Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
T |
C |
19: 55,268,924 (GRCm39) |
V195A |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,452,466 (GRCm39) |
M211V |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,994,098 (GRCm39) |
M5127I |
probably benign |
Het |
Akr1c13 |
T |
C |
13: 4,244,111 (GRCm39) |
Y55H |
probably damaging |
Het |
Ap3d1 |
A |
T |
10: 80,544,313 (GRCm39) |
H1161Q |
probably benign |
Het |
Armh3 |
A |
T |
19: 45,922,307 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
C |
T |
6: 113,750,349 (GRCm39) |
R625H |
probably damaging |
Het |
Bdnf |
G |
A |
2: 109,554,463 (GRCm39) |
C239Y |
probably damaging |
Het |
Bpifa5 |
G |
T |
2: 154,007,539 (GRCm39) |
|
probably null |
Het |
C9 |
T |
A |
15: 6,516,243 (GRCm39) |
F349I |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,927,975 (GRCm39) |
V1170A |
possibly damaging |
Het |
Celsr1 |
A |
G |
15: 85,815,477 (GRCm39) |
V1846A |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,190,652 (GRCm39) |
L120H |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Cpne1 |
G |
T |
2: 155,919,339 (GRCm39) |
Q343K |
probably benign |
Het |
Dlc1 |
A |
T |
8: 37,405,702 (GRCm39) |
I29K |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,786,827 (GRCm39) |
D3602G |
possibly damaging |
Het |
Dock1 |
A |
G |
7: 134,475,879 (GRCm39) |
S885G |
probably benign |
Het |
Evpl |
T |
A |
11: 116,118,549 (GRCm39) |
Q686L |
probably damaging |
Het |
Gli1 |
A |
T |
10: 127,168,446 (GRCm39) |
M469K |
probably damaging |
Het |
Grin2c |
G |
A |
11: 115,141,472 (GRCm39) |
P882L |
probably damaging |
Het |
H2-Ob |
C |
T |
17: 34,461,588 (GRCm39) |
T109I |
probably damaging |
Het |
Jpt2 |
C |
A |
17: 25,167,647 (GRCm39) |
A101S |
probably benign |
Het |
Krt1c |
A |
G |
15: 101,724,932 (GRCm39) |
V226A |
probably damaging |
Het |
Lamc1 |
T |
G |
1: 153,110,341 (GRCm39) |
Q1111H |
probably damaging |
Het |
Lamc1 |
T |
C |
1: 153,110,358 (GRCm39) |
S1106G |
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,110,326 (GRCm39) |
Q1116H |
possibly damaging |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,411,155 (GRCm39) |
D1399E |
probably benign |
Het |
Ltbp4 |
G |
T |
7: 27,024,485 (GRCm39) |
P715Q |
probably damaging |
Het |
Mtor |
T |
C |
4: 148,547,367 (GRCm39) |
V450A |
probably benign |
Het |
Muc6 |
G |
A |
7: 141,223,981 (GRCm39) |
|
probably benign |
Het |
Myom1 |
A |
T |
17: 71,428,131 (GRCm39) |
I1450F |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,420,274 (GRCm39) |
I1332T |
possibly damaging |
Het |
Ncstn |
A |
G |
1: 171,899,072 (GRCm39) |
V353A |
possibly damaging |
Het |
Nt5c3 |
T |
C |
6: 56,863,734 (GRCm39) |
T149A |
probably benign |
Het |
Or5ac21 |
A |
T |
16: 59,124,352 (GRCm39) |
I280F |
probably damaging |
Het |
Or5p81 |
A |
G |
7: 108,267,364 (GRCm39) |
H247R |
probably damaging |
Het |
Paip1 |
T |
C |
13: 119,566,854 (GRCm39) |
S54P |
possibly damaging |
Het |
Prdm14 |
G |
T |
1: 13,195,968 (GRCm39) |
A31E |
probably benign |
Het |
Prr14l |
A |
G |
5: 32,985,767 (GRCm39) |
S1243P |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,435,878 (GRCm39) |
M1T |
probably null |
Het |
Raver2 |
T |
A |
4: 100,960,147 (GRCm39) |
V209D |
probably damaging |
