Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn3 |
C |
T |
19: 4,921,644 (GRCm39) |
V179I |
probably benign |
Het |
Adra1b |
A |
G |
11: 43,667,151 (GRCm39) |
I362T |
possibly damaging |
Het |
B3galnt1 |
T |
C |
3: 69,482,950 (GRCm39) |
K104E |
probably benign |
Het |
Bnc2 |
T |
C |
4: 84,474,101 (GRCm39) |
Y15C |
probably benign |
Het |
C2cd2l |
C |
A |
9: 44,228,960 (GRCm39) |
A124S |
possibly damaging |
Het |
Camsap3 |
T |
A |
8: 3,654,116 (GRCm39) |
F595L |
probably damaging |
Het |
Cct2 |
A |
T |
10: 116,897,464 (GRCm39) |
D93E |
probably benign |
Het |
Cd200l2 |
A |
T |
16: 45,348,030 (GRCm39) |
I169N |
possibly damaging |
Het |
Cemip |
A |
T |
7: 83,598,012 (GRCm39) |
|
probably null |
Het |
Ciapin1 |
T |
C |
8: 95,550,338 (GRCm39) |
T34A |
|
Het |
Dop1a |
G |
A |
9: 86,397,431 (GRCm39) |
V912I |
probably damaging |
Het |
Efcab3 |
A |
T |
11: 104,790,093 (GRCm39) |
Q2832L |
probably benign |
Het |
Eif3c |
T |
C |
7: 126,151,495 (GRCm39) |
T610A |
possibly damaging |
Het |
Ephb3 |
A |
G |
16: 21,033,231 (GRCm39) |
R106G |
probably damaging |
Het |
Ephx3 |
T |
A |
17: 32,404,328 (GRCm39) |
|
probably null |
Het |
Etv2 |
A |
T |
7: 30,334,455 (GRCm39) |
S93T |
probably benign |
Het |
Fbxo34 |
T |
A |
14: 47,767,841 (GRCm39) |
D451E |
probably benign |
Het |
Fmo9 |
A |
G |
1: 166,504,140 (GRCm39) |
F141L |
probably damaging |
Het |
Fryl |
T |
C |
5: 73,265,821 (GRCm39) |
K500R |
possibly damaging |
Het |
Gnptg |
T |
C |
17: 25,458,897 (GRCm39) |
N34S |
possibly damaging |
Het |
Golga5 |
T |
A |
12: 102,441,034 (GRCm39) |
|
probably null |
Het |
Herc2 |
G |
T |
7: 55,734,828 (GRCm39) |
L139F |
probably benign |
Het |
Ikzf2 |
T |
A |
1: 69,578,240 (GRCm39) |
N423I |
probably benign |
Het |
Il31ra |
A |
T |
13: 112,660,439 (GRCm39) |
*717R |
probably null |
Het |
Itga2 |
G |
T |
13: 115,014,227 (GRCm39) |
Q234K |
probably benign |
Het |
Kcnt1 |
A |
T |
2: 25,799,951 (GRCm39) |
|
probably null |
Het |
Kif19b |
G |
T |
5: 140,457,400 (GRCm39) |
A390S |
probably benign |
Het |
Man2a2 |
T |
C |
7: 80,018,653 (GRCm39) |
S69G |
probably damaging |
Het |
Mccc1 |
A |
G |
3: 36,037,944 (GRCm39) |
V294A |
probably benign |
Het |
Mphosph8 |
T |
A |
14: 56,911,754 (GRCm39) |
I259K |
possibly damaging |
Het |
Mrpl15 |
A |
T |
1: 4,846,711 (GRCm39) |
N288K |
probably benign |
Het |
Msantd2 |
T |
C |
9: 37,400,965 (GRCm39) |
W116R |
probably damaging |
Het |
Msantd5f9 |
G |
T |
4: 73,835,808 (GRCm39) |
L219M |
probably benign |
Het |
Mtmr10 |
T |
C |
7: 63,963,932 (GRCm39) |
|
probably benign |
Het |
Mylk |
A |
T |
16: 34,742,899 (GRCm39) |
D1137V |
probably damaging |
Het |
Nhsl1 |
A |
G |
10: 18,401,512 (GRCm39) |
K879E |
probably damaging |
Het |
Or8j3c |
A |
T |
2: 86,253,533 (GRCm39) |
C162* |
probably null |
Het |
Pak6 |
A |
G |
2: 118,523,909 (GRCm39) |
T355A |
probably benign |
Het |
Patj |
C |
T |
4: 98,299,294 (GRCm39) |
R139C |
probably damaging |
Het |
Pcdhb3 |
C |
T |
18: 37,434,505 (GRCm39) |
A157V |
probably damaging |
Het |
Phkg1 |
C |
A |
5: 129,895,802 (GRCm39) |
D150Y |
probably damaging |
Het |
Ppp2r5c |
C |
T |
12: 110,432,323 (GRCm39) |
S45L |
probably benign |
Het |
Prl4a1 |
A |
C |
13: 28,202,556 (GRCm39) |
T44P |
probably benign |
Het |
Ptpro |
G |
A |
6: 137,345,335 (GRCm39) |
V114M |
probably damaging |
Het |
Pwp1 |
A |
G |
10: 85,715,147 (GRCm39) |
N211S |
probably benign |
Het |
Ralgapb |
A |
G |
2: 158,282,747 (GRCm39) |
D504G |
probably benign |
Het |
Rock2 |
A |
T |
12: 16,979,003 (GRCm39) |
I98F |
probably damaging |
Het |
Senp6 |
G |
T |
9: 80,040,247 (GRCm39) |
