Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,248,235 (GRCm39) |
F2661L |
probably benign |
Het |
Acadsb |
A |
G |
7: 131,031,836 (GRCm39) |
D224G |
probably benign |
Het |
Acsm1 |
A |
G |
7: 119,239,920 (GRCm39) |
H288R |
probably damaging |
Het |
Adamts2 |
A |
G |
11: 50,667,457 (GRCm39) |
D465G |
probably damaging |
Het |
Akap9 |
A |
T |
5: 4,022,851 (GRCm39) |
|
probably benign |
Het |
Alms1 |
A |
G |
6: 85,679,582 (GRCm39) |
T3240A |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,555,075 (GRCm39) |
W417R |
probably damaging |
Het |
Arfgef1 |
C |
A |
1: 10,250,212 (GRCm39) |
|
probably benign |
Het |
Cacna1s |
T |
A |
1: 136,016,746 (GRCm39) |
|
probably benign |
Het |
Clcn1 |
T |
C |
6: 42,287,515 (GRCm39) |
F740L |
probably benign |
Het |
Clec12a |
T |
A |
6: 129,341,016 (GRCm39) |
D265E |
probably benign |
Het |
Clic3 |
T |
A |
2: 25,347,797 (GRCm39) |
|
probably benign |
Het |
Cntnap3 |
T |
G |
13: 64,909,859 (GRCm39) |
T749P |
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,261,186 (GRCm39) |
D45E |
probably null |
Het |
Cplane1 |
T |
A |
15: 8,211,727 (GRCm39) |
S356T |
probably damaging |
Het |
Crxos |
T |
A |
7: 15,632,460 (GRCm39) |
S89T |
probably benign |
Het |
Cxcr1 |
G |
T |
1: 74,231,468 (GRCm39) |
P185T |
possibly damaging |
Het |
Cyp20a1 |
T |
A |
1: 60,410,486 (GRCm39) |
N262K |
possibly damaging |
Het |
Dennd2b |
T |
A |
7: 109,156,411 (GRCm39) |
Q113L |
probably benign |
Het |
Dpy19l2 |
T |
C |
9: 24,607,324 (GRCm39) |
R46G |
probably benign |
Het |
Dpysl2 |
A |
T |
14: 67,045,411 (GRCm39) |
L454Q |
probably damaging |
Het |
Dvl3 |
C |
T |
16: 20,346,173 (GRCm39) |
|
probably benign |
Het |
Eppin |
T |
A |
2: 164,431,332 (GRCm39) |
E98V |
possibly damaging |
Het |
Fancm |
A |
T |
12: 65,152,835 (GRCm39) |
H1097L |
probably benign |
Het |
Fkbp4 |
A |
G |
6: 128,412,705 (GRCm39) |
I75T |
probably damaging |
Het |
Fmn2 |
A |
G |
1: 174,409,525 (GRCm39) |
H586R |
unknown |
Het |
Gm973 |
C |
T |
1: 59,597,393 (GRCm39) |
|
probably benign |
Het |
Haus6 |
A |
C |
4: 86,521,083 (GRCm39) |
V185G |
possibly damaging |
Het |
Herc2 |
T |
A |
7: 55,772,114 (GRCm39) |
C1098S |
possibly damaging |
Het |
Hic1 |
C |
A |
11: 75,057,136 (GRCm39) |
L584F |
possibly damaging |
Het |
Itgb1bp1 |
C |
A |
12: 21,326,896 (GRCm39) |
|
probably benign |
Het |
Kbtbd2 |
G |
A |
6: 56,757,374 (GRCm39) |
R121* |
probably null |
Het |
Lgr4 |
C |
T |
2: 109,837,626 (GRCm39) |
|
probably benign |
Het |
Lrrc55 |
T |
C |
2: 85,022,264 (GRCm39) |
E309G |
probably damaging |
Het |
Mertk |
T |
C |
2: 128,635,027 (GRCm39) |
|
probably null |
Het |
Micu3 |
A |
G |
8: 40,819,294 (GRCm39) |
|
probably benign |
Het |
Mmp11 |
G |
A |
10: 75,762,592 (GRCm39) |
A287V |
probably benign |
Het |
Mpzl2 |
A |
G |
9: 44,954,039 (GRCm39) |
Y47C |
probably damaging |
Het |
Muc5b |
A |
C |
7: 141,415,752 (GRCm39) |
R2899S |
probably benign |
Het |
Myo1b |
A |
G |
1: 51,794,857 (GRCm39) |
Y1078H |
probably benign |
Het |
Naip1 |
A |
T |
13: 100,559,727 (GRCm39) |
D1092E |
probably benign |
Het |
Ncapd3 |
T |
G |
9: 26,969,179 (GRCm39) |
V611G |
probably damaging |
Het |
Ntpcr |
C |
T |
8: 126,464,093 (GRCm39) |
R73* |
probably null |
Het |
Or4c120 |
A |
T |
2: 89,000,704 (GRCm39) |
V284E |
probably benign |
Het |
Or5b119 |
G |
A |
19: 13,456,857 (GRCm39) |
A235V |
probably damaging |
Het |
Osbp2 |
A |
G |
11: 3,664,709 (GRCm39) |
F88S |
probably damaging |
Het |
Pkn3 |
A |
T |
2: 29,979,889 (GRCm39) |
T711S |
probably damaging |
Het |
Plekhm1 |
T |
C |
11: 103,285,602 (GRCm39) |
K278E |
probably benign |
Het |
Ppp1r36 |
A |
G |
12: 76,486,065 (GRCm39) |
T408A |
probably benign |
Het |
Prss41 |
T |
C |
17: 24,061,477 (GRCm39) |
T105A |
possibly damaging |
Het |
Psme1 |
G |
T |
14: 55,817,378 (GRCm39) |
|
probably benign |
Het |
Ptprq |
A |
T |
10: 107,444,036 (GRCm39) |
Y1523N |
probably damaging |
Het |
Ric8b |
A |
G |
10: 84,828,086 (GRCm39) |
D470G |
probably damaging |
Het |
Scarb1 |
A |
G |
5: 125,375,795 (GRCm39) |
|
probably benign |
Het |
Slc25a54 |
G |
A |
3: 109,010,112 (GRCm39) |
A204T |
