Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkbh3 |
C |
A |
2: 93,826,706 (GRCm39) |
R165L |
possibly damaging |
Het |
Arap3 |
A |
G |
18: 38,120,855 (GRCm39) |
V730A |
possibly damaging |
Het |
Arcn1 |
A |
C |
9: 44,662,614 (GRCm39) |
I344S |
probably damaging |
Het |
Ascc3 |
A |
C |
10: 50,643,470 (GRCm39) |
D1807A |
possibly damaging |
Het |
Atp2b3 |
A |
G |
X: 72,585,811 (GRCm39) |
S615G |
probably benign |
Het |
Ccdc40 |
A |
G |
11: 119,128,904 (GRCm39) |
N450S |
probably benign |
Het |
Cep41 |
T |
C |
6: 30,658,867 (GRCm39) |
E160G |
probably benign |
Het |
Cxxc1 |
T |
C |
18: 74,354,254 (GRCm39) |
L654P |
probably damaging |
Het |
Dusp29 |
T |
A |
14: 21,753,123 (GRCm39) |
T8S |
probably damaging |
Het |
Gnb4 |
C |
T |
3: 32,645,374 (GRCm39) |
A106T |
probably benign |
Het |
Gosr1 |
T |
C |
11: 76,645,603 (GRCm39) |
N59S |
probably benign |
Het |
Itgav |
A |
G |
2: 83,622,283 (GRCm39) |
T622A |
probably benign |
Het |
Lamc2 |
A |
G |
1: 153,027,803 (GRCm39) |
I207T |
probably damaging |
Het |
Lce1c |
C |
A |
3: 92,587,845 (GRCm39) |
|
probably benign |
Het |
Mcm3ap |
G |
T |
10: 76,342,255 (GRCm39) |
D1583Y |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,453,563 (GRCm39) |
F220I |
possibly damaging |
Het |
Or14j2 |
A |
G |
17: 37,885,912 (GRCm39) |
V134A |
possibly damaging |
Het |
Or2ag16 |
A |
T |
7: 106,352,559 (GRCm39) |
F12Y |
probably damaging |
Het |
Plcb1 |
T |
G |
2: 135,062,779 (GRCm39) |
|
probably benign |
Het |
Polr3c |
G |
A |
3: 96,624,002 (GRCm39) |
T312M |
probably damaging |
Het |
Ppp4r3c2 |
T |
C |
X: 88,796,210 (GRCm39) |
V14A |
probably benign |
Het |
Ptpn12 |
G |
T |
5: 21,224,244 (GRCm39) |
D116E |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,174,569 (GRCm39) |
D747G |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,366,440 (GRCm39) |
|
probably null |
Het |
Slit3 |
T |
C |
11: 35,591,172 (GRCm39) |
V1328A |
probably benign |
Het |
Sucla2 |
C |
A |
14: 73,819,246 (GRCm39) |
S264Y |
probably benign |
Het |
Tbck |
A |
G |
3: 132,480,247 (GRCm39) |
T709A |
probably benign |
Het |
Tead1 |
C |
T |
7: 112,460,663 (GRCm39) |
A189V |
probably benign |
Het |
Tmem234 |
A |
G |
4: 129,494,896 (GRCm39) |
Q46R |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 63,868,881 (GRCm39) |
L395Q |
probably damaging |
Het |
Tti2 |
T |
A |
8: 31,645,942 (GRCm39) |
W419R |
probably damaging |
Het |
Vmn2r3 |
A |
T |
3: 64,194,816 (GRCm39) |
M34K |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,793,530 (GRCm39) |
|
probably benign |
Het |
Zfp521 |
A |
T |
18: 13,977,987 (GRCm39) |
Y809N |
probably benign |
Het |
|
Other mutations in Tagln3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00816:Tagln3
|
APN |
16 |
45,544,556 (GRCm39) |
nonsense |
probably null |
|
IGL02715:Tagln3
|
APN |
16 |
45,544,588 (GRCm39) |
missense |
probably benign |
|
R0619:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1118:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1119:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1865:Tagln3
|
UTSW |
16 |
45,532,013 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2111:Tagln3
|
UTSW |
16 |
45,531,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Tagln3
|
UTSW |
16 |
45,544,701 (GRCm39) |
start gained |
probably benign |
|
R6329:Tagln3
|
UTSW |
16 |
45,533,365 (GRCm39) |
missense |
probably benign |
0.03 |
R6857:Tagln3
|
UTSW |
16 |
45,544,599 (GRCm39) |
missense |
probably benign |
|
R6995:Tagln3
|
UTSW |
16 |
45,543,321 (GRCm39) |
missense |
probably benign |
0.01 |
R7398:Tagln3
|
UTSW |
16 |
45,543,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R8144:Tagln3
|
UTSW |
16 |
45,544,554 (GRCm39) |
missense |
probably benign |
0.00 |
R9678:Tagln3
|
UTSW |
16 |
45,544,605 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Tagln3
|
UTSW |
16 |
45,543,460 (GRCm39) |
missense |
probably benign |
|
|