Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1190005I06Rik |
A |
T |
8: 121,335,735 (GRCm39) |
D69E |
probably damaging |
Het |
AAdacl4fm3 |
T |
A |
4: 144,430,437 (GRCm39) |
D184V |
probably damaging |
Het |
Adgrv1 |
G |
T |
13: 81,723,220 (GRCm39) |
|
probably null |
Het |
Ahr |
A |
T |
12: 35,554,031 (GRCm39) |
V696E |
probably benign |
Het |
Akap13 |
A |
G |
7: 75,376,792 (GRCm39) |
T2007A |
probably benign |
Het |
Arid1b |
T |
C |
17: 5,377,953 (GRCm39) |
F753S |
probably damaging |
Het |
C2cd2 |
A |
G |
16: 97,680,822 (GRCm39) |
C331R |
probably benign |
Het |
Chrm1 |
T |
A |
19: 8,655,542 (GRCm39) |
Y82* |
probably null |
Het |
Clcn3 |
A |
C |
8: 61,382,595 (GRCm39) |
V331G |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,413,748 (GRCm39) |
D1022E |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,430,241 (GRCm39) |
T106S |
probably benign |
Het |
Fam171a2 |
T |
A |
11: 102,330,711 (GRCm39) |
D256V |
probably damaging |
Het |
Firrm |
G |
T |
1: 163,781,734 (GRCm39) |
R898S |
probably benign |
Het |
Fmn2 |
T |
A |
1: 174,437,149 (GRCm39) |
|
probably benign |
Het |
Fut11 |
C |
T |
14: 20,745,377 (GRCm39) |
R103W |
probably damaging |
Het |
Gas2l2 |
A |
C |
11: 83,320,179 (GRCm39) |
S26A |
probably damaging |
Het |
Gramd1a |
A |
T |
7: 30,843,221 (GRCm39) |
I29N |
probably benign |
Het |
Grem2 |
A |
G |
1: 174,664,450 (GRCm39) |
V133A |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,233,600 (GRCm39) |
S1813T |
possibly damaging |
Het |
Igkv3-2 |
T |
C |
6: 70,676,023 (GRCm39) |
F111L |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,252,878 (GRCm39) |
Q68R |
probably damaging |
Het |
Irx5 |
A |
G |
8: 93,086,354 (GRCm39) |
I146V |
probably damaging |
Het |
Kcnh3 |
T |
C |
15: 99,136,124 (GRCm39) |
L707P |
probably damaging |
Het |
Kcnk4 |
T |
A |
19: 6,905,665 (GRCm39) |
I101F |
probably damaging |
Het |
Klhl9 |
A |
G |
4: 88,639,399 (GRCm39) |
Y281H |
probably benign |
Het |
Klra9 |
G |
T |
6: 130,155,995 (GRCm39) |
Y253* |
probably null |
Het |
Lmbr1 |
C |
T |
5: 29,583,166 (GRCm39) |
A9T |
probably benign |
Het |
Map10 |
G |
T |
8: 126,399,123 (GRCm39) |
E839* |
probably null |
Het |
Nectin4 |
C |
A |
1: 171,214,321 (GRCm39) |
A492D |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,082,140 (GRCm39) |
|
probably null |
Het |
Or5p5 |
A |
G |
7: 107,413,901 (GRCm39) |
T37A |
probably benign |
Het |
Plec |
A |
G |
15: 76,062,084 (GRCm39) |
Y2608H |
probably benign |
Het |
Pold3 |
A |
G |
7: 99,749,839 (GRCm39) |
S42P |
probably benign |
Het |
Ppp2r1a |
G |
T |
17: 21,180,893 (GRCm39) |
G432* |
probably null |
Het |
Qki |
T |
C |
17: 10,434,394 (GRCm39) |
E315G |
probably benign |
Het |
Rfx2 |
C |
T |
17: 57,091,397 (GRCm39) |
V354I |
probably benign |
Het |
Rp1 |
T |
C |
1: 4,418,109 (GRCm39) |
Y1001C |
probably benign |
Het |
Sez6l |
A |
G |
5: 112,609,007 (GRCm39) |
|
probably null |
Het |
Slc39a14 |
A |
G |
14: 70,547,335 (GRCm39) |
I337T |
probably damaging |
Het |
Slc3a2 |
G |
T |