V785L |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,672,609 (GRCm39) |
D319G |
probably benign |
Het |
Tas2r105 |
A |
T |
6: 131,663,723 (GRCm39) |
I235N |
probably damaging |
Het |
Tas2r110 |
A |
T |
6: 132,845,667 (GRCm39) |
M233L |
possibly damaging |
Het |
Tmem260 |
C |
T |
14: 48,746,647 (GRCm39) |
|
probably null |
Het |
Trank1 |
G |
T |
9: 111,202,142 (GRCm39) |
V1590L |
possibly damaging |
Het |
Tsc2 |
A |
T |
17: 24,842,568 (GRCm39) |
M286K |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,697,796 (GRCm39) |
T202A |
|
Het |
Ttyh1 |
A |
G |
7: 4,136,663 (GRCm39) |
N424D |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,263,502 (GRCm39) |
|
probably null |
Het |
Utp20 |
G |
T |
10: 88,585,204 (GRCm39) |
P2620Q |
probably benign |
Het |
Vmn1r45 |
A |
G |
6: 89,910,133 (GRCm39) |
M279T |
probably benign |
Het |
Vmn2r115 |
T |
A |
17: 23,578,576 (GRCm39) |
I683K |
probably benign |
Het |
Vmn2r34 |
T |
C |
7: 7,684,750 (GRCm39) |
K481E |
probably damaging |
Het |
Vmn2r54 |
T |
A |
7: 12,365,917 (GRCm39) |
H339L |
possibly damaging |
Het |
Vmn2r94 |
T |
A |
17: 18,477,811 (GRCm39) |
N200I |
possibly damaging |
Het |
Wdfy3 |
A |
G |
5: 101,984,074 (GRCm39) |
Y3493H |
probably damaging |
Het |
Wdr5b |
A |
G |
16: 35,862,208 (GRCm39) |
D109G |
possibly damaging |
Het |
Zfp286 |
A |
T |
11: 62,674,496 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gfra3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Gfra3
|
APN |
18 |
34,824,601 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01778:Gfra3
|
APN |
18 |
34,824,644 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02051:Gfra3
|
APN |
18 |
34,828,894 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0107:Gfra3
|
UTSW |
18 |
34,844,359 (GRCm39) |
missense |
probably benign |
0.04 |
R0573:Gfra3
|
UTSW |
18 |
34,824,668 (GRCm39) |
missense |
probably benign |
|
R1029:Gfra3
|
UTSW |
18 |
34,823,892 (GRCm39) |
missense |
probably benign |
0.01 |
R1870:Gfra3
|
UTSW |
18 |
34,844,373 (GRCm39) |
missense |
probably damaging |
0.97 |
R2512:Gfra3
|
UTSW |
18 |
34,837,564 (GRCm39) |
missense |
probably benign |
0.04 |
R4689:Gfra3
|
UTSW |
18 |
34,823,640 (GRCm39) |
missense |
unknown |
|
R4801:Gfra3
|
UTSW |
18 |
34,853,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R4802:Gfra3
|
UTSW |
18 |
34,853,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Gfra3
|
UTSW |
18 |
34,844,304 (GRCm39) |
missense |
probably benign |
0.00 |
R5824:Gfra3
|
UTSW |
18 |
34,844,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Gfra3
|
UTSW |
18 |
34,823,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Gfra3
|
UTSW |
18 |
34,837,582 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6228:Gfra3
|
UTSW |
18 |
34,828,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Gfra3
|
UTSW |
18 |
34,828,864 (GRCm39) |
frame shift |
probably null |
|
R6759:Gfra3
|
UTSW |
18 |
34,828,926 (GRCm39) |
nonsense |
probably null |
|
R6781:Gfra3
|
UTSW |
18 |
34,844,375 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6894:Gfra3
|
UTSW |
18 |
34,828,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7021:Gfra3
|
UTSW |
18 |
34,823,933 (GRCm39) |
missense |
probably benign |
0.00 |
R7232:Gfra3
|
UTSW |
18 |
34,844,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Gfra3
|
UTSW |
18 |
34,844,189 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8987:Gfra3
|
UTSW |
18 |
34,823,879 (GRCm39) |
missense |
probably benign |
0.14 |
R9329:Gfra3
|
UTSW |
18 |
34,837,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Gfra3
|
UTSW |
18 |
34,837,591 (GRCm39) |
missense |
probably benign |
0.00 |
|