Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,551 (GRCm39) |
Y195C |
probably damaging |
Het |
Abcb1a |
T |
A |
5: 8,735,371 (GRCm39) |
F159L |
probably damaging |
Het |
Adam6b |
A |
G |
12: 113,454,371 (GRCm39) |
N396S |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,823,055 (GRCm39) |
M338V |
possibly damaging |
Het |
Adamts7 |
T |
A |
9: 90,077,321 (GRCm39) |
H1329Q |
probably damaging |
Het |
Aim2 |
C |
T |
1: 173,289,786 (GRCm39) |
P243L |
probably damaging |
Het |
Ankdd1a |
T |
C |
9: 65,412,418 (GRCm39) |
D311G |
probably damaging |
Het |
Apon |
A |
T |
10: 128,090,428 (GRCm39) |
E35D |
probably benign |
Het |
Atp6v0a1 |
T |
A |
11: 100,953,229 (GRCm39) |
*839R |
probably null |
Het |
Bco2 |
A |
G |
9: 50,461,878 (GRCm39) |
L42P |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,141,873 (GRCm39) |
|
probably benign |
Het |
Ccna1 |
T |
C |
3: 54,955,878 (GRCm39) |
Q306R |
probably benign |
Het |
Cep152 |
G |
T |
2: 125,406,131 (GRCm39) |
S1467* |
probably null |
Het |
Cfap44 |
T |
A |
16: 44,225,085 (GRCm39) |
V110E |
probably damaging |
Het |
Clip2 |
G |
A |
5: 134,531,462 (GRCm39) |
A781V |
probably benign |
Het |
Cps1 |
A |
T |
1: 67,243,772 (GRCm39) |
I1083F |
probably damaging |
Het |
Cux1 |
A |
G |
5: 136,336,710 (GRCm39) |
V934A |
possibly damaging |
Het |
Depdc5 |
T |
C |
5: 33,101,382 (GRCm39) |
F891L |
possibly damaging |
Het |
Dnai7 |
T |
A |
6: 145,127,542 (GRCm39) |
I456F |
probably benign |
Het |
Dnajc13 |
A |
G |
9: 104,057,338 (GRCm39) |
V1554A |
probably benign |
Het |
Echs1 |
A |
T |
7: 139,690,499 (GRCm39) |
M191K |
probably damaging |
Het |
Eif6 |
T |
A |
2: 155,664,772 (GRCm39) |
D238V |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,144,692 (GRCm39) |
L4061F |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,908,703 (GRCm39) |
D2433G |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,320,265 (GRCm39) |
V33A |
probably benign |
Het |
Garin2 |
TGATGTCACAGATGTCAC |
TGATGTCAC |
12: 78,762,057 (GRCm39) |
|
probably benign |
Het |
Gpr155 |
T |
C |
2: 73,174,039 (GRCm39) |
E790G |
probably damaging |
Het |
Ighv1-67 |
A |
T |
12: 115,567,861 (GRCm39) |
V17E |
probably damaging |
Het |
Klra9 |
T |
A |
6: 130,165,639 (GRCm39) |
R125S |
probably damaging |
Het |
Leo1 |
T |
C |
9: 75,353,277 (GRCm39) |
|
probably null |
Het |
Map2 |
G |
T |
1: 66,460,872 (GRCm39) |
R1556L |
probably damaging |
Het |
Megf8 |
A |
G |
7: 25,059,166 (GRCm39) |
|
probably null |
Het |
Meikin |
T |
C |
11: 54,317,477 (GRCm39) |
I426T |
possibly damaging |
Het |
Muc16 |
A |
T |
9: 18,556,015 (GRCm39) |
V3426E |
unknown |
Het |
Or4a15 |
T |
A |
2: 89,193,065 (GRCm39) |
Y236F |
probably benign |
Het |
Or51af1 |
G |
A |
7: 103,142,029 (GRCm39) |
L19F |
probably damaging |
Het |
Or52n2c |
A |
G |
7: 104,574,620 (GRCm39) |
L117P |
probably damaging |
Het |
Or7e168 |
T |
G |
9: 19,720,105 (GRCm39) |
S164A |
possibly damaging |
Het |
Or8k25 |
T |
C |
2: 86,243,935 (GRCm39) |
I154V |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,547,643 (GRCm39) |
V5A |
probably benign |
Het |
Otogl |
A |
G |
10: 107,747,936 (GRCm39) |
|
probably null |
Het |
Palm3 |
T |
C |
8: 84,756,504 (GRCm39) |
L672P |
probably damaging |
Het |
Perm1 |
A |
G |
4: 156,302,091 (GRCm39) |
T212A |
probably benign |
Het |
Poc1a |
T |
C |
9: 106,226,960 (GRCm39) |
M400T |
probably benign |
Het |
Pou6f2 |
T |
A |
13: 18,414,196 (GRCm39) |
Q193L |
unknown |
Het |
Ppl |
C |
T |
16: 4,905,300 (GRCm39) |
R1665H |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,123,449 (GRCm39) |
|
probably null |
Het |
Ptger1 |
T |
C |
8: 84,394,654 (GRCm39) |
