Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
A |
G |
17: 84,989,453 (GRCm39) |
I85T |
probably damaging |
Het |
Amer2 |
A |
G |
14: 60,617,356 (GRCm39) |
D391G |
possibly damaging |
Het |
Atp13a3 |
A |
T |
16: 30,180,781 (GRCm39) |
C83S |
probably benign |
Het |
Bdh2 |
A |
T |
3: 134,994,080 (GRCm39) |
Q54L |
probably benign |
Het |
Cep128 |
A |
G |
12: 90,975,628 (GRCm39) |
S1051P |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,396,138 (GRCm39) |
T865A |
probably damaging |
Het |
Epha8 |
C |
A |
4: 136,658,360 (GRCm39) |
*1005L |
probably null |
Het |
Etl4 |
T |
C |
2: 20,811,493 (GRCm39) |
V1509A |
probably benign |
Het |
Gucy1b1 |
T |
C |
3: 81,953,833 (GRCm39) |
E161G |
possibly damaging |
Het |
Hepacam |
T |
A |
9: 37,291,912 (GRCm39) |
V80E |
probably damaging |
Het |
Ireb2 |
A |
G |
9: 54,772,641 (GRCm39) |
K24E |
probably benign |
Het |
Itch |
T |
A |
2: 155,014,467 (GRCm39) |
D101E |
possibly damaging |
Het |
Itch |
T |
A |
2: 155,014,406 (GRCm39) |
F81Y |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,390,373 (GRCm39) |
I115M |
probably damaging |
Het |
Klf7 |
C |
A |
1: 64,117,933 (GRCm39) |
Q221H |
probably benign |
Het |
Kptn |
A |
G |
7: 15,857,897 (GRCm39) |
T242A |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,334,485 (GRCm39) |
F4420S |
probably benign |
Het |
Mthfd2 |
A |
G |
6: 83,288,792 (GRCm39) |
|
probably null |
Het |
Mtrf1l |
A |
C |
10: 5,764,112 (GRCm39) |
L284V |
probably null |
Het |
Neb |
C |
T |
2: 52,060,561 (GRCm39) |
V2259I |
probably benign |
Het |
Or4c111 |
A |
T |
2: 88,843,814 (GRCm39) |
V198E |
possibly damaging |
Het |
Or9i14 |
A |
T |
19: 13,792,180 (GRCm39) |
M258K |
possibly damaging |
Het |
Padi1 |
A |
T |
4: 140,556,746 (GRCm39) |
C154S |
probably damaging |
Het |
Paxip1 |
T |
C |
5: 27,956,036 (GRCm39) |
T903A |
probably benign |
Het |
Phactr2 |
T |
A |
10: 13,129,181 (GRCm39) |
L292F |
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,362,796 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
C |
2: 24,940,985 (GRCm39) |
|
probably null |
Het |
Rif1 |
T |
A |
2: 52,002,555 (GRCm39) |
I2003K |
probably benign |
Het |
Rxfp3 |
A |
T |
15: 11,037,132 (GRCm39) |
V80E |
probably damaging |
Het |
Sart3 |
T |
A |
5: 113,883,709 (GRCm39) |
K768* |
probably null |
Het |
Slc35f5 |
C |
T |
1: 125,517,612 (GRCm39) |
T470I |
probably damaging |
Het |
Smg8 |
A |
T |
11: 86,971,102 (GRCm39) |
Y890N |
probably damaging |
Het |
Spata31 |
T |
C |
13: 65,068,968 (GRCm39) |
V372A |
possibly damaging |
Het |
Tbc1d30 |
A |
T |
10: 121,103,084 (GRCm39) |
D649E |
probably benign |
Het |
Tctn3 |
G |
A |
19: 40,600,581 (GRCm39) |
T3I |
probably damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,434,135 (GRCm39) |
*856C |
probably null |
Het |
Vmn2r61 |
A |
T |
7: 41,909,639 (GRCm39) |
I55F |
probably benign |
Het |
Zbtb41 |
C |
T |
1: 139,375,065 (GRCm39) |
P842S |
probably benign |
Het |
Zc3h13 |
A |
G |
14: 75,581,209 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tns3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Tns3
|
APN |
11 |
8,401,066 (GRCm39) |
missense |
probably benign |
0.42 |
IGL00822:Tns3
|
APN |
11 |
8,393,976 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01075:Tns3
|
APN |
11 |
