Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
3110082I17Rik |
G |
T |
5: 139,441,197 (GRCm39) |
P35Q |
probably damaging |
Het |
Adam11 |
T |
C |
11: 102,665,193 (GRCm39) |
|
probably null |
Het |
Ank2 |
A |
G |
3: 126,746,842 (GRCm39) |
L581P |
probably damaging |
Het |
Armc2 |
T |
C |
10: 41,798,190 (GRCm39) |
I779V |
probably benign |
Het |
C3 |
A |
G |
17: 57,533,067 (GRCm39) |
V146A |
probably damaging |
Het |
Cfap206 |
A |
T |
4: 34,716,445 (GRCm39) |
I340N |
probably damaging |
Het |
Col3a1 |
A |
G |
1: 45,386,295 (GRCm39) |
D145G |
probably damaging |
Het |
Drosha |
A |
G |
15: 12,890,615 (GRCm39) |
D954G |
possibly damaging |
Het |
Fam161b |
A |
T |
12: 84,408,464 (GRCm39) |
|
probably null |
Het |
Fat2 |
C |
T |
11: 55,147,012 (GRCm39) |
A3995T |
probably benign |
Het |
Foxg1 |
A |
G |
12: 49,432,382 (GRCm39) |
T372A |
probably benign |
Het |
Heatr1 |
G |
T |
13: 12,449,341 (GRCm39) |
L1946F |
probably damaging |
Het |
Hook1 |
T |
C |
4: 95,877,888 (GRCm39) |
F55L |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,019,328 (GRCm39) |
K986R |
probably benign |
Het |
Inpp5k |
T |
C |
11: 75,538,512 (GRCm39) |
L461P |
probably damaging |
Het |
Klra8 |
T |
A |
6: 130,102,018 (GRCm39) |
D139V |
probably benign |
Het |
Mical3 |
T |
C |
6: 120,998,298 (GRCm39) |
Y20C |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,368,398 (GRCm39) |
Y386F |
probably damaging |
Het |
Ncoa6 |
G |
A |
2: 155,249,677 (GRCm39) |
T1209I |
probably damaging |
Het |
Nsa2 |
G |
T |
13: 97,272,042 (GRCm39) |
Q60K |
possibly damaging |
Het |
Olfml2b |
A |
G |
1: 170,509,551 (GRCm39) |
D633G |
probably damaging |
Het |
Plekhg3 |
T |
C |
12: 76,607,294 (GRCm39) |
|
probably null |
Het |
Plxna2 |
T |
A |
1: 194,326,925 (GRCm39) |
D286E |
probably benign |
Het |
Pmepa1 |
G |
A |
2: 173,069,926 (GRCm39) |
R210W |
probably damaging |
Het |
Prmt7 |
C |
A |
8: 106,968,768 (GRCm39) |
Q361K |
probably benign |
Het |
Prrc2c |
T |
C |
1: 162,537,238 (GRCm39) |
|
probably benign |
Het |
Psg27 |
T |
A |
7: 18,294,279 (GRCm39) |
Q376L |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rad51b |
C |
T |
12: 79,347,419 (GRCm39) |
Q28* |
probably null |
Het |
Rala |
T |
A |
13: 18,057,031 (GRCm39) |
E185V |
probably benign |
Het |
Sall4 |
A |
G |
2: 168,598,043 (GRCm39) |
S266P |
probably damaging |
Het |
Senp6 |
T |
G |
9: 79,999,568 (GRCm39) |
I74S |
probably benign |
Het |
Spats2l |
A |
G |
1: 57,924,938 (GRCm39) |
E112G |
probably damaging |
Het |
Synrg |
T |
C |
11: 83,892,746 (GRCm39) |
F613S |
probably damaging |
Het |
Taf15 |
G |
A |
11: 83,397,248 (GRCm39) |
D313N |
unknown |
Het |
Tekt1 |
A |
G |
11: 72,235,720 (GRCm39) |
I376T |
probably damaging |
Het |
Thbs4 |
T |
C |
13: 92,909,672 (GRCm39) |
N375S |
probably benign |
Het |
Tubb6 |
A |
G |
18: 67,526,063 (GRCm39) |
T72A |
possibly damaging |
Het |
Txndc16 |
A |
T |
14: 45,403,343 (GRCm39) |
V32E |
probably damaging |
Het |
Vmn1r200 |
A |
T |
13: 22,580,025 (GRCm39) |
Y276F |
possibly 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 |
IGL02571:Atp8a2
|
APN |
14 |
60,249,907 (GRCm39) |
splice site |
probably benign |
|
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 |
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 |
|