Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
C |
T |
10: 78,902,325 (GRCm39) |
V664M |
possibly damaging |
Het |
Abca4 |
A |
G |
3: 121,967,663 (GRCm39) |
T2238A |
probably damaging |
Het |
Adss2 |
G |
A |
1: 177,595,263 (GRCm39) |
Q426* |
probably null |
Het |
Afap1l2 |
T |
C |
19: 56,933,199 (GRCm39) |
E71G |
probably damaging |
Het |
Afg1l |
T |
C |
10: 42,194,607 (GRCm39) |
D395G |
probably damaging |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,592,302 (GRCm39) |
T385A |
probably benign |
Het |
Ank3 |
C |
T |
10: 69,828,402 (GRCm39) |
T2357I |
|
Het |
Ankfn1 |
T |
A |
11: 89,394,797 (GRCm39) |
S263C |
probably benign |
Het |
Atpsckmt |
C |
T |
15: 31,606,186 (GRCm39) |
A48V |
probably damaging |
Het |
Azin1 |
C |
T |
15: 38,501,665 (GRCm39) |
V29I |
probably benign |
Het |
B3galt2 |
T |
C |
1: 143,523,042 (GRCm39) |
Y393H |
probably damaging |
Het |
Cnbd2 |
G |
T |
2: 156,170,296 (GRCm39) |
R127L |
possibly damaging |
Het |
Col6a5 |
A |
T |
9: 105,741,887 (GRCm39) |
L2344* |
probably null |
Het |
Csn3 |
T |
C |
5: 88,077,821 (GRCm39) |
V109A |
not run |
Het |
Cxcr2 |
C |
G |
1: 74,198,074 (GRCm39) |
N189K |
probably benign |
Het |
Dclre1a |
A |
G |
19: 56,517,965 (GRCm39) |
F1038S |
probably damaging |
Het |
Ddx21 |
T |
C |
10: 62,426,449 (GRCm39) |
Q468R |
probably benign |
Het |
Dlx6 |
A |
G |
6: 6,863,423 (GRCm39) |
D15G |
probably damaging |
Het |
Dnajb14 |
T |
C |
3: 137,610,558 (GRCm39) |
V262A |
possibly damaging |
Het |
Dpp7 |
A |
G |
2: 25,245,603 (GRCm39) |
V161A |
probably benign |
Het |
Enkur |
C |
T |
2: 21,209,913 (GRCm39) |
S16N |
probably benign |
Het |
Ensa |
C |
A |
3: 95,535,956 (GRCm39) |
H96Q |
probably damaging |
Het |
Ero1b |
T |
G |
13: 12,617,254 (GRCm39) |
C393G |
probably damaging |
Het |
Fbxo3 |
T |
C |
2: 103,881,543 (GRCm39) |
F292L |
possibly damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,853,848 (GRCm39) |
D1604G |
possibly damaging |
Het |
Fos |
T |
C |
12: 85,521,871 (GRCm39) |
S102P |
probably benign |
Het |
Foxs1 |
C |
T |
2: 152,774,361 (GRCm39) |
G231S |
probably benign |
Het |
Furin |
T |
C |
7: 80,046,734 (GRCm39) |
D174G |
probably damaging |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Git2 |
C |
T |
5: 114,904,550 (GRCm39) |
R123H |
probably damaging |
Het |
Gm32687 |
T |
A |
10: 81,716,023 (GRCm39) |
C472S |
probably damaging |
Het |
Gmip |
A |
G |
8: 70,267,085 (GRCm39) |
E327G |
probably benign |
Het |
Gpld1 |
A |
G |
13: 25,146,388 (GRCm39) |
T211A |
probably benign |
Het |
Grin2d |
T |
C |
7: 45,511,803 (GRCm39) |
H214R |
probably benign |
Het |
Hfm1 |
T |
C |
5: 107,043,909 (GRCm39) |
T576A |
probably benign |
Het |
Hnrnpd |
A |
T |
5: 100,115,113 (GRCm39) |
F142I |
probably damaging |
Het |
Krt32 |
T |
A |
11: 99,972,047 (GRCm39) |
T434S |
probably benign |
Het |
Lct |
T |
G |
1: 128,228,469 (GRCm39) |
D1008A |
probably damaging |
Het |
Man1c1 |
A |
G |
4: 134,291,814 (GRCm39) |
|
probably null |
Het |
Marchf7 |
T |
A |
2: 60,060,048 (GRCm39) |
C58* |
