Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cacna2d2 |
G |
A |
9: 107,402,845 (GRCm39) |
E885K |
possibly damaging |
Het |
Cyp4f17 |
A |
G |
17: 32,743,878 (GRCm39) |
E352G |
probably benign |
Het |
Dip2b |
T |
C |
15: 100,055,766 (GRCm39) |
W373R |
possibly damaging |
Het |
Garin3 |
G |
T |
11: 46,296,072 (GRCm39) |
R148L |
probably damaging |
Het |
Gem |
C |
A |
4: 11,713,628 (GRCm39) |
Q255K |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,341,887 (GRCm39) |
|
probably benign |
Het |
Herc2 |
A |
T |
7: 55,803,134 (GRCm39) |
N2161I |
probably damaging |
Het |
Ift172 |
A |
G |
5: 31,415,235 (GRCm39) |
F1325L |
probably damaging |
Het |
Irgc |
T |
C |
7: 24,132,016 (GRCm39) |
K267R |
probably damaging |
Het |
Kif1a |
A |
G |
1: 92,948,178 (GRCm39) |
|
probably null |
Het |
Lifr |
G |
T |
15: 7,219,592 (GRCm39) |
|
probably benign |
Het |
Mrpl12 |
A |
G |
11: 120,376,258 (GRCm39) |
|
probably null |
Het |
Mrps18c |
A |
G |
5: 100,949,841 (GRCm39) |
D74G |
probably damaging |
Het |
Mtus1 |
C |
T |
8: 41,536,519 (GRCm39) |
G399D |
possibly damaging |
Het |
Nf1 |
T |
C |
11: 79,319,453 (GRCm39) |
I536T |
probably damaging |
Het |
Or5a3 |
C |
A |
19: 12,400,250 (GRCm39) |
S192R |
possibly damaging |
Het |
Pcdh9 |
A |
G |
14: 93,798,023 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Rubcnl |
A |
T |
14: 75,269,576 (GRCm39) |
Q78L |
possibly damaging |
Het |
Sis |
C |
A |
3: 72,863,637 (GRCm39) |
|
probably benign |
Het |
Tbc1d2 |
T |
C |
4: 46,628,370 (GRCm39) |
M320V |
probably benign |
Het |
Vmn1r178 |
C |
T |
7: 23,593,660 (GRCm39) |
T236I |
probably damaging |
Het |
Xpc |
T |
C |
6: 91,481,053 (GRCm39) |
D273G |
probably benign |
Het |
Zfhx4 |
A |
C |
3: 5,394,583 (GRCm39) |
N1033T |
probably damaging |
Het |
Zfp646 |
A |
G |
7: 127,478,584 (GRCm39) |
T254A |
probably damaging |
Het |
|
Other mutations in Atp8a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01289:Atp8a2
|
APN |
14 |
59,928,910 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01505:Atp8a2
|
APN |
14 |
60,265,512 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01614:Atp8a2
|
APN |
14 |
60,282,437 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01621:Atp8a2
|
APN |
14 |
60,253,317 (GRCm39) |
splice site |
probably benign |
|
IGL01634:Atp8a2
|
APN |
14 |
60,235,511 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01672:Atp8a2
|
APN |
14 |
59,928,982 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01898:Atp8a2
|
APN |
14 |
60,260,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01945:Atp8a2
|
APN |
14 |
60,263,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02006:Atp8a2
|
APN |
14 |
60,094,497 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02089:Atp8a2
|
APN |
14 |
60,264,369 (GRCm39) |
splice site |
probably null |
|
IGL02211:Atp8a2
|
APN |
14 |
60,265,425 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02283:Atp8a2
|
APN |
14 |
60,254,248 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02337:Atp8a2
|
APN |
14 |
60,235,451 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02795:Atp8a2
|
APN |
14 |
60,271,191 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02874:Atp8a2
|
APN |
14 |
60,039,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02999:Atp8a2
|
APN |
14 |
60,162,571 (GRCm39) |
nonsense |
probably null |
|
IGL03307:Atp8a2
|
APN |
14 |
60,253,321 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03345:Atp8a2
|
APN |
14 |
60,011,460 (GRCm39) |
missense |
probably benign |
|
PIT4431001:Atp8a2
|
UTSW |
14 |
59,892,075 (GRCm39) |
missense |
probably benign |
|
R0334:Atp8a2
|
UTSW |
14 |
59,928,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0368:Atp8a2
|
UTSW |
14 |
60,097,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Atp8a2
|
UTSW |
14 |
60,011,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0684:Atp8a2
|
UTSW |
14 |
60,260,593 (GRCm39) |
missense |
probably benign |
0.00 |
R0755:Atp8a2
|
UTSW |
14 |
60,247,330 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0853:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R0908:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R0991:Atp8a2
|
UTSW |
14 |
60,031,378 (GRCm39) |
missense |
probably benign |
0.33 |
R1025:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1190:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1387:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1426:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1442:Atp8a2
|
UTSW |
14 |
60,097,772 (GRCm39) |
splice site |
probably benign |
|
