Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl4 |
T |
G |
3: 151,203,467 (GRCm39) |
I59R |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,593,363 (GRCm39) |
D4208V |
probably damaging |
Het |
Aimp2 |
A |
T |
5: 143,843,347 (GRCm39) |
|
probably benign |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Ankib1 |
A |
G |
5: 3,779,693 (GRCm39) |
V392A |
probably benign |
Het |
Ap2b1 |
A |
G |
11: 83,227,563 (GRCm39) |
|
probably null |
Het |
Arsg |
A |
G |
11: 109,418,700 (GRCm39) |
E232G |
probably benign |
Het |
Axdnd1 |
A |
G |
1: 156,162,920 (GRCm39) |
F144S |
probably benign |
Het |
Bud13 |
T |
A |
9: 46,203,498 (GRCm39) |
M111K |
probably damaging |
Het |
Cav2 |
T |
C |
6: 17,287,012 (GRCm39) |
F152S |
possibly damaging |
Het |
Ccdc180 |
A |
G |
4: 45,928,046 (GRCm39) |
T1194A |
probably damaging |
Het |
Ccdc192 |
G |
A |
18: 57,671,156 (GRCm39) |
|
probably null |
Het |
Ccdc88c |
T |
C |
12: 100,911,290 (GRCm39) |
K848R |
probably damaging |
Het |
Ceacam15 |
A |
G |
7: 16,406,024 (GRCm39) |
W176R |
probably damaging |
Het |
Cenpf |
A |
T |
1: 189,415,100 (GRCm39) |
D136E |
probably benign |
Het |
Dclk2 |
T |
C |
3: 86,813,344 (GRCm39) |
I201V |
possibly damaging |
Het |
Defa24 |
T |
A |
8: 22,224,612 (GRCm39) |
D20E |
probably damaging |
Het |
Dgcr8 |
T |
C |
16: 18,095,039 (GRCm39) |
N566D |
probably damaging |
Het |
Dido1 |
C |
A |
2: 180,326,966 (GRCm39) |
V386L |
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dtx3 |
G |
A |
10: 127,028,807 (GRCm39) |
P141S |
probably benign |
Het |
Fmn1 |
T |
C |
2: 113,426,714 (GRCm39) |
Y1144H |
probably damaging |
Het |
Gabbr2 |
A |
G |
4: 46,734,113 (GRCm39) |
L535P |
probably damaging |
Het |
Gimap3 |
T |
A |
6: 48,742,183 (GRCm39) |
E249V |
possibly damaging |
Het |
Git2 |
A |
T |
5: 114,881,835 (GRCm39) |
|
probably null |
Het |
Gm4922 |
T |
C |
10: 18,659,745 (GRCm39) |
T326A |
probably benign |
Het |
Gsdmc2 |
T |
G |
15: 63,700,045 (GRCm39) |
E242D |
probably benign |
Het |
Hdgfl2 |
G |
A |
17: 56,389,118 (GRCm39) |
G31S |
possibly damaging |
Het |
Herc2 |
A |
T |
7: 55,856,519 (GRCm39) |
I3956F |
probably damaging |
Het |
Hsf2bp |
G |
A |
17: 32,165,721 (GRCm39) |
R134C |
unknown |
Het |
Igf1r |
G |
C |
7: 67,843,107 (GRCm39) |
R739S |
probably benign |
Het |
Igkv4-51 |
T |
C |
6: 69,658,443 (GRCm39) |
E102G |
probably damaging |
Het |
Kif1a |
T |
G |
1: 92,969,414 (GRCm39) |
I1156L |
possibly damaging |
Het |
Kti12 |
T |
C |
4: 108,705,821 (GRCm39) |
L245S |
probably damaging |
Het |
Med17 |
A |
G |
9: 15,181,700 (GRCm39) |
S17P |
probably benign |
Het |
Mllt6 |
G |
A |
11: 97,560,326 (GRCm39) |
S210N |
possibly damaging |
Het |
Mrps18b |
A |
G |
17: 36,225,215 (GRCm39) |
|
probably benign |
Het |
Ms4a8a |
A |
G |
19: 11,056,828 (GRCm39) |
S85P |
probably benign |
Het |
Msln |
T |
C |
17: 25,968,847 (GRCm39) |
