Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
C |
5: 113,331,692 (GRCm39) |
S841G |
probably benign |
Het |
4933427I04Rik |
G |
T |
4: 123,753,879 (GRCm39) |
|
probably benign |
Het |
Aak1 |
A |
G |
6: 86,921,399 (GRCm39) |
T199A |
probably damaging |
Het |
Acnat2 |
C |
A |
4: 49,380,254 (GRCm39) |
V375L |
probably benign |
Het |
Aldh1a7 |
T |
C |
19: 20,677,320 (GRCm39) |
T434A |
possibly damaging |
Het |
Aldh3a2 |
T |
C |
11: 61,156,088 (GRCm39) |
T63A |
probably benign |
Het |
Anxa2 |
T |
C |
9: 69,391,103 (GRCm39) |
S97P |
probably damaging |
Het |
Apip |
T |
C |
2: 102,922,191 (GRCm39) |
S186P |
probably benign |
Het |
Apob |
A |
G |
12: 8,061,049 (GRCm39) |
K3177R |
probably benign |
Het |
Atm |
C |
T |
9: 53,429,859 (GRCm39) |
W392* |
probably null |
Het |
Atp8b1 |
T |
A |
18: 64,679,161 (GRCm39) |
R773S |
probably benign |
Het |
Bicdl2 |
T |
A |
17: 23,885,718 (GRCm39) |
|
probably null |
Het |
Bltp1 |
C |
T |
3: 37,042,234 (GRCm39) |
T2740I |
possibly damaging |
Het |
Cacng3 |
G |
A |
7: 122,361,547 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
G |
T |
3: 144,455,450 (GRCm39) |
L448M |
probably damaging |
Het |
Clk4 |
A |
G |
11: 51,166,401 (GRCm39) |
I94M |
possibly damaging |
Het |
Cnot3 |
G |
T |
7: 3,654,918 (GRCm39) |
V124F |
probably damaging |
Het |
Cyp4a30b |
C |
T |
4: 115,318,571 (GRCm39) |
A426V |
probably benign |
Het |
Dact1 |
T |
A |
12: 71,364,911 (GRCm39) |
L564* |
probably null |
Het |
Dnah8 |
T |
A |
17: 30,882,266 (GRCm39) |
|
probably null |
Het |
Dock5 |
T |
A |
14: 68,033,445 (GRCm39) |
T975S |
probably benign |
Het |
Dock8 |
C |
A |
19: 25,104,848 (GRCm39) |
H739Q |
probably damaging |
Het |
Efr3b |
T |
A |
12: 4,034,613 (GRCm39) |
N186Y |
probably damaging |
Het |
Enam |
G |
A |
5: 88,649,550 (GRCm39) |
G278D |
probably damaging |
Het |
Fgl2 |
A |
G |
5: 21,578,256 (GRCm39) |
D181G |
probably benign |
Het |
Jam3 |
G |
C |
9: 27,013,276 (GRCm39) |
T98S |
probably benign |
Het |
Ltbp2 |
A |
T |
12: 84,834,184 (GRCm39) |
I1435N |
probably damaging |
Het |
Man2a1 |
G |
A |
17: 64,932,383 (GRCm39) |
A157T |
probably benign |
Het |
Mcm3ap |
T |
A |
10: 76,337,148 (GRCm39) |
V1361E |
probably benign |
Het |
Nobox |
A |
T |
6: 43,284,538 (GRCm39) |
L36Q |
possibly damaging |
Het |
Or2ag12 |
T |
A |
7: 106,277,100 (GRCm39) |
M198L |
probably benign |
Het |
Or51a10 |
A |
G |
7: 103,699,334 (GRCm39) |
S76P |
probably damaging |
Het |
Parp4 |
G |
A |
14: 56,857,947 (GRCm39) |
V860I |
probably benign |
Het |
Pim3 |
T |
A |
15: 88,747,296 (GRCm39) |
|
probably null |
Het |
Ptpn13 |
A |
T |
5: 103,713,121 (GRCm39) |
N1748I |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,145 (GRCm39) |
T356A |
possibly damaging |
Het |
Ranbp2 |
C |
T |
10: 58,293,559 (GRCm39) |
R310* |
probably null |
Het |
Rassf5 |
C |
T |
1: 131,109,988 (GRCm39) |
V190I |
probably benign |
Het |
Rgl1 |
T |
G |
1: 152,409,281 (GRCm39) |
Q481P |
probably damaging |
Het |
Rrp1b |
A |
G |
17: 32,276,063 (GRCm39) |
T537A |
probably benign |
Het |
Smok3c |
T |
A |
5: 138,063,699 (GRCm39) |
S395R |
probably benign |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Strn4 |
A |
T |
7: 16,556,978 (GRCm39) |
E145V |
probably damaging |
Het |
Tex21 |
T |
A |
12: 76,251,086 (GRCm39) |
|
probably null |
Het |
Usp37 |
G |
A |
1: 74,534,908 (GRCm39) |
R13* |
probably null |
Het |
Uty |
G |
T |
Y: 1,174,735 (GRCm39) |
L222I |
probably damaging |
Homo |
Wwp2 |
A |
G |
8: 108,267,314 (GRCm39) |
T309A |
probably damaging |
Het |
Zfp40 |
C |
T |
17: 23,395,510 (GRCm39) |
R359H |
possibly damaging |
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 |
|
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 |
R7236:Gfra3
|
UTSW |
18 |
34,828,884 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|