Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
C |
A |
10: 79,834,123 (GRCm39) |
H116Q |
probably benign |
Het |
Akap12 |
G |
T |
10: 4,303,947 (GRCm39) |
E252D |
probably benign |
Het |
Apobr |
A |
G |
7: 126,184,188 (GRCm39) |
D2G |
probably damaging |
Het |
Arhgef12 |
A |
T |
9: 42,931,982 (GRCm39) |
H168Q |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,031,357 (GRCm39) |
|
probably null |
Het |
Brip1 |
T |
C |
11: 85,968,710 (GRCm39) |
Y825C |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,525,143 (GRCm39) |
Y1679N |
probably damaging |
Het |
Ccdc69 |
C |
T |
11: 54,951,296 (GRCm39) |
A42T |
probably benign |
Het |
Cds1 |
G |
T |
5: 101,929,286 (GRCm39) |
D55Y |
possibly damaging |
Het |
Cep135 |
C |
A |
5: 76,784,873 (GRCm39) |
D989E |
probably benign |
Het |
Cpsf6 |
C |
A |
10: 117,197,189 (GRCm39) |
|
probably benign |
Het |
Ctif |
C |
T |
18: 75,770,290 (GRCm39) |
V32M |
probably damaging |
Het |
Cylc2 |
T |
C |
4: 51,228,587 (GRCm39) |
|
probably benign |
Het |
Dao |
T |
C |
5: 114,158,070 (GRCm39) |
|
probably null |
Het |
Dop1a |
T |
A |
9: 86,403,868 (GRCm39) |
N1689K |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,536,931 (GRCm39) |
Y14C |
probably damaging |
Het |
Fam187a |
C |
T |
11: 102,777,290 (GRCm39) |
R365C |
probably damaging |
Het |
Fastkd2 |
A |
G |
1: 63,770,598 (GRCm39) |
|
probably benign |
Het |
Fhip2a |
A |
G |
19: 57,359,613 (GRCm39) |
N51S |
probably damaging |
Het |
Fkbp15 |
G |
T |
4: 62,230,560 (GRCm39) |
L718I |
possibly damaging |
Het |
Gabbr2 |
C |
A |
4: 46,681,208 (GRCm39) |
V118F |
probably damaging |
Het |
Gm13991 |
T |
A |
2: 116,358,508 (GRCm39) |
|
noncoding transcript |
Het |
H2-M9 |
T |
C |
17: 36,952,523 (GRCm39) |
I174M |
probably damaging |
Het |
Ift70a2 |
T |
C |
2: 75,807,421 (GRCm39) |
M364V |
probably benign |
Het |
Insr |
T |
A |
8: 3,208,742 (GRCm39) |
M1240L |
probably benign |
Het |
Ints15 |
G |
T |
5: 143,300,830 (GRCm39) |
S7* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Mad2l1bp |
T |
A |
17: 46,463,738 (GRCm39) |
E95D |
probably benign |
Het |
Marchf9 |
T |
C |
10: 126,895,319 (GRCm39) |
D102G |
probably benign |
Het |
Muc19 |
A |
G |
15: 91,776,374 (GRCm39) |
|
noncoding transcript |
Het |
Nr1h4 |
T |
A |
10: 89,334,117 (GRCm39) |
Y91F |
probably benign |
Het |
Nr5a2 |
A |
T |
1: 136,876,540 (GRCm39) |
M1K |
probably null |
Het |
Oprd1 |
T |
C |
4: 131,841,104 (GRCm39) |
T285A |
probably benign |
Het |
Optc |
T |
C |
1: 133,829,822 (GRCm39) |
N196S |
probably benign |
Het |
Or51f5 |
T |
A |
7: 102,424,513 (GRCm39) |
S261T |
probably damaging |
Het |
Or7g21 |
A |
T |
9: 19,032,656 (GRCm39) |
Y132F |
probably damaging |
Het |
Panx2 |
G |
T |
15: 88,944,431 (GRCm39) |
R52L |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,333,389 (GRCm39) |
F211L |
probably damaging |
Het |
Pot1b |
T |
A |
17: 56,006,995 (GRCm39) |
T41S |
probably benign |
Het |
Prss56 |
T |
C |
1: 87,111,880 (GRCm39) |
L37S |
probably damaging |
Het |
Ptk2b |
T |
C |
14: 66,393,864 (GRCm39) |
T870A |
probably damaging |
Het |
Rabep2 |
C |
A |
7: 126,033,465 (GRCm39) |
|
probably benign |
Het |
Rbm48 |
A |
C |
5: 3,645,444 (GRCm39) |
V80G |
probably damaging |
Het |
Rhou |
G |
T |
8: 124,380,848 (GRCm39) |
C55F |
possibly damaging |
Het |
Rnaseh2c |
A |
G |
19: 5,652,070 (GRCm39) |
