Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
C |
4: 62,461,022 (GRCm39) |
|
probably null |
Het |
Adamts6 |
T |
A |
13: 104,616,027 (GRCm39) |
C1030S |
probably damaging |
Het |
Adamtsl3 |
C |
A |
7: 82,253,007 (GRCm39) |
T1527K |
possibly damaging |
Het |
Akap9 |
G |
A |
5: 3,998,897 (GRCm39) |
|
probably null |
Het |
Ankle2 |
C |
A |
5: 110,389,909 (GRCm39) |
P457T |
possibly damaging |
Het |
Ankrd7 |
A |
G |
6: 18,868,007 (GRCm39) |
N91S |
probably damaging |
Het |
Ascc3 |
C |
A |
10: 50,494,173 (GRCm39) |
Q203K |
probably benign |
Het |
Baz2b |
A |
T |
2: 59,742,137 (GRCm39) |
D61E |
|
Het |
Bmpr1a |
T |
A |
14: 34,136,759 (GRCm39) |
K477N |
probably benign |
Het |
Cacna1d |
T |
C |
14: 29,824,364 (GRCm39) |
I1040V |
probably damaging |
Het |
Castor2 |
T |
C |
5: 134,166,955 (GRCm39) |
F304L |
possibly damaging |
Het |
Cdkn2a |
C |
A |
4: 89,200,291 (GRCm39) |
V20L |
possibly damaging |
Het |
Chd5 |
A |
G |
4: 152,445,173 (GRCm39) |
S385G |
probably damaging |
Het |
Cntrob |
A |
G |
11: 69,190,679 (GRCm39) |
F46L |
unknown |
Het |
Cth |
T |
C |
3: 157,630,657 (GRCm39) |
D4G |
probably benign |
Het |
Cyld |
C |
T |
8: 89,456,197 (GRCm39) |
H416Y |
probably damaging |
Het |
Dennd6a |
C |
A |
14: 26,328,098 (GRCm39) |
H264Q |
possibly damaging |
Het |
Dnah1 |
T |
C |
14: 31,015,682 (GRCm39) |
Y1672C |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,892,814 (GRCm39) |
I800V |
probably benign |
Het |
Esrp2 |
A |
G |
8: 106,858,853 (GRCm39) |
Y595H |
probably damaging |
Het |
F12 |
T |
A |
13: 55,566,301 (GRCm39) |
Y497F |
probably benign |
Het |
Fggy |
A |
G |
4: 95,732,427 (GRCm39) |
T473A |
probably benign |
Het |
Garre1 |
A |
T |
7: 33,984,569 (GRCm39) |
L18Q |
probably damaging |
Het |
Gstt2 |
C |
A |
10: 75,668,526 (GRCm39) |
R107L |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,358,319 (GRCm39) |
|
probably benign |
Het |
Helb |
A |
G |
10: 119,938,791 (GRCm39) |
F561S |
probably damaging |
Het |
Ints2 |
T |
C |
11: 86,146,249 (GRCm39) |
T120A |
probably benign |
Het |
Kdm5d |
G |
A |
Y: 914,056 (GRCm39) |
R331H |
probably benign |
Het |
Krt6b |
A |
G |
15: 101,586,455 (GRCm39) |
Y345H |
probably damaging |
Het |
Limch1 |
A |
G |
5: 67,159,825 (GRCm39) |
K418E |
probably damaging |
Het |
Lrrc37 |
T |
A |
11: 103,511,726 (GRCm39) |
T81S |
unknown |
Het |
Med17 |
C |
T |
9: 15,173,735 (GRCm39) |
|
probably null |
Het |
Met |
A |
T |
6: 17,571,799 (GRCm39) |
I1373F |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,436,894 (GRCm39) |
Q543L |
possibly damaging |
Het |
Nat9 |
T |
C |
11: 115,075,902 (GRCm39) |
T40A |
probably damaging |
Het |
Notch4 |
A |
T |
17: 34,805,763 (GRCm39) |
|
probably null |
Het |
Ogdh |
A |
G |
11: 6,292,619 (GRCm39) |
N455S |
probably damaging |
Het |
Or52k2 |
C |
A |
7: 102,254,207 (GRCm39) |
F215L |
probably benign |
Het |
Pde4a |
T |
C |
9: 21,117,534 (GRCm39) |
F599L |
probably benign |
Het |
Pga5 |
T |
C |
19: 10,649,173 (GRCm39) |
Y249C |
probably damaging |
Het |
Plekha8 |
A |
T |
6: 54,607,539 (GRCm39) |
K382M |
probably damaging |
Het |
Pnp |
A |
T |
14: 51,185,356 (GRCm39) |
H20L |
probably benign |
Het |
Polq |
A |
T |
16: 36,837,559 (GRCm39) |
|
probably null |
Het |
Psma3 |
T |
G |
12: 71,035,250 (GRCm39) |
I177R |
probably damaging |
Het |
Ptpn3 |
A |
G |
4: 57,240,784 (GRCm39) |
|
probably null |
Het |
Ptprt |
A |
T |
2: 161,400,806 (GRCm39) |
L1077Q |
probably damaging |
Het |
Ralgps2 |
A |
T |
1: 156,651,744 (GRCm39) |
|
probably null |
Het |
Rbm47 |
A |
T |
5: 66,184,573 (GRCm39) |
M10K |
possibly damaging |
Het |
Rere |
A |
G |
4: 150,703,653 (GRCm39) |
D186G |
probably damaging |
Het |
Rpl24 |
T |
C |
16: 55,787,453 (GRCm39) |
S38P |
probably damaging |
Het |
Slco1a1 |
A |
T |
6: 141,885,787 (GRCm39) |
F79L |
possibly damaging |
