Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
T |
C |
15: 91,033,232 (GRCm39) |
D728G |
probably benign |
Het |
Adig |
A |
T |
2: 158,347,727 (GRCm39) |
D48V |
probably damaging |
Het |
Adig |
A |
C |
2: 158,349,890 (GRCm39) |
*57S |
probably null |
Het |
Amigo3 |
A |
G |
9: 107,932,020 (GRCm39) |
D481G |
probably damaging |
Het |
Atf6b |
T |
A |
17: 34,872,968 (GRCm39) |
M628K |
probably damaging |
Het |
Atoh8 |
A |
G |
6: 72,212,129 (GRCm39) |
L7P |
probably damaging |
Het |
Bcl9 |
A |
G |
3: 97,115,959 (GRCm39) |
S912P |
probably damaging |
Het |
Card9 |
T |
A |
2: 26,247,310 (GRCm39) |
I280F |
probably damaging |
Het |
Ccr9 |
A |
G |
9: 123,609,085 (GRCm39) |
T256A |
probably benign |
Het |
Cd300lg |
T |
C |
11: 101,939,590 (GRCm39) |
I306T |
probably damaging |
Het |
Cfap65 |
T |
A |
1: 74,960,769 (GRCm39) |
M734L |
probably benign |
Het |
Cobll1 |
A |
G |
2: 64,929,356 (GRCm39) |
S657P |
probably damaging |
Het |
Comp |
A |
G |
8: 70,831,285 (GRCm39) |
N384S |
probably damaging |
Het |
Cps1 |
T |
A |
1: 67,191,445 (GRCm39) |
V209D |
possibly damaging |
Het |
Cwc22 |
A |
T |
2: 77,759,803 (GRCm39) |
D81E |
possibly damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,167,512 (GRCm39) |
P1030L |
possibly damaging |
Het |
Dcn |
A |
G |
10: 97,343,637 (GRCm39) |
Y199C |
probably damaging |
Het |
Exosc3 |
A |
T |
4: 45,316,969 (GRCm39) |
I228N |
probably damaging |
Het |
Fbxo21 |
T |
A |
5: 118,146,108 (GRCm39) |
I577N |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,447,815 (GRCm39) |
Q1206L |
probably benign |
Het |
Fubp3 |
T |
C |
2: 31,503,056 (GRCm39) |
F480L |
probably benign |
Het |
Fzd5 |
T |
C |
1: 64,775,110 (GRCm39) |
N217S |
possibly damaging |
Het |
Garem1 |
G |
A |
18: 21,281,274 (GRCm39) |
R361C |
probably damaging |
Het |
Gcg |
T |
C |
2: 62,306,133 (GRCm39) |
M155V |
probably null |
Het |
Gm7298 |
G |
A |
6: 121,756,604 (GRCm39) |
|
probably benign |
Het |
Gpr160 |
T |
A |
3: 30,950,038 (GRCm39) |
L37I |
probably benign |
Het |
Grik1 |
G |
A |
16: 87,848,379 (GRCm39) |
H130Y |
|
Het |
Hydin |
T |
A |
8: 111,233,580 (GRCm39) |
I1806N |
probably damaging |
Het |
Isl1 |
A |
T |
13: 116,444,902 (GRCm39) |
C42* |
probably null |
Het |
Itpr2 |
T |
C |
6: 146,226,529 (GRCm39) |
D1405G |
probably damaging |
Het |
Kat6b |
A |
G |
14: 21,711,551 (GRCm39) |
N682D |
probably benign |
Het |
Kcnh6 |
C |
G |
11: 105,924,860 (GRCm39) |
H941Q |
possibly damaging |
Het |
Kprp |
A |
C |
3: 92,733,000 (GRCm39) |
C17G |
probably damaging |
Het |
Lsm14a |
T |
C |
7: 34,088,225 (GRCm39) |
|
probably benign |
Het |
Mrgpra2a |
G |
T |
7: 47,076,307 (GRCm39) |
T317K |
probably benign |
Het |
Myh11 |
A |
G |
16: 14,054,283 (GRCm39) |
V360A |
|
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Oaf |
G |
A |
9: 43,133,966 (GRCm39) |
P252S |
probably benign |
Het |
Obox2 |
T |
G |
7: 15,131,290 (GRCm39) |
V132G |
unknown |
Het |
Or51v8 |
T |
A |
7: 103,319,633 (GRCm39) |
T202S |
probably benign |
Het |
Or52b1 |
A |
G |
7: 104,978,646 (GRCm39) |
L251P |
probably damaging |
Het |
Or5b109 |
C |
T |
19: 13,212,268 (GRCm39) |
S218L |
probably damaging |
Het |
Or5b12 |
T |
C |
19: 12,897,446 (GRCm39) |
