Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn3 |
T |
C |
19: 4,915,468 (GRCm39) |
E428G |
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,732,211 (GRCm39) |
I1600T |
probably benign |
Het |
Arid3b |
A |
T |
9: 57,697,713 (GRCm39) |
|
probably benign |
Het |
Asgr2 |
C |
A |
11: 69,989,057 (GRCm39) |
T167K |
probably benign |
Het |
Atf6b |
T |
A |
17: 34,871,648 (GRCm39) |
M428K |
probably benign |
Het |
Atpaf1 |
A |
T |
4: 115,645,556 (GRCm39) |
M142L |
probably benign |
Het |
Bivm |
A |
T |
1: 44,177,793 (GRCm39) |
R364S |
probably damaging |
Het |
Bms1 |
T |
C |
6: 118,382,308 (GRCm39) |
|
probably null |
Het |
Brwd1 |
G |
A |
16: 95,818,804 (GRCm39) |
P1343S |
probably damaging |
Het |
Cdca2 |
T |
C |
14: 67,952,299 (GRCm39) |
D24G |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,300,993 (GRCm39) |
R2767G |
probably benign |
Het |
Cip2a |
T |
A |
16: 48,833,612 (GRCm39) |
F571Y |
probably benign |
Het |
Cyp2c55 |
A |
T |
19: 39,000,235 (GRCm39) |
I145F |
probably damaging |
Het |
Ddx18 |
T |
C |
1: 121,489,121 (GRCm39) |
T309A |
probably benign |
Het |
Dlg3 |
A |
T |
X: 99,840,288 (GRCm39) |
|
probably benign |
Het |
Fbf1 |
A |
G |
11: 116,039,720 (GRCm39) |
L713P |
probably damaging |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Fnbp1 |
A |
G |
2: 30,995,362 (GRCm39) |
F24S |
probably damaging |
Het |
Gm16686 |
A |
T |
4: 88,673,710 (GRCm39) |
|
probably benign |
Het |
Gmps |
A |
G |
3: 63,898,040 (GRCm39) |
M275V |
probably damaging |
Het |
Igdcc4 |
A |
G |
9: 65,031,892 (GRCm39) |
|
probably null |
Het |
Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
Kif18a |
T |
C |
2: 109,123,398 (GRCm39) |
V224A |
probably benign |
Het |
Lbr |
C |
T |
1: 181,648,267 (GRCm39) |
C398Y |
probably damaging |
Het |
Lmf1 |
T |
C |
17: 25,873,455 (GRCm39) |
L320P |
probably damaging |
Het |
Mapkapk3 |
T |
C |
9: 107,136,131 (GRCm39) |
|
probably benign |
Het |
Mettl18 |
A |
G |
1: 163,824,171 (GRCm39) |
D164G |
probably damaging |
Het |
Myo5a |
A |
T |
9: 75,051,453 (GRCm39) |
T349S |
probably benign |
Het |
Or1ad6 |
T |
C |
11: 50,860,253 (GRCm39) |
M136T |
probably damaging |
Het |
Or8d2b |
A |
G |
9: 38,788,609 (GRCm39) |
I46V |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,734 (GRCm39) |
S705T |
possibly damaging |
Het |
Phf14 |
C |
T |
6: 11,987,096 (GRCm39) |
P559S |
probably damaging |
Het |
Pik3c3 |
G |
A |
18: 30,477,043 (GRCm39) |
A855T |
probably damaging |
Het |
Rev1 |
A |
T |
1: 38,147,500 (GRCm39) |
D13E |
possibly damaging |
Het |
Sec16a |
A |
G |
2: 26,312,167 (GRCm39) |
Y1998H |
probably benign |
Het |
Slc4a5 |
C |
T |
6: 83,237,511 (GRCm39) |
R165C |
probably damaging |
Het |
Slfn10-ps |
T |
C |
11: 82,926,260 (GRCm39) |
|
noncoding transcript |
Het |
Slfn9 |
T |
C |
11: 82,873,334 (GRCm39) |
N523S |
probably benign |
Het |
Spata13 |
T |
A |
14: 60,947,004 (GRCm39) |
M684K |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,776,636 (GRCm39) |
|
probably benign |
Het |
Stk32c |
T |
C |
7: 138,700,704 (GRCm39) |
|
probably null |
Het |
Tenm3 |
T |
C |
8: 48,848,693 (GRCm39) |
T49A |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,084,318 (GRCm39) |
I954V |
probably benign |
Het |
Tmem237 |
A |
G |
1: 59,158,995 (GRCm39) |
|
probably benign |
Het |
Vmn2r101 |
A |
T |
17: 19,832,303 (GRCm39) |
R766S |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,636,996 (GRCm39) |
T693A |
probably benign |
Het |
Xpr1 |
A |
G |
1: 155,188,542 (GRCm39) |
F366S |
possibly damaging |
Het |
Zfp317 |
A |
G |
9: 19,557,990 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Plpp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00661:Plpp4
|
APN |
7 |
128,918,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00885:Plpp4
|
APN |
7 |
128,923,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Plpp4
|
UTSW |
7 |
128,925,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Plpp4
|
UTSW |
7 |
128,925,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Plpp4
|
UTSW |
7 |
128,981,095 (GRCm39) |
missense |
probably benign |
0.08 |
R4290:Plpp4
|
UTSW |
7 |
128,909,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Plpp4
|
UTSW |
7 |
128,909,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4439:Plpp4
|
UTSW |
7 |
128,858,813 (GRCm39) |
start gained |
probably benign |
|
R5185:Plpp4
|
UTSW |
7 |
128,918,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Plpp4
|
UTSW |
7 |
128,992,616 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7122:Plpp4
|
UTSW |
7 |
128,981,207 (GRCm39) |
missense |
unknown |
|
R8048:Plpp4
|
UTSW |
7 |
128,981,201 (GRCm39) |
missense |
unknown |
|
R8854:Plpp4
|
UTSW |
7 |
128,909,362 (GRCm39) |
nonsense |
probably null |
|
R8926:Plpp4
|
UTSW |
7 |
128,923,211 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8994:Plpp4
|
UTSW |
7 |
128,981,157 (GRCm39) |
missense |
probably damaging |
0.99 |
R9575:Plpp4
|
UTSW |
7 |
128,925,211 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Plpp4
|
UTSW |
7 |
128,981,201 (GRCm39) |
missense |
unknown |
|
|