Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
G |
17: 36,270,144 (GRCm39) |
F638S |
possibly damaging |
Het |
Actl6b |
T |
A |
5: 137,562,762 (GRCm39) |
N159K |
probably damaging |
Het |
Adam6a |
T |
G |
12: 113,508,655 (GRCm39) |
S343A |
probably benign |
Het |
Ankrd17 |
G |
A |
5: 90,380,173 (GRCm39) |
T2505I |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,433,382 (GRCm39) |
T728A |
probably benign |
Het |
Asap2 |
G |
T |
12: 21,315,964 (GRCm39) |
E919* |
probably null |
Het |
Atp10b |
A |
T |
11: 43,136,291 (GRCm39) |
I1140F |
probably damaging |
Het |
Cep126 |
A |
T |
9: 8,103,383 (GRCm39) |
V209E |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,965,792 (GRCm39) |
R406Q |
probably benign |
Het |
Cldn1 |
T |
C |
16: 26,190,376 (GRCm39) |
M1V |
probably null |
Het |
Cryl1 |
C |
T |
14: 57,512,956 (GRCm39) |
D304N |
probably benign |
Het |
D3Ertd751e |
T |
C |
3: 41,708,212 (GRCm39) |
|
probably null |
Het |
D630044L22Rik |
A |
T |
17: 26,181,090 (GRCm39) |
M156L |
probably benign |
Het |
Ddx21 |
T |
C |
10: 62,427,634 (GRCm39) |
D423G |
possibly damaging |
Het |
Dock2 |
T |
A |
11: 34,260,363 (GRCm39) |
M993L |
probably benign |
Het |
Dusp29 |
A |
T |
14: 21,727,129 (GRCm39) |
I173N |
probably damaging |
Het |
Eif4g1 |
C |
T |
16: 20,500,252 (GRCm39) |
A675V |
probably damaging |
Het |
Eml1 |
C |
T |
12: 108,472,810 (GRCm39) |
S206L |
probably benign |
Het |
Farp2 |
A |
C |
1: 93,531,181 (GRCm39) |
I560L |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,223,969 (GRCm39) |
D593E |
probably benign |
Het |
Fetub |
A |
G |
16: 22,748,007 (GRCm39) |
D61G |
possibly damaging |
Het |
Fpgs |
T |
C |
2: 32,576,641 (GRCm39) |
K329E |
probably benign |
Het |
Fpgt |
T |
C |
3: 154,797,120 (GRCm39) |
Y45C |
probably damaging |
Het |
Gas2l1 |
A |
T |
11: 5,011,106 (GRCm39) |
C574* |
probably null |
Het |
Gm9747 |
G |
T |
1: 82,211,837 (GRCm39) |
C12F |
unknown |
Het |
H2-T23 |
T |
C |
17: 36,342,709 (GRCm39) |
Y143C |
probably damaging |
Het |
Hhip |
A |
T |
8: 80,719,142 (GRCm39) |
S462T |
probably benign |
Het |
Hnf1a |
C |
T |
5: 115,091,446 (GRCm39) |
G416R |
probably damaging |
Het |
Hoxa5 |
C |
T |
6: 52,181,023 (GRCm39) |
C103Y |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,390,848 (GRCm39) |
D395E |
possibly damaging |
Het |
Marchf10 |
A |
G |
11: 105,299,502 (GRCm39) |
S116P |
probably benign |
Het |
Med12l |
C |
T |
3: 59,001,180 (GRCm39) |
Q748* |
probably null |
Het |
Mroh7 |
T |
A |
4: 106,577,791 (GRCm39) |
N296Y |
probably damaging |
Het |
Mtbp |
T |
G |
15: 55,421,961 (GRCm39) |
D61E |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,391 (GRCm39) |
I1446L |
unknown |
Het |
Myh15 |
T |
C |
16: 48,901,705 (GRCm39) |
V266A |
possibly damaging |
Het |
Nap1l1 |
G |
A |
10: 111,330,655 (GRCm39) |
|
probably null |
Het |
Napsa |
A |
G |
7: 44,235,159 (GRCm39) |
T315A |
probably benign |
Het |
Nlrc5 |
A |
T |
8: 95,206,350 (GRCm39) |
I734F |
probably damaging |
Het |
Nnt |
A |
G |
13: 119,531,198 (GRCm39) |
V183A |
probably damaging |
Het |
Nploc4 |
A |
T |
11: 120,276,614 (GRCm39) |
D477E |
probably benign |
Het |
Nrip3 |
A |
G |
7: 109,364,695 (GRCm39) |
S144P |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 109,842,445 (GRCm39) |
F109L |
probably benign |
Het |
Or5p61 |
A |
G |
7: 107,758,883 (GRCm39) |
Y66H |
probably damaging |
Het |
Or5v1 |
T |
A |
17: 37,809,776 (GRCm39) |
V78D |
probably damaging |
Het |
Or6aa1 |
G |
A |
7: 86,044,752 (GRCm39) |
|
probably benign |
Het |
Or8b36 |
A |
G |
9: 37,937,795 (GRCm39) |
E231G |
probably benign |
Het |
Pacsin1 |
G |
A |
17: 27,921,707 (GRCm39) |
D30N |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,860,368 (GRCm39) |
|
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,613,750 (GRCm39) |
T565I |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,763,246 (GRCm39) |
T225S |
probably benign |
Het |