T76A |
possibly damaging |
Het |
Pld2 |
T |
A |
11: 70,448,234 (GRCm39) |
S894T |
probably benign |
Het |
Plxna1 |
G |
T |
6: 89,296,364 (GRCm39) |
S1893R |
possibly damaging |
Het |
Prkd1 |
T |
C |
12: 50,472,232 (GRCm39) |
E227G |
possibly damaging |
Het |
Prox1 |
T |
C |
1: 189,893,242 (GRCm39) |
N401S |
possibly damaging |
Het |
Prune2 |
T |
C |
19: 17,095,690 (GRCm39) |
V398A |
possibly damaging |
Het |
Rasgef1a |
A |
G |
6: 118,063,223 (GRCm39) |
N285D |
probably benign |
Het |
Rbbp5 |
A |
G |
1: 132,420,304 (GRCm39) |
K179R |
probably benign |
Het |
Rp9 |
G |
A |
9: 22,379,573 (GRCm39) |
|
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,574,090 (GRCm39) |
F588L |
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,880,977 (GRCm39) |
D415E |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 4,990,901 (GRCm39) |
K593E |
probably benign |
Het |
Tab1 |
A |
G |
15: 80,041,904 (GRCm39) |
T341A |
probably benign |
Het |
Tmc4 |
T |
C |
7: 3,670,552 (GRCm39) |
E513G |
probably damaging |
Het |
Tmem131l |
A |
C |
3: 83,848,244 (GRCm39) |
V302G |
probably damaging |
Het |
Tnip1 |
G |
A |
11: 54,807,783 (GRCm39) |
H553Y |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,021,478 (GRCm39) |
P1048S |
probably damaging |
Het |
Twsg1 |
C |
T |
17: 66,233,306 (GRCm39) |
V215I |
probably damaging |
Het |
Txnl1 |
G |
A |
18: 63,825,325 (GRCm39) |
|
probably benign |
Het |
Unc13c |
A |
G |
9: 73,839,862 (GRCm39) |
Y330H |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,509,707 (GRCm39) |
W2422R |
probably damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,837,721 (GRCm39) |
D727E |
probably damaging |
Het |
Vmn2r59 |
G |
T |
7: 41,695,286 (GRCm39) |
C375* |
probably null |
Het |
Vopp1 |
G |
T |
6: 57,731,575 (GRCm39) |
Q139K |
possibly damaging |
Het |
Vwa5b1 |
T |
C |
4: 138,316,005 (GRCm39) |
D579G |
probably damaging |
Het |
Wdr6 |
A |
G |
9: 108,450,691 (GRCm39) |
Y971H |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,706,059 (GRCm39) |
F339L |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,317,610 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Fbxo10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Fbxo10
|
APN |
4 |
45,058,684 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02073:Fbxo10
|
APN |
4 |
45,046,349 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02097:Fbxo10
|
APN |
4 |
45,048,527 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02315:Fbxo10
|
APN |
4 |
45,062,469 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02403:Fbxo10
|
APN |
4 |
45,062,517 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02408:Fbxo10
|
APN |
4 |
45,058,361 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02496:Fbxo10
|
APN |
4 |
45,043,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02583:Fbxo10
|
APN |
4 |
45,044,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Fbxo10
|
APN |
4 |
45,041,928 (GRCm39) |
missense |
probably benign |
0.20 |
N/A - 287:Fbxo10
|
UTSW |
4 |
45,044,708 (GRCm39) |
splice site |
probably benign |
|
R1033:Fbxo10
|
UTSW |
4 |
45,062,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Fbxo10
|
UTSW |
4 |