probably null |
Het |
Mccc1 |
C |
T |
3: 36,029,943 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
A |
10: 88,385,187 (GRCm39) |
D484V |
probably damaging |
Het |
Myh10 |
T |
A |
11: 68,636,806 (GRCm39) |
C227S |
unknown |
Het |
Niban1 |
T |
A |
1: 151,594,063 (GRCm39) |
V916E |
probably benign |
Het |
Nin |
T |
C |
12: 70,109,480 (GRCm39) |
E153G |
|
Het |
Nr1h2 |
G |
A |
7: 44,200,216 (GRCm39) |
T313M |
probably damaging |
Het |
Or4g7 |
T |
A |
2: 111,309,477 (GRCm39) |
I116K |
probably damaging |
Het |
Or5k15 |
G |
T |
16: 58,709,629 (GRCm39) |
A318D |
probably benign |
Het |
Otog |
C |
A |
7: 45,937,279 (GRCm39) |
H1663N |
possibly damaging |
Het |
Piezo2 |
G |
T |
18: 63,186,081 (GRCm39) |
T1696K |
probably benign |
Het |
Plekhg4 |
T |
A |
8: 106,102,031 (GRCm39) |
C7S |
probably benign |
Het |
Pnma2 |
A |
G |
14: 67,153,428 (GRCm39) |
|
probably benign |
Het |
Potegl |
A |
G |
2: 23,097,837 (GRCm39) |
Y5C |
probably benign |
Het |
Prag1 |
A |
G |
8: 36,614,096 (GRCm39) |
Y1216C |
probably damaging |
Het |
Prima1 |
T |
C |
12: 103,163,566 (GRCm39) |
Y135C |
probably damaging |
Het |
Prkce |
C |
A |
17: 86,800,721 (GRCm39) |
S379* |
probably null |
Het |
Prmt7 |
A |
G |
8: 106,968,835 (GRCm39) |
N383S |
probably damaging |
Het |
Ptafr |
A |
G |
4: 132,307,063 (GRCm39) |
Y151C |
probably damaging |
Het |
Ptprn2 |
T |
C |
12: 116,449,486 (GRCm39) |
M1T |
probably null |
Het |
Rad23a |
A |
T |
8: 85,565,108 (GRCm39) |
S136T |
probably benign |
Het |
Rnf123 |
A |
T |
9: 107,947,818 (GRCm39) |
Y137N |
probably damaging |
Het |
Sfxn4 |
A |
C |
19: 60,842,324 (GRCm39) |
I126S |
probably benign |
Het |
Slc4a4 |
A |
G |
5: 89,373,726 (GRCm39) |
H935R |
probably damaging |
Het |
Slitrk3 |
T |
G |
3: 72,958,448 (GRCm39) |
N108T |
probably damaging |
Het |
Spred1 |
T |
A |
2: 117,007,806 (GRCm39) |
H237Q |
probably benign |
Het |
Syne1 |
T |
A |
10: 5,074,820 (GRCm39) |
K1168N |
probably damaging |
Het |
Syt14 |
T |
C |
1: 192,665,885 (GRCm39) |
K340E |
unknown |
Het |
Tespa1 |
T |
C |
10: 130,190,624 (GRCm39) |
S84P |
probably damaging |
Het |
Tmem268 |
G |
T |
4: 63,480,681 (GRCm39) |
|
probably benign |
Het |
Tmem52b |
T |
A |
6: 129,493,040 (GRCm39) |
Y48* |
probably null |
Het |
Tox2 |
C |
A |
2: 163,157,822 (GRCm39) |
Y295* |
probably null |
Het |
Trp53bp1 |
T |
G |
2: 121,067,119 (GRCm39) |
T536P |
possibly damaging |
Het |
Tysnd1 |
T |
C |
10: 61,531,665 (GRCm39) |
C106R |
probably benign |
Het |
Unc5d |
T |
C |
8: 29,381,449 (GRCm39) |
I63V |
probably damaging |
Het |
Vmn1r235 |
A |
G |
17: 21,481,881 (GRCm39) |
N69D |
possibly damaging |
Het |
Vps11 |
A |
T |
9: 44,260,258 (GRCm39) |
M868K |
probably benign |
Het |
Wipf3 |
A |
G |
6: 54,462,509 (GRCm39) |
T240A |
possibly damaging |
Het |
Xirp2 |
G |
A |
2: 67,345,309 (GRCm39) |
E2517K |
possibly damaging |
Het |
Ylpm1 |
T |
A |
12: 85,043,994 (GRCm39) |
L244Q |
unknown |
Het |
Zdhhc18 |
G |
T |
4: 133,342,520 (GRCm39) |
S198* |
probably null |
Het |
Zfp760 |
T |
A |
17: 21,941,242 (GRCm39) |