Q487R |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,228,549 (GRCm39) |
N363S |
probably benign |
Het |
Myo6 |
T |
C |
9: 80,152,942 (GRCm39) |
F192L |
probably damaging |
Het |
Nfkbiz |
T |
C |
16: 55,634,383 (GRCm39) |
D688G |
probably damaging |
Het |
Nsun4 |
C |
T |
4: 115,908,974 (GRCm39) |
V529I |
possibly damaging |
Het |
Or12d15 |
A |
T |
17: 37,694,192 (GRCm39) |
M245L |
probably benign |
Het |
Or1j16 |
G |
A |
2: 36,530,975 (GRCm39) |
R308K |
probably benign |
Het |
Or5p70 |
G |
A |
7: 107,994,332 (GRCm39) |
A2T |
probably benign |
Het |
Phf11a |
C |
A |
14: 59,516,834 (GRCm39) |
C208F |
probably damaging |
Het |
Plekhh2 |
G |
A |
17: 84,874,275 (GRCm39) |
C520Y |
probably benign |
Het |
Plxna4 |
C |
A |
6: 32,155,293 (GRCm39) |
M1550I |
probably damaging |
Het |
Pnpla6 |
A |
T |
8: 3,571,397 (GRCm39) |
Y140F |
probably damaging |
Het |
Ppp1r12a |
T |
A |
10: 108,085,488 (GRCm39) |
S478T |
possibly damaging |
Het |
Prkcz |
C |
A |
4: 155,357,393 (GRCm39) |
|
probably null |
Het |
Prss55 |
T |
A |
14: 64,314,574 (GRCm39) |
M199L |
probably damaging |
Het |
Qrich1 |
G |
A |
9: 108,433,659 (GRCm39) |
V651I |
possibly damaging |
Het |
Ralyl |
T |
C |
3: 13,842,005 (GRCm39) |
V47A |
probably damaging |
Het |
Raph1 |
A |
T |
1: 60,562,105 (GRCm39) |
|
probably benign |
Het |
Rgs12 |
T |
C |
5: 35,123,383 (GRCm39) |
Y389H |
probably damaging |
Het |
Sec24b |
C |
A |
3: 129,834,544 (GRCm39) |
G82V |
probably damaging |
Het |
Sema4a |
A |
G |
3: 88,357,293 (GRCm39) |
|
probably null |
Het |
Slc25a11 |
A |
T |
11: 70,536,361 (GRCm39) |
W149R |
probably damaging |
Het |
Slc32a1 |
T |
A |
2: 158,456,716 (GRCm39) |
M457K |
probably damaging |
Het |
Spata31d1e |
T |
C |
13: 59,890,234 (GRCm39) |
|
probably null |
Het |
Spint4 |
C |
T |
2: 164,542,812 (GRCm39) |
T135M |
probably damaging |
Het |
Sult2a2 |
A |
C |
7: 13,472,228 (GRCm39) |
N142H |
probably damaging |
Het |
Tbc1d1 |
G |
A |
5: 64,490,738 (GRCm39) |
G863D |
probably damaging |
Het |
Tmem156 |
G |
A |
5: 65,232,917 (GRCm39) |
T151M |
probably benign |
Het |
Trip12 |
T |
C |
1: 84,746,401 (GRCm39) |
Q459R |
probably damaging |
Het |
Vmn2r116 |
G |
A |
17: 23,605,095 (GRCm39) |
C136Y |
probably damaging |
Het |
Vmn2r51 |
C |
T |
7: 9,836,545 (GRCm39) |
V79M |
possibly damaging |
Het |
Vmn2r67 |
A |
T |
7: 84,801,023 (GRCm39) |
D304E |
probably benign |
Het |
Wdr93 |
T |
A |
7: 79,399,779 (GRCm39) |
F123I |
probably damaging |
Het |
Zfp672 |
A |
T |
11: 58,207,456 (GRCm39) |
C288* |
probably null |
Het |
Zp1 |
T |
C |
19: 10,896,769 (GRCm39) |
Y90C |
probably damaging |
Het |
|
Other mutations in Slc2a7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01302:Slc2a7
|
APN |
4 |
150,242,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01990:Slc2a7
|
APN |
4 |
150,239,141 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02480:Slc2a7