8,428,399 (GRCm39) |
missense |
probably benign |
0.45 |
IGL01286:Tns3
|
APN |
11 |
8,442,617 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01680:Tns3
|
APN |
11 |
8,498,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01687:Tns3
|
APN |
11 |
8,442,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01734:Tns3
|
APN |
11 |
8,469,192 (GRCm39) |
splice site |
probably benign |
|
IGL01984:Tns3
|
APN |
11 |
8,498,992 (GRCm39) |
nonsense |
probably null |
|
IGL02137:Tns3
|
APN |
11 |
8,442,578 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02273:Tns3
|
APN |
11 |
8,384,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Tns3
|
APN |
11 |
8,387,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02697:Tns3
|
APN |
11 |
8,442,346 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02829:Tns3
|
APN |
11 |
8,469,564 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU74:Tns3
|
UTSW |
11 |
8,442,149 (GRCm39) |
missense |
probably benign |
0.38 |
R0020:Tns3
|
UTSW |
11 |
8,495,227 (GRCm39) |
critical splice donor site |
probably null |
|
R0064:Tns3
|
UTSW |
11 |
8,385,856 (GRCm39) |
nonsense |
probably null |
|
R0064:Tns3
|
UTSW |
11 |
8,385,856 (GRCm39) |
nonsense |
probably null |
|
R0370:Tns3
|
UTSW |
11 |
8,395,730 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0388:Tns3
|
UTSW |
11 |
8,395,703 (GRCm39) |
missense |
probably benign |
0.07 |
R0410:Tns3
|
UTSW |
11 |
8,385,852 (GRCm39) |
missense |
probably benign |
0.02 |
R0496:Tns3
|
UTSW |
11 |
8,497,262 (GRCm39) |
splice site |
probably benign |
|
R0562:Tns3
|
UTSW |
11 |
8,443,262 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0626:Tns3
|
UTSW |
11 |
8,443,121 (GRCm39) |
missense |
probably benign |
0.04 |
R0736:Tns3
|
UTSW |
11 |
8,469,474 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0893:Tns3
|
UTSW |
11 |
8,443,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1367:Tns3
|
UTSW |
11 |
8,398,704 (GRCm39) |
missense |
probably benign |
0.01 |
R1386:Tns3
|
UTSW |
11 |
8,468,261 (GRCm39) |
missense |
probably benign |
0.02 |
R1975:Tns3
|
UTSW |
11 |
8,385,738 (GRCm39) |
missense |
probably benign |
0.04 |
R2205:Tns3
|
UTSW |
11 |
8,481,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R2319:Tns3
|
UTSW |
11 |
8,491,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R2830:Tns3
|
UTSW |
11 |
8,385,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R3720:Tns3
|
UTSW |
11 |
8,442,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R3765:Tns3
|
UTSW |
11 |
8,401,133 (GRCm39) |
missense |
probably benign |
0.00 |
R3817:Tns3
|
UTSW |
11 |
8,384,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R4058:Tns3
|
UTSW |
11 |
8,442,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Tns3
|
UTSW |
11 |
8,481,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Tns3
|
UTSW |
11 |
8,401,119 (GRCm39) |
missense |
probably benign |
0.30 |
R4731:Tns3
|
UTSW |
11 |
8,400,986 (GRCm39) |
missense |
probably benign |
0.28 |
R4732:Tns3
|
UTSW |
11 |
8,400,986 (GRCm39) |
missense |
probably benign |
0.28 |
R4733:Tns3
|
UTSW |
11 |
8,400,986 (GRCm39) |
missense |
probably benign |
0.28 |
R5472:Tns3
|
UTSW |
11 |
8,401,092 (GRCm39) |
missense |
probably benign |
|
R5749:Tns3
|
UTSW |
11 |
8,401,177 (GRCm39) |