S44P |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,473,009 (GRCm39) |
T787A |
probably benign |
Het |
Rab44 |
A |
T |
17: 29,358,642 (GRCm39) |
R277* |
probably null |
Het |
Rasgef1a |
T |
A |
6: 118,064,088 (GRCm39) |
I334K |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,818,084 (GRCm39) |
V554A |
possibly damaging |
Het |
Ripk1 |
T |
A |
13: 34,214,032 (GRCm39) |
I518K |
possibly damaging |
Het |
Rpl22 |
A |
G |
4: 152,416,763 (GRCm39) |
Y90C |
probably damaging |
Het |
Rps27a |
C |
A |
11: 29,495,998 (GRCm39) |
R118L |
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,319,331 (GRCm39) |
S19T |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,520,509 (GRCm39) |
|
probably null |
Het |
Sema4c |
A |
T |
1: 36,589,867 (GRCm39) |
S496T |
probably benign |
Het |
Serpina3i |
T |
C |
12: 104,231,387 (GRCm39) |
V8A |
possibly damaging |
Het |
Sis |
G |
A |
3: 72,867,628 (GRCm39) |
T139M |
probably damaging |
Het |
Skic3 |
A |
T |
13: 76,303,587 (GRCm39) |
H1227L |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,000,972 (GRCm39) |
S24T |
probably benign |
Het |
Slc5a11 |
A |
G |
7: 122,866,975 (GRCm39) |
I423M |
probably benign |
Het |
Slc7a10 |
G |
A |
7: 34,885,997 (GRCm39) |
G31S |
probably benign |
Het |
Sowahc |
A |
G |
10: 59,059,001 (GRCm39) |
N379S |
probably benign |
Het |
Stat5a |
T |
C |
11: 100,774,714 (GRCm39) |
M741T |
unknown |
Het |
Tcf15 |
T |
C |
2: 151,986,020 (GRCm39) |
S159P |
probably benign |
Het |
Tdrd5 |
C |
A |
1: 156,098,788 (GRCm39) |
R669L |
possibly damaging |
Het |
Tln1 |
T |
C |
4: 43,553,041 (GRCm39) |
E350G |
possibly damaging |
Het |
Trim12c |
T |
G |
7: 103,997,271 (GRCm39) |
N95T |
|
Het |
Urb1 |
T |
C |
16: 90,571,513 (GRCm39) |
T1099A |
probably benign |
Het |
Vmn1r44 |
T |
A |
6: 89,870,578 (GRCm39) |
V108D |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,589,388 (GRCm39) |
Y843H |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,871,321 (GRCm39) |
I654T |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,623,270 (GRCm39) |
N2797S |
possibly damaging |
Het |
Wscd2 |
T |
C |
5: 113,712,235 (GRCm39) |
Y385H |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,229,500 (GRCm39) |
I318V |
probably benign |
Het |
Xrcc3 |
T |
A |
12: 111,774,313 (GRCm39) |
K172M |
probably damaging |
Het |
|
Other mutations in Atp1a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00419:Atp1a4
|
APN |
1 |
172,067,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00924:Atp1a4
|
APN |
1 |
172,074,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Atp1a4
|
APN |
1 |
172,085,474 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01665:Atp1a4
|
APN |
1 |
172,074,291 (GRCm39) |
missense |
probably benign |
|
IGL02156:Atp1a4
|
APN |
1 |
172,085,529 (GRCm39) |
missense |
probably benign |
|
IGL02170:Atp1a4
|
APN |
1 |
172,062,103 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02228:Atp1a4
|
APN |
1 |
172,082,452 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02505:Atp1a4
|
APN |
1 |
172,062,642 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Atp1a4
|
APN |
1 |
172,078,973 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02792:Atp1a4
|
APN |
1 |
172,054,866 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02794:Atp1a4
|
APN |
1 |
172,071,653 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03102:Atp1a4
|
APN |
1 |
172,058,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Atp1a4
|
UTSW |
1 |
172,067,664 (GRCm39) |
missense |
probably benign |
0.09 |
R0046:Atp1a4
|
UTSW |
1 |
172,067,664 (GRCm39) |
missense |
probably benign |
0.09 |
R0276:Atp1a4
|
UTSW |
1 |
172,085,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Atp1a4