|
APN |
4 |
150,244,569 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02607:Slc2a7
|
APN |
4 |
150,239,162 (GRCm39) |
missense |
probably benign |
|
IGL02716:Slc2a7
|
APN |
4 |
150,244,467 (GRCm39) |
splice site |
probably benign |
|
IGL02861:Slc2a7
|
APN |
4 |
150,252,836 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03343:Slc2a7
|
APN |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
anhedonic
|
UTSW |
4 |
150,243,015 (GRCm39) |
nonsense |
probably null |
|
Anorectic
|
UTSW |
4 |
150,242,667 (GRCm39) |
splice site |
probably null |
|
paunch
|
UTSW |
4 |
150,242,605 (GRCm39) |
missense |
probably damaging |
1.00 |
tablemuscle
|
UTSW |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Slc2a7
|
UTSW |
4 |
150,252,721 (GRCm39) |
missense |
probably benign |
0.31 |
R0302:Slc2a7
|
UTSW |
4 |
150,233,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R0309:Slc2a7
|
UTSW |
4 |
150,242,528 (GRCm39) |
splice site |
probably benign |
|
R0367:Slc2a7
|
UTSW |
4 |
150,250,823 (GRCm39) |
missense |
probably benign |
0.03 |
R1485:Slc2a7
|
UTSW |
4 |
150,250,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Slc2a7
|
UTSW |
4 |
150,252,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Slc2a7
|
UTSW |
4 |
150,239,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R3973:Slc2a7
|
UTSW |
4 |
150,242,667 (GRCm39) |
splice site |
probably null |
|
R4399:Slc2a7
|
UTSW |
4 |
150,243,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4467:Slc2a7
|
UTSW |
4 |
150,247,731 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4712:Slc2a7
|
UTSW |
4 |
150,252,926 (GRCm39) |
missense |
probably benign |
0.00 |
R5066:Slc2a7
|
UTSW |
4 |
150,244,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Slc2a7
|
UTSW |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Slc2a7
|
UTSW |
4 |
150,249,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R6062:Slc2a7
|
UTSW |
4 |
150,252,884 (GRCm39) |
missense |
probably benign |
|
R6185:Slc2a7
|
UTSW |
4 |
150,233,450 (GRCm39) |
missense |
probably benign |
0.00 |
R6730:Slc2a7
|
UTSW |
4 |
150,242,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Slc2a7
|
UTSW |
4 |
150,239,141 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8145:Slc2a7
|
UTSW |
4 |
150,252,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R8203:Slc2a7
|
UTSW |
4 |
150,243,015 (GRCm39) |
nonsense |
probably null |
|
R8512:Slc2a7
|
UTSW |
4 |
150,247,752 (GRCm39) |
missense |
probably benign |
0.23 |
R9066:Slc2a7
|
UTSW |
4 |
150,250,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Slc2a7
|
UTSW |
4 |
150,242,625 (GRCm39) |
missense |
probably benign |
0.44 |
R9129:Slc2a7
|
UTSW |
4 |
150,243,001 (GRCm39) |
missense |
probably benign |
0.31 |
R9773:Slc2a7
|
UTSW |
4 |
150,234,044 (GRCm39) |
missense |
possibly damaging |
0.63 |
|