Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anxa2 |
A |
T |
9: 69,387,410 (GRCm39) |
K6N |
unknown |
Het |
Arhgap20 |
T |
A |
9: 51,743,050 (GRCm39) |
M296K |
possibly damaging |
Het |
Bdh1 |
G |
A |
16: 31,256,910 (GRCm39) |
V20I |
not run |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Cct4 |
A |
G |
11: 22,940,814 (GRCm39) |
K21E |
probably benign |
Het |
Cercam |
G |
A |
2: 29,762,574 (GRCm39) |
|
probably null |
Het |
Clip2 |
A |
T |
5: 134,546,853 (GRCm39) |
Y238* |
probably null |
Het |
Col19a1 |
A |
T |
1: 24,309,525 (GRCm39) |
S1043T |
possibly damaging |
Het |
Ctcf |
A |
G |
8: 106,390,468 (GRCm39) |
Y25C |
probably damaging |
Het |
Dennd4c |
C |
T |
4: 86,704,330 (GRCm39) |
R282C |
probably benign |
Het |
Eef1g |
T |
A |
19: 8,955,427 (GRCm39) |
H425Q |
probably benign |
Het |
Fam131b |
C |
T |
6: 42,295,476 (GRCm39) |
A234T |
probably benign |
Het |
Fam184a |
C |
A |
10: 53,509,802 (GRCm39) |
E126* |
probably null |
Het |
Fam187b |
A |
G |
7: 30,677,139 (GRCm39) |
D216G |
possibly damaging |
Het |
Gabra1 |
A |
T |
11: 42,026,270 (GRCm39) |
Y341N |
possibly damaging |
Het |
Glb1l3 |
T |
A |
9: 26,739,659 (GRCm39) |
|
probably null |
Het |
Gm3667 |
T |
A |
14: 18,271,599 (GRCm39) |
Q52L |
probably damaging |
Het |
Gpr179 |
C |
T |
11: 97,242,118 (GRCm39) |
R242H |
probably damaging |
Het |
Gulo |
T |
C |
14: 66,245,522 (GRCm39) |
Y24C |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,358,680 (GRCm39) |
E49V |
unknown |
Het |
Htra4 |
A |
G |
8: 25,527,169 (GRCm39) |
S209P |
possibly damaging |
Het |
Lmntd1 |
A |
G |
6: 145,489,196 (GRCm39) |
S22P |
probably benign |
Het |
Lypd8l |
A |
T |
11: 58,499,325 (GRCm39) |
N164K |
probably benign |
Het |
Med12l |
A |
G |
3: 59,163,413 (GRCm39) |
K1347E |
probably damaging |
Het |
Mrc1 |
C |
A |
2: 14,284,788 (GRCm39) |
D592E |
probably benign |
Het |
Muc15 |
A |
G |
2: 110,562,143 (GRCm39) |
D193G |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,100,630 (GRCm39) |
V1316A |
|
Het |
Odad1 |
T |
A |
7: 45,597,835 (GRCm39) |
S582T |
probably damaging |
Het |
Or2t43 |
A |
G |
11: 58,457,593 (GRCm39) |
Y193H |
probably damaging |
Het |
Or2y10 |
A |
T |
11: 49,455,359 (GRCm39) |
I204L |
probably benign |
Het |
Or5t16 |
T |
C |
2: 86,819,323 (GRCm39) |
I66V |
probably benign |
Het |
Serpina6 |
A |
T |
12: 103,614,936 (GRCm39) |
Y303* |
probably null |
Het |
Shld2 |
T |
G |
14: 33,990,661 (GRCm39) |
T82P |
possibly damaging |
Het |
Shroom3 |
T |
C |
5: 93,089,512 (GRCm39) |
L754P |
probably benign |
Het |
Skint5 |
C |
A |
4: 113,685,099 (GRCm39) |
L539F |
unknown |
Het |
St3gal4 |
C |
A |
9: 34,964,375 (GRCm39) |
R209L |
possibly damaging |
Het |
Tex14 |
A |
C |
11: 87,385,868 (GRCm39) |
T243P |
probably damaging |
Het |
Ttc12 |
T |
A |
9: 49,351,602 (GRCm39) |
M632L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,738,116 (GRCm39) |
E4187G |
unknown |
Het |
Txk |
G |
A |
5: 72,864,900 (GRCm39) |
A379V |
probably damaging |
Het |
Wdr43 |
A |
G |
17: 71,923,338 (GRCm39) |
Y28C |
probably benign |
Het |
Zfp1005 |
A |
G |
2: 150,110,468 (GRCm39) |
Y386C |
unknown |
Het |
Zfp40 |
A |
G |
17: 23,397,251 (GRCm39) |
V82A |
probably benign |
Het |
Zfp994 |
A |
T |
17: 22,419,091 (GRCm39) |
N619K |
probably benign |
Het |
|
Other mutations in Bop1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00436:Bop1
|
APN |
15 |
76,338,728 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01085:Bop1
|
APN |
15 |
76,337,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02157:Bop1
|
APN |
15 |
76,339,772 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0332:Bop1
|
UTSW |
15 |
76,340,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R2148:Bop1
|
UTSW |
15 |
76,339,487 (GRCm39) |
missense |
probably damaging |
0.96 |
R3979:Bop1
|
UTSW |
15 |
76,338,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Bop1
|
UTSW |
15 |
76,338,535 (GRCm39) |
missense |
probably benign |
0.24 |
R5396:Bop1
|
UTSW |
15 |
76,339,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5434:Bop1
|
UTSW |
15 |
76,339,611 (GRCm39) |
missense |
probably benign |
0.01 |
R5666:Bop1
|
UTSW |
15 |
76,338,433 (GRCm39) |
missense |
probably benign |
0.00 |
R5820:Bop1
|
UTSW |
15 |
76,339,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5883:Bop1
|
UTSW |
15 |
76,339,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5907:Bop1
|
UTSW |
15 |
76,340,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Bop1
|
UTSW |
15 |
76,339,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R6947:Bop1
|
UTSW |
15 |
76,338,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Bop1
|
UTSW |
15 |
76,337,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Bop1
|
UTSW |
15 |
76,338,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Bop1
|
UTSW |
15 |
76,339,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Bop1
|
UTSW |
15 |
76,338,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Bop1
|
UTSW |
15 |
76,338,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R9292:Bop1
|
UTSW |
15 |
76,351,031 (GRCm39) |
missense |
probably benign |
|
R9487:Bop1
|
UTSW |
15 |
76,338,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Bop1
|
UTSW |
15 |
76,338,688 (GRCm39) |
missense |
probably benign |
0.16 |
R9781:Bop1
|
UTSW |
15 |
76,338,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|