R1472:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1538:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1573:Atp8a2
|
UTSW |
14 |
60,097,655 (GRCm39) |
missense |
probably benign |
0.00 |
R1620:Atp8a2
|
UTSW |
14 |
60,028,632 (GRCm39) |
missense |
probably benign |
|
R1661:Atp8a2
|
UTSW |
14 |
60,097,635 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1673:Atp8a2
|
UTSW |
14 |
60,028,689 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Atp8a2
|
UTSW |
14 |
60,097,623 (GRCm39) |
nonsense |
probably null |
|
R1796:Atp8a2
|
UTSW |
14 |
60,258,207 (GRCm39) |
critical splice donor site |
probably null |
|
R1815:Atp8a2
|
UTSW |
14 |
60,324,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Atp8a2
|
UTSW |
14 |
60,243,815 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1935:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1936:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1937:Atp8a2
|
UTSW |
14 |
60,097,719 (GRCm39) |
missense |
probably benign |
0.01 |
R2416:Atp8a2
|
UTSW |
14 |
60,162,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Atp8a2
|
UTSW |
14 |
60,097,641 (GRCm39) |
missense |
probably benign |
0.43 |
R3029:Atp8a2
|
UTSW |
14 |
59,928,914 (GRCm39) |
frame shift |
probably null |
|
R3621:Atp8a2
|
UTSW |
14 |
60,263,587 (GRCm39) |
splice site |
probably null |
|
R3768:Atp8a2
|
UTSW |
14 |
60,281,785 (GRCm39) |
missense |
probably benign |
0.19 |
R3784:Atp8a2
|
UTSW |
14 |
60,011,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R3896:Atp8a2
|
UTSW |
14 |
60,263,589 (GRCm39) |
critical splice donor site |
probably null |
|
R4009:Atp8a2
|
UTSW |
14 |
60,265,434 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4591:Atp8a2
|
UTSW |
14 |
59,892,078 (GRCm39) |
missense |
probably benign |
0.03 |
R4866:Atp8a2
|
UTSW |
14 |
59,928,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Atp8a2
|
UTSW |
14 |
60,245,918 (GRCm39) |
nonsense |
probably null |
|
R5059:Atp8a2
|
UTSW |
14 |
59,928,986 (GRCm39) |
missense |
probably benign |
0.00 |
R5529:Atp8a2
|
UTSW |
14 |
60,031,314 (GRCm39) |
critical splice donor site |
probably null |
|
R5788:Atp8a2
|
UTSW |
14 |
60,258,242 (GRCm39) |
missense |
probably damaging |
0.96 |
R6126:Atp8a2
|
UTSW |
14 |
60,281,775 (GRCm39) |
missense |
probably benign |
|
R6295:Atp8a2
|
UTSW |
14 |
60,249,848 (GRCm39) |
nonsense |
probably null |
|
R6393:Atp8a2
|
UTSW |
14 |
60,011,204 (GRCm39) |
nonsense |
probably null |
|
R6454:Atp8a2
|
UTSW |
14 |
60,245,948 (GRCm39) |
splice site |
probably null |
|
R6651:Atp8a2
|
UTSW |
14 |
60,011,470 (GRCm39) |
missense |
probably benign |
0.00 |
R6763:Atp8a2
|
UTSW |
14 |
60,245,857 (GRCm39) |
missense |
probably benign |
0.12 |
R6767:Atp8a2
|
UTSW |
14 |
60,284,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Atp8a2
|
UTSW |
14 |
60,249,859 (GRCm39) |
missense |
probably benign |
0.33 |
R7032:Atp8a2
|
UTSW |
14 |
60,255,289 (GRCm39) |
splice site |
probably null |
|
R7243:Atp8a2
|
UTSW |
14 |
59,885,291 (GRCm39) |
missense |
probably benign |
|
R7352:Atp8a2
|
UTSW |
14 |
60,028,653 (GRCm39) |
missense |
probably benign |
|
R7355:Atp8a2
|
UTSW |
14 |
60,282,453 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7382:Atp8a2
|
UTSW |
14 |
59,892,043 (GRCm39) |
missense |
probably benign |
0.00 |
R7451:Atp8a2
|
UTSW |
14 |
60,028,630 (GRCm39) |
missense |
probably null |
0.00 |
R7483:Atp8a2
|
UTSW |
14 |
60,245,824 (GRCm39) |
missense |
probably benign |
0.00 |
R7516:Atp8a2
|
UTSW |
14 |
60,094,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Atp8a2
|
UTSW |
14 |
60,011,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R8116:Atp8a2
|
UTSW |
14 |
60,263,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Atp8a2
|
UTSW |
14 |
60,283,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Atp8a2
|
UTSW |
14 |
59,885,366 (GRCm39) |
nonsense |
probably null |
|
R8516:Atp8a2
|
UTSW |
14 |
59,928,921 (GRCm39) |
missense |
probably benign |
0.00 |
R8552:Atp8a2
|
UTSW |
14 |
60,011,431 (GRCm39) |
missense |
probably benign |
0.00 |
R8852:Atp8a2
|
UTSW |
14 |
60,162,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Atp8a2
|
UTSW |
14 |
60,249,827 (GRCm39) |
critical splice donor site |
probably null |
|
R9469:Atp8a2
|
UTSW |
14 |
60,028,668 (GRCm39) |
missense |
probably benign |
0.32 |
R9691:Atp8a2
|
UTSW |
14 |
60,245,829 (GRCm39) |
missense |
probably damaging |
0.96 |
R9709:Atp8a2
|
UTSW |
14 |
60,271,187 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1088:Atp8a2
|
UTSW |
14 |
60,265,419 (GRCm39) |
missense |
probably benign |
|
Z1177:Atp8a2
|
UTSW |
14 |
60,243,779 (GRCm39) |
missense |
possibly damaging |
0.93 |
|