missense |
probably benign |
0.01 |
R5807:Tns3
|
UTSW |
11 |
8,443,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Tns3
|
UTSW |
11 |
8,384,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5942:Tns3
|
UTSW |
11 |
8,385,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Tns3
|
UTSW |
11 |
8,442,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R6025:Tns3
|
UTSW |
11 |
8,442,578 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6266:Tns3
|
UTSW |
11 |
8,442,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6322:Tns3
|
UTSW |
11 |
8,442,147 (GRCm39) |
missense |
probably benign |
0.01 |
R6536:Tns3
|
UTSW |
11 |
8,384,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R6577:Tns3
|
UTSW |
11 |
8,499,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R6577:Tns3
|
UTSW |
11 |
8,499,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6864:Tns3
|
UTSW |
11 |
8,443,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Tns3
|
UTSW |
11 |
8,481,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Tns3
|
UTSW |
11 |
8,387,251 (GRCm39) |
missense |
probably benign |
0.00 |
R7443:Tns3
|
UTSW |
11 |
8,401,442 (GRCm39) |
missense |
probably benign |
0.01 |
R7459:Tns3
|
UTSW |
11 |
8,442,793 (GRCm39) |
missense |
probably benign |
0.16 |
R7474:Tns3
|
UTSW |
11 |
8,480,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Tns3
|
UTSW |
11 |
8,491,192 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7979:Tns3
|
UTSW |
11 |
8,442,701 (GRCm39) |
missense |
probably benign |
0.01 |
R8055:Tns3
|
UTSW |
11 |
8,495,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Tns3
|
UTSW |
11 |
8,442,773 (GRCm39) |
missense |
probably benign |
|
R8077:Tns3
|
UTSW |
11 |
8,395,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Tns3
|
UTSW |
11 |
8,442,971 (GRCm39) |
missense |
probably damaging |
0.96 |
R8523:Tns3
|
UTSW |
11 |
8,398,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R8790:Tns3
|
UTSW |
11 |
8,468,273 (GRCm39) |
missense |
probably damaging |
0.99 |
R9228:Tns3
|
UTSW |
11 |
8,400,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R9374:Tns3
|
UTSW |
11 |
8,442,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Tns3
|
UTSW |
11 |
8,395,702 (GRCm39) |
missense |
probably damaging |
0.99 |
R9510:Tns3
|
UTSW |
11 |
8,395,702 (GRCm39) |
missense |
probably damaging |
0.99 |
R9594:Tns3
|
UTSW |
11 |
8,401,142 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9595:Tns3
|
UTSW |
11 |
8,401,142 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9596:Tns3
|
UTSW |
11 |
8,401,142 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9624:Tns3
|
UTSW |
11 |
8,401,142 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9629:Tns3
|
UTSW |
11 |
8,401,142 (GRCm39) |
missense |
possibly damaging |
0.79 |
T0975:Tns3
|
UTSW |
11 |
8,401,146 (GRCm39) |
missense |
probably benign |
0.00 |
T0975:Tns3
|
UTSW |
11 |
8,499,100 (GRCm39) |
start gained |
probably benign |
|
T0975:Tns3
|
UTSW |
11 |
8,429,518 (GRCm39) |
missense |
probably benign |
|
X0005:Tns3
|
UTSW |
11 |
8,429,518 (GRCm39) |
missense |
probably benign |
|
X0005:Tns3
|
UTSW |
11 |
8,401,224 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tns3
|
UTSW |
11 |
8,401,014 (GRCm39) |
nonsense |
probably null |
|
|