Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,078,698 (GRCm39) |
D1264G |
probably benign |
Het |
Ace |
T |
C |
11: 105,876,884 (GRCm39) |
F1122S |
probably damaging |
Het |
Actr10 |
T |
G |
12: 70,990,283 (GRCm39) |
Y112D |
probably benign |
Het |
Cacnb1 |
T |
G |
11: 97,900,121 (GRCm39) |
I346L |
possibly damaging |
Het |
Camsap2 |
T |
C |
1: 136,209,639 (GRCm39) |
T607A |
probably damaging |
Het |
Cby3 |
T |
C |
11: 50,250,175 (GRCm39) |
F32S |
probably damaging |
Het |
Cers5 |
G |
T |
15: 99,634,122 (GRCm39) |
H409N |
probably benign |
Het |
Ces1h |
A |
T |
8: 94,106,322 (GRCm39) |
L11H |
|
Het |
Clcnkb |
T |
C |
4: 141,141,833 (GRCm39) |
Y51C |
probably benign |
Het |
Cnnm2 |
A |
G |
19: 46,866,420 (GRCm39) |
E856G |
probably benign |
Het |
Cnot1 |
A |
G |
8: 96,491,690 (GRCm39) |
V378A |
probably benign |
Het |
Crisp4 |
A |
C |
1: 18,198,973 (GRCm39) |
S154A |
probably benign |
Het |
Disp1 |
C |
T |
1: 182,880,550 (GRCm39) |
R241Q |
probably benign |
Het |
Ermard |
G |
A |
17: 15,277,065 (GRCm39) |
R429H |
probably benign |
Het |
Extl1 |
C |
T |
4: 134,098,929 (GRCm39) |
G34D |
probably benign |
Het |
Gen1 |
T |
C |
12: 11,291,863 (GRCm39) |
D707G |
probably benign |
Het |
H1f3 |
C |
A |
13: 23,739,541 (GRCm39) |
T93N |
possibly damaging |
Het |
Igkv5-37 |
A |
C |
6: 69,940,499 (GRCm39) |
S48R |
possibly damaging |
Het |
Ilvbl |
C |
T |
10: 78,419,809 (GRCm39) |
A571V |
possibly damaging |
Het |
Itgb1 |
A |
G |
8: 129,439,718 (GRCm39) |
K136E |
possibly damaging |
Het |
Lhx8 |
A |
G |
3: 154,027,284 (GRCm39) |
F253L |
probably damaging |
Het |
Naa25 |
A |
G |
5: 121,562,594 (GRCm39) |
T459A |
possibly damaging |
Het |
Nr3c2 |
A |
G |
8: 77,636,621 (GRCm39) |
Y574C |
probably damaging |
Het |
Nrxn1 |
C |
T |
17: 91,396,635 (GRCm39) |
|
probably benign |
Het |
Ntrk3 |
T |
A |
7: 77,952,488 (GRCm39) |
R576S |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,041,904 (GRCm39) |
Y403C |
probably damaging |
Het |
Or2ag12 |
A |
G |
7: 106,276,781 (GRCm39) |
V304A |
probably benign |
Het |
Or8b53 |
T |
G |
9: 38,667,914 (GRCm39) |
L310W |
probably damaging |
Het |
Otogl |
T |
A |
10: 107,722,376 (GRCm39) |
Y326F |
probably damaging |
Het |
Pcdha1 |
T |
A |
18: 37,064,426 (GRCm39) |
D363E |
probably damaging |
Het |
Pcdhb3 |
T |
A |
18: 37,434,974 (GRCm39) |
N313K |
probably benign |
Het |
Pcdhb9 |
A |
C |
18: 37,534,602 (GRCm39) |
S199R |
probably benign |
Het |
Pde4dip |
C |
T |
3: 97,622,599 (GRCm39) |
D1537N |
probably damaging |
Het |
Pinx1 |
A |
G |
14: 64,156,984 (GRCm39) |
K304E |
probably benign |
Het |
Pnlip |
T |
C |
19: 58,670,134 (GRCm39) |
V458A |
probably benign |
Het |
Polr3a |
C |
A |
14: 24,534,455 (GRCm39) |
M60I |
probably null |
Het |
Qrich2 |
G |
T |
11: 116,347,686 (GRCm39) |
S1046* |
probably null |
Het |
Rigi |
T |
C |
4: 40,211,618 (GRCm39) |
E650G |
probably benign |
Het |
Rps6ka5 |
G |
A |
12: 100,524,824 (GRCm39) |
P638S |
probably damaging |
Het |
Slc6a13 |
T |
A |
6: 121,298,658 (GRCm39) |
N158K |
probably damaging |
Het |
Sord |
T |
C |
2: 122,089,561 (GRCm39) |
V187A |
probably damaging |
Het |
Thbs2 |
T |
C |
17: 14,896,558 (GRCm39) |
D777G |
probably damaging |
Het |
Tmed9 |
A |
G |
13: 55,743,345 (GRCm39) |
D159G |
probably benign |
Het |
Trbc1 |
A |
G |
6: 41,516,195 (GRCm39) |
I142V |
|
Het |
Usp17ld |
A |
G |
7: 102,900,041 (GRCm39) |
V297A |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,069 (GRCm39) |
*316R |
probably null |
Het |
Wdr59 |
C |
A |
8: 112,248,570 (GRCm39) |
R15L |
|
Het |
Zfp189 |
C |
T |
4: 49,529,367 (GRCm39) |
P157S |
possibly damaging |
Het |
Zfp407 |
C |
T |
18: 84,578,800 (GRCm39) |
G771D |
probably damaging |
Het |
|
Other mutations in Sult2a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00541:Sult2a2
|
APN |
7 |
13,468,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01504:Sult2a2
|
APN |
7 |
13,472,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01833:Sult2a2
|
APN |
7 |
13,468,721 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03162:Sult2a2
|
APN |
7 |
13,468,822 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03408:Sult2a2
|
APN |
7 |
13,472,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R0941:Sult2a2
|
UTSW |
7 |
13,468,815 (GRCm39) |
nonsense |
probably null |
|
R1109:Sult2a2
|
UTSW |
7 |
13,468,798 (GRCm39) |
missense |
probably benign |
0.01 |
R1376:Sult2a2
|
UTSW |
7 |
13,468,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R1376:Sult2a2
|
UTSW |
7 |
13,468,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R4114:Sult2a2
|
UTSW |
7 |
13,468,708 (GRCm39) |
missense |
probably benign |
0.00 |
R4116:Sult2a2
|
UTSW |
7 |
13,468,708 (GRCm39) |
missense |
probably benign |
0.00 |
R4940:Sult2a2
|
UTSW |
7 |
13,472,223 (GRCm39) |
missense |
probably benign |
0.03 |
R5023:Sult2a2
|
UTSW |
7 |
13,468,785 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5510:Sult2a2
|
UTSW |
7 |
13,472,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R7424:Sult2a2
|
UTSW |
7 |
13,468,822 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7569:Sult2a2
|
UTSW |
7 |
13,513,430 (GRCm39) |
missense |
probably benign |
|
R8842:Sult2a2
|
UTSW |
7 |
13,472,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R8948:Sult2a2
|
UTSW |
7 |
13,467,484 (GRCm39) |
start codon destroyed |
probably damaging |
0.96 |
R8950:Sult2a2
|
UTSW |
7 |
13,467,484 (GRCm39) |
start codon destroyed |
probably damaging |
0.96 |
|