Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,547,500 (GRCm39) |
|
probably null |
Het |
Apoa4 |
A |
G |
9: 46,153,822 (GRCm39) |
D141G |
probably benign |
Het |
Atg9a |
T |
C |
1: 75,161,143 (GRCm39) |
Y701C |
probably damaging |
Het |
Baz2b |
C |
T |
2: 59,762,510 (GRCm39) |
R922Q |
probably damaging |
Het |
Bmal2 |
T |
G |
6: 146,731,216 (GRCm39) |
V507G |
probably benign |
Het |
Brms1 |
T |
A |
19: 5,096,727 (GRCm39) |
C136* |
probably null |
Het |
Ccdc180 |
T |
A |
4: 45,890,900 (GRCm39) |
V24E |
probably benign |
Het |
Clec4f |
C |
T |
6: 83,629,911 (GRCm39) |
V216M |
probably benign |
Het |
Cpd |
C |
G |
11: 76,681,664 (GRCm39) |
G1160R |
probably damaging |
Het |
Creb5 |
A |
G |
6: 53,424,642 (GRCm39) |
M128V |
probably benign |
Het |
Ddb2 |
G |
T |
2: 91,065,165 (GRCm39) |
Q87K |
probably benign |
Het |
Defb41 |
A |
G |
1: 18,321,471 (GRCm39) |
Y48H |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,303,267 (GRCm39) |
N1546D |
probably benign |
Het |
Dmac1 |
A |
G |
4: 75,196,337 (GRCm39) |
V51A |
possibly damaging |
Het |
Dnajb11 |
C |
T |
16: 22,681,369 (GRCm39) |
A49V |
probably damaging |
Het |
Dnajc14 |
G |
A |
10: 128,643,448 (GRCm39) |
D457N |
probably damaging |
Het |
Eif3a |
C |
A |
19: 60,755,264 (GRCm39) |
D973Y |
unknown |
Het |
Farsb |
T |
A |
1: 78,439,011 (GRCm39) |
K395* |
probably null |
Het |
Fem1b |
A |
G |
9: 62,704,082 (GRCm39) |
S393P |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,817,299 (GRCm39) |
N4344T |
possibly damaging |
Het |
Gphn |
A |
G |
12: 78,684,277 (GRCm39) |
S558G |
probably damaging |
Het |
Gpr142 |
C |
A |
11: 114,689,755 (GRCm39) |
H2Q |
probably benign |
Het |
Grhpr |
T |
C |
4: 44,988,915 (GRCm39) |
|
probably benign |
Het |
Grik3 |
C |
A |
4: 125,517,368 (GRCm39) |
N70K |
probably damaging |
Het |
Gsap |
T |
A |
5: 21,455,933 (GRCm39) |
|
probably benign |
Het |
Iars1 |
T |
A |
13: 49,846,611 (GRCm39) |
C237S |
probably damaging |
Het |
Ighv1-9 |
A |
T |
12: 114,547,602 (GRCm39) |
F7L |
probably benign |
Het |
Ints8 |
A |
G |
4: 11,204,595 (GRCm39) |
|
probably benign |
Het |
Kcnj16 |
G |
T |
11: 110,915,549 (GRCm39) |
W70C |
probably damaging |
Het |
Kpna6 |
T |
C |
4: 129,551,251 (GRCm39) |
M85V |
probably benign |
Het |
Kri1 |
G |
A |
9: 21,186,661 (GRCm39) |
S447L |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,632,829 (GRCm39) |
V3528A |
probably benign |
Het |
Lrrc46 |
A |
T |
11: 96,929,605 (GRCm39) |
L77Q |
probably damaging |
Het |
Mrpl44 |
T |
C |
1: 79,757,212 (GRCm39) |
L219S |
probably damaging |
Het |
Ms4a14 |
T |
C |
19: 11,281,303 (GRCm39) |
I418M |
probably benign |
Het |
Myo7a |
T |
C |
7: 97,714,905 (GRCm39) |
D112G |
probably damaging |
Het |
Ncoa3 |
A |
G |
2: 165,897,098 (GRCm39) |
T630A |
possibly damaging |
Het |
Nsl1 |
T |
C |
1: 190,814,381 (GRCm39) |
L194P |
probably damaging |
Het |
Or8u10 |
T |
C |
2: 85,915,705 (GRCm39) |
K139E |
probably benign |
Het |
Pde4d |
A |
G |
13: 109,876,955 (GRCm39) |
S159G |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,142,978 (GRCm39) |
R845G |
probably null |
Het |
Pld1 |
A |
G |
3: 28,150,033 (GRCm39) |
|
probably benign |
Het |
Psd |
T |
A |
19: 46,311,781 (GRCm39) |
I300F |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 22,986,195 (GRCm39) |
W332R |
probably damaging |
Het |
Rnf212 |
T |
A |
5: 108,893,530 (GRCm39) |
M70L |
possibly damaging |
Het |
Sema4f |
A |
G |
6: 82,896,674 (GRCm39) |
|
probably benign |