Phyhip |
T |
G |
14: 70,704,639 (GRCm39) |
I286S |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,813,086 (GRCm39) |
Y3903N |
probably damaging |
Het |
Plcd4 |
T |
A |
1: 74,593,662 (GRCm39) |
H262Q |
probably benign |
Het |
Plekhh1 |
C |
T |
12: 79,109,390 (GRCm39) |
A474V |
probably benign |
Het |
Plppr3 |
T |
C |
10: 79,701,537 (GRCm39) |
E435G |
probably damaging |
Het |
Poln |
T |
A |
5: 34,276,340 (GRCm39) |
N305I |
possibly damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,874 (GRCm39) |
T420A |
probably benign |
Het |
Ppdpf |
T |
C |
2: 180,829,523 (GRCm39) |
Y17H |
probably damaging |
Het |
Prrx2 |
C |
A |
2: 30,768,485 (GRCm39) |
T104K |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,294,822 (GRCm39) |
L462H |
probably benign |
Het |
Radil |
T |
C |
5: 142,471,304 (GRCm39) |
T991A |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,178,608 (GRCm39) |
E147G |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,300,742 (GRCm39) |
V35M |
probably benign |
Het |
Rps6ka1 |
T |
C |
4: 133,599,373 (GRCm39) |
Q18R |
probably benign |
Het |
Setbp1 |
T |
A |
18: 78,902,734 (GRCm39) |
D311V |
possibly damaging |
Het |
Setd2 |
C |
T |
9: 110,377,865 (GRCm39) |
S560L |
possibly damaging |
Het |
Slc12a5 |
A |
T |
2: 164,816,878 (GRCm39) |
I134F |
probably damaging |
Het |
Speer1h |
C |
T |
5: 11,647,706 (GRCm39) |
T148I |
possibly damaging |
Het |
Svil |
A |
G |
18: 5,116,080 (GRCm39) |
D2035G |
probably damaging |
Het |
Syngap1 |
T |
C |
17: 27,178,985 (GRCm39) |
Y665H |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,043,519 (GRCm39) |
Y547H |
possibly damaging |
Het |
Tgm2 |
A |
G |
2: 157,980,812 (GRCm39) |
V83A |
probably benign |
Het |
Tmem233 |
T |
C |
5: 116,189,429 (GRCm39) |
I117V |
probably benign |
Het |
Tsen34 |
A |
G |
7: 3,703,640 (GRCm39) |
T293A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,709,023 (GRCm39) |
V8752A |
unknown |
Het |
Ubac1 |
A |
G |
2: 25,904,974 (GRCm39) |
V88A |
probably benign |
Het |
Uchl4 |
T |
C |
9: 64,142,621 (GRCm39) |
V34A |
probably damaging |
Het |
Ugt2a2 |
C |
T |
5: 87,608,435 (GRCm39) |
R468H |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,749 (GRCm39) |
T255S |
probably benign |
Het |
Wdr6 |
T |
A |
9: 108,450,564 (GRCm39) |
N988I |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,903,389 (GRCm39) |
I2359N |
unknown |
Het |
Ybey |
A |
G |
10: 76,304,025 (GRCm39) |
V59A |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,349,375 (GRCm39) |
C271S |
possibly damaging |
Het |
Zfp397 |
A |
G |
18: 24,090,122 (GRCm39) |
N142S |
probably benign |
Het |
Zfy1 |
A |
T |
Y: 725,788 (GRCm39) |
V659E |
probably damaging |
Het |
|
Other mutations in Plcb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01092:Plcb3
|
APN |
19 |
6,932,690 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01370:Plcb3
|
APN |
19 |
6,940,192 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01385:Plcb3
|
APN |
19 |
6,935,276 (GRCm39) |
missense |
probably benign |
|
IGL01511:Plcb3
|
APN |
19 |
6,933,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02182:Plcb3
|
APN |
19 |
6,946,988 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02240:Plcb3
|
APN |
19 |
6,935,448 (GRCm39) |
splice site |
probably benign |
|
IGL02350:Plcb3
|
APN |
19 |
6,935,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Plcb3
|
APN |
19 |
6,935,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Plcb3
|
APN |
19 |
6,937,544 (GRCm39) |
nonsense |
probably null |
|
IGL02866:Plcb3
|
APN |
19 |
6,935,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Plcb3
|
APN |
19 |
6,933,521 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03327:Plcb3
|
APN |
19 |
6,932,420 (GRCm39) |
missense |
probably benign |
|
IGL03346:Plcb3
|
APN |
19 |
6,932,420 (GRCm39) |
missense |
probably benign |
|
Multifarious
|
UTSW |
19 |
6,932,071 (GRCm39) |
critical splice donor site |
