Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl5 |
A |
G |
10: 80,178,065 (GRCm39) |
|
probably benign |
Het |
Brd3 |
A |
G |
2: 27,349,753 (GRCm39) |
S267P |
possibly damaging |
Het |
Btaf1 |
A |
G |
19: 36,946,468 (GRCm39) |
T425A |
probably benign |
Het |
Caskin1 |
A |
T |
17: 24,721,383 (GRCm39) |
E544D |
probably benign |
Het |
Col20a1 |
C |
T |
2: 180,630,905 (GRCm39) |
Q58* |
probably null |
Het |
Eif2ak1 |
G |
A |
5: 143,826,270 (GRCm39) |
V428I |
probably damaging |
Het |
Fez2 |
A |
G |
17: 78,692,184 (GRCm39) |
I345T |
probably benign |
Het |
Focad |
A |
T |
4: 88,310,234 (GRCm39) |
M1388L |
probably benign |
Het |
Gfer |
T |
C |
17: 24,914,921 (GRCm39) |
R41G |
probably benign |
Het |
Gm9956 |
C |
T |
10: 56,621,350 (GRCm39) |
S4L |
unknown |
Het |
Krtap6-1 |
G |
A |
16: 88,828,643 (GRCm39) |
G13D |
unknown |
Het |
Megf8 |
A |
G |
7: 25,045,933 (GRCm39) |
E1492G |
possibly damaging |
Het |
Myh7 |
T |
C |
14: 55,221,197 (GRCm39) |
I909V |
probably damaging |
Het |
Or11g25 |
T |
A |
14: 50,723,643 (GRCm39) |
S243T |
probably damaging |
Het |
Or1e21 |
T |
A |
11: 73,344,561 (GRCm39) |
H159L |
probably damaging |
Het |
Otog |
A |
G |
7: 45,959,562 (GRCm39) |
E717G |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,527,605 (GRCm39) |
I319M |
probably benign |
Het |
Piwil4 |
A |
T |
9: 14,617,583 (GRCm39) |
|
probably benign |
Het |
Plekho1 |
T |
A |
3: 95,899,493 (GRCm39) |
H100L |
probably damaging |
Het |
Prr30 |
T |
G |
14: 101,435,917 (GRCm39) |
D215A |
probably benign |
Het |
Ralgps2 |
C |
A |
1: 156,645,314 (GRCm39) |
K514N |
probably benign |
Het |
Robo4 |
T |
C |
9: 37,319,472 (GRCm39) |
I463T |
probably damaging |
Het |
Sars1 |
A |
T |
3: 108,336,579 (GRCm39) |
F268Y |
probably damaging |
Het |
Sidt1 |
C |
T |
16: 44,102,858 (GRCm39) |
R289Q |
possibly damaging |
Het |
Slco1a8 |
T |
A |
6: 141,940,023 (GRCm39) |
Y140F |
probably benign |
Het |
Slco2a1 |
T |
C |
9: 102,956,805 (GRCm39) |
V539A |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,058,676 (GRCm39) |
|
probably benign |
Het |
Spag17 |
A |
G |
3: 100,008,702 (GRCm39) |
D1944G |
probably benign |
Het |
Spata1 |
C |
T |
3: 146,181,094 (GRCm39) |
R288Q |
possibly damaging |
Het |
Tatdn3 |
T |
C |
1: 190,778,507 (GRCm39) |
*233W |
probably null |
Het |
Ttc3 |
T |
A |
16: 94,220,285 (GRCm39) |
V536E |
probably damaging |
Het |
V1rd19 |
A |
C |
7: 23,702,854 (GRCm39) |
T107P |
probably damaging |
Het |
|
Other mutations in Prss52 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0021:Prss52
|
UTSW |
14 |
64,341,857 (GRCm39) |
missense |
probably benign |
|
R0271:Prss52
|
UTSW |
14 |
64,351,127 (GRCm39) |
missense |
probably benign |
0.23 |
R0480:Prss52
|
UTSW |
14 |
64,351,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R1770:Prss52
|
UTSW |
14 |
64,351,082 (GRCm39) |
missense |
probably damaging |
0.96 |
R2216:Prss52
|
UTSW |
14 |
64,351,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R3157:Prss52
|
UTSW |
14 |
64,350,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R3158:Prss52
|
UTSW |
14 |
64,350,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5613:Prss52
|
UTSW |
14 |
64,346,951 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7049:Prss52
|
UTSW |
14 |
64,350,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Prss52
|
UTSW |
14 |
64,347,037 (GRCm39) |
missense |
probably benign |
0.02 |
R8425:Prss52
|
UTSW |
14 |
64,350,009 (GRCm39) |
nonsense |
probably null |
|
R9482:Prss52
|
UTSW |
14 |
64,351,129 (GRCm39) |
missense |
probably damaging |
0.98 |
RF012:Prss52
|
UTSW |
14 |
64,350,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|