Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam21 |
A |
G |
12: 81,606,380 (GRCm39) |
F461L |
probably benign |
Het |
Adamtsl3 |
C |
A |
7: 82,227,818 (GRCm39) |
H1334Q |
probably benign |
Het |
Adgrf1 |
A |
G |
17: 43,621,263 (GRCm39) |
N500S |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,042,634 (GRCm39) |
D335G |
possibly damaging |
Het |
Arhgap19 |
G |
A |
19: 41,775,077 (GRCm39) |
T178M |
probably damaging |
Het |
Chac2 |
T |
C |
11: 30,927,625 (GRCm39) |
D86G |
probably damaging |
Het |
Clhc1 |
T |
C |
11: 29,510,542 (GRCm39) |
S209P |
possibly damaging |
Het |
Col1a2 |
G |
A |
6: 4,515,517 (GRCm39) |
G127S |
unknown |
Het |
Coro2b |
A |
G |
9: 62,396,606 (GRCm39) |
F51L |
probably benign |
Het |
Cux2 |
A |
G |
5: 122,002,789 (GRCm39) |
S1139P |
probably benign |
Het |
Cyth3 |
A |
T |
5: 143,693,595 (GRCm39) |
I379F |
probably damaging |
Het |
Dock2 |
A |
T |
11: 34,312,822 (GRCm39) |
L240H |
possibly damaging |
Het |
Ercc6 |
A |
G |
14: 32,248,780 (GRCm39) |
K444E |
probably damaging |
Het |
Fam3b |
A |
G |
16: 97,302,101 (GRCm39) |
L52P |
possibly damaging |
Het |
Fat4 |
T |
G |
3: 39,035,418 (GRCm39) |
Y3023* |
probably null |
Het |
Gad1 |
A |
T |
2: 70,423,780 (GRCm39) |
N396Y |
probably damaging |
Het |
Gbp2b |
A |
G |
3: 142,317,252 (GRCm39) |
E536G |
probably benign |
Het |
Gm11564 |
G |
A |
11: 99,706,061 (GRCm39) |
T123I |
unknown |
Het |
Herc2 |
G |
T |
7: 55,796,393 (GRCm39) |
E1922* |
probably null |
Het |
Hrh4 |
G |
T |
18: 13,155,525 (GRCm39) |
V355F |
probably damaging |
Het |
Isyna1 |
A |
G |
8: 71,047,339 (GRCm39) |
I21V |
probably damaging |
Het |
Jak1 |
T |
C |
4: 101,039,130 (GRCm39) |
D165G |
probably benign |
Het |
Klhl38 |
C |
A |
15: 58,185,809 (GRCm39) |
G307* |
probably null |
Het |
Krt77 |
T |
C |
15: 101,772,772 (GRCm39) |
N269S |
probably damaging |
Het |
Lrp4 |
T |
A |
2: 91,322,765 (GRCm39) |
I1118N |
possibly damaging |
Het |
Ly6i |
T |
C |
15: 74,853,833 (GRCm39) |
Y30C |
probably damaging |
Het |
Magi2 |
A |
G |
5: 20,807,345 (GRCm39) |
E620G |
possibly damaging |
Het |
Mbl2 |
A |
G |
19: 30,216,839 (GRCm39) |
D217G |
possibly damaging |
Het |
Mogat2 |
T |
A |
7: 98,871,553 (GRCm39) |
I253F |
probably benign |
Het |
Mpped2 |
T |
C |
2: 106,691,925 (GRCm39) |
L210P |
probably damaging |
Het |
Nav3 |
C |
A |
10: 109,600,617 (GRCm39) |
A1337S |
probably damaging |
Het |
Ncaph2 |
T |
A |
15: 89,248,407 (GRCm39) |
V206E |
probably benign |
Het |
Nlgn1 |
T |
C |
3: 25,488,094 (GRCm39) |
E747G |
possibly damaging |
Het |
Nlrc3 |
C |
T |
16: 3,770,308 (GRCm39) |
G237D |
possibly damaging |
Het |
Nsun7 |
A |
G |
5: 66,452,827 (GRCm39) |
D514G |
probably benign |
Het |
Or10al5 |
C |
G |
17: 38,063,577 (GRCm39) |
D277E |
probably damaging |
Het |
Pals2 |
A |
G |
6: 50,175,146 (GRCm39) |
K500E |
possibly damaging |
Het |
Pcnx2 |
C |
A |
8: 126,480,224 (GRCm39) |
V2028F |
probably damaging |
Het |
Pdx1 |
G |
T |
5: 147,207,440 (GRCm39) |
W131L |
probably damaging |