Het |
Scube1 |
T |
A |
15: 83,512,277 (GRCm39) |
|
probably null |
Het |
Serpina3c |
T |
A |
12: 104,117,805 (GRCm39) |
I178F |
probably damaging |
Het |
Slc16a13 |
A |
T |
11: 70,111,457 (GRCm39) |
V16E |
probably damaging |
Het |
Slc30a6 |
T |
C |
17: 74,722,640 (GRCm39) |
S236P |
possibly damaging |
Het |
Sobp |
A |
C |
10: 42,898,689 (GRCm39) |
S299A |
probably damaging |
Het |
Sorcs3 |
C |
A |
19: 48,694,448 (GRCm39) |
T574K |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,942,820 (GRCm39) |
M862K |
probably benign |
Het |
Ubox5 |
A |
T |
2: 130,442,630 (GRCm39) |
V19E |
probably damaging |
Het |
Vmn1r173 |
A |
G |
7: 23,402,160 (GRCm39) |
T132A |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,218,711 (GRCm39) |
M244V |
probably benign |
Het |
Zfp820 |
T |
C |
17: 22,038,509 (GRCm39) |
D273G |
probably benign |
Het |
|
Other mutations in Fmo6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01392:Fmo6
|
APN |
1 |
162,757,580 (GRCm39) |
nonsense |
probably null |
|
IGL02083:Fmo6
|
APN |
1 |
162,748,033 (GRCm39) |
nonsense |
probably null |
|
adventure
|
UTSW |
1 |
162,750,379 (GRCm39) |
missense |
probably benign |
|
R0940:Fmo6
|
UTSW |
1 |
162,753,795 (GRCm39) |
missense |
probably benign |
0.07 |
R1173:Fmo6
|
UTSW |
1 |
162,753,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1268:Fmo6
|
UTSW |
1 |
162,748,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1538:Fmo6
|
UTSW |
1 |
162,753,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Fmo6
|
UTSW |
1 |
162,750,241 (GRCm39) |
missense |
probably benign |
|
R1717:Fmo6
|
UTSW |
1 |
162,753,821 (GRCm39) |
nonsense |
probably null |
|
R1837:Fmo6
|
UTSW |
1 |
162,750,379 (GRCm39) |
missense |
probably benign |
|
R2125:Fmo6
|
UTSW |
1 |
162,757,527 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2434:Fmo6
|
UTSW |
1 |
162,744,439 (GRCm39) |
missense |
probably benign |
0.00 |
R2894:Fmo6
|
UTSW |
1 |
162,750,293 (GRCm39) |
nonsense |
probably null |
|
R4864:Fmo6
|
UTSW |
1 |
162,751,964 (GRCm39) |
missense |
probably benign |
0.34 |
R6414:Fmo6
|
UTSW |
1 |
162,748,014 (GRCm39) |
missense |
probably damaging |
0.97 |
R6576:Fmo6
|
UTSW |
1 |
162,750,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R6883:Fmo6
|
UTSW |
1 |
162,757,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7013:Fmo6
|
UTSW |
1 |
162,745,817 (GRCm39) |
missense |
probably benign |
0.00 |
R7014:Fmo6
|
UTSW |
1 |
162,753,877 (GRCm39) |
missense |
probably benign |
0.13 |
R7657:Fmo6
|
UTSW |
1 |
162,750,285 (GRCm39) |
missense |
probably benign |
|
R8351:Fmo6
|
UTSW |
1 |
162,748,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R8451:Fmo6
|
UTSW |
1 |
162,748,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Fmo6
|
UTSW |
1 |
162,748,114 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9217:Fmo6
|
UTSW |
1 |
162,748,046 (GRCm39) |
missense |
probably benign |
0.02 |
R9274:Fmo6
|
UTSW |
1 |
162,747,921 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Fmo6
|
UTSW |
1 |
162,750,427 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Fmo6
|
UTSW |
1 |
162,748,065 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Fmo6
|
UTSW |
1 |
162,753,701 (GRCm39) |
nonsense |
probably null |
|
|