19: 8,686,683 (GRCm39) |
L76M |
probably damaging |
Het |
Slco1a5 |
T |
C |
6: 142,183,260 (GRCm39) |
T555A |
probably benign |
Het |
Sprr2e |
A |
T |
3: 92,260,341 (GRCm39) |
K57N |
unknown |
Het |
Syne2 |
A |
G |
12: 75,990,675 (GRCm39) |
T1886A |
probably damaging |
Het |
Tenm3 |
A |
T |
8: 48,689,098 (GRCm39) |
I2147N |
probably damaging |
Het |
Thbs1 |
G |
T |
2: 117,950,328 (GRCm39) |
G654W |
probably damaging |
Het |
Tigd5 |
A |
G |
15: 75,782,352 (GRCm39) |
Y238C |
possibly damaging |
Het |
Tmem221 |
A |
G |
8: 72,010,493 (GRCm39) |
F126S |
probably damaging |
Het |
Trp63 |
C |
A |
16: 25,582,108 (GRCm39) |
P52Q |
probably damaging |
Het |
Ugp2 |
A |
T |
11: 21,278,883 (GRCm39) |
S434R |
probably benign |
Het |
Vmn2r69 |
A |
C |
7: 85,056,378 (GRCm39) |
F587V |
probably benign |
Het |
Vps13d |
T |
A |
4: 144,784,065 (GRCm39) |
N3872I |
possibly damaging |
Het |
Wdfy2 |
A |
G |
14: 63,186,115 (GRCm39) |
Y250C |
probably damaging |
Het |
Zbtb16 |
T |
C |
9: 48,576,619 (GRCm39) |
D487G |
possibly damaging |
Het |
|
Other mutations in Bpifb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01982:Bpifb3
|
APN |
2 |
153,767,521 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02568:Bpifb3
|
APN |
2 |
153,766,721 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02817:Bpifb3
|
APN |
2 |
153,761,566 (GRCm39) |
missense |
unknown |
|
IGL03175:Bpifb3
|
APN |
2 |
153,761,568 (GRCm39) |
missense |
unknown |
|
R0478:Bpifb3
|
UTSW |
2 |
153,773,400 (GRCm39) |
splice site |
probably benign |
|
R0538:Bpifb3
|
UTSW |
2 |
153,765,789 (GRCm39) |
missense |
probably benign |
0.05 |
R1633:Bpifb3
|
UTSW |
2 |
153,764,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1850:Bpifb3
|
UTSW |
2 |
153,771,264 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1874:Bpifb3
|
UTSW |
2 |
153,767,760 (GRCm39) |
missense |
probably benign |
0.01 |
R5993:Bpifb3
|
UTSW |
2 |
153,771,234 (GRCm39) |
missense |
probably benign |
0.20 |
R6120:Bpifb3
|
UTSW |
2 |
153,773,363 (GRCm39) |
missense |
probably benign |
0.12 |
R6170:Bpifb3
|
UTSW |
2 |
153,761,557 (GRCm39) |
missense |
unknown |
|
R6216:Bpifb3
|
UTSW |
2 |
153,767,773 (GRCm39) |
missense |
probably benign |
0.17 |
R6274:Bpifb3
|
UTSW |
2 |
153,771,243 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6431:Bpifb3
|
UTSW |
2 |
153,766,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6609:Bpifb3
|
UTSW |
2 |
153,762,568 (GRCm39) |
critical splice donor site |
probably null |
|
R7334:Bpifb3
|
UTSW |
2 |
153,761,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R8111:Bpifb3
|
UTSW |
2 |
153,764,609 (GRCm39) |
missense |
probably benign |
0.00 |
R8375:Bpifb3
|
UTSW |
2 |
153,767,715 (GRCm39) |
missense |
probably benign |
0.01 |
R8812:Bpifb3
|
UTSW |
2 |
153,764,516 (GRCm39) |
missense |
probably benign |
0.00 |
R9049:Bpifb3
|
UTSW |
2 |
153,767,810 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Bpifb3
|
UTSW |
2 |
153,767,709 (GRCm39) |
missense |
probably benign |
0.36 |
|