Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
T |
A |
15: 94,251,521 (GRCm39) |
H422L |
probably benign |
Het |
Adgra3 |
G |
T |
5: 50,145,013 (GRCm39) |
P527T |
probably damaging |
Het |
Afg1l |
A |
G |
10: 42,302,517 (GRCm39) |
V161A |
probably damaging |
Het |
Als2cl |
A |
C |
9: 110,714,025 (GRCm39) |
E65A |
probably damaging |
Het |
Arl3 |
A |
C |
19: 46,546,709 (GRCm39) |
S39A |
probably benign |
Het |
Cacna1a |
T |
C |
8: 85,276,087 (GRCm39) |
V560A |
probably damaging |
Het |
Ccr10 |
C |
T |
11: 101,064,982 (GRCm39) |
G183R |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,218 (GRCm39) |
T2029S |
probably benign |
Het |
Chkb |
A |
T |
15: 89,312,376 (GRCm39) |
V213E |
possibly damaging |
Het |
Chst5 |
A |
G |
8: 112,617,422 (GRCm39) |
V66A |
probably damaging |
Het |
Crx |
C |
A |
7: 15,602,031 (GRCm39) |
A216S |
possibly damaging |
Het |
Ctnnd1 |
T |
C |
2: 84,444,287 (GRCm39) |
D556G |
probably damaging |
Het |
Cyp4a14 |
C |
A |
4: 115,353,129 (GRCm39) |
G61V |
probably damaging |
Het |
Cyp4f17 |
T |
A |
17: 32,739,550 (GRCm39) |
F157L |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,548,849 (GRCm39) |
|
probably null |
Het |
Dnah14 |
A |
C |
1: 181,633,577 (GRCm39) |
H4P |
|
Het |
Dnah7a |
T |
C |
1: 53,657,142 (GRCm39) |
D878G |
probably benign |
Het |
Epb41l1 |
C |
T |
2: 156,363,684 (GRCm39) |
T731I |
probably benign |
Het |
Epg5 |
G |
C |
18: 77,991,946 (GRCm39) |
E214D |
probably benign |
Het |
Fam171b |
A |
G |
2: 83,690,864 (GRCm39) |
T276A |
probably benign |
Het |
Fat4 |
G |
A |
3: 39,035,702 (GRCm39) |
R3118H |
probably benign |
Het |
Fbrs |
C |
T |
7: 127,082,329 (GRCm39) |
R327W |
probably damaging |
Het |
Fmo3 |
A |
G |
1: 162,794,509 (GRCm39) |
V187A |
possibly damaging |
Het |
Gins1 |
T |
C |
2: 150,772,807 (GRCm39) |
V190A |
probably benign |
Het |
Gm17067 |
T |
C |
7: 42,358,155 (GRCm39) |
S116G |
probably damaging |
Het |
Gm5478 |
A |
G |
15: 101,553,862 (GRCm39) |
V250A |
probably benign |
Het |
Gpr85 |
T |
C |
6: 13,836,848 (GRCm39) |
T19A |
probably benign |
Het |
Hepacam2 |
T |
C |
6: 3,483,358 (GRCm39) |
N217S |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,845,377 (GRCm39) |
Y889H |
probably benign |
Het |
Itpr2 |
T |
G |
6: 146,135,464 (GRCm39) |
R1822S |
possibly damaging |
Het |
Kcnk7 |
C |
T |
19: 5,754,407 (GRCm39) |
|
probably benign |
Het |
Klk1 |
T |
C |
7: 43,874,933 (GRCm39) |
S11P |
probably damaging |
Het |
Klra7 |
C |
T |
6: 130,201,109 (GRCm39) |
G216R |
probably damaging |
Het |
Krt34 |
T |
C |
11: 99,930,901 (GRCm39) |
D167G |
probably damaging |
Het |
Larp1b |
A |
C |
3: 40,930,995 (GRCm39) |
E291D |
probably benign |
Het |
Lats1 |
T |
A |
10: 7,586,688 (GRCm39) |
L950* |
probably null |
Het |
Lrrc2 |
A |
C |
9: 110,799,218 (GRCm39) |
D255A |
probably damaging |
Het |
Lrrc49 |
A |
T |
9: 60,505,456 (GRCm39) |
M605K |
probably benign |
Het |
Mocos |
A |
G |
18: 24,799,314 (GRCm39) |
K183E |
probably benign |
Het |
Mpl |
C |
A |
4: 118,301,213 (GRCm39) |
|
probably null |
Het |
Mroh9 |
T |
A |
1: 162,883,250 (GRCm39) |
T410S |
probably damaging |
Het |
Notch3 |
T |
C |
17: 32,375,024 (GRCm39) |
E430G |
probably damaging |
Het |
Nsun6 |
T |
C |
2: 15,034,863 (GRCm39) |
T252A |
probably benign |
Het |
Ntrk1 |
C |
A |
3: 87,698,976 (GRCm39) |
|
probably null |
Het |
Nts |
G |
T |
10: 102,320,921 (GRCm39) |
T56N |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,092,874 (GRCm39) |
D1276G |
probably null |
Het |
Or4c12b |
G |
T |
2: 89,647,494 (GRCm39) |
V269F |
probably damaging |
Het |
Or51a10 |
C |
A |
7: 103,698,875 (GRCm39) |
A229S |
possibly damaging |
Het |
Or5b105 |
T |
C |
19: 13,079,840 (GRCm39) |
Y276C |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,113,177 (GRCm39) |
S535G |
possibly damaging |
Het |
Pax9 |
A |
G |
12: 56,743,550 (GRCm39) |
I66V |
possibly damaging |
Het |
Pja2 |
A |
G |
17: 64,599,843 (GRCm39) |
V547A |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,608,540 (GRCm39) |
|
probably null |
Het |
Ptgdr2 |
A |
T |
19: 10,917,785 (GRCm39) |
T101S |
possibly damaging |
Het |
Ptprd |
T |
C |
4: 75,984,496 (GRCm39) |
D550G |
probably benign |
Het |
Ptx3 |
