Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl1 |
C |
T |
8: 46,980,228 (GRCm39) |
S423L |
probably benign |
Het |
Ankmy1 |
T |
G |
1: 92,813,874 (GRCm39) |
E435A |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,216,052 (GRCm39) |
M343K |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
C3 |
T |
C |
17: 57,524,173 (GRCm39) |
|
probably null |
Het |
Cdk17 |
T |
C |
10: 93,047,939 (GRCm39) |
|
probably null |
Het |
Cntn2 |
A |
G |
1: 132,456,677 (GRCm39) |
V123A |
probably damaging |
Het |
Cracd |
T |
A |
5: 77,004,421 (GRCm39) |
W261R |
unknown |
Het |
Dchs1 |
A |
G |
7: 105,411,770 (GRCm39) |
Y1449H |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,138,518 (GRCm39) |
N772K |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,942,188 (GRCm39) |
|
probably benign |
Het |
Edn1 |
T |
A |
13: 42,455,382 (GRCm39) |
F4L |
probably benign |
Het |
Epb41l3 |
C |
T |
17: 69,581,111 (GRCm39) |
R552* |
probably null |
Het |
Epc1 |
T |
C |
18: 6,452,258 (GRCm39) |
D267G |
possibly damaging |
Het |
Fbxo22 |
A |
T |
9: 55,130,546 (GRCm39) |
T169S |
probably benign |
Het |
Fmnl1 |
A |
G |
11: 103,072,940 (GRCm39) |
N144D |
probably damaging |
Het |
Folh1 |
A |
G |
7: 86,424,864 (GRCm39) |
L35P |
possibly damaging |
Het |
Gm10220 |
A |
C |
5: 26,321,908 (GRCm39) |
S255A |
possibly damaging |
Het |
Gm15446 |
G |
T |
5: 110,088,313 (GRCm39) |
V9L |
probably damaging |
Het |
Hipk2 |
A |
G |
6: 38,676,200 (GRCm39) |
L1011P |
probably damaging |
Het |
Kif4-ps |
G |
T |
12: 101,112,473 (GRCm39) |
V201L |
probably damaging |
Het |
Lgsn |
C |
A |
1: 31,215,540 (GRCm39) |
D3E |
probably benign |
Het |
Mavs |
T |
C |
2: 131,087,218 (GRCm39) |
S239P |
probably benign |
Het |
Mrtfb |
T |
A |
16: 13,219,322 (GRCm39) |
V667D |
probably damaging |
Het |
Mtrf1 |
A |
G |
14: 79,656,707 (GRCm39) |
Y403C |
probably damaging |
Het |
Mycbp2 |
A |
C |
14: 103,532,686 (GRCm39) |
L390V |
probably damaging |
Het |
Neto2 |
A |
G |
8: 86,389,894 (GRCm39) |
S190P |
probably damaging |
Het |
Ngly1 |
A |
G |
14: 16,270,574 (GRCm38) |
I195V |
probably damaging |
Het |
Or10d4c |
A |
G |
9: 39,558,420 (GRCm39) |
I133V |
probably benign |
Het |
Or13p5 |
T |
C |
4: 118,591,882 (GRCm39) |
I52T |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,620,504 (GRCm39) |
K1632E |
probably damaging |
Het |
Pigk |
T |
C |
3: 152,419,832 (GRCm39) |
S21P |
probably benign |
Het |
Rabggtb |
A |
G |
3: 153,616,417 (GRCm39) |
F82L |
probably damaging |
Het |
Reep6 |
G |
A |
10: 80,171,369 (GRCm39) |
R415Q |
probably benign |
Het |
Serpinb13 |
T |
C |
1: 106,926,302 (GRCm39) |
V159A |
probably benign |
Het |
Slc5a8 |
T |
A |
10: 88,738,325 (GRCm39) |
M196K |
possibly damaging |
Het |
Sprr1a |
G |
A |
3: 92,391,827 (GRCm39) |
P58L |
probably damaging |
Het |
Taf1a |
A |
T |
1: 183,172,288 (GRCm39) |
T10S |
possibly damaging |
Het |
Tap1 |
T |
A |
17: 34,412,232 (GRCm39) |
V479E |
probably damaging |
Het |
Trpm4 |
C |
T |
7: 44,971,422 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 187,995,579 (GRCm39) |
Y117H |
probably benign |
Het |
Vmn2r58 |
A |
T |
7: 41,513,914 (GRCm39) |
L243* |
probably null |
Het |
Zbtb32 |
A |
G |
7: 30,290,569 (GRCm39) |
I242T |
probably benign |
Het |
Zbtb7a |
T |
C |
10: 80,983,859 (GRCm39) |
C434R |
probably damaging |
Het |
|
Other mutations in Klk1b16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01068:Klk1b16
|
APN |
7 |
43,790,102 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01529:Klk1b16
|
APN |
7 |
43,790,163 (GRCm39) |
missense |
probably benign |
0.18 |
R1105:Klk1b16
|
UTSW |
7 |
43,788,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R1106:Klk1b16
|
UTSW |
7 |
43,788,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R1559:Klk1b16
|
UTSW |
7 |
43,790,425 (GRCm39) |
missense |
probably benign |
0.00 |
R3884:Klk1b16
|
UTSW |
7 |
43,788,887 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4152:Klk1b16
|
UTSW |
7 |
43,789,973 (GRCm39) |
missense |
probably benign |
0.09 |
R4398:Klk1b16
|
UTSW |
7 |
43,790,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Klk1b16
|
UTSW |
7 |
43,786,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Klk1b16
|
UTSW |
7 |
43,790,412 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5470:Klk1b16
|
UTSW |
7 |
43,786,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R5532:Klk1b16
|
UTSW |
7 |
43,790,950 (GRCm39) |
missense |
probably benign |
0.00 |
R5690:Klk1b16
|
UTSW |
7 |
43,790,318 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5717:Klk1b16
|
UTSW |
7 |
43,788,913 (GRCm39) |
missense |
probably benign |
0.00 |
R5749:Klk1b16
|
UTSW |
7 |
43,790,210 (GRCm39) |
missense |
probably benign |
0.03 |
R6589:Klk1b16
|
UTSW |
7 |
43,790,894 (GRCm39) |
missense |
probably benign |
0.03 |
R7084:Klk1b16
|
UTSW |
7 |
43,788,910 (GRCm39) |
missense |
probably benign |
0.01 |
R7336:Klk1b16
|
UTSW |
7 |
43,790,907 (GRCm39) |
missense |
probably benign |
0.05 |
R8281:Klk1b16
|
UTSW |
7 |
43,790,971 (GRCm39) |
missense |
probably benign |
|
R8358:Klk1b16
|
UTSW |
7 |
43,790,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9002:Klk1b16
|
UTSW |
7 |
43,790,189 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9010:Klk1b16
|
UTSW |
7 |
43,790,177 (GRCm39) |
missense |
probably benign |
0.40 |
R9013:Klk1b16
|
UTSW |
7 |
43,790,332 (GRCm39) |
missense |
probably benign |
0.03 |
X0026:Klk1b16
|
UTSW |
7 |
43,790,368 (GRCm39) |
missense |
probably damaging |
0.99 |
|