Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
T |
5: 88,119,774 (GRCm39) |
Y177F |
possibly damaging |
Het |
Als2 |
C |
A |
1: 59,255,189 (GRCm39) |
|
probably benign |
Het |
Arhgap44 |
A |
G |
11: 64,915,038 (GRCm39) |
L410P |
probably damaging |
Het |
Atp13a2 |
C |
T |
4: 140,727,666 (GRCm39) |
A481V |
possibly damaging |
Het |
Bod1l |
C |
A |
5: 41,988,927 (GRCm39) |
L393F |
probably benign |
Het |
Cflar |
T |
A |
1: 58,780,179 (GRCm39) |
I258N |
probably damaging |
Het |
Col24a1 |
T |
C |
3: 145,244,458 (GRCm39) |
|
probably null |
Het |
Csmd2 |
A |
T |
4: 128,412,834 (GRCm39) |
N2542I |
probably benign |
Het |
Cyp2b9 |
T |
C |
7: 25,898,025 (GRCm39) |
|
probably benign |
Het |
Dip2c |
A |
T |
13: 9,601,814 (GRCm39) |
I258F |
probably damaging |
Het |
Dock7 |
A |
G |
4: 98,854,585 (GRCm39) |
S1560P |
probably benign |
Het |
Drc7 |
C |
T |
8: 95,802,875 (GRCm39) |
|
probably benign |
Het |
Gm3667 |
T |
A |
14: 18,269,522 (GRCm39) |
S203C |
probably null |
Het |
Gramd2a |
A |
G |
9: 59,619,410 (GRCm39) |
E190G |
probably benign |
Het |
Gstm4 |
T |
C |
3: 107,951,263 (GRCm39) |
D8G |
probably damaging |
Het |
Heatr5b |
A |
T |
17: 79,067,928 (GRCm39) |
M1820K |
probably benign |
Het |
Irs4 |
A |
G |
X: 140,505,794 (GRCm39) |
Y801H |
unknown |
Het |
Loxhd1 |
C |
T |
18: 77,374,169 (GRCm39) |
T80I |
possibly damaging |
Het |
Lrrc40 |
G |
A |
3: 157,747,302 (GRCm39) |
|
probably benign |
Het |
Mapk8ip1 |
T |
G |
2: 92,216,958 (GRCm39) |
K446Q |
probably damaging |
Het |
Mmp8 |
T |
A |
9: 7,558,530 (GRCm39) |
|
probably benign |
Het |
Muc19 |
A |
T |
15: 91,808,424 (GRCm39) |
|
noncoding transcript |
Het |
Nipsnap3b |
T |
A |
4: 53,015,016 (GRCm39) |
V21E |
possibly damaging |
Het |
Or1j15 |
C |
A |
2: 36,458,716 (GRCm39) |
Y35* |
probably null |
Het |
Or5al6 |
A |
G |
2: 85,977,043 (GRCm39) |
F12L |
probably damaging |
Het |
Or7a38 |
A |
T |
10: 78,753,471 (GRCm39) |
I266F |
probably benign |
Het |
Parp12 |
G |
A |
6: 39,064,520 (GRCm39) |
|
probably null |
Het |
Pramel14 |
C |
A |
4: 143,719,815 (GRCm39) |
L183F |
probably damaging |
Het |
Rgsl1 |
T |
A |
1: 153,701,948 (GRCm39) |
T169S |
possibly damaging |
Het |
Rnf38 |
T |
C |
4: 44,152,529 (GRCm39) |
R12G |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,363,624 (GRCm39) |
|
probably benign |
Het |
Slpi |
T |
C |
2: 164,197,367 (GRCm39) |
|
probably benign |
Het |
Snx17 |
G |
A |
5: 31,353,355 (GRCm39) |
V165I |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 18,880,357 (GRCm39) |
V570A |
probably benign |
Het |
Vmn1r63 |
A |
G |
7: 5,806,350 (GRCm39) |
M94T |
probably benign |
Het |
Vmn2r95 |
A |
G |
17: 18,672,575 (GRCm39) |
I771V |
probably benign |
Het |
Wiz |
A |
G |
17: 32,575,532 (GRCm39) |
V868A |
probably benign |
Het |
|
Other mutations in Mettl21e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00660:Mettl21e
|
APN |
1 |
44,245,530 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01878:Mettl21e
|
APN |
1 |
44,250,193 (GRCm39) |
missense |
probably null |
1.00 |
IGL02194:Mettl21e
|
APN |
1 |
44,250,343 (GRCm39) |
missense |
probably benign |
|
IGL03396:Mettl21e
|
APN |
1 |
44,245,759 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0165:Mettl21e
|
UTSW |
1 |
44,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Mettl21e
|
UTSW |
1 |
44,250,190 (GRCm39) |
critical splice donor site |
probably null |
|
R0525:Mettl21e
|
UTSW |
1 |
44,245,542 (GRCm39) |
missense |
probably damaging |
0.98 |
R2078:Mettl21e
|
UTSW |
1 |
44,245,662 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2143:Mettl21e
|
UTSW |
1 |
44,249,398 (GRCm39) |
missense |
probably benign |
0.06 |
R3623:Mettl21e
|
UTSW |
1 |
44,245,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R3870:Mettl21e
|
UTSW |
1 |
44,245,524 (GRCm39) |
missense |
probably benign |
0.01 |
R4780:Mettl21e
|
UTSW |
1 |
44,250,303 (GRCm39) |
missense |
probably benign |
|
R5488:Mettl21e
|
UTSW |
1 |
44,257,276 (GRCm39) |
missense |
probably benign |
|
R5654:Mettl21e
|
UTSW |
1 |
44,250,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Mettl21e
|
UTSW |
1 |
44,249,425 (GRCm39) |
missense |
probably damaging |
0.97 |
R6697:Mettl21e
|
UTSW |
1 |
44,249,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R6804:Mettl21e
|
UTSW |
1 |
44,257,295 (GRCm39) |
missense |
probably benign |
0.01 |
R6862:Mettl21e
|
UTSW |
1 |
44,245,526 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Mettl21e
|
UTSW |
1 |
44,249,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R7870:Mettl21e
|
UTSW |
1 |
44,249,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Mettl21e
|
UTSW |
1 |
44,245,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Mettl21e
|
UTSW |
1 |
44,245,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Mettl21e
|
UTSW |
1 |
44,245,857 (GRCm39) |
missense |
probably benign |
0.01 |
R9507:Mettl21e
|
UTSW |
1 |
44,245,536 (GRCm39) |
missense |
probably benign |
0.05 |
R9641:Mettl21e
|
UTSW |
1 |
44,250,351 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Mettl21e
|
UTSW |
1 |
44,245,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|