probably damaging |
Het |
Spink10 |
T |
C |
18: 62,793,036 (GRCm39) |
C67R |
probably damaging |
Het |
Tmtc1 |
A |
T |
6: 148,314,138 (GRCm39) |
|
probably null |
Het |
Tprkb |
A |
G |
6: 85,901,446 (GRCm39) |
D28G |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,910,098 (GRCm39) |
H747R |
probably benign |
Het |
Usp24 |
A |
G |
4: 106,259,302 (GRCm39) |
S1608G |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,596,774 (GRCm39) |
F2115L |
probably damaging |
Het |
Vmn1r200 |
A |
T |
13: 22,579,361 (GRCm39) |
I46L |
probably benign |
Het |
Zdhhc8 |
A |
T |
16: 18,046,254 (GRCm39) |
M103K |
probably damaging |
Het |
Zfp595 |
C |
T |
13: 67,465,369 (GRCm39) |
G298E |
probably damaging |
Het |
Zfp738 |
T |
G |
13: 67,818,140 (GRCm39) |
H617P |
possibly damaging |
Het |
Zfp9 |
A |
T |
6: 118,442,163 (GRCm39) |
H166Q |
probably damaging |
Het |
Zp3r |
C |
A |
1: 130,546,071 (GRCm39) |
D80Y |
probably damaging |
Het |
|
Other mutations in Atf6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01327:Atf6
|
APN |
1 |
170,616,175 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01431:Atf6
|
APN |
1 |
170,680,571 (GRCm39) |
splice site |
probably benign |
|
IGL01755:Atf6
|
APN |
1 |
170,616,180 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02060:Atf6
|
APN |
1 |
170,646,989 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02416:Atf6
|
APN |
1 |
170,574,726 (GRCm39) |
nonsense |
probably null |
|
IGL02903:Atf6
|
APN |
1 |
170,627,283 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02989:Atf6
|
APN |
1 |
170,616,252 (GRCm39) |
splice site |
probably benign |
|
IGL03209:Atf6
|
APN |
1 |
170,662,463 (GRCm39) |
missense |
probably benign |
|
R0455:Atf6
|
UTSW |
1 |
170,662,492 (GRCm39) |
missense |
probably benign |
0.00 |
R0467:Atf6
|
UTSW |
1 |
170,621,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Atf6
|
UTSW |
1 |
170,537,516 (GRCm39) |
missense |
probably benign |
0.19 |
R1486:Atf6
|
UTSW |
1 |
170,622,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1850:Atf6
|
UTSW |
1 |
170,646,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Atf6
|
UTSW |
1 |
170,682,710 (GRCm39) |
missense |
probably benign |
0.00 |
R2164:Atf6
|
UTSW |
1 |
170,622,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R3782:Atf6
|
UTSW |
1 |
170,622,336 (GRCm39) |
nonsense |
probably null |
|
R4454:Atf6
|
UTSW |
1 |
170,621,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R4631:Atf6
|
UTSW |
1 |
170,574,766 (GRCm39) |
splice site |
probably null |
|
R4676:Atf6
|
UTSW |
1 |
170,614,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Atf6
|
UTSW |
1 |
170,574,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Atf6
|
UTSW |
1 |
170,669,345 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5860:Atf6
|
UTSW |
1 |
170,669,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Atf6
|
UTSW |
1 |
170,662,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Atf6
|
UTSW |
1 |
170,621,545 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6520:Atf6
|
UTSW |
1 |
170,695,238 (GRCm39) |
missense |
probably benign |
0.00 |
R7032:Atf6
|
UTSW |
1 |
170,627,181 (GRCm39) |
critical splice donor site |
probably null |
|
R7472:Atf6
|
UTSW |
1 |
170,643,060 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7923:Atf6
|
UTSW |
1 |
170,622,275 (GRCm39) |
missense |
probably benign |
|
R8002:Atf6
|
UTSW |
1 |
170,646,823 (GRCm39) |
missense |
probably benign |
0.43 |
R8860:Atf6
|
UTSW |
1 |
170,680,535 (GRCm39) |
missense |
probably null |
0.95 |
R8956:Atf6
|
UTSW |
1 |
170,621,576 (GRCm39) |
missense |
probably damaging |
0.98 |
R9090:Atf6
|
UTSW |
1 |
170,622,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Atf6
|
UTSW |
1 |
170,622,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9323:Atf6
|
UTSW |
1 |
170,682,682 (GRCm39) |
nonsense |
probably null |
|
R9500:Atf6
|
UTSW |
1 |
170,574,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R9594:Atf6
|
UTSW |
1 |
170,668,402 (GRCm39) |
missense |
probably benign |
0.18 |
R9733:Atf6
|
UTSW |
1 |
170,662,402 (GRCm39) |
missense |
probably benign |
0.00 |
|