Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam10 |
C |
T |
9: 70,685,371 (GRCm39) |
R749C |
probably damaging |
Het |
Atp9a |
A |
G |
2: 168,481,879 (GRCm39) |
F872L |
probably damaging |
Het |
Cacna1e |
A |
C |
1: 154,317,997 (GRCm39) |
Y1462D |
probably damaging |
Het |
Ccna1 |
T |
C |
3: 54,958,041 (GRCm39) |
T7A |
probably benign |
Het |
Ces1d |
A |
G |
8: 93,901,816 (GRCm39) |
|
probably benign |
Het |
Cmtm8 |
A |
T |
9: 114,619,794 (GRCm39) |
V117D |
probably benign |
Het |
Cnot1 |
A |
G |
8: 96,462,308 (GRCm39) |
|
probably benign |
Het |
Col24a1 |
A |
T |
3: 145,019,744 (GRCm39) |
|
probably benign |
Het |
Crispld1 |
T |
C |
1: 17,815,701 (GRCm39) |
|
probably benign |
Het |
Dnaja2 |
A |
T |
8: 86,275,534 (GRCm39) |
N140K |
probably benign |
Het |
Fktn |
A |
T |
4: 53,720,120 (GRCm39) |
K6* |
probably null |
Het |
Fryl |
C |
A |
5: 73,293,659 (GRCm39) |
|
probably benign |
Het |
Gm5117 |
T |
A |
8: 32,228,836 (GRCm39) |
|
noncoding transcript |
Het |
Gucy2c |
A |
C |
6: 136,728,044 (GRCm39) |
S319R |
probably benign |
Het |
Helz2 |
G |
A |
2: 180,873,597 (GRCm39) |
A2299V |
probably benign |
Het |
Hivep2 |
T |
C |
10: 14,019,411 (GRCm39) |
S2061P |
probably damaging |
Het |
Irx4 |
A |
G |
13: 73,415,850 (GRCm39) |
N213S |
possibly damaging |
Het |
Mark3 |
A |
G |
12: 111,614,104 (GRCm39) |
T649A |
probably benign |
Het |
Nav3 |
C |
T |
10: 109,660,433 (GRCm39) |
|
probably null |
Het |
Npr1 |
C |
T |
3: 90,363,298 (GRCm39) |
E861K |
probably benign |
Het |
Or52a5 |
A |
C |
7: 103,426,634 (GRCm39) |
V306G |
probably benign |
Het |
Or5a3 |
T |
C |
19: 12,400,291 (GRCm39) |
V206A |
probably benign |
Het |
Pcdhb10 |
C |
T |
18: 37,545,374 (GRCm39) |
T150I |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,684,151 (GRCm39) |
C2009R |
possibly damaging |
Het |
Ttc16 |
T |
C |
2: 32,652,409 (GRCm39) |
|
probably benign |
Het |
Ttc39b |
T |
A |
4: 83,165,896 (GRCm39) |
Y230F |
probably benign |
Het |
Ubr1 |
A |
T |
2: 120,694,898 (GRCm39) |
I1678N |
probably damaging |
Het |
|
Other mutations in Trgv7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01640:Trgv7
|
APN |
13 |
19,362,260 (GRCm39) |
splice site |
probably benign |
|
IGL02320:Trgv7
|
APN |
13 |
19,362,249 (GRCm39) |
missense |
unknown |
|
IGL03178:Trgv7
|
APN |
13 |
19,362,211 (GRCm39) |
utr 5 prime |
probably benign |
|
R0069:Trgv7
|
UTSW |
13 |
19,362,592 (GRCm39) |
missense |
probably benign |
0.19 |
R3925:Trgv7
|
UTSW |
13 |
19,362,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Trgv7
|
UTSW |
13 |
19,362,558 (GRCm39) |
missense |
probably damaging |
0.97 |
R5085:Trgv7
|
UTSW |
13 |
19,362,598 (GRCm39) |
nonsense |
probably null |
|
R9456:Trgv7
|
UTSW |
13 |
19,362,385 (GRCm39) |
nonsense |
probably null |
|
|