Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Amer3 |
A |
G |
1: 34,625,820 (GRCm39) |
K20E |
probably damaging |
Het |
Arhgap31 |
A |
G |
16: 38,421,818 (GRCm39) |
L1416P |
probably damaging |
Het |
Avpr1a |
G |
A |
10: 122,285,434 (GRCm39) |
C242Y |
probably damaging |
Het |
Bclaf3 |
T |
C |
X: 158,336,415 (GRCm39) |
Y281H |
probably benign |
Het |
Cdc14a |
T |
A |
3: 116,068,361 (GRCm39) |
|
probably benign |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Cntn4 |
T |
C |
6: 106,595,239 (GRCm39) |
|
probably benign |
Het |
Cyp3a44 |
T |
A |
5: 145,731,149 (GRCm39) |
D217V |
possibly damaging |
Het |
Eprs1 |
A |
G |
1: 185,111,812 (GRCm39) |
E274G |
probably benign |
Het |
Ercc6l2 |
G |
T |
13: 63,995,268 (GRCm39) |
Q354H |
probably null |
Het |
Glb1l |
A |
T |
1: 75,177,882 (GRCm39) |
I392N |
probably damaging |
Het |
Gm3173 |
T |
C |
14: 15,728,472 (GRCm39) |
|
probably null |
Het |
Hadh |
C |
T |
3: 131,034,640 (GRCm39) |
V219M |
probably damaging |
Het |
Hspb9 |
A |
G |
11: 100,604,761 (GRCm39) |
H29R |
possibly damaging |
Het |
Iqgap3 |
G |
T |
3: 88,017,429 (GRCm39) |
V240L |
probably benign |
Het |
Jmjd1c |
T |
C |
10: 67,062,494 (GRCm39) |
S1616P |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,907,461 (GRCm39) |
I1662V |
probably benign |
Het |
Maco1 |
A |
T |
4: 134,560,608 (GRCm39) |
V125E |
probably damaging |
Het |
Mapre3 |
A |
G |
5: 31,022,240 (GRCm39) |
I236V |
probably benign |
Het |
Med17 |
T |
C |
9: 15,190,917 (GRCm39) |
E58G |
probably benign |
Het |
Myh6 |
T |
C |
14: 55,189,749 (GRCm39) |
E1099G |
probably damaging |
Het |
Myt1 |
T |
A |
2: 181,439,522 (GRCm39) |
V348D |
probably damaging |
Het |
Nat10 |
A |
T |
2: 103,573,393 (GRCm39) |
I368N |
probably damaging |
Het |
Nol6 |
T |
C |
4: 41,118,205 (GRCm39) |
I811V |
probably benign |
Het |
Oas1d |
C |
A |
5: 121,057,127 (GRCm39) |
Y244* |
probably null |
Het |
Or6e1 |
A |
T |
14: 54,520,181 (GRCm39) |
M57K |
probably damaging |
Het |
Osbpl1a |
A |
G |
18: 13,038,132 (GRCm39) |
V273A |
probably benign |
Het |
Pigw |
T |
C |
11: 84,768,769 (GRCm39) |
R187G |
probably benign |
Het |
Plekhg5 |
G |
A |
4: 152,192,953 (GRCm39) |
D603N |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,456,414 (GRCm39) |
V1058A |
probably damaging |
Het |
Robo4 |
G |
A |
9: 37,317,296 (GRCm39) |
S537N |
probably benign |
Het |
Rptn |
T |
A |
3: 93,304,489 (GRCm39) |
F607L |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,759,972 (GRCm39) |
V44A |
probably damaging |
Het |
Sh3bp4 |
C |
A |
1: 89,071,682 (GRCm39) |
Q177K |
probably benign |
Het |
Skic3 |
T |
A |
13: 76,303,581 (GRCm39) |
L1225* |
probably null |
Het |
Spmip6 |
T |
A |
4: 41,511,433 (GRCm39) |
E93D |
probably damaging |
Het |
Srrt |
C |
A |
5: 137,294,569 (GRCm39) |
G779V |
probably damaging |
Het |
Tamalin |
A |
G |
15: 101,126,777 (GRCm39) |
|
probably benign |
Het |
Vmn1r10 |
A |
G |
6: 57,090,821 (GRCm39) |
S138G |
possibly damaging |
Het |
Yars2 |
C |
T |
16: 16,124,406 (GRCm39) |
R338* |
probably null |
Het |
Zfp454 |
T |
C |
11: 50,765,033 (GRCm39) |
E22G |
probably benign |
Het |
Zzef1 |
T |
A |
11: 72,765,795 (GRCm39) |
C1441S |
probably benign |
Het |
|
Other mutations in Tex21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00472:Tex21
|
APN |
12 |
76,253,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00923:Tex21
|
APN |
12 |
76,291,885 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01063:Tex21
|
APN |
12 |
76,245,592 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02624:Tex21
|
APN |
12 |
76,261,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Tex21
|
APN |
12 |
76,268,365 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03387:Tex21
|
APN |
12 |
76,245,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Tex21
|
APN |
12 |
76,291,780 (GRCm39) |
critical splice donor site |
probably null |
|
ihop
|
UTSW |
12 |
76,286,229 (GRCm39) |
critical splice donor site |
probably null |
|
R0189:Tex21
|
UTSW |
12 |
76,286,307 (GRCm39) |
missense |
probably benign |
0.13 |
R0730:Tex21
|
UTSW |
12 |
76,250,940 (GRCm39) |
missense |
probably benign |
0.25 |
R1521:Tex21
|
UTSW |
12 |
76,251,044 (GRCm39) |
missense |
probably benign |
0.38 |
R1572:Tex21
|
UTSW |
12 |
76,253,665 (GRCm39) |
missense |
probably benign |
0.03 |
R1700:Tex21
|
UTSW |
12 |
76,268,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R1941:Tex21
|
UTSW |
12 |
76,268,458 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4654:Tex21
|
UTSW |
12 |
76,263,860 (GRCm39) |
missense |
probably benign |
0.32 |
R4943:Tex21
|
UTSW |
12 |
76,268,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Tex21
|
UTSW |
12 |
76,245,707 (GRCm39) |
missense |
probably benign |
0.00 |
R6262:Tex21
|
UTSW |
12 |
76,259,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R6738:Tex21
|
UTSW |
12 |
76,286,283 (GRCm39) |
missense |
probably benign |
0.12 |
R6759:Tex21
|
UTSW |
12 |
76,251,086 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6890:Tex21
|
UTSW |
12 |
76,286,229 (GRCm39) |
critical splice donor site |
probably null |
|
R8910:Tex21
|
UTSW |
12 |
76,263,533 (GRCm39) |
unclassified |
probably benign |
|
R9547:Tex21
|
UTSW |
12 |
76,253,591 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Tex21
|
UTSW |
12 |
76,250,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|