Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
G |
3: 59,836,354 (GRCm39) |
|
probably benign |
Het |
Abr |
A |
C |
11: 76,313,987 (GRCm39) |
M720R |
probably benign |
Het |
Acad10 |
G |
A |
5: 121,768,273 (GRCm39) |
T761M |
probably damaging |
Het |
Agxt |
G |
T |
1: 93,065,623 (GRCm39) |
G164V |
possibly damaging |
Het |
Ankar |
C |
T |
1: 72,689,390 (GRCm39) |
G1247D |
probably damaging |
Het |
Bptf |
A |
C |
11: 106,945,658 (GRCm39) |
L2527R |
probably damaging |
Het |
Brinp2 |
T |
C |
1: 158,094,117 (GRCm39) |
H195R |
possibly damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,213,624 (GRCm39) |
R14S |
probably benign |
Het |
Cep126 |
A |
T |
9: 8,100,988 (GRCm39) |
C515* |
probably null |
Het |
Chia1 |
A |
T |
3: 106,039,236 (GRCm39) |
N442I |
probably damaging |
Het |
Clasp2 |
A |
G |
9: 113,681,825 (GRCm39) |
D327G |
probably damaging |
Het |
Cnbd2 |
T |
C |
2: 156,215,581 (GRCm39) |
F519L |
probably benign |
Het |
Cntrl |
T |
A |
2: 35,041,869 (GRCm39) |
F1214I |
possibly damaging |
Het |
Cul9 |
A |
T |
17: 46,839,491 (GRCm39) |
M829K |
probably damaging |
Het |
Cyp4b1 |
T |
C |
4: 115,493,175 (GRCm39) |
Q223R |
possibly damaging |
Het |
Defb37 |
A |
T |
8: 19,040,988 (GRCm39) |
M1K |
probably null |
Het |
Dnah7c |
A |
T |
1: 46,494,937 (GRCm39) |
Q55L |
possibly damaging |
Het |
Efcab3 |
A |
G |
11: 104,791,432 (GRCm39) |
N2882S |
probably benign |
Het |
Eif2b4 |
A |
T |
5: 31,345,131 (GRCm39) |
D463E |
possibly damaging |
Het |
Elapor1 |
T |
G |
3: 108,382,317 (GRCm39) |
D232A |
possibly damaging |
Het |
Elovl1 |
C |
T |
4: 118,288,811 (GRCm39) |
H167Y |
probably damaging |
Het |
Emb |
T |
A |
13: 117,404,013 (GRCm39) |
L255Q |
probably damaging |
Het |
Eogt |
T |
C |
6: 97,089,685 (GRCm39) |
Y465C |
probably damaging |
Het |
Erc2 |
A |
G |
14: 27,375,115 (GRCm39) |
H111R |
probably damaging |
Het |
Fam234b |
T |
C |
6: 135,205,529 (GRCm39) |
F498S |
probably damaging |
Het |
Fgfr3 |
GAGGCTGGCAGCGTGTACGCAGGC |
GAGGC |
5: 33,890,092 (GRCm39) |
|
probably null |
Het |
Flrt3 |
T |
A |
2: 140,503,090 (GRCm39) |
E179D |
probably damaging |
Het |
Fndc3a |
T |
C |
14: 72,793,597 (GRCm39) |
R993G |
probably benign |
Het |
Gm14325 |
T |
C |
2: 177,476,403 (GRCm39) |
T14A |
probably damaging |
Het |
Gm5464 |
T |
A |
14: 67,106,681 (GRCm39) |
V106D |
unknown |
Het |
Gpatch11 |
T |
A |
17: 79,149,546 (GRCm39) |
I182N |
possibly damaging |
Het |
Grm6 |
A |
G |
11: 50,753,870 (GRCm39) |
R725G |
probably damaging |
Het |
Hap1 |
A |
T |
11: 100,239,655 (GRCm39) |
M588K |
probably benign |
Het |
Icam2 |
A |
G |
11: 106,273,268 (GRCm39) |
F15L |
probably benign |
Het |
Ints8 |
A |
G |
4: 11,225,613 (GRCm39) |
M648T |
probably benign |
Het |
Ipo11 |
A |
T |
13: 107,029,065 (GRCm39) |
L296Q |
probably damaging |
Het |
Kirrel1 |
G |
A |
3: 86,993,704 (GRCm39) |
Q518* |
probably null |
Het |
Krt18 |
G |
T |
15: 101,937,967 (GRCm39) |
D155Y |
possibly damaging |
Het |
Lctl |
A |
T |
9: 64,026,217 (GRCm39) |
K91* |
probably null |
Het |
Marf1 |
C |
A |
16: 13,960,349 (GRCm39) |
R565L |
probably damaging |
Het |
Med13 |
A |
T |
11: 86,178,921 (GRCm39) |
D1458E |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,071,837 (GRCm39) |
Y556F |
probably benign |
Het |
Muc16 |
C |
T |
9: 18,553,495 (GRCm39) |
G4266D |
probably benign |
Het |
Nsrp1 |
A |
T |
11: 76,939,249 (GRCm39) |
F182I |
probably damaging |
Het |
Obox3 |
A |
T |
7: 15,359,983 (GRCm39) |
Y229N |
probably benign |
Het |
Or11h7 |
A |
T |
14: 50,891,528 (GRCm39) |
Y278F |
probably damaging |
Het |
Or2b2 |
T |
C |
13: 21,887,272 (GRCm39) |
S34P |
probably damaging |
Het |
Or2b4 |
A |
G |
17: 38,116,452 (GRCm39) |
K139E |
probably benign |
Het |
Or4a74 |
T |
C |
2: 89,440,272 (GRCm39) |
Y58C |
probably damaging |
Het |
Or4c108 |
A |
G |
2: 88,803,497 (GRCm39) |
V246A |
probably damaging |
Het |
Or4p22 |
T |
A |
2: 88,317,973 (GRCm39) |
V299D |
probably damaging |
Het |
Or8d1 |
A |
G |
9: 38,766,538 (GRCm39) |
Y60C |
probably damaging |
Het |
Pabpc2 |
