Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
C |
T |
17: 46,623,827 (GRCm39) |
E770K |
possibly damaging |
Het |
Abhd17a |
C |
A |
10: 80,422,395 (GRCm39) |
A22S |
probably benign |
Het |
Actbl2 |
A |
G |
13: 111,392,225 (GRCm39) |
T187A |
probably benign |
Het |
Adgrl3 |
G |
A |
5: 81,660,064 (GRCm39) |
G278R |
probably damaging |
Het |
Atp2b2 |
A |
G |
6: 113,790,828 (GRCm39) |
F192S |
probably damaging |
Het |
Bdh1 |
T |
C |
16: 31,268,754 (GRCm39) |
I163T |
possibly damaging |
Het |
Bmp1 |
G |
T |
14: 70,723,660 (GRCm39) |
N725K |
probably damaging |
Het |
Bmp1 |
T |
A |
14: 70,727,547 (GRCm39) |
I679F |
probably damaging |
Het |
Bmp2 |
T |
A |
2: 133,402,844 (GRCm39) |
F132I |
probably benign |
Het |
Bpifb5 |
T |
C |
2: 154,069,103 (GRCm39) |
L140P |
probably damaging |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Carmil3 |
T |
C |
14: 55,731,279 (GRCm39) |
|
probably benign |
Het |
Ccdc57 |
T |
C |
11: 120,764,586 (GRCm39) |
T730A |
possibly damaging |
Het |
Cdh10 |
G |
T |
15: 19,013,342 (GRCm39) |
K647N |
probably damaging |
Het |
Cdh17 |
A |
C |
4: 11,771,373 (GRCm39) |
|
probably benign |
Het |
Cep126 |
A |
G |
9: 8,099,925 (GRCm39) |
S870P |
probably benign |
Het |
Col6a4 |
T |
C |
9: 105,954,302 (GRCm39) |
T346A |
probably damaging |
Het |
Csmd3 |
A |
C |
15: 47,530,024 (GRCm39) |
V2592G |
probably damaging |
Het |
Dnajc16 |
A |
T |
4: 141,504,244 (GRCm39) |
F239I |
probably damaging |
Het |
Entrep3 |
C |
T |
3: 89,095,903 (GRCm39) |
R545* |
probably null |
Het |
F5 |
G |
A |
1: 164,017,695 (GRCm39) |
V591M |
probably damaging |
Het |
Fchsd2 |
T |
G |
7: 100,826,429 (GRCm39) |
|
probably null |
Het |
Flad1 |
A |
T |
3: 89,316,294 (GRCm39) |
D89E |
probably damaging |
Het |
Fsd1 |
C |
A |
17: 56,303,499 (GRCm39) |
P457Q |
probably damaging |
Het |
Gm21985 |
A |
G |
2: 112,187,929 (GRCm39) |
D1012G |
possibly damaging |
Het |
Gon4l |
A |
G |
3: 88,764,517 (GRCm39) |
D366G |
probably null |
Het |
Hadha |
A |
G |
5: 30,347,843 (GRCm39) |
|
probably benign |
Het |
Kdr |
A |
G |
5: 76,122,513 (GRCm39) |
|
probably benign |
Het |
Kyat3 |
A |
G |
3: 142,426,136 (GRCm39) |
K24R |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,668,397 (GRCm39) |
D661G |
probably benign |
Het |
Mical1 |
A |
T |
10: 41,360,407 (GRCm39) |
K615N |
possibly damaging |
Het |
Ncor1 |
T |
C |
11: 62,310,435 (GRCm39) |
K204E |
possibly damaging |
Het |
Nmral1 |
T |
A |
16: 4,534,346 (GRCm39) |
I32F |
probably benign |
Het |
Nrros |
T |
C |
16: 31,963,492 (GRCm39) |
D175G |
possibly damaging |
Het |
Or10ak8 |
G |
A |
4: 118,773,968 (GRCm39) |
T232I |
probably benign |
Het |
Or12j5 |
T |
C |
7: 140,084,077 (GRCm39) |
I98M |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,587,143 (GRCm39) |
F4713L |
possibly damaging |
Het |
Serpinb1b |
G |
A |
13: 33,275,301 (GRCm39) |
G142D |
possibly damaging |
Het |
Slc10a1 |
A |
G |
12: 81,007,248 (GRCm39) |
S178P |
possibly damaging |
Het |
Spint1 |
G |
A |
2: 119,068,698 (GRCm39) |
R144H |
probably benign |
