Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
A |
T |
11: 23,467,378 (GRCm39) |
V85D |
probably benign |
Het |
Abcb8 |
A |
G |
5: 24,605,159 (GRCm39) |
N115S |
probably benign |
Het |
Appl1 |
C |
A |
14: 26,684,823 (GRCm39) |
L75F |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,100,760 (GRCm39) |
|
probably null |
Het |
Atp2c2 |
T |
A |
8: 120,479,801 (GRCm39) |
|
probably null |
Het |
Cfap54 |
T |
A |
10: 92,864,979 (GRCm39) |
I94F |
probably damaging |
Het |
Clasp1 |
A |
G |
1: 118,395,643 (GRCm39) |
I194V |
possibly damaging |
Het |
Crebbp |
A |
C |
16: 3,932,777 (GRCm39) |
D1000E |
probably benign |
Het |
Ctdnep1 |
C |
T |
11: 69,872,316 (GRCm39) |
R3W |
possibly damaging |
Het |
Dgkb |
T |
C |
12: 38,177,363 (GRCm39) |
V230A |
probably damaging |
Het |
Duoxa2 |
T |
C |
2: 122,129,633 (GRCm39) |
F38L |
possibly damaging |
Het |
Ecd |
T |
C |
14: 20,388,273 (GRCm39) |
S172G |
probably benign |
Het |
Endog |
G |
T |
2: 30,061,663 (GRCm39) |
|
probably benign |
Het |
Eqtn |
G |
A |
4: 94,813,193 (GRCm39) |
P131L |
possibly damaging |
Het |
Gabbr1 |
T |
A |
17: 37,367,767 (GRCm39) |
S290T |
possibly damaging |
Het |
Glt8d2 |
T |
A |
10: 82,487,282 (GRCm39) |
R319S |
possibly damaging |
Het |
Gm16686 |
A |
G |
4: 88,673,641 (GRCm39) |
|
probably benign |
Het |
Gm5709 |
A |
T |
3: 59,542,983 (GRCm39) |
|
noncoding transcript |
Het |
Gm7381 |
T |
C |
8: 3,892,161 (GRCm39) |
|
noncoding transcript |
Het |
Gorab |
T |
G |
1: 163,213,871 (GRCm39) |
D353A |
possibly damaging |
Het |
Gstm1 |
A |
G |
3: 107,924,720 (GRCm39) |
L20P |
probably damaging |
Het |
Hexim2 |
A |
G |
11: 103,029,884 (GRCm39) |
D312G |
probably benign |
Het |
Hfm1 |
A |
G |
5: 106,995,528 (GRCm39) |
|
probably null |
Het |
Mbd4 |
C |
A |
6: 115,827,679 (GRCm39) |
A66S |
probably benign |
Het |
Mmp27 |
T |
A |
9: 7,573,363 (GRCm39) |
W152R |
probably damaging |
Het |
Mogat1 |
A |
G |
1: 78,500,307 (GRCm39) |
T124A |
probably benign |
Het |
Mrps18b |
A |
T |
17: 36,225,236 (GRCm39) |
V102D |
probably damaging |
Het |
Or10g3b |
A |
T |
14: 52,586,776 (GRCm39) |
C242* |
probably null |
Het |
Peg10 |
T |
A |
6: 4,755,565 (GRCm39) |
M47K |
probably benign |
Het |
Plxnc1 |
T |
G |
10: 94,758,604 (GRCm39) |
Q364P |
probably benign |
Het |
Psd |
A |
T |
19: 46,304,528 (GRCm39) |
|
probably null |
Het |
Rims1 |
T |
G |
1: 22,522,289 (GRCm39) |
I470L |
possibly damaging |
Het |
Sbsn |
T |
C |
7: 30,452,542 (GRCm39) |
V519A |
possibly damaging |
Het |
Senp1 |
A |
G |
15: 97,964,377 (GRCm39) |
V279A |
probably benign |
Het |
Sfxn5 |
T |
A |
6: 85,309,582 (GRCm39) |
|
probably benign |
Het |
Slc6a13 |
T |
A |
6: 121,313,032 (GRCm39) |
M483K |
probably damaging |
Het |