|
UTSW |
1 |
172,062,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Atp1a4
|
UTSW |
1 |
172,067,255 (GRCm39) |
splice site |
probably benign |
|
R0615:Atp1a4
|
UTSW |
1 |
172,059,627 (GRCm39) |
splice site |
probably benign |
|
R0730:Atp1a4
|
UTSW |
1 |
172,067,774 (GRCm39) |
splice site |
probably benign |
|
R1412:Atp1a4
|
UTSW |
1 |
172,059,576 (GRCm39) |
missense |
probably damaging |
0.97 |
R1652:Atp1a4
|
UTSW |
1 |
172,082,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Atp1a4
|
UTSW |
1 |
172,062,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R1968:Atp1a4
|
UTSW |
1 |
172,067,731 (GRCm39) |
missense |
probably benign |
|
R2291:Atp1a4
|
UTSW |
1 |
172,072,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Atp1a4
|
UTSW |
1 |
172,074,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R2908:Atp1a4
|
UTSW |
1 |
172,062,044 (GRCm39) |
missense |
probably benign |
|
R3119:Atp1a4
|
UTSW |
1 |
172,067,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R3731:Atp1a4
|
UTSW |
1 |
172,061,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Atp1a4
|
UTSW |
1 |
172,061,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R4602:Atp1a4
|
UTSW |
1 |
172,067,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4670:Atp1a4
|
UTSW |
1 |
172,062,567 (GRCm39) |
missense |
probably benign |
0.07 |
R4674:Atp1a4
|
UTSW |
1 |
172,085,223 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4675:Atp1a4
|
UTSW |
1 |
172,085,223 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4785:Atp1a4
|
UTSW |
1 |
172,081,677 (GRCm39) |
nonsense |
probably null |
|
R4958:Atp1a4
|
UTSW |
1 |
172,058,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Atp1a4
|
UTSW |
1 |
172,081,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5149:Atp1a4
|
UTSW |
1 |
172,059,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Atp1a4
|
UTSW |
1 |
172,054,737 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5501:Atp1a4
|
UTSW |
1 |
172,074,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5682:Atp1a4
|
UTSW |
1 |
172,081,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R5872:Atp1a4
|
UTSW |
1 |
172,071,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Atp1a4
|
UTSW |
1 |
172,059,841 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6722:Atp1a4
|
UTSW |
1 |
172,085,617 (GRCm39) |
unclassified |
probably benign |
|
R7087:Atp1a4
|
UTSW |
1 |
172,074,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7122:Atp1a4
|
UTSW |
1 |
172,059,503 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7381:Atp1a4
|
UTSW |
1 |
172,067,682 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7431:Atp1a4
|
UTSW |
1 |
172,078,474 (GRCm39) |
missense |
probably benign |
0.31 |
R8269:Atp1a4
|
UTSW |
1 |
172,059,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8400:Atp1a4
|
UTSW |
1 |
172,062,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Atp1a4
|
UTSW |
1 |
172,078,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Atp1a4
|
UTSW |
1 |
172,059,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Atp1a4
|
UTSW |
1 |
172,059,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Atp1a4
|
UTSW |
1 |
172,072,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R8869:Atp1a4
|
UTSW |
1 |
172,054,690 (GRCm39) |
missense |
probably benign |
|
R9260:Atp1a4
|
UTSW |
1 |
172,074,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R9300:Atp1a4
|
UTSW |
1 |
172,067,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R9545:Atp1a4
|
UTSW |
1 |
172,078,464 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Atp1a4
|
UTSW |
1 |
172,059,521 (GRCm39) |
missense |
probably benign |
0.44 |
|