G |
T |
3: 66,128,419 (GRCm39) |
R160L |
probably benign |
Het |
Rdh16f1 |
A |
C |
10: 127,624,714 (GRCm39) |
E184A |
probably damaging |
Het |
Rfx3 |
C |
T |
19: 27,771,072 (GRCm39) |
E560K |
possibly damaging |
Het |
Scgb2b24 |
T |
C |
7: 33,436,779 (GRCm39) |
Q111R |
probably benign |
Het |
Spart |
A |
G |
3: 55,032,315 (GRCm39) |
D383G |
probably damaging |
Het |
Stpg3 |
C |
A |
2: 25,103,333 (GRCm39) |
R252L |
probably damaging |
Het |
Tcp11l2 |
C |
T |
10: 84,449,396 (GRCm39) |
Q454* |
probably null |
Het |
Trav10d |
A |
G |
14: 53,048,780 (GRCm39) |
Y57C |
probably damaging |
Het |
Vmn1r170 |
T |
A |
7: 23,306,321 (GRCm39) |
M241K |
possibly damaging |
Het |
Vwa8 |
T |
A |
14: 79,302,332 (GRCm39) |
N1000K |
probably damaging |
Het |
Wdsub1 |
T |
C |
2: 59,692,045 (GRCm39) |
E329G |
probably benign |
Het |
Wnk4 |
C |
A |
11: 101,166,147 (GRCm39) |
C891* |
probably null |
Het |
Zdhhc16 |
G |
T |
19: 41,928,093 (GRCm39) |
C204F |
probably damaging |
Het |
Zfp868 |
T |
C |
8: 70,064,559 (GRCm39) |
I259V |
possibly damaging |
Het |
Zranb3 |
G |
T |
1: 127,920,647 (GRCm39) |
Q426K |
probably damaging |
Het |
|
Other mutations in Plekhs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Plekhs1
|
APN |
19 |
56,453,031 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01387:Plekhs1
|
APN |
19 |
56,459,403 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02506:Plekhs1
|
APN |
19 |
56,460,198 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Plekhs1
|
UTSW |
19 |
56,468,290 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Plekhs1
|
UTSW |
19 |
56,468,290 (GRCm39) |
unclassified |
probably benign |
|
FR4342:Plekhs1
|
UTSW |
19 |
56,468,293 (GRCm39) |
unclassified |
probably benign |
|
FR4342:Plekhs1
|
UTSW |
19 |
56,468,290 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Plekhs1
|
UTSW |
19 |
56,468,295 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Plekhs1
|
UTSW |
19 |
56,468,295 (GRCm39) |
unclassified |
probably benign |
|
IGL03052:Plekhs1
|
UTSW |
19 |
56,459,189 (GRCm39) |
missense |
probably benign |
0.43 |
R0023:Plekhs1
|
UTSW |
19 |
56,466,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R0023:Plekhs1
|
UTSW |
19 |
56,466,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R0100:Plekhs1
|
UTSW |
19 |
56,466,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Plekhs1
|
UTSW |
19 |
56,466,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R0129:Plekhs1
|
UTSW |
19 |
56,465,722 (GRCm39) |
critical splice donor site |
probably null |
|
R0498:Plekhs1
|
UTSW |
19 |
56,469,536 (GRCm39) |
splice site |
probably null |
|
R1264:Plekhs1
|
UTSW |
19 |
56,474,195 (GRCm39) |
missense |
probably benign |
|
R1528:Plekhs1
|
UTSW |
19 |
56,468,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Plekhs1
|
UTSW |
19 |
56,459,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Plekhs1
|
UTSW |
19 |
56,466,954 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2884:Plekhs1
|
UTSW |
19 |
56,459,258 (GRCm39) |
missense |
probably benign |
0.01 |
R3237:Plekhs1
|
UTSW |
19 |
56,453,032 (GRCm39) |
splice site |
probably null |
|
R4395:Plekhs1
|
UTSW |
19 |
56,468,326 (GRCm39) |
missense |
probably benign |
|
R4825:Plekhs1
|
UTSW |
19 |
56,461,700 (GRCm39) |
splice site |
probably null |
|
R5484:Plekhs1
|
UTSW |
19 |
56,468,260 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5511:Plekhs1
|
UTSW |
19 |
56,474,224 (GRCm39) |
missense |
probably damaging |
0.97 |
R7105:Plekhs1
|
UTSW |
19 |
56,465,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R7267:Plekhs1
|
UTSW |
19 |
56,459,209 (GRCm39) |
missense |
probably damaging |
0.96 |
R8212:Plekhs1
|
UTSW |
19 |
56,460,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Plekhs1
|
UTSW |
19 |
56,471,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Plekhs1
|
UTSW |
19 |
56,461,680 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9564:Plekhs1
|
UTSW |
19 |
56,461,628 (GRCm39) |
missense |
probably damaging |
1.00 |
RF025:Plekhs1
|
UTSW |
19 |
56,468,290 (GRCm39) |
unclassified |
probably benign |
|
RF043:Plekhs1
|
UTSW |
19 |
56,468,290 (GRCm39) |
unclassified |
probably benign |
|
|