T |
A |
18: 39,906,963 (GRCm39) |
V76D |
possibly damaging |
Het |
Parp9 |
T |
C |
16: 35,774,071 (GRCm39) |
W348R |
probably benign |
Het |
Pdp1 |
T |
C |
4: 11,961,004 (GRCm39) |
T455A |
probably damaging |
Het |
Phactr2 |
A |
C |
10: 13,122,783 (GRCm39) |
D446E |
possibly damaging |
Het |
Pi4kb |
T |
C |
3: 94,901,500 (GRCm39) |
L389P |
probably damaging |
Het |
Pla2g4f |
C |
T |
2: 120,131,476 (GRCm39) |
R749H |
probably benign |
Het |
Plec |
A |
G |
15: 76,059,974 (GRCm39) |
V3321A |
probably damaging |
Het |
Plod2 |
T |
C |
9: 92,466,580 (GRCm39) |
V180A |
probably damaging |
Het |
Potefam3d |
T |
G |
8: 69,975,316 (GRCm39) |
D50A |
probably benign |
Het |
Rubcn |
T |
C |
16: 32,687,293 (GRCm39) |
|
probably null |
Het |
Sacs |
T |
C |
14: 61,446,255 (GRCm39) |
V2767A |
probably damaging |
Het |
Selenbp2 |
C |
G |
3: 94,611,133 (GRCm39) |
Y414* |
probably null |
Het |
Slc45a4 |
A |
T |
15: 73,458,259 (GRCm39) |
M430K |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,782,020 (GRCm39) |
L1145P |
possibly damaging |
Het |
Spns2 |
A |
G |
11: 72,347,742 (GRCm39) |
V316A |
probably benign |
Het |
Srl |
T |
A |
16: 4,300,811 (GRCm39) |
E753D |
probably damaging |
Het |
Thada |
T |
C |
17: 84,771,794 (GRCm39) |
T23A |
possibly damaging |
Het |
Tmem231 |
T |
C |
8: 112,660,308 (GRCm39) |
T31A |
probably benign |
Het |
Tpr |
C |
T |
1: 150,321,929 (GRCm39) |
T2321M |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,772,195 (GRCm39) |
N2615I |
unknown |
Het |
Vmn1r41 |
A |
G |
6: 89,724,034 (GRCm39) |
I192V |
probably benign |
Het |
Vmn2r83 |
A |
T |
10: 79,316,001 (GRCm39) |
T466S |
probably benign |
Het |
Vnn1 |
A |
G |
10: 23,770,952 (GRCm39) |
D60G |
probably benign |
Het |
Wiz |
G |
A |
17: 32,578,139 (GRCm39) |
P449S |
probably benign |
Het |
Zic1 |
A |
G |
9: 91,246,785 (GRCm39) |
S96P |
probably damaging |
Het |
Zw10 |
T |
A |
9: 48,981,012 (GRCm39) |
S471T |
probably benign |
Het |
|
Other mutations in Plppr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Plppr5
|
APN |
3 |
117,465,592 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01081:Plppr5
|
APN |
3 |
117,480,298 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01315:Plppr5
|
APN |
3 |
117,456,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02802:Plppr5
|
UTSW |
3 |
117,456,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Plppr5
|
UTSW |
3 |
117,465,538 (GRCm39) |
splice site |
probably null |
|
R0044:Plppr5
|
UTSW |
3 |
117,465,538 (GRCm39) |
splice site |
probably null |
|
R0332:Plppr5
|
UTSW |
3 |
117,465,581 (GRCm39) |
missense |
probably benign |
0.05 |
R0757:Plppr5
|
UTSW |
3 |
117,369,540 (GRCm39) |
missense |
probably benign |
0.16 |
R1101:Plppr5
|
UTSW |
3 |
117,456,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R1354:Plppr5
|
UTSW |
3 |
117,369,496 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1498:Plppr5
|
UTSW |
3 |
117,456,261 (GRCm39) |
missense |
probably damaging |
0.97 |
R1967:Plppr5
|
UTSW |
3 |
117,419,555 (GRCm39) |
critical splice donor site |
probably null |
|
R2090:Plppr5
|
UTSW |
3 |
117,369,520 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4661:Plppr5
|
UTSW |
3 |
117,414,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5143:Plppr5
|
UTSW |
3 |
117,419,552 (GRCm39) |
missense |
probably benign |
|
R5441:Plppr5
|
UTSW |
3 |
117,456,120 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5722:Plppr5
|
UTSW |
3 |
117,414,714 (GRCm39) |
missense |
probably benign |
0.00 |
R6560:Plppr5
|
UTSW |
3 |
117,465,639 (GRCm39) |
missense |
probably benign |
0.09 |
R8556:Plppr5
|
UTSW |
3 |
117,465,679 (GRCm39) |
missense |
probably benign |
|
R8925:Plppr5
|
UTSW |
3 |
117,369,532 (GRCm39) |
missense |
probably benign |
0.41 |
R8927:Plppr5
|
UTSW |
3 |
117,369,532 (GRCm39) |
missense |
probably benign |
0.41 |
R9015:Plppr5
|
UTSW |
3 |
117,456,103 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Plppr5
|
UTSW |
3 |
117,419,428 (GRCm39) |
missense |
probably damaging |
0.99 |
|