Het |
Sult6b1 |
C |
T |
17: 79,196,504 (GRCm39) |
G213R |
probably damaging |
Het |
Themis3 |
G |
T |
17: 66,862,900 (GRCm39) |
H353N |
probably benign |
Het |
Tpr |
T |
C |
1: 150,289,525 (GRCm39) |
S619P |
probably benign |
Het |
Ttn |
A |
T |
2: 76,645,134 (GRCm39) |
V11161E |
probably damaging |
Het |
Usp13 |
G |
A |
3: 32,987,314 (GRCm39) |
V837I |
probably damaging |
Het |
Usp25 |
T |
C |
16: 76,880,670 (GRCm39) |
V677A |
probably benign |
Het |
Wdr62 |
A |
G |
7: 29,942,894 (GRCm39) |
V1001A |
possibly damaging |
Het |
Whrn |
A |
T |
4: 63,336,822 (GRCm39) |
I580N |
possibly damaging |
Het |
Wls |
T |
A |
3: 159,616,993 (GRCm39) |
V344D |
probably damaging |
Het |
Zan |
A |
T |
5: 137,385,222 (GRCm39) |
Y5070* |
probably null |
Het |
|
Other mutations in Apoh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Apoh
|
APN |
11 |
108,286,660 (GRCm39) |
missense |
probably benign |
0.45 |
IGL01327:Apoh
|
APN |
11 |
108,288,187 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01353:Apoh
|
APN |
11 |
108,288,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01464:Apoh
|
APN |
11 |
108,286,716 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02646:Apoh
|
APN |
11 |
108,302,968 (GRCm39) |
missense |
probably benign |
0.15 |
R0125:Apoh
|
UTSW |
11 |
108,302,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Apoh
|
UTSW |
11 |
108,288,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Apoh
|
UTSW |
11 |
108,298,288 (GRCm39) |
missense |
probably benign |
0.00 |
R2280:Apoh
|
UTSW |
11 |
108,300,006 (GRCm39) |
nonsense |
probably null |
|
R2568:Apoh
|
UTSW |
11 |
108,295,697 (GRCm39) |
missense |
probably benign |
0.00 |
R4369:Apoh
|
UTSW |
11 |
108,288,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Apoh
|
UTSW |
11 |
108,300,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R4824:Apoh
|
UTSW |
11 |
108,305,087 (GRCm39) |
missense |
probably benign |
0.37 |
R4937:Apoh
|
UTSW |
11 |
108,298,204 (GRCm39) |
missense |
probably benign |
0.19 |
R5634:Apoh
|
UTSW |
11 |
108,302,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R5900:Apoh
|
UTSW |
11 |
108,302,843 (GRCm39) |
missense |
probably damaging |
0.99 |
R5951:Apoh
|
UTSW |
11 |
108,286,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Apoh
|
UTSW |
11 |
108,286,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Apoh
|
UTSW |
11 |
108,288,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Apoh
|
UTSW |
11 |
108,286,674 (GRCm39) |
missense |
probably benign |
0.14 |
R7471:Apoh
|
UTSW |
11 |
108,298,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Apoh
|
UTSW |
11 |
108,300,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R9310:Apoh
|
UTSW |
11 |
108,298,307 (GRCm39) |
critical splice donor site |
probably null |
|
R9671:Apoh
|
UTSW |
11 |
108,286,792 (GRCm39) |
nonsense |
probably null |
|
X0065:Apoh
|
UTSW |
11 |
108,286,176 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Apoh
|
UTSW |
11 |
108,234,285 (GRCm39) |
start gained |
probably benign |
|
|