Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
C |
12: 118,838,379 (GRCm39) |
V1061G |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,781,413 (GRCm39) |
|
probably null |
Het |
Apbb1 |
A |
G |
7: 105,215,902 (GRCm39) |
F112L |
probably benign |
Het |
Atg9a |
A |
G |
1: 75,161,702 (GRCm39) |
S615P |
probably benign |
Het |
Bbof1 |
A |
T |
12: 84,457,942 (GRCm39) |
N69I |
possibly damaging |
Het |
Bcl2l14 |
T |
A |
6: 134,404,370 (GRCm39) |
V186D |
probably benign |
Het |
Bmp1 |
T |
G |
14: 70,728,823 (GRCm39) |
Y583S |
possibly damaging |
Het |
Boc |
A |
C |
16: 44,312,711 (GRCm39) |
S586R |
probably benign |
Het |
Btbd9 |
A |
T |
17: 30,518,710 (GRCm39) |
|
probably null |
Het |
Cacna1e |
T |
C |
1: 154,317,919 (GRCm39) |
M1180V |
probably damaging |
Het |
Ciao1 |
T |
C |
2: 127,088,376 (GRCm39) |
H149R |
probably damaging |
Het |
Cops5 |
T |
C |
1: 10,100,920 (GRCm39) |
|
probably benign |
Het |
Doc2b |
C |
T |
11: 75,671,093 (GRCm39) |
R209Q |
probably damaging |
Het |
Doc2b |
T |
C |
11: 75,686,451 (GRCm39) |
Y90C |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,901,675 (GRCm39) |
F481L |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,061,229 (GRCm39) |
|
probably null |
Het |
Fbxw16 |
T |
A |
9: 109,277,837 (GRCm39) |
|
probably benign |
Het |
Fbxw27 |
T |
C |
9: 109,601,154 (GRCm39) |
E17G |
possibly damaging |
Het |
Gm29735 |
G |
A |
7: 141,710,367 (GRCm39) |
P162S |
unknown |
Het |
Gypa |
T |
G |
8: 81,222,969 (GRCm39) |
S24R |
unknown |
Het |
Hdhd5 |
T |
C |
6: 120,495,485 (GRCm39) |
N153D |
probably benign |
Het |
Ibsp |
C |
A |
5: 104,449,987 (GRCm39) |
|
probably null |
Het |
Klhdc3 |
C |
T |
17: 46,988,972 (GRCm39) |
V73I |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,388,459 (GRCm39) |
E2322G |
unknown |
Het |
Lrrtm3 |
T |
C |
10: 63,765,913 (GRCm39) |
H558R |
probably benign |
Het |
Mbtd1 |
C |
T |
11: 93,823,058 (GRCm39) |
H493Y |
possibly damaging |
Het |
Mphosph9 |
A |
G |
5: 124,458,978 (GRCm39) |
V64A |
possibly damaging |
Het |
Nthl1 |
C |
T |
17: 24,857,475 (GRCm39) |
R251C |
probably damaging |
Het |
Numa1 |
G |
A |
7: 101,649,974 (GRCm39) |
R1235H |
probably benign |
Het |
Opn1sw |
T |
A |
6: 29,379,413 (GRCm39) |
Y197F |
possibly damaging |
Het |
Or10a3m |
T |
C |
7: 108,312,845 (GRCm39) |
V95A |
probably damaging |
Het |
Pcca |
A |
T |
14: 122,896,187 (GRCm39) |
I268F |
probably benign |
Het |
Per2 |
A |
T |
1: 91,377,594 (GRCm39) |
D76E |
unknown |
Het |
Pfas |
T |
C |
11: 68,888,825 (GRCm39) |
N374S |
probably benign |
Het |
Pomk |
C |
A |
8: 26,472,955 (GRCm39) |
V333F |
probably damaging |
Het |
Ptgfr |
T |
C |
3: 151,540,926 (GRCm39) |
E194G |
probably benign |
Het |
Ptpn14 |
C |
T |
1: 189,582,997 (GRCm39) |
P615S |
probably damaging |
Het |
Pyroxd1 |
T |
C |
6: 142,300,479 (GRCm39) |
I203T |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,087,520 (GRCm39) |
N466S |
probably benign |
Het |
Rpl3l |
G |
A |
17: 24,952,966 (GRCm39) |
V309I |
probably benign |
Het |
Rtkn2 |
C |
T |
10: 67,815,529 (GRCm39) |
|
probably benign |
Het |
Sec16a |
C |
T |
2: 26,318,253 (GRCm39) |
A1613T |
probably damaging |
Het |
Sis |
T |
A |
3: 72,874,103 (GRCm39) |
T33S |
probably damaging |
Het |
Slc22a4 |
C |
A |
11: 53,898,634 (GRCm39) |
V153F |
possibly damaging |
Het |
Stxbp1 |
C |
G |
2: 32,684,621 (GRCm39) |
E603Q |
probably damaging |
Het |
Tiam2 |
A |
G |
17: 3,559,831 (GRCm39) |
S1291G |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,687,572 (GRCm39) |
L1144M |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,579,673 (GRCm39) |
T23740M |
probably damaging |
Het |
Vmn1r201 |
T |
C |
13: 22,659,533 (GRCm39) |
V249A |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,888,182 (GRCm39) |
C552S |
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 |
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 |
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 |
|
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 |
|