Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap35 |
A |
T |
7: 16,299,000 (GRCm39) |
S22T |
probably damaging |
Het |
Cad |
T |
A |
5: 31,232,890 (GRCm39) |
|
probably null |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Defa41 |
C |
T |
8: 21,691,753 (GRCm39) |
S45F |
probably damaging |
Het |
Dhx15 |
G |
A |
5: 52,324,074 (GRCm39) |
P406L |
probably benign |
Het |
Dnah17 |
T |
A |
11: 117,995,352 (GRCm39) |
M999L |
probably benign |
Het |
Dpysl4 |
A |
G |
7: 138,676,672 (GRCm39) |
E374G |
probably damaging |
Het |
Gatad2a |
T |
C |
8: 70,368,930 (GRCm39) |
|
probably null |
Het |
Gm826 |
C |
A |
2: 160,155,423 (GRCm39) |
|
probably benign |
Het |
H2-M10.1 |
T |
A |
17: 36,636,216 (GRCm39) |
H117L |
probably damaging |
Het |
Klhl9 |
A |
T |
4: 88,639,830 (GRCm39) |
V137D |
possibly damaging |
Het |
Limch1 |
A |
G |
5: 67,186,183 (GRCm39) |
Y828C |
probably damaging |
Het |
Med1 |
T |
C |
11: 98,046,341 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
A |
T |
7: 141,361,212 (GRCm39) |
T1507S |
possibly damaging |
Het |
Pak6 |
A |
T |
2: 118,526,958 (GRCm39) |
Q651L |
probably damaging |
Het |
Plscr2 |
T |
A |
9: 92,173,133 (GRCm39) |
V90D |
probably damaging |
Het |
Rbbp4 |
G |
A |
4: 129,228,344 (GRCm39) |
T2I |
probably damaging |
Het |
Rnf121 |
G |
A |
7: 101,673,244 (GRCm39) |
T223M |
probably damaging |
Het |
Rsph6a |
A |
G |
7: 18,789,256 (GRCm39) |
K196R |
probably damaging |
Het |
Tex47 |
A |
T |
5: 7,355,529 (GRCm39) |
I237L |
probably benign |
Het |
Ulk1 |
C |
T |
5: 110,937,223 (GRCm39) |
R691Q |
probably benign |
Het |
Vmn1r30 |
C |
A |
6: 58,412,278 (GRCm39) |
V185L |
probably benign |
Het |
Vmn2r103 |
A |
T |
17: 20,032,411 (GRCm39) |
E728D |
probably damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,368,033 (GRCm39) |
Y320N |
probably benign |
Het |
Zc3h14 |
T |
A |
12: 98,724,902 (GRCm39) |
F188Y |
probably damaging |
Het |
|
Other mutations in Atp2b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Atp2b1
|
APN |
10 |
98,850,882 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00972:Atp2b1
|
APN |
10 |
98,850,906 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00977:Atp2b1
|
APN |
10 |
98,822,837 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01154:Atp2b1
|
APN |
10 |
98,832,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03073:Atp2b1
|
APN |
10 |
98,835,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03081:Atp2b1
|
APN |
10 |
98,830,675 (GRCm39) |
splice site |
probably benign |
|
PIT4453001:Atp2b1
|
UTSW |
10 |
98,852,840 (GRCm39) |
missense |
probably benign |
0.00 |
R0157:Atp2b1
|
UTSW |
10 |
98,835,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R0200:Atp2b1
|
UTSW |
10 |
98,815,676 (GRCm39) |
nonsense |
probably null |
|
R0899:Atp2b1
|
UTSW |
10 |
98,852,893 (GRCm39) |
critical splice donor site |
probably null |
|
R0981:Atp2b1
|
UTSW |
10 |
98,851,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Atp2b1
|
UTSW |
10 |
98,815,713 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1569:Atp2b1
|
UTSW |
10 |
98,823,188 (GRCm39) |
missense |
probably benign |
0.02 |
R1572:Atp2b1
|
UTSW |
10 |
98,830,537 (GRCm39) |
missense |
probably benign |
0.10 |
R1574:Atp2b1
|
UTSW |
10 |
98,832,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Atp2b1
|
UTSW |
10 |
98,832,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Atp2b1
|
UTSW |
10 |