D45G |
probably benign |
Het |
Rusc1 |
A |
G |
3: 88,996,389 (GRCm39) |
S109P |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,588,012 (GRCm39) |
D2643G |
possibly damaging |
Het |
Septin4 |
T |
A |
11: 87,458,358 (GRCm39) |
M244K |
probably benign |
Het |
Sik2 |
T |
C |
9: 50,810,703 (GRCm39) |
E471G |
probably benign |
Het |
Sipa1 |
A |
G |
19: 5,709,406 (GRCm39) |
S310P |
probably damaging |
Het |
Sp140l1 |
C |
T |
1: 85,066,521 (GRCm39) |
|
probably benign |
Het |
Spen |
T |
C |
4: 141,203,587 (GRCm39) |
E1680G |
unknown |
Het |
Steap3 |
C |
T |
1: 120,171,497 (GRCm39) |
|
probably null |
Het |
Tmeff2 |
T |
A |
1: 51,110,700 (GRCm39) |
C171* |
probably null |
Het |
Tmem138 |
A |
T |
19: 10,552,634 (GRCm39) |
M33K |
probably benign |
Het |
Trappc11 |
C |
A |
8: 47,963,998 (GRCm39) |
V601L |
possibly damaging |
Het |
Ttll4 |
C |
A |
1: 74,718,445 (GRCm39) |
H99N |
probably damaging |
Het |
Uchl4 |
A |
T |
9: 64,143,022 (GRCm39) |
K168* |
probably null |
Het |
Wdr17 |
C |
T |
8: 55,106,913 (GRCm39) |
|
probably null |
Het |
Xpo1 |
A |
G |
11: 23,245,977 (GRCm39) |
D1029G |
probably damaging |
Het |
Zfp719 |
G |
T |
7: 43,240,549 (GRCm39) |
K712N |
probably damaging |
Het |
|
Other mutations in Or5g29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01763:Or5g29
|
APN |
2 |
85,421,691 (GRCm39) |
missense |
probably benign |
0.00 |
R0091:Or5g29
|
UTSW |
2 |
85,421,696 (GRCm39) |
missense |
probably benign |
0.38 |
R0241:Or5g29
|
UTSW |
2 |
85,421,154 (GRCm39) |
missense |
probably benign |
0.20 |
R0241:Or5g29
|
UTSW |
2 |
85,421,154 (GRCm39) |
missense |
probably benign |
0.20 |
R0268:Or5g29
|
UTSW |
2 |
85,421,645 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0481:Or5g29
|
UTSW |
2 |
85,421,448 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1816:Or5g29
|
UTSW |
2 |
85,421,269 (GRCm39) |
missense |
probably benign |
0.00 |
R1988:Or5g29
|
UTSW |
2 |
85,420,985 (GRCm39) |
missense |
probably benign |
0.00 |
R2008:Or5g29
|
UTSW |
2 |
85,421,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Or5g29
|
UTSW |
2 |
85,421,627 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2273:Or5g29
|
UTSW |
2 |
85,420,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4409:Or5g29
|
UTSW |
2 |
85,421,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Or5g29
|
UTSW |
2 |
85,421,282 (GRCm39) |
missense |
probably benign |
0.03 |
R4785:Or5g29
|
UTSW |
2 |
85,421,282 (GRCm39) |
missense |
probably benign |
0.03 |
R5098:Or5g29
|
UTSW |
2 |
85,420,976 (GRCm39) |
missense |
probably benign |
0.00 |
R5462:Or5g29
|
UTSW |
2 |
85,421,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Or5g29
|
UTSW |
2 |
85,420,950 (GRCm39) |
missense |
probably benign |
0.14 |
R6278:Or5g29
|
UTSW |
2 |
85,421,342 (GRCm39) |
missense |
probably benign |
0.00 |
R7022:Or5g29
|
UTSW |
2 |
85,420,942 (GRCm39) |
missense |
probably benign |
0.01 |
R7673:Or5g29
|
UTSW |
2 |
85,421,406 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8054:Or5g29
|
UTSW |
2 |
85,421,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Or5g29
|
UTSW |
2 |
85,421,332 (GRCm39) |
nonsense |
probably null |
|
R8940:Or5g29
|
UTSW |
2 |
85,421,528 (GRCm39) |
missense |
probably benign |
|
R9617:Or5g29
|
UTSW |
2 |
85,421,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|