Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
C |
A |
10: 85,490,366 (GRCm39) |
Q1011K |
probably damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,907,522 (GRCm39) |
H174L |
possibly damaging |
Het |
Auts2 |
G |
T |
5: 131,501,198 (GRCm39) |
Q72K |
probably damaging |
Het |
Ccdc7b |
A |
T |
8: 129,863,049 (GRCm39) |
|
probably benign |
Het |
Frem3 |
A |
G |
8: 81,342,372 (GRCm39) |
E1555G |
probably benign |
Het |
Gm5263 |
T |
G |
1: 146,296,302 (GRCm39) |
|
noncoding transcript |
Het |
Gm5828 |
A |
G |
1: 16,840,208 (GRCm39) |
|
noncoding transcript |
Het |
Gm6605 |
T |
C |
7: 38,147,630 (GRCm39) |
|
noncoding transcript |
Het |
Gvin3 |
T |
A |
7: 106,201,516 (GRCm39) |
N576I |
possibly damaging |
Het |
Hps3 |
T |
C |
3: 20,065,130 (GRCm39) |
D638G |
probably damaging |
Het |
Igdcc4 |
A |
T |
9: 65,039,014 (GRCm39) |
N887I |
probably damaging |
Het |
Itpkc |
G |
A |
7: 26,912,491 (GRCm39) |
|
probably benign |
Het |
Mfge8 |
A |
G |
7: 78,786,403 (GRCm39) |
|
probably null |
Het |
Mrc2 |
G |
T |
11: 105,216,560 (GRCm39) |
L116F |
probably benign |
Het |
Necab1 |
T |
C |
4: 14,978,171 (GRCm39) |
D226G |
probably damaging |
Het |
Neurod2 |
T |
C |
11: 98,218,201 (GRCm39) |
E321G |
possibly damaging |
Het |
Obp2b |
G |
T |
2: 25,627,760 (GRCm39) |
V59L |
possibly damaging |
Het |
Olr1 |
T |
C |
6: 129,465,811 (GRCm39) |
N65S |
possibly damaging |
Het |
Or14c39 |
A |
T |
7: 86,343,997 (GRCm39) |
Q111L |
probably benign |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or5d43 |
A |
T |
2: 88,104,977 (GRCm39) |
C139S |
possibly damaging |
Het |
Or8b48 |
C |
T |
9: 38,492,809 (GRCm39) |
P79S |
probably damaging |
Het |
Rock1 |
A |
G |
18: 10,079,113 (GRCm39) |
|
probably null |
Het |
Scn3a |
T |
A |
2: 65,291,596 (GRCm39) |
M1717L |
possibly damaging |
Het |
Smg7 |
T |
C |
1: 152,719,812 (GRCm39) |
D903G |
possibly damaging |
Het |
Tlr1 |
A |
T |
5: 65,083,290 (GRCm39) |
L429* |
probably null |
Het |
Ttll9 |
A |
T |
2: 152,825,025 (GRCm39) |
N68I |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,567,943 (GRCm39) |
V25904A |
possibly damaging |
Het |
Uaca |
G |
A |
9: 60,777,139 (GRCm39) |
V507M |
probably damaging |
Het |
Vmn1r195 |
G |
T |
13: 22,463,421 (GRCm39) |
C297F |
probably benign |
Het |
Zdhhc2 |
G |
A |
8: 40,926,042 (GRCm39) |
A346T |
probably benign |
Het |
|
Other mutations in 1700018F24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01625:1700018F24Rik
|
APN |
5 |
144,979,957 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02928:1700018F24Rik
|
APN |
5 |
144,980,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03324:1700018F24Rik
|
APN |
5 |
144,982,261 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4486001:1700018F24Rik
|
UTSW |
5 |
144,980,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:1700018F24Rik
|
UTSW |
5 |
144,982,181 (GRCm39) |
nonsense |
probably null |
|
R0554:1700018F24Rik
|
UTSW |
5 |
144,982,181 (GRCm39) |
nonsense |
probably null |
|
R0724:1700018F24Rik
|
UTSW |
5 |
144,981,573 (GRCm39) |
missense |
probably benign |
0.10 |
R1774:1700018F24Rik
|
UTSW |
5 |
144,982,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R2041:1700018F24Rik
|
UTSW |
5 |
144,982,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R4625:1700018F24Rik
|
UTSW |
5 |
144,981,693 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5043:1700018F24Rik
|
UTSW |
5 |
144,980,910 (GRCm39) |
nonsense |
probably null |
|
R5610:1700018F24Rik
|
UTSW |
5 |
144,982,156 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5712:1700018F24Rik
|
UTSW |
5 |
144,981,563 (GRCm39) |
missense |
probably benign |
0.32 |
R6163:1700018F24Rik
|
UTSW |
5 |
144,982,098 (GRCm39) |
nonsense |
probably null |
|
R6799:1700018F24Rik
|
UTSW |
5 |
144,981,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R7174:1700018F24Rik
|
UTSW |
5 |
144,981,627 (GRCm39) |
missense |
probably benign |
0.27 |
R8127:1700018F24Rik
|
UTSW |
5 |
144,980,249 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8688:1700018F24Rik
|
UTSW |
5 |
144,982,183 (GRCm39) |
missense |
probably damaging |
0.98 |
R8975:1700018F24Rik
|
UTSW |
5 |
144,980,192 (GRCm39) |
missense |
probably damaging |
0.97 |
R9289:1700018F24Rik
|
UTSW |
5 |
144,982,333 (GRCm39) |
missense |
probably benign |
0.00 |
R9473:1700018F24Rik
|
UTSW |
5 |
144,980,912 (GRCm39) |
missense |
probably benign |
0.01 |
|