probably null |
|
R0042:Plcb3
|
UTSW |
19 |
6,943,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Plcb3
|
UTSW |
19 |
6,936,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Plcb3
|
UTSW |
19 |
6,940,363 (GRCm39) |
missense |
probably benign |
0.16 |
R0240:Plcb3
|
UTSW |
19 |
6,940,363 (GRCm39) |
missense |
probably benign |
0.16 |
R0724:Plcb3
|
UTSW |
19 |
6,940,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Plcb3
|
UTSW |
19 |
6,939,281 (GRCm39) |
nonsense |
probably null |
|
R0945:Plcb3
|
UTSW |
19 |
6,932,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Plcb3
|
UTSW |
19 |
6,939,281 (GRCm39) |
nonsense |
probably null |
|
R1414:Plcb3
|
UTSW |
19 |
6,940,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Plcb3
|
UTSW |
19 |
6,932,414 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1533:Plcb3
|
UTSW |
19 |
6,935,041 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1652:Plcb3
|
UTSW |
19 |
6,932,664 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Plcb3
|
UTSW |
19 |
6,933,381 (GRCm39) |
unclassified |
probably benign |
|
R1870:Plcb3
|
UTSW |
19 |
6,940,353 (GRCm39) |
missense |
probably benign |
0.04 |
R1934:Plcb3
|
UTSW |
19 |
6,941,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Plcb3
|
UTSW |
19 |
6,943,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4397:Plcb3
|
UTSW |
19 |
6,943,193 (GRCm39) |
missense |
probably damaging |
0.96 |
R4533:Plcb3
|
UTSW |
19 |
6,933,640 (GRCm39) |
missense |
probably benign |
0.08 |
R4576:Plcb3
|
UTSW |
19 |
6,936,415 (GRCm39) |
splice site |
probably benign |
|
R4815:Plcb3
|
UTSW |
19 |
6,940,352 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4903:Plcb3
|
UTSW |
19 |
6,933,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R5093:Plcb3
|
UTSW |
19 |
6,943,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5555:Plcb3
|
UTSW |
19 |
6,943,587 (GRCm39) |
missense |
probably benign |
0.19 |
R5593:Plcb3
|
UTSW |
19 |
6,932,117 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5626:Plcb3
|
UTSW |
19 |
6,932,643 (GRCm39) |
missense |
probably benign |
0.24 |
R5661:Plcb3
|
UTSW |
19 |
6,940,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R5713:Plcb3
|
UTSW |
19 |
6,935,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R5741:Plcb3
|
UTSW |
19 |
6,931,790 (GRCm39) |
nonsense |
probably null |
|
R6025:Plcb3
|
UTSW |
19 |
6,933,547 (GRCm39) |
missense |
probably benign |
0.03 |
R6063:Plcb3
|
UTSW |
19 |
6,940,202 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6155:Plcb3
|
UTSW |
19 |
6,943,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6157:Plcb3
|
UTSW |
19 |
6,943,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Plcb3
|
UTSW |
19 |
6,932,071 (GRCm39) |
critical splice donor site |
probably null |
|
R7085:Plcb3
|
UTSW |
19 |
6,937,501 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7117:Plcb3
|
UTSW |
19 |
6,941,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7153:Plcb3
|
UTSW |
19 |
6,935,452 (GRCm39) |
critical splice donor site |
probably null |
|
R7316:Plcb3
|
UTSW |
19 |
6,943,753 (GRCm39) |
critical splice donor site |
probably null |
|
R7366:Plcb3
|
UTSW |
19 |
6,939,389 (GRCm39) |
missense |
probably benign |
|
R7399:Plcb3
|
UTSW |
19 |
6,940,235 (GRCm39) |
missense |
probably benign |
|
R7736:Plcb3
|
UTSW |
19 |
6,946,991 (GRCm39) |
missense |
probably benign |
0.00 |
R8057:Plcb3
|
UTSW |
19 |
6,936,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R8057:Plcb3
|
UTSW |
19 |
6,932,463 (GRCm39) |
missense |
probably benign |
|
R8376:Plcb3
|
UTSW |
19 |
6,944,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R9103:Plcb3
|
UTSW |
19 |
6,936,288 (GRCm39) |
missense |
probably benign |
0.06 |
R9292:Plcb3
|
UTSW |
19 |
6,942,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R9366:Plcb3
|
UTSW |
19 |
6,937,658 (GRCm39) |
critical splice donor site |
probably null |
|
|