Het |
Sorl1 |
T |
A |
9: 41,903,041 (GRCm39) |
D1551V |
probably benign |
Het |
Sos1 |
C |
A |
17: 80,741,548 (GRCm39) |
M412I |
probably benign |
Het |
Spast |
G |
A |
17: 74,666,293 (GRCm39) |
V209I |
probably benign |
Het |
Spindoc |
G |
T |
19: 7,335,769 (GRCm39) |
Q340K |
possibly damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,185 (GRCm39) |
Y574C |
probably damaging |
Het |
Tnrc6a |
A |
G |
7: 122,791,346 (GRCm39) |
N1748S |
possibly damaging |
Het |
Trbv13-2 |
A |
T |
6: 41,098,474 (GRCm39) |
K16N |
probably benign |
Het |
Triobp |
C |
T |
15: 78,878,326 (GRCm39) |
H1750Y |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,225,933 (GRCm39) |
D659G |
possibly damaging |
Het |
Vmn2r88 |
T |
A |
14: 51,656,253 (GRCm39) |
C821S |
probably damaging |
Het |
Whamm |
T |
A |
7: 81,224,295 (GRCm39) |
V197D |
probably damaging |
Het |
Zfp777 |
A |
G |
6: 48,006,101 (GRCm39) |
F431S |
probably damaging |
Het |
|
Other mutations in Plekhd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02882:Plekhd1
|
APN |
12 |
80,765,781 (GRCm39) |
critical splice donor site |
probably null |
|
R0377:Plekhd1
|
UTSW |
12 |
80,753,210 (GRCm39) |
splice site |
probably benign |
|
R0462:Plekhd1
|
UTSW |
12 |
80,768,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Plekhd1
|
UTSW |
12 |
80,764,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1125:Plekhd1
|
UTSW |
12 |
80,753,998 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1344:Plekhd1
|
UTSW |
12 |
80,739,659 (GRCm39) |
missense |
probably benign |
|
R1418:Plekhd1
|
UTSW |
12 |
80,739,659 (GRCm39) |
missense |
probably benign |
|
R1694:Plekhd1
|
UTSW |
12 |
80,769,095 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2070:Plekhd1
|
UTSW |
12 |
80,739,681 (GRCm39) |
nonsense |
probably null |
|
R2073:Plekhd1
|
UTSW |
12 |
80,768,066 (GRCm39) |
missense |
probably benign |
0.19 |
R2231:Plekhd1
|
UTSW |
12 |
80,768,725 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2326:Plekhd1
|
UTSW |
12 |
80,768,873 (GRCm39) |
splice site |
probably null |
|
R3615:Plekhd1
|
UTSW |
12 |
80,764,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Plekhd1
|
UTSW |
12 |
80,764,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Plekhd1
|
UTSW |
12 |
80,769,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Plekhd1
|
UTSW |
12 |
80,768,795 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5028:Plekhd1
|
UTSW |
12 |
80,739,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R5446:Plekhd1
|
UTSW |
12 |
80,767,410 (GRCm39) |
missense |
probably benign |
0.00 |
R5615:Plekhd1
|
UTSW |
12 |
80,767,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Plekhd1
|
UTSW |
12 |
80,767,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Plekhd1
|
UTSW |
12 |
80,769,140 (GRCm39) |
missense |
probably benign |
|
R6534:Plekhd1
|
UTSW |
12 |
80,754,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R7003:Plekhd1
|
UTSW |
12 |
80,768,734 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7615:Plekhd1
|
UTSW |
12 |
80,769,219 (GRCm39) |
missense |
probably benign |
0.02 |
R7656:Plekhd1
|
UTSW |
12 |
80,768,934 (GRCm39) |
splice site |
probably null |
|
R8348:Plekhd1
|
UTSW |
12 |
80,753,149 (GRCm39) |
missense |
probably damaging |
0.97 |
R8750:Plekhd1
|
UTSW |
12 |
80,752,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Plekhd1
|
UTSW |
12 |
80,767,368 (GRCm39) |
missense |
probably benign |
0.13 |
R9220:Plekhd1
|
UTSW |
12 |
80,768,726 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9235:Plekhd1
|
UTSW |
12 |
80,768,791 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9553:Plekhd1
|
UTSW |
12 |
80,753,977 (GRCm39) |
missense |
probably benign |
0.09 |
R9604:Plekhd1
|
UTSW |
12 |
80,739,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|