Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
A |
T |
1: 11,868,716 (GRCm39) |
D332V |
probably damaging |
Het |
Akr1c12 |
T |
C |
13: 4,326,322 (GRCm39) |
Y53C |
probably benign |
Het |
Arhgap23 |
T |
C |
11: 97,383,498 (GRCm39) |
|
probably benign |
Het |
AU040320 |
T |
C |
4: 126,710,276 (GRCm39) |
|
probably benign |
Het |
B4galnt2 |
A |
G |
11: 95,782,767 (GRCm39) |
L15P |
probably benign |
Het |
Cadps2 |
A |
G |
6: 23,583,472 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dppa4 |
T |
C |
16: 48,113,343 (GRCm39) |
F244S |
possibly damaging |
Het |
Exoc1 |
A |
G |
5: 76,702,035 (GRCm39) |
K445R |
probably benign |
Het |
Fgf12 |
A |
T |
16: 27,981,202 (GRCm39) |
N171K |
possibly damaging |
Het |
Fyb2 |
G |
A |
4: 104,852,903 (GRCm39) |
V528M |
possibly damaging |
Het |
Ghr |
A |
G |
15: 3,349,337 (GRCm39) |
S614P |
probably damaging |
Het |
Gm10985 |
A |
C |
3: 53,752,674 (GRCm39) |
Y19S |
probably damaging |
Het |
Gpr152 |
T |
A |
19: 4,193,554 (GRCm39) |
V365D |
possibly damaging |
Het |
Guca1a |
A |
G |
17: 47,706,637 (GRCm39) |
|
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,310,997 (GRCm39) |
G1079D |
probably benign |
Het |
Hnrnpm |
T |
C |
17: 33,868,687 (GRCm39) |
D580G |
probably damaging |
Het |
Ints6 |
A |
T |
14: 62,945,147 (GRCm39) |
D394E |
probably damaging |
Het |
Kat6b |
T |
A |
14: 21,672,108 (GRCm39) |
Y339* |
probably null |
Het |
Kcnj11 |
C |
A |
7: 45,749,285 (GRCm39) |
V13L |
probably benign |
Het |
Lama3 |
C |
T |
18: 12,554,191 (GRCm39) |
|
probably benign |
Het |
Mtrex |
A |
G |
13: 113,050,876 (GRCm39) |
|
probably benign |
Het |
Myo18a |
A |
G |
11: 77,709,473 (GRCm39) |
T161A |
probably benign |
Het |
Ncapg |
G |
T |
5: 45,857,261 (GRCm39) |
S991I |
possibly damaging |
Het |
Nrde2 |
G |
A |
12: 100,116,069 (GRCm39) |
|
probably benign |
Het |
Or4c127 |
T |
A |
2: 89,832,822 (GRCm39) |
I24N |
probably benign |
Het |
Or5d18 |
T |
C |
2: 87,864,602 (GRCm39) |
R294G |
probably damaging |
Het |
Pcdhb7 |
A |
T |
18: 37,476,927 (GRCm39) |
T688S |
probably damaging |
Het |
Pla2g6 |
T |
C |
15: 79,190,635 (GRCm39) |
D309G |
probably benign |
Het |
Plod1 |
A |
T |
4: 148,005,584 (GRCm39) |
V404D |
probably damaging |
Het |
Ppp2r2a |
G |
T |
14: 67,266,447 (GRCm39) |
Y71* |
probably null |
Het |
Prcp |
A |
G |
7: 92,566,954 (GRCm39) |
N222S |
probably benign |
Het |
Rad21 |
T |
C |
15: 51,833,532 (GRCm39) |
T316A |
possibly damaging |
Het |
Ranbp2 |
T |
C |
10: 58,319,034 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
C |
A |
2: 72,038,492 (GRCm39) |
P548T |
possibly damaging |
Het |
Ric1 |
G |
T |
19: 29,555,135 (GRCm39) |
M416I |
probably benign |
Het |
Slc9a8 |
T |
C |
2: 167,266,041 (GRCm39) |
F6S |
probably benign |
Het |
Smpdl3a |
T |
G |
10: 57,678,575 (GRCm39) |
I126S |
probably null |
Het |
Sphkap |
A |
T |
1: 83,268,698 (GRCm39) |
L98Q |
probably damaging |
Het |
Spink4 |
T |
G |
4: 40,924,974 (GRCm39) |
|
probably benign |
Het |
Taar5 |
A |
T |
10: 23,847,605 (GRCm39) |
L334F |
probably damaging |
Het |
Tecta |
A |
T |
9: 42,289,203 (GRCm39) |
I454K |
probably benign |
Het |
Ttc7 |
C |
T |
17: 87,654,006 (GRCm39) |
T561M |
possibly damaging |
Het |
Vmn2r9 |
G |
T |
5: 108,995,440 (GRCm39) |
H403N |
probably damaging |
Het |
Zdbf2 |
G |
A |
1: 63,342,161 (GRCm39) |
C180Y |
possibly damaging |
Het |
|
Other mutations in Fam47e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Fam47e
|
APN |
5 |
92,727,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Fam47e
|
UTSW |
5 |
92,726,317 (GRCm39) |
intron |
probably benign |
|
R1170:Fam47e
|
UTSW |
5 |
92,713,781 (GRCm39) |
splice site |
probably benign |
|
R1926:Fam47e
|
UTSW |
5 |
92,733,244 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3434:Fam47e
|
UTSW |
5 |
92,733,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R3435:Fam47e
|
UTSW |
5 |
92,733,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R4899:Fam47e
|
UTSW |
5 |
92,722,528 (GRCm39) |
missense |
probably benign |
0.23 |
R4925:Fam47e
|
UTSW |
5 |
92,733,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R5885:Fam47e
|
UTSW |
5 |
92,713,827 (GRCm39) |
missense |
probably damaging |
0.97 |
R6060:Fam47e
|
UTSW |
5 |
92,727,472 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6278:Fam47e
|
UTSW |
5 |
92,710,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Fam47e
|
UTSW |
5 |
92,713,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7661:Fam47e
|
UTSW |
5 |
92,735,384 (GRCm39) |
missense |
probably damaging |
0.97 |
R7992:Fam47e
|
UTSW |
5 |
92,722,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8349:Fam47e
|
UTSW |
5 |
92,702,990 (GRCm39) |
missense |
probably benign |
0.27 |
R8449:Fam47e
|
UTSW |
5 |
92,702,990 (GRCm39) |
missense |
probably benign |
0.27 |
R9058:Fam47e
|
UTSW |
5 |
92,719,367 (GRCm39) |
start gained |
probably benign |
|
R9260:Fam47e
|
UTSW |
5 |
92,735,384 (GRCm39) |
missense |
probably damaging |
0.97 |
R9595:Fam47e
|
UTSW |
5 |
92,726,395 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Fam47e
|
UTSW |
5 |
92,726,395 (GRCm39) |
missense |
probably benign |
0.00 |
R9624:Fam47e
|
UTSW |
5 |
92,726,395 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Fam47e
|
UTSW |
5 |
92,727,527 (GRCm39) |
missense |
possibly damaging |
0.86 |
|