45,043,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1583:Fbxo10
|
UTSW |
4 |
45,062,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Fbxo10
|
UTSW |
4 |
45,042,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1789:Fbxo10
|
UTSW |
4 |
45,046,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R2187:Fbxo10
|
UTSW |
4 |
45,058,531 (GRCm39) |
missense |
probably benign |
0.09 |
R2191:Fbxo10
|
UTSW |
4 |
45,044,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R2377:Fbxo10
|
UTSW |
4 |
45,044,719 (GRCm39) |
missense |
probably benign |
0.18 |
R2425:Fbxo10
|
UTSW |
4 |
45,051,642 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2495:Fbxo10
|
UTSW |
4 |
45,040,545 (GRCm39) |
missense |
probably benign |
0.00 |
R4105:Fbxo10
|
UTSW |
4 |
45,059,054 (GRCm39) |
missense |
probably benign |
0.01 |
R4472:Fbxo10
|
UTSW |
4 |
45,043,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4480:Fbxo10
|
UTSW |
4 |
45,048,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Fbxo10
|
UTSW |
4 |
45,040,692 (GRCm39) |
missense |
probably benign |
0.33 |
R5193:Fbxo10
|
UTSW |
4 |
45,051,573 (GRCm39) |
nonsense |
probably null |
|
R5309:Fbxo10
|
UTSW |
4 |
45,042,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5312:Fbxo10
|
UTSW |
4 |
45,042,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5348:Fbxo10
|
UTSW |
4 |
45,058,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Fbxo10
|
UTSW |
4 |
45,035,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Fbxo10
|
UTSW |
4 |
45,058,760 (GRCm39) |
missense |
probably benign |
0.09 |
R5974:Fbxo10
|
UTSW |
4 |
45,040,631 (GRCm39) |
missense |
probably benign |
0.18 |
R5990:Fbxo10
|
UTSW |
4 |
45,061,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R6197:Fbxo10
|
UTSW |
4 |
45,043,857 (GRCm39) |
missense |
probably benign |
0.03 |
R6359:Fbxo10
|
UTSW |
4 |
45,041,796 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6808:Fbxo10
|
UTSW |
4 |
45,059,035 (GRCm39) |
missense |
probably benign |
0.00 |
R6873:Fbxo10
|
UTSW |
4 |
45,041,787 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6921:Fbxo10
|
UTSW |
4 |
45,044,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7089:Fbxo10
|
UTSW |
4 |
45,062,230 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7120:Fbxo10
|
UTSW |
4 |
45,040,533 (GRCm39) |
nonsense |
probably null |
|
R7498:Fbxo10
|
UTSW |
4 |
45,062,194 (GRCm39) |
missense |
probably benign |
0.04 |
R7872:Fbxo10
|
UTSW |
4 |
45,051,699 (GRCm39) |
missense |
not run |
|
R8022:Fbxo10
|
UTSW |
4 |
45,062,062 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8161:Fbxo10
|
UTSW |
4 |
45,044,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R8416:Fbxo10
|
UTSW |
4 |
45,058,942 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8419:Fbxo10
|
UTSW |
4 |
45,041,809 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8744:Fbxo10
|
UTSW |
4 |
45,043,880 (GRCm39) |
missense |
probably benign |
|
R8798:Fbxo10
|
UTSW |
4 |
45,051,605 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8887:Fbxo10
|
UTSW |
4 |
45,058,887 (GRCm39) |
missense |
probably benign |
|
R9548:Fbxo10
|
UTSW |
4 |
45,058,970 (GRCm39) |
missense |
probably damaging |
1.00 |
|