Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,903,743 (GRCm39) |
E163G |
probably damaging |
Het |
4921513D11Rik |
A |
G |
17: 79,935,562 (GRCm39) |
|
probably benign |
Het |
Acox3 |
T |
A |
5: 35,749,459 (GRCm39) |
F195I |
possibly damaging |
Het |
Acsl6 |
T |
C |
11: 54,216,417 (GRCm39) |
Y135H |
probably damaging |
Het |
Ankhd1 |
C |
A |
18: 36,781,083 (GRCm39) |
A2045E |
probably benign |
Het |
Ap5z1 |
A |
G |
5: 142,458,096 (GRCm39) |
H423R |
probably benign |
Het |
Arsk |
T |
A |
13: 76,214,985 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
A |
G |
14: 55,739,861 (GRCm39) |
T983A |
probably damaging |
Het |
Ccdc192 |
A |
T |
18: 57,666,959 (GRCm39) |
D12V |
probably damaging |
Het |
Chmp2b |
A |
T |
16: 65,342,213 (GRCm39) |
M125K |
possibly damaging |
Het |
Clca3a2 |
T |
A |
3: 144,511,491 (GRCm39) |
I26L |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,315,337 (GRCm39) |
Y3032C |
probably damaging |
Het |
Ehbp1 |
T |
A |
11: 22,101,850 (GRCm39) |
D226V |
probably damaging |
Het |
Enpp6 |
A |
T |
8: 47,535,541 (GRCm39) |
D362V |
probably damaging |
Het |
Fam53b |
A |
G |
7: 132,317,521 (GRCm39) |
S374P |
probably damaging |
Het |
Fmn1 |
T |
C |
2: 113,260,066 (GRCm39) |
|
probably benign |
Het |
Fndc7 |
C |
T |
3: 108,784,003 (GRCm39) |
R202H |
probably benign |
Het |
Frmd4b |
T |
G |
6: 97,265,415 (GRCm39) |
D951A |
probably benign |
Het |
Git2 |
A |
G |
5: 114,877,162 (GRCm39) |
Y107H |
probably damaging |
Het |
Gm11595 |
A |
T |
11: 99,663,365 (GRCm39) |
V105E |
unknown |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
Lrriq4 |
C |
A |
3: 30,713,242 (GRCm39) |
Q448K |
probably benign |
Het |
Ly6g5c |
A |
G |
17: 35,330,863 (GRCm39) |
I128M |
possibly damaging |
Het |
Mroh9 |
T |
A |
1: 162,903,860 (GRCm39) |
S51C |
probably damaging |
Het |
Myh3 |
A |
G |
11: 66,970,828 (GRCm39) |
S2G |
probably benign |
Het |
Nat8f4 |
A |
G |
6: 85,878,497 (GRCm39) |
Y9H |
probably damaging |
Het |
Negr1 |
T |
C |
3: 156,267,836 (GRCm39) |
V2A |
probably benign |
Het |
Or2y1 |
C |
T |
11: 49,386,131 (GRCm39) |
T257I |
probably damaging |
Het |
Or7g19 |
C |
T |
9: 18,856,781 (GRCm39) |
T279I |
probably benign |
Het |
Or8k32 |
T |
G |
2: 86,368,857 (GRCm39) |
Y132S |
probably damaging |
Het |
Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
Pdgfra |
C |
A |
5: 75,324,394 (GRCm39) |
T83K |
probably benign |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Retreg1 |
A |
G |
15: 25,969,924 (GRCm39) |
D109G |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,189,613 (GRCm39) |
W674R |
probably damaging |
Het |
Rgs18 |
T |
C |
1: 144,631,818 (GRCm39) |
D98G |
possibly damaging |
Het |
Rnf146 |
A |
G |
10: 29,223,715 (GRCm39) |
F57S |
probably damaging |
Het |
Skic3 |
T |
A |
13: 76,282,889 (GRCm39) |
V737D |
probably damaging |
Het |
Slc22a20 |
C |
A |
19: 6,021,464 (GRCm39) |
V513L |
probably benign |
Het |
Stox2 |
G |
T |
8: 47,646,661 (GRCm39) |
F266L |
probably damaging |
Het |
Tbx21 |
C |
T |
11: 96,990,863 (GRCm39) |
V272M |
probably damaging |
Het |
Tmc7 |
A |
G |
7: 118,144,850 (GRCm39) |
F570S |
probably benign |
Het |
Tmem236 |
T |
C |
2: 14,224,117 (GRCm39) |
I302T |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,862,776 (GRCm39) |
L506S |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,218,694 (GRCm39) |
I78V |
probably damaging |
Het |
Xpo4 |
A |
T |
14: 57,828,328 (GRCm39) |
V844D |
probably damaging |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
|
Other mutations in Bpi |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Bpi
|
APN |
2 |
158,116,716 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00327:Bpi
|
APN |
2 |
158,116,764 (GRCm39) |
critical splice donor site |
probably benign |
|
IGL01614:Bpi
|
APN |
2 |
158,113,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Bpi
|
APN |
2 |
158,116,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02516:Bpi
|
APN |
2 |
158,109,651 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02752:Bpi
|
APN |
2 |
158,104,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R0077:Bpi
|
UTSW |
2 |
158,103,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R0085:Bpi
|
UTSW |
2 |
158,115,072 (GRCm39) |
nonsense |
probably null |
|
R0433:Bpi
|
UTSW |
2 |
158,100,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Bpi
|
UTSW |
2 |
158,100,215 (GRCm39) |
start codon destroyed |
probably damaging |
0.98 |
R0605:Bpi
|
UTSW |
2 |
158,103,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Bpi
|
UTSW |
2 |
158,103,346 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0930:Bpi
|
UTSW |
2 |
158,103,346 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1173:Bpi
|
UTSW |
2 |
158,109,660 (GRCm39) |
missense |
probably benign |
0.04 |
R1530:Bpi
|
UTSW |
2 |
158,103,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Bpi
|
UTSW |
2 |
158,116,635 (GRCm39) |
missense |
probably damaging |
0.98 |
R2011:Bpi
|
UTSW |
2 |
158,103,272 (GRCm39) |
missense |
probably damaging |
0.97 |
R4748:Bpi
|
UTSW |
2 |
158,113,941 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6005:Bpi
|
UTSW |
2 |
158,104,400 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6374:Bpi
|
UTSW |
2 |
158,113,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Bpi
|
UTSW |
2 |
158,100,164 (GRCm39) |
start gained |
probably benign |
|
R7072:Bpi
|
UTSW |
2 |
158,113,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:Bpi
|
UTSW |
2 |
158,103,093 (GRCm39) |
missense |
probably benign |
0.02 |
R8825:Bpi
|
UTSW |
2 |
158,109,670 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Bpi
|
UTSW |
2 |
158,116,608 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Bpi
|
UTSW |
2 |
158,114,022 (GRCm39) |
missense |
possibly damaging |
0.95 |
|