Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,018,194 (GRCm39) |
F1142S |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,973,806 (GRCm39) |
T2503A |
possibly damaging |
Het |
Bpi |
A |
G |
2: 158,104,344 (GRCm39) |
D149G |
probably damaging |
Het |
Cntnap5a |
A |
G |
1: 116,508,261 (GRCm39) |
T1258A |
probably benign |
Het |
Col4a3 |
A |
G |
1: 82,637,946 (GRCm39) |
D256G |
unknown |
Het |
Cul5 |
T |
C |
9: 53,546,278 (GRCm39) |
T338A |
probably damaging |
Het |
Efs |
A |
G |
14: 55,154,880 (GRCm39) |
V453A |
probably damaging |
Het |
Fbxw19 |
T |
A |
9: 109,323,709 (GRCm39) |
N89Y |
probably benign |
Het |
Fbxw8 |
A |
G |
5: 118,280,815 (GRCm39) |
F114S |
probably damaging |
Het |
Flnb |
A |
G |
14: 7,917,338 (GRCm38) |
I1606V |
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,831,638 (GRCm39) |
T913A |
possibly damaging |
Het |
Gtf2f1 |
A |
T |
17: 57,316,682 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,387,678 (GRCm39) |
*1059L |
probably null |
Het |
Hmgb4 |
T |
C |
4: 128,154,134 (GRCm39) |
K145E |
probably damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,898,860 (GRCm39) |
M250L |
probably benign |
Het |
Igkv14-111 |
A |
G |
6: 68,233,561 (GRCm39) |
K21E |
probably benign |
Het |
Il6st |
C |
T |
13: 112,616,729 (GRCm39) |
T92I |
probably damaging |
Het |
Jak3 |
G |
T |
8: 72,135,595 (GRCm39) |
V581L |
possibly damaging |
Het |
Kank2 |
C |
T |
9: 21,706,329 (GRCm39) |
V230M |
probably damaging |
Het |
Kif1a |
G |
A |
1: 92,967,569 (GRCm39) |
A1123V |
possibly damaging |
Het |
Kpna4 |
T |
A |
3: 69,002,863 (GRCm39) |
R125* |
probably null |
Het |
Mybpc3 |
A |
T |
2: 90,962,982 (GRCm39) |
|
probably null |
Het |
Ntn4 |
T |
C |
10: 93,546,421 (GRCm39) |
V358A |
possibly damaging |
Het |
Pacsin1 |
A |
T |
17: 27,921,672 (GRCm39) |
|
probably null |
Het |
Pcsk2 |
A |
G |
2: 143,615,865 (GRCm39) |
N221S |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,254,262 (GRCm39) |
L575P |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,623,815 (GRCm39) |
V760E |
possibly damaging |
Het |
Plxnc1 |
T |
C |
10: 94,630,542 (GRCm39) |
|
probably null |
Het |
Ppfia1 |
T |
C |
7: 144,073,341 (GRCm39) |
T217A |
probably benign |
Het |
Rictor |
A |
G |
15: 6,816,852 (GRCm39) |
T1375A |
probably benign |
Het |
Scn1a |
A |
G |
2: 66,161,756 (GRCm39) |
I264T |
probably damaging |
Het |
Sez6l2 |
T |
C |
7: 126,552,905 (GRCm39) |
S164P |
probably damaging |
Het |
Slc31a1 |
C |
T |
4: 62,303,869 (GRCm39) |
|
probably benign |
Het |
Slc45a1 |
T |
C |
4: 150,722,478 (GRCm39) |
N469D |
probably benign |
Het |
Slco1a5 |
T |
C |
6: 142,208,438 (GRCm39) |
T76A |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Stfa3 |
G |
A |
16: 36,270,999 (GRCm39) |
T95I |
probably damaging |
Het |
Stk11ip |
A |
C |
1: 75,501,325 (GRCm39) |
|
probably null |
Het |
Tcn2 |
C |
A |
11: 3,876,158 (GRCm39) |
S90I |
possibly damaging |
Het |
Traf1 |
A |
G |
2: 34,848,020 (GRCm39) |
S25P |
probably benign |
Het |
Ttn |
G |
T |
2: 76,622,125 (GRCm39) |
|
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,798,283 (GRCm39) |
I2041N |
probably damaging |
Het |
Zfp512b |
A |
T |
2: 181,229,864 (GRCm39) |
D556E |
possibly damaging |
Het |
Zfpm2 |
T |
A |
15: 40,965,415 (GRCm39) |
D633E |
probably benign |
Het |
|
Other mutations in 5031439G07Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00910:5031439G07Rik
|
APN |
15 |
84,840,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:5031439G07Rik
|
UTSW |
15 |
84,838,201 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0899:5031439G07Rik
|
UTSW |
15 |
84,833,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1302:5031439G07Rik
|
UTSW |
15 |
84,837,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:5031439G07Rik
|
UTSW |
15 |
84,839,833 (GRCm39) |
splice site |
probably benign |
|
R1468:5031439G07Rik
|
UTSW |
15 |
84,837,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:5031439G07Rik
|
UTSW |
15 |
84,837,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R2299:5031439G07Rik
|
UTSW |
15 |
84,837,486 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5721:5031439G07Rik
|
UTSW |
15 |
84,844,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:5031439G07Rik
|
UTSW |
15 |
84,839,897 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5971:5031439G07Rik
|
UTSW |
15 |
84,871,863 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6131:5031439G07Rik
|
UTSW |
15 |
84,844,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R6981:5031439G07Rik
|
UTSW |
15 |
84,833,798 (GRCm39) |
nonsense |
probably null |
|
R7173:5031439G07Rik
|
UTSW |
15 |
84,833,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7220:5031439G07Rik
|
UTSW |
15 |
84,837,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7554:5031439G07Rik
|
UTSW |
15 |
84,839,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7956:5031439G07Rik
|
UTSW |
15 |
84,834,963 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8218:5031439G07Rik
|
UTSW |
15 |
84,839,668 (GRCm39) |
missense |
probably damaging |
0.99 |
R8500:5031439G07Rik
|
UTSW |
15 |
84,871,836 (GRCm39) |
missense |
probably benign |
|
R8501:5031439G07Rik
|
UTSW |
15 |
84,844,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:5031439G07Rik
|
UTSW |
15 |
84,839,867 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9032:5031439G07Rik
|
UTSW |
15 |
84,844,782 (GRCm39) |
missense |
probably benign |
0.34 |
Z1177:5031439G07Rik
|
UTSW |
15 |
84,834,843 (GRCm39) |
missense |
possibly damaging |
0.52 |
|