Het |
Sez6 |
C |
A |
11: 77,844,699 (GRCm39) |
T7K |
possibly damaging |
Het |
Skint2 |
T |
C |
4: 112,502,660 (GRCm39) |
I290T |
probably benign |
Het |
Slc5a3 |
T |
A |
16: 91,874,522 (GRCm39) |
I193N |
probably damaging |
Het |
Snip1 |
T |
A |
4: 124,966,633 (GRCm39) |
Y354* |
probably null |
Het |
Tmco5 |
A |
G |
2: 116,717,768 (GRCm39) |
Y200C |
probably damaging |
Het |
Tmem87b |
T |
A |
2: 128,673,361 (GRCm39) |
|
probably benign |
Het |
Trim60 |
T |
C |
8: 65,453,973 (GRCm39) |
E92G |
probably benign |
Het |
Ttn |
A |
T |
2: 76,626,804 (GRCm39) |
D13067E |
possibly damaging |
Het |
Ufl1 |
A |
T |
4: 25,269,087 (GRCm39) |
I168N |
probably damaging |
Het |
Zfp385c |
G |
A |
11: 100,520,782 (GRCm39) |
P293S |
probably benign |
Het |
Zfp473 |
T |
A |
7: 44,383,899 (GRCm39) |
S144C |
probably damaging |
Het |
|
Other mutations in Or5ac23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02475:Or5ac23
|
APN |
16 |
59,149,088 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03236:Or5ac23
|
APN |
16 |
59,149,200 (GRCm39) |
missense |
probably damaging |
0.97 |
R0054:Or5ac23
|
UTSW |
16 |
59,149,428 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0167:Or5ac23
|
UTSW |
16 |
59,149,337 (GRCm39) |
nonsense |
probably null |
|
R0178:Or5ac23
|
UTSW |
16 |
59,149,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Or5ac23
|
UTSW |
16 |
59,149,585 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0577:Or5ac23
|
UTSW |
16 |
59,149,061 (GRCm39) |
missense |
probably benign |
0.01 |
R0597:Or5ac23
|
UTSW |
16 |
59,149,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Or5ac23
|
UTSW |
16 |
59,149,546 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1670:Or5ac23
|
UTSW |
16 |
59,149,607 (GRCm39) |
missense |
probably benign |
0.03 |
R1702:Or5ac23
|
UTSW |
16 |
59,149,504 (GRCm39) |
missense |
probably benign |
0.12 |
R1995:Or5ac23
|
UTSW |
16 |
59,149,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Or5ac23
|
UTSW |
16 |
59,149,738 (GRCm39) |
missense |
probably damaging |
0.99 |
R4063:Or5ac23
|
UTSW |
16 |
59,149,243 (GRCm39) |
missense |
probably benign |
0.05 |
R4400:Or5ac23
|
UTSW |
16 |
59,148,961 (GRCm39) |
missense |
probably benign |
|
R4666:Or5ac23
|
UTSW |
16 |
59,149,573 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4795:Or5ac23
|
UTSW |
16 |
59,149,213 (GRCm39) |
missense |
probably benign |
0.09 |
R5327:Or5ac23
|
UTSW |
16 |
59,149,461 (GRCm39) |
missense |
probably benign |
0.01 |
R5471:Or5ac23
|
UTSW |
16 |
59,148,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R5770:Or5ac23
|
UTSW |
16 |
59,149,514 (GRCm39) |
nonsense |
probably null |
|
R6195:Or5ac23
|
UTSW |
16 |
59,149,785 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6702:Or5ac23
|
UTSW |
16 |
59,148,961 (GRCm39) |
missense |
probably benign |
|
R7686:Or5ac23
|
UTSW |
16 |
59,149,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7911:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7912:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7913:Or5ac23
|
UTSW |
16 |
59,149,606 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7998:Or5ac23
|
UTSW |
16 |
59,149,633 (GRCm39) |
missense |
probably benign |
0.09 |
R8772:Or5ac23
|
UTSW |
16 |
59,149,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Or5ac23
|
UTSW |
16 |
59,149,765 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Or5ac23
|
UTSW |
16 |
59,149,713 (GRCm39) |
missense |
probably benign |
0.09 |
|