Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933421I07Rik |
T |
C |
7: 42,096,398 (GRCm39) |
D119G |
probably damaging |
Het |
Apol7c |
A |
G |
15: 77,410,500 (GRCm39) |
C149R |
probably damaging |
Het |
Arfgef1 |
G |
A |
1: 10,230,133 (GRCm39) |
R1235* |
probably null |
Het |
Bpifb4 |
A |
G |
2: 153,786,703 (GRCm39) |
D285G |
probably damaging |
Het |
Cep192 |
T |
A |
18: 67,986,043 (GRCm39) |
H1682Q |
possibly damaging |
Het |
Cerk |
G |
T |
15: 86,033,552 (GRCm39) |
Y290* |
probably null |
Het |
Cyld |
A |
T |
8: 89,467,998 (GRCm39) |
I544F |
probably damaging |
Het |
Dcp1a |
T |
C |
14: 30,227,528 (GRCm39) |
S134P |
possibly damaging |
Het |
Epha6 |
A |
C |
16: 59,659,666 (GRCm39) |
N817K |
probably benign |
Het |
Ephb4 |
A |
G |
5: 137,364,003 (GRCm39) |
|
probably benign |
Het |
Fcgr3 |
A |
T |
1: 170,886,849 (GRCm39) |
L25Q |
probably damaging |
Het |
Heatr3 |
A |
G |
8: 88,871,245 (GRCm39) |
I83V |
probably benign |
Het |
Hormad1 |
T |
A |
3: 95,485,608 (GRCm39) |
N265K |
possibly damaging |
Het |
Kpna1 |
A |
G |
16: 35,840,562 (GRCm39) |
T201A |
probably benign |
Het |
Krt6b |
T |
A |
15: 101,587,549 (GRCm39) |
T182S |
probably damaging |
Het |
Macc1 |
A |
G |
12: 119,414,088 (GRCm39) |
K755E |
probably damaging |
Het |
Med12l |
C |
T |
3: 59,169,314 (GRCm39) |
T1568M |
probably damaging |
Het |
Muc4 |
G |
T |
16: 32,581,722 (GRCm39) |
|
probably null |
Het |
Myt1l |
T |
C |
12: 29,960,770 (GRCm39) |
S1028P |
unknown |
Het |
Nhlrc2 |
C |
T |
19: 56,559,282 (GRCm39) |
R256C |
probably benign |
Het |
Or4c123 |
T |
A |
2: 89,127,471 (GRCm39) |
T48S |
probably benign |
Het |
Or5a3 |
G |
A |
19: 12,399,736 (GRCm39) |
R21H |
probably benign |
Het |
Pfkfb4 |
G |
A |
9: 108,828,202 (GRCm39) |
R79H |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,315,904 (GRCm39) |
|
probably benign |
Het |
Pramel5 |
C |
T |
4: 144,000,429 (GRCm39) |
R49H |
probably benign |
Het |
Ralgapb |
T |
A |
2: 158,304,079 (GRCm39) |
S613T |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,778,022 (GRCm39) |
E2158G |
probably damaging |
Het |
Slc17a6 |
A |
G |
7: 51,317,770 (GRCm39) |
T468A |
possibly damaging |
Het |
Slc36a1 |
A |
G |
11: 55,119,147 (GRCm39) |
D374G |
possibly damaging |
Het |
Wdtc1 |
T |
C |
4: 133,022,543 (GRCm39) |
D601G |
probably damaging |
Het |
Zfp1007 |
A |
C |
5: 109,825,182 (GRCm39) |
Y89* |
probably null |
Het |
|
Other mutations in Scgb2b19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4515001:Scgb2b19
|
UTSW |
7 |
32,979,036 (GRCm39) |
critical splice donor site |
probably null |
|
R0580:Scgb2b19
|
UTSW |
7 |
32,977,995 (GRCm39) |
missense |
probably benign |
0.15 |
R1437:Scgb2b19
|
UTSW |
7 |
32,977,980 (GRCm39) |
missense |
probably benign |
0.08 |
R1445:Scgb2b19
|
UTSW |
7 |
32,979,037 (GRCm39) |
critical splice donor site |
probably null |
|
R5332:Scgb2b19
|
UTSW |
7 |
32,978,006 (GRCm39) |
missense |
probably benign |
0.07 |
R6424:Scgb2b19
|
UTSW |
7 |
32,978,022 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7102:Scgb2b19
|
UTSW |
7 |
32,979,711 (GRCm39) |
missense |
probably null |
|
R7576:Scgb2b19
|
UTSW |
7 |
32,979,211 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9551:Scgb2b19
|
UTSW |
7 |
32,979,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9552:Scgb2b19
|
UTSW |
7 |
32,979,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Scgb2b19
|
UTSW |
7 |
32,978,039 (GRCm39) |
missense |
probably benign |
0.04 |
|