Het |
Pkdrej |
C |
T |
15: 85,703,747 (GRCm39) |
V730I |
probably damaging |
Het |
Plcg1 |
T |
A |
2: 160,596,487 (GRCm39) |
Y669N |
probably damaging |
Het |
Sfxn1 |
G |
A |
13: 54,242,918 (GRCm39) |
V59I |
probably benign |
Het |
Shank1 |
T |
C |
7: 43,976,645 (GRCm39) |
I581T |
unknown |
Het |
Slc35f6 |
A |
C |
5: 30,814,164 (GRCm39) |
K150N |
possibly damaging |
Het |
Slc5a7 |
A |
T |
17: 54,591,231 (GRCm39) |
S234T |
probably benign |
Het |
Smg6 |
C |
T |
11: 74,821,331 (GRCm39) |
T534I |
possibly damaging |
Het |
Ush2a |
C |
T |
1: 188,573,724 (GRCm39) |
T3649I |
probably benign |
Het |
Vmn1r158 |
T |
C |
7: 22,490,078 (GRCm39) |
T44A |
possibly damaging |
Het |
Vmn1r217 |
A |
T |
13: 23,298,073 (GRCm39) |
Y276* |
probably null |
Het |
Vmn2r100 |
T |
A |
17: 19,742,355 (GRCm39) |
I243N |
probably damaging |
Het |
Vwde |
T |
C |
6: 13,208,404 (GRCm39) |
|
probably null |
Het |
Washc4 |
C |
A |
10: 83,394,687 (GRCm39) |
P306T |
probably damaging |
Het |
Wdhd1 |
C |
T |
14: 47,488,217 (GRCm39) |
|
probably null |
Het |
Xpo6 |
T |
C |
7: 125,770,262 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Plpp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Plpp1
|
APN |
13 |
112,988,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:Plpp1
|
APN |
13 |
112,993,433 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02269:Plpp1
|
APN |
13 |
112,993,526 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4260001:Plpp1
|
UTSW |
13 |
112,993,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0550:Plpp1
|
UTSW |
13 |
112,971,519 (GRCm39) |
missense |
probably benign |
0.02 |
R1301:Plpp1
|
UTSW |
13 |
112,971,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Plpp1
|
UTSW |
13 |
112,996,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5224:Plpp1
|
UTSW |
13 |
112,988,046 (GRCm39) |
nonsense |
probably null |
|
R5306:Plpp1
|
UTSW |
13 |
112,988,089 (GRCm39) |
critical splice donor site |
probably null |
|
R6108:Plpp1
|
UTSW |
13 |
113,003,399 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6111:Plpp1
|
UTSW |
13 |
113,003,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R7520:Plpp1
|
UTSW |
13 |
112,937,781 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7716:Plpp1
|
UTSW |
13 |
112,996,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7716:Plpp1
|
UTSW |
13 |
112,993,323 (GRCm39) |
missense |
probably benign |
0.27 |
R8080:Plpp1
|
UTSW |
13 |
113,004,002 (GRCm39) |
missense |
probably benign |
0.19 |
R8209:Plpp1
|
UTSW |
13 |
113,003,465 (GRCm39) |
missense |
probably benign |
0.44 |
R8226:Plpp1
|
UTSW |
13 |
113,003,465 (GRCm39) |
missense |
probably benign |
0.44 |
R8514:Plpp1
|
UTSW |
13 |
112,971,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Plpp1
|
UTSW |
13 |
112,943,057 (GRCm39) |
intron |
probably benign |
|
R8948:Plpp1
|
UTSW |
13 |
112,993,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R9130:Plpp1
|
UTSW |
13 |
112,988,038 (GRCm39) |
missense |
|
|
|