Slc6a21 |
G |
A |
7: 44,931,966 (GRCm39) |
|
probably null |
Het |
Slco6c1 |
T |
C |
1: 97,053,481 (GRCm39) |
Y140C |
probably damaging |
Het |
Spata32 |
A |
G |
11: 103,100,122 (GRCm39) |
S128P |
probably damaging |
Het |
Spty2d1 |
G |
T |
7: 46,647,633 (GRCm39) |
T432K |
possibly damaging |
Het |
Stx8 |
A |
G |
11: 67,911,792 (GRCm39) |
Q170R |
probably benign |
Het |
Sytl3 |
G |
A |
17: 6,982,879 (GRCm39) |
V112I |
probably benign |
Het |
Tdrkh |
A |
G |
3: 94,336,019 (GRCm39) |
I420V |
probably benign |
Het |
Tmem117 |
T |
C |
15: 94,992,711 (GRCm39) |
V457A |
probably benign |
Het |
Trpc2 |
GTGTCCTA |
GTGTCCTATGTCCTA |
7: 101,744,420 (GRCm39) |
|
probably null |
Het |
Tsen54 |
A |
G |
11: 115,706,048 (GRCm39) |
E90G |
probably benign |
Het |
Ugt1a2 |
A |
T |
1: 88,128,968 (GRCm39) |
M204L |
probably damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,567,972 (GRCm39) |
I32F |
probably benign |
Het |
Xkr6 |
T |
C |
14: 64,056,833 (GRCm39) |
V248A |
unknown |
Het |
Zfhx4 |
C |
A |
3: 5,308,067 (GRCm39) |
S431Y |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,723,180 (GRCm39) |
S1728T |
possibly damaging |
Het |
Zfp563 |
T |
C |
17: 33,308,540 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tpk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0084:Tpk1
|
UTSW |
6 |
43,323,763 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1736:Tpk1
|
UTSW |
6 |
43,588,284 (GRCm39) |
missense |
probably benign |
0.09 |
R2348:Tpk1
|
UTSW |
6 |
43,323,778 (GRCm39) |
missense |
probably damaging |
0.97 |
R4664:Tpk1
|
UTSW |
6 |
43,588,269 (GRCm39) |
missense |
probably benign |
0.08 |
R4804:Tpk1
|
UTSW |
6 |
43,570,012 (GRCm39) |
intron |
probably benign |
|
R5172:Tpk1
|
UTSW |
6 |
43,536,951 (GRCm39) |
splice site |
probably null |
|
R5230:Tpk1
|
UTSW |
6 |
43,400,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Tpk1
|
UTSW |
6 |
43,400,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Tpk1
|
UTSW |
6 |
43,400,635 (GRCm39) |
missense |
probably benign |
0.00 |
R6326:Tpk1
|
UTSW |
6 |
43,323,736 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6460:Tpk1
|
UTSW |
6 |
43,445,961 (GRCm39) |
missense |
probably benign |
0.01 |
R6767:Tpk1
|
UTSW |
6 |
43,323,727 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8061:Tpk1
|
UTSW |
6 |
43,323,778 (GRCm39) |
missense |
probably damaging |
0.97 |
R8120:Tpk1
|
UTSW |
6 |
43,445,930 (GRCm39) |
splice site |
probably null |
|
R8308:Tpk1
|
UTSW |
6 |
43,642,711 (GRCm39) |
missense |
probably benign |
0.14 |
R9335:Tpk1
|
UTSW |
6 |
43,446,084 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9468:Tpk1
|
UTSW |
6 |
43,536,901 (GRCm39) |
missense |
probably benign |
0.18 |
|