Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,846,184 (GRCm39) |
T612A |
probably damaging |
Het |
Acacb |
G |
A |
5: 114,383,161 (GRCm39) |
A2115T |
possibly damaging |
Het |
Adam32 |
T |
C |
8: 25,388,510 (GRCm39) |
K398R |
probably benign |
Het |
Adam9 |
T |
A |
8: 25,441,002 (GRCm39) |
I824F |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,986,395 (GRCm39) |
I2560V |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,542,644 (GRCm39) |
M1I |
probably null |
Het |
Anks1b |
T |
G |
10: 90,348,699 (GRCm39) |
I789S |
probably damaging |
Het |
Ap2b1 |
T |
A |
11: 83,241,931 (GRCm39) |
N641K |
probably benign |
Het |
Arhgap33 |
A |
G |
7: 30,228,146 (GRCm39) |
L412P |
probably damaging |
Het |
Atp13a3 |
T |
A |
16: 30,171,095 (GRCm39) |
M317L |
possibly damaging |
Het |
B4galt5 |
A |
G |
2: 167,148,617 (GRCm39) |
L167P |
probably damaging |
Het |
Bace2 |
T |
C |
16: 97,237,998 (GRCm39) |
I483T |
possibly damaging |
Het |
C2cd3 |
A |
C |
7: 100,056,257 (GRCm39) |
K177T |
|
Het |
Ccr4 |
T |
C |
9: 114,322,024 (GRCm39) |
T14A |
probably benign |
Het |
Cep250 |
A |
T |
2: 155,833,472 (GRCm39) |
H1799L |
probably benign |
Het |
Cgnl1 |
T |
C |
9: 71,632,052 (GRCm39) |
Q433R |
probably benign |
Het |
Copb1 |
C |
T |
7: 113,836,591 (GRCm39) |
V384M |
probably damaging |
Het |
Cyp2c50 |
T |
A |
19: 40,079,012 (GRCm39) |
N118K |
probably benign |
Het |
Cyp4a32 |
A |
G |
4: 115,459,499 (GRCm39) |
I78V |
probably benign |
Het |
Cyth4 |
A |
G |
15: 78,491,245 (GRCm39) |
K108R |
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,986,896 (GRCm39) |
H3632R |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,542,856 (GRCm39) |
I540V |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,844,859 (GRCm39) |
Y1174C |
probably damaging |
Het |
Drd5 |
A |
G |
5: 38,477,879 (GRCm39) |
T291A |
probably damaging |
Het |
Eeig1 |
A |
G |
2: 32,448,076 (GRCm39) |
R62G |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,148,415 (GRCm39) |
N2611S |
possibly damaging |
Het |
Fcsk |
A |
G |
8: 111,622,529 (GRCm39) |
I133T |
probably benign |
Het |
Fhod3 |
A |
G |
18: 25,193,409 (GRCm39) |
E640G |
probably damaging |
Het |
Flvcr2 |
T |
A |
12: 85,852,013 (GRCm39) |
D522E |
probably benign |
Het |
Ganc |
T |
A |
2: 120,272,010 (GRCm39) |
I556K |
probably damaging |
Het |
Gjc2 |
T |
A |
11: 59,067,960 (GRCm39) |
E174V |
unknown |
Het |
Gzmd |
G |
A |
14: 56,368,799 (GRCm39) |
R32C |
probably damaging |
Het |
Hltf |
T |
A |
3: 20,119,556 (GRCm39) |
H200Q |
probably benign |
Het |
Ift88 |
A |
G |
14: 57,717,454 (GRCm39) |
I559M |
probably damaging |
Het |
Ighv1-62-1 |
C |
A |
12: 115,350,322 (GRCm39) |
C115F |
probably damaging |
Het |
Impdh2 |
A |
G |
9: 108,440,636 (GRCm39) |
N279S |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,494,581 (GRCm39) |
|
probably null |
Het |
Kansl1l |
T |
C |
1: 66,840,787 (GRCm39) |
N171S |
possibly damaging |
Het |
Kif14 |
T |
A |
1: 136,396,491 (GRCm39) |
C266S |
probably benign |