98,832,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Atp2b1
|
UTSW |
10 |
98,839,063 (GRCm39) |
missense |
probably benign |
0.01 |
R1840:Atp2b1
|
UTSW |
10 |
98,858,791 (GRCm39) |
missense |
probably benign |
0.00 |
R1867:Atp2b1
|
UTSW |
10 |
98,832,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Atp2b1
|
UTSW |
10 |
98,832,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Atp2b1
|
UTSW |
10 |
98,858,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R1984:Atp2b1
|
UTSW |
10 |
98,850,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2055:Atp2b1
|
UTSW |
10 |
98,850,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R2325:Atp2b1
|
UTSW |
10 |
98,854,757 (GRCm39) |
nonsense |
probably null |
|
R2399:Atp2b1
|
UTSW |
10 |
98,835,785 (GRCm39) |
missense |
probably benign |
0.02 |
R2876:Atp2b1
|
UTSW |
10 |
98,835,607 (GRCm39) |
missense |
probably damaging |
0.96 |
R3776:Atp2b1
|
UTSW |
10 |
98,815,731 (GRCm39) |
frame shift |
probably null |
|
R3808:Atp2b1
|
UTSW |
10 |
98,839,010 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3978:Atp2b1
|
UTSW |
10 |
98,832,795 (GRCm39) |
splice site |
probably null |
|
R4391:Atp2b1
|
UTSW |
10 |
98,839,076 (GRCm39) |
missense |
probably benign |
0.00 |
R4825:Atp2b1
|
UTSW |
10 |
98,845,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R5755:Atp2b1
|
UTSW |
10 |
98,830,671 (GRCm39) |
critical splice donor site |
probably null |
|
R5755:Atp2b1
|
UTSW |
10 |
98,839,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R6018:Atp2b1
|
UTSW |
10 |
98,846,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R6179:Atp2b1
|
UTSW |
10 |
98,858,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Atp2b1
|
UTSW |
10 |
98,852,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6496:Atp2b1
|
UTSW |
10 |
98,839,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R6786:Atp2b1
|
UTSW |
10 |
98,852,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6814:Atp2b1
|
UTSW |
10 |
98,858,877 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7034:Atp2b1
|
UTSW |
10 |
98,823,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7036:Atp2b1
|
UTSW |
10 |
98,823,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7079:Atp2b1
|
UTSW |
10 |
98,854,595 (GRCm39) |
missense |
probably benign |
0.01 |
R7216:Atp2b1
|
UTSW |
10 |
98,822,839 (GRCm39) |
missense |
probably benign |
0.30 |
R7510:Atp2b1
|
UTSW |
10 |
98,829,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7562:Atp2b1
|
UTSW |
10 |
98,858,667 (GRCm39) |
splice site |
probably null |
|
R7651:Atp2b1
|
UTSW |
10 |
98,852,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7739:Atp2b1
|
UTSW |
10 |
98,837,227 (GRCm39) |
missense |
probably benign |
0.01 |
R8005:Atp2b1
|
UTSW |
10 |
98,830,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R8111:Atp2b1
|
UTSW |
10 |
98,832,786 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8904:Atp2b1
|
UTSW |
10 |
98,804,866 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9419:Atp2b1
|
UTSW |
10 |
98,837,178 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9495:Atp2b1
|
UTSW |
10 |
98,835,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R9506:Atp2b1
|
UTSW |
10 |
98,858,862 (GRCm39) |
missense |
probably benign |
0.01 |
R9682:Atp2b1
|
UTSW |
10 |
98,815,662 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Atp2b1
|
UTSW |
10 |
98,854,710 (GRCm39) |
missense |
probably damaging |
0.99 |
|