
T |
7: 104,806,006 (GRCm39) |
Y294* |
probably null |
Het |
Or5g24-ps1 |
T |
C |
2: 85,464,367 (GRCm39) |
V198A |
probably benign |
Het |
Or5t18 |
A |
G |
2: 86,637,160 (GRCm39) |
L61P |
possibly damaging |
Het |
P2rx2 |
A |
T |
5: 110,488,138 (GRCm39) |
M472K |
probably benign |
Het |
Pbxip1 |
A |
G |
3: 89,354,941 (GRCm39) |
K487E |
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,045,122 (GRCm39) |
V1108A |
probably benign |
Het |
Polq |
A |
G |
16: 36,881,394 (GRCm39) |
N1186S |
probably benign |
Het |
Por |
T |
A |
5: 135,754,597 (GRCm39) |
W6R |
unknown |
Het |
Prex2 |
G |
A |
1: 11,207,028 (GRCm39) |
V529I |
probably benign |
Het |
Rgs6 |
T |
G |
12: 82,698,615 (GRCm39) |
S5A |
probably benign |
Het |
Rp9 |
G |
T |
9: 22,360,082 (GRCm39) |
S171* |
probably null |
Het |
Sec11c |
T |
A |
18: 65,942,568 (GRCm39) |
I47N |
possibly damaging |
Het |
Sh2b1 |
GCCACGGGGACCAGCTC |
GCCACGGGGACCAGCTCATCCACGGGGACCAGCTC |
7: 126,066,756 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
GACCAGCTCAGCCACGGG |
GACCAGCTCAGCCACGGGTACCAGCTCAGCCACGGG |
7: 126,066,746 (GRCm39) |
|
probably benign |
Het |
Slco1a8 |
A |
G |
6: 141,940,511 (GRCm39) |
S137P |
possibly damaging |
Het |
Sorcs1 |
A |
G |
19: 50,213,651 (GRCm39) |
M692T |
possibly damaging |
Het |
Sult1d1 |
T |
A |
5: 87,713,954 (GRCm39) |
Q30L |
probably benign |
Het |
Tcea2 |
A |
G |
2: 181,322,243 (GRCm39) |
D15G |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,066,429 (GRCm39) |
S2344G |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,784,404 (GRCm39) |
Y1824* |
probably null |
Het |
Ubqln5 |
T |
C |
7: 103,777,985 (GRCm39) |
T280A |
probably benign |
Het |
Ush1c |
T |
C |
7: 45,869,934 (GRCm39) |
R342G |
probably benign |
Het |
Vmn1r185 |
T |
A |
7: 26,311,056 (GRCm39) |
I150F |
probably benign |
Het |
Vmn1r43 |
G |
A |
6: 89,846,877 (GRCm39) |
T203M |
probably damaging |
Het |
Vmn1r86 |
A |
G |
7: 12,836,261 (GRCm39) |
M205T |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,896,956 (GRCm39) |
Y321* |
probably null |
Het |
|
Other mutations in Or5p76 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02260:Or5p76
|
APN |
7 |
108,122,492 (GRCm39) |
missense |
probably benign |
0.00 |
R0007:Or5p76
|
UTSW |
7 |
108,122,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Or5p76
|
UTSW |
7 |
108,122,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Or5p76
|
UTSW |
7 |
108,122,525 (GRCm39) |
missense |
probably benign |
|
R1469:Or5p76
|
UTSW |
7 |
108,122,411 (GRCm39) |
missense |
probably benign |
0.14 |
R1469:Or5p76
|
UTSW |
7 |
108,122,411 (GRCm39) |
missense |
probably benign |
0.14 |
R1701:Or5p76
|
UTSW |
7 |
108,122,731 (GRCm39) |
missense |
probably benign |
0.01 |
R3736:Or5p76
|
UTSW |
7 |
108,122,626 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5030:Or5p76
|
UTSW |
7 |
108,122,384 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5315:Or5p76
|
UTSW |
7 |
108,123,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Or5p76
|
UTSW |
7 |
108,122,945 (GRCm39) |
missense |
probably benign |
0.34 |
R6548:Or5p76
|
UTSW |
7 |
108,122,423 (GRCm39) |
missense |
probably benign |
0.00 |
R6866:Or5p76
|
UTSW |
7 |
108,122,377 (GRCm39) |
missense |
probably damaging |
0.96 |
R6946:Or5p76
|
UTSW |
7 |
108,122,528 (GRCm39) |
missense |
probably benign |
0.02 |
R7582:Or5p76
|
UTSW |
7 |
108,123,058 (GRCm39) |
missense |
probably benign |
0.00 |
R8771:Or5p76
|
UTSW |
7 |
108,122,632 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8824:Or5p76
|
UTSW |
7 |
108,122,350 (GRCm39) |
missense |
probably benign |
0.28 |
R8854:Or5p76
|
UTSW |
7 |
108,122,936 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Or5p76
|
UTSW |
7 |
108,122,605 (GRCm39) |
missense |
probably damaging |
0.99 |
|