Het |
Kif19b |
A |
G |
5: 140,447,943 (GRCm39) |
T137A |
probably damaging |
Het |
Lrriq1 |
A |
C |
10: 103,051,834 (GRCm39) |
V306G |
probably damaging |
Het |
Mast4 |
G |
A |
13: 103,470,508 (GRCm39) |
R65W |
possibly damaging |
Het |
Mex3d |
T |
C |
10: 80,223,091 (GRCm39) |
D55G |
|
Het |
Mrps27 |
A |
T |
13: 99,547,788 (GRCm39) |
K233* |
probably null |
Het |
Myo1f |
A |
G |
17: 33,798,902 (GRCm39) |
N189S |
probably damaging |
Het |
Nbn |
A |
T |
4: 15,991,190 (GRCm39) |
K729N |
probably benign |
Het |
Or1e35 |
T |
C |
11: 73,798,058 (GRCm39) |
S87G |
probably benign |
Het |
Or8k35 |
C |
A |
2: 86,424,498 (GRCm39) |
V225F |
possibly damaging |
Het |
Pgghg |
T |
C |
7: 140,525,633 (GRCm39) |
S479P |
|
Het |
Plaat5 |
A |
G |
19: 7,591,946 (GRCm39) |
T121A |
probably benign |
Het |
Polr1e |
A |
C |
4: 45,029,340 (GRCm39) |
H315P |
probably damaging |
Het |
Pou6f2 |
A |
G |
13: 18,299,874 (GRCm39) |
V595A |
|
Het |
Prdm15 |
T |
C |
16: 97,596,941 (GRCm39) |
D960G |
possibly damaging |
Het |
Prkcz |
A |
T |
4: 155,353,516 (GRCm39) |
M460K |
probably benign |
Het |
Prkd2 |
G |
T |
7: 16,591,730 (GRCm39) |
R587L |
probably benign |
Het |
Rabep1 |
C |
A |
11: 70,830,815 (GRCm39) |
T829N |
probably damaging |
Het |
Rptn |
A |
G |
3: 93,303,261 (GRCm39) |
E198G |
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,680,799 (GRCm39) |
I3182N |
possibly damaging |
Het |
Sectm1a |
T |
A |
11: 120,960,708 (GRCm39) |
I36F |
possibly damaging |
Het |
Sez6l |
T |
C |
5: 112,621,346 (GRCm39) |
S243G |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,122,876 (GRCm39) |
E3378G |
probably benign |
Het |
Taf2 |
T |
A |
15: 54,925,537 (GRCm39) |
H235L |
probably benign |
Het |
Tbc1d7 |
T |
C |
13: 43,306,493 (GRCm39) |
Q161R |
probably benign |
Het |
Tfcp2 |
T |
C |
15: 100,416,468 (GRCm39) |
T271A |
possibly damaging |
Het |
Thrsp |
G |
T |
7: 97,066,295 (GRCm39) |
T139K |
probably damaging |
Het |
Timm10 |
T |
A |
2: 84,660,333 (GRCm39) |
*91R |
probably null |
Het |
Tlr11 |
T |
A |
14: 50,599,598 (GRCm39) |
I528N |
possibly damaging |
Het |
Tnnt2 |
T |
A |
1: 135,779,444 (GRCm39) |
L278Q |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,664,715 (GRCm39) |
M1K |
probably null |
Het |
Trpv5 |
G |
A |
6: 41,652,242 (GRCm39) |
R148* |
probably null |
Het |
Ttll13 |
A |
C |
7: 79,903,911 (GRCm39) |
K280Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,783,550 (GRCm39) |
V860A |
unknown |
Het |
Txnip |
T |
C |
3: 96,466,991 (GRCm39) |
Y222H |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,170,725 (GRCm39) |
S1600N |
probably damaging |
Het |
Uhrf1 |
T |
C |
17: 56,622,193 (GRCm39) |
Y364H |
probably damaging |
Het |
Unc5a |
A |
T |
13: 55,138,833 (GRCm39) |
T71S |
probably damaging |
Het |
Vmn1r123 |
A |
T |
7: 20,896,537 (GRCm39) |
Y143F |
possibly damaging |
Het |
Vmn1r180 |
T |
A |
7: 23,651,891 (GRCm39) |
I18N |
probably damaging |
Het |
Washc2 |
A |
G |
6: 116,185,168 (GRCm39) |
M1V |