L139* |
probably null |
Het |
|
Other mutations in Plcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:Plcd1
|
APN |
9 |
118,905,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01634:Plcd1
|
APN |
9 |
118,902,857 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01992:Plcd1
|
APN |
9 |
118,905,053 (GRCm39) |
missense |
probably benign |
|
IGL02246:Plcd1
|
APN |
9 |
118,901,677 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02266:Plcd1
|
APN |
9 |
118,903,855 (GRCm39) |
splice site |
probably benign |
|
IGL02270:Plcd1
|
APN |
9 |
118,913,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02281:Plcd1
|
APN |
9 |
118,903,841 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02324:Plcd1
|
APN |
9 |
118,901,710 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02936:Plcd1
|
APN |
9 |
118,903,267 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03348:Plcd1
|
APN |
9 |
118,901,558 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0366:Plcd1
|
UTSW |
9 |
118,910,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R1765:Plcd1
|
UTSW |
9 |
118,900,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R3704:Plcd1
|
UTSW |
9 |
118,905,277 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5143:Plcd1
|
UTSW |
9 |
118,903,519 (GRCm39) |
nonsense |
probably null |
|
R5587:Plcd1
|
UTSW |
9 |
118,902,900 (GRCm39) |
missense |
probably benign |
|
R5877:Plcd1
|
UTSW |
9 |
118,905,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Plcd1
|
UTSW |
9 |
118,901,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R6103:Plcd1
|
UTSW |
9 |
118,901,109 (GRCm39) |
missense |
probably benign |
0.16 |
R6338:Plcd1
|
UTSW |
9 |
118,904,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Plcd1
|
UTSW |
9 |
118,904,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Plcd1
|
UTSW |
9 |
118,901,709 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6516:Plcd1
|
UTSW |
9 |
118,905,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R6646:Plcd1
|
UTSW |
9 |
118,904,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R6854:Plcd1
|
UTSW |
9 |
118,903,389 (GRCm39) |
splice site |
probably null |
|
R6955:Plcd1
|
UTSW |
9 |
118,900,924 (GRCm39) |
missense |
probably benign |
0.01 |
R7382:Plcd1
|
UTSW |
9 |
118,903,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Plcd1
|
UTSW |
9 |
118,903,720 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8089:Plcd1
|
UTSW |
9 |
118,905,060 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9027:Plcd1
|
UTSW |
9 |
118,913,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R9217:Plcd1
|
UTSW |
9 |
118,901,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9434:Plcd1
|
UTSW |
9 |
118,905,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R9596:Plcd1
|
UTSW |
9 |
118,917,183 (GRCm39) |
missense |
probably benign |
0.10 |
R9667:Plcd1
|
UTSW |
9 |
118,901,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R9739:Plcd1
|
UTSW |
9 |
118,901,195 (GRCm39) |
missense |
possibly damaging |
0.69 |
|