probably null |
Het |
Zfp174 |
C |
A |
16: 3,666,111 (GRCm39) |
H125Q |
probably benign |
Het |
Zfpl1 |
T |
C |
19: 6,131,943 (GRCm39) |
H227R |
possibly damaging |
Het |
|
Other mutations in Prkn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4304:Prkn
|
UTSW |
17 |
12,073,650 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Prkn
|
UTSW |
17 |
12,073,650 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Prkn
|
UTSW |
17 |
12,073,650 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Prkn
|
UTSW |
17 |
11,286,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0333:Prkn
|
UTSW |
17 |
11,286,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0543:Prkn
|
UTSW |
17 |
11,286,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4460:Prkn
|
UTSW |
17 |
12,280,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Prkn
|
UTSW |
17 |
12,073,720 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4742:Prkn
|
UTSW |
17 |
11,456,591 (GRCm39) |
critical splice donor site |
probably null |
|
R4752:Prkn
|
UTSW |
17 |
12,223,010 (GRCm39) |
missense |
probably benign |
|
R4911:Prkn
|
UTSW |
17 |
11,059,359 (GRCm39) |
utr 5 prime |
probably benign |
|
R5653:Prkn
|
UTSW |
17 |
11,456,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Prkn
|
UTSW |
17 |
11,456,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Prkn
|
UTSW |
17 |
11,456,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360:Prkn
|
UTSW |
17 |
12,222,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Prkn
|
UTSW |
17 |
11,286,183 (GRCm39) |
splice site |
probably null |
|
R7163:Prkn
|
UTSW |
17 |
12,280,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Prkn
|
UTSW |
17 |
11,653,501 (GRCm39) |
missense |
probably benign |
|
R7630:Prkn
|
UTSW |
17 |
11,456,455 (GRCm39) |
missense |
probably benign |
|
R8278:Prkn
|
UTSW |
17 |
12,269,609 (GRCm39) |
missense |
probably benign |
0.26 |
R8299:Prkn
|
UTSW |
17 |
11,456,408 (GRCm39) |
missense |
probably benign |
0.25 |
R8551:Prkn
|
UTSW |
17 |
11,286,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R8558:Prkn
|
UTSW |
17 |
11,456,472 (GRCm39) |
missense |
probably benign |
|
R8706:Prkn
|
UTSW |
17 |
11,456,472 (GRCm39) |
missense |
probably benign |
|
R8867:Prkn
|
UTSW |
17 |
11,456,448 (GRCm39) |
missense |
probably benign |
0.00 |
R9241:Prkn
|
UTSW |
17 |
11,456,382 (GRCm39) |
missense |
probably benign |
0.10 |
R9272:Prkn
|
UTSW |
17 |
11,456,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Prkn
|
UTSW |
17 |
12,057,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9607:Prkn
|
UTSW |
17 |
12,222,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R9665:Prkn
|
UTSW |
17 |
11,286,062 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9779:Prkn
|
UTSW |
17 |
11,854,318 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9796:Prkn
|
UTSW |
17 |
11,456,554 (GRCm39) |
missense |
possibly damaging |
0.84 |
X0010:Prkn
|
UTSW |
17 |
11,456,463 (GRCm39) |
missense |
probably benign |
|
|