Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l2 |
T |
C |
19: 56,902,881 (GRCm39) |
N748S |
probably benign |
Het |
Aox1 |
T |
A |
1: 58,086,326 (GRCm39) |
I77N |
probably damaging |
Het |
Ap1s1 |
A |
T |
5: 137,072,095 (GRCm39) |
M20K |
probably damaging |
Het |
Atad3a |
A |
T |
4: 155,835,892 (GRCm39) |
|
probably null |
Het |
Atp1b1 |
G |
T |
1: 164,265,889 (GRCm39) |
R291S |
probably damaging |
Het |
Birc7 |
T |
C |
2: 180,570,974 (GRCm39) |
V12A |
possibly damaging |
Het |
Btnl2 |
T |
C |
17: 34,582,211 (GRCm39) |
V259A |
probably damaging |
Het |
Cdh11 |
A |
T |
8: 103,377,343 (GRCm39) |
N434K |
probably benign |
Het |
Cel |
G |
T |
2: 28,450,479 (GRCm39) |
|
probably benign |
Het |
Col10a1 |
A |
G |
10: 34,271,074 (GRCm39) |
K349E |
probably damaging |
Het |
Ddhd2 |
A |
G |
8: 26,239,768 (GRCm39) |
V315A |
probably benign |
Het |
Dnah17 |
C |
A |
11: 117,994,324 (GRCm39) |
|
probably benign |
Het |
Dock2 |
T |
C |
11: 34,595,474 (GRCm39) |
T441A |
probably benign |
Het |
Ermap |
A |
T |
4: 119,041,152 (GRCm39) |
I286N |
probably damaging |
Het |
Fbxl17 |
T |
C |
17: 63,794,813 (GRCm39) |
K423R |
probably damaging |
Het |
Frem2 |
T |
C |
3: 53,561,940 (GRCm39) |
T856A |
probably benign |
Het |
Gas6 |
T |
C |
8: 13,543,901 (GRCm39) |
E64G |
probably damaging |
Het |
Gzma |
T |
A |
13: 113,232,331 (GRCm39) |
N190I |
probably damaging |
Het |
Ifngr1 |
C |
T |
10: 19,485,090 (GRCm39) |
T363M |
probably damaging |
Het |
Itga7 |
A |
G |
10: 128,782,732 (GRCm39) |
T690A |
probably benign |
Het |
Kif15 |
A |
G |
9: 122,823,074 (GRCm39) |
E485G |
probably benign |
Het |
Kif18a |
A |
G |
2: 109,123,336 (GRCm39) |
I203M |
probably damaging |
Het |
Klhl1 |
A |
T |
14: 96,438,647 (GRCm39) |
|
probably null |
Het |
Lrch3 |
C |
T |
16: 32,770,781 (GRCm39) |
Q128* |
probably null |
Het |
Lrriq4 |
C |
G |
3: 30,705,037 (GRCm39) |
P355R |
probably damaging |
Het |
Mcm10 |
A |
T |
2: 5,003,563 (GRCm39) |
H551Q |
probably damaging |
Het |
Mcm3ap |
T |
C |
10: 76,319,060 (GRCm39) |
F763L |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,156,758 (GRCm39) |
V55E |
probably damaging |
Het |
Me2 |
A |
T |
18: 73,931,016 (GRCm39) |
N92K |
probably damaging |
Het |
Mtss1 |
A |
G |
15: 58,815,560 (GRCm39) |
S667P |
probably damaging |
Het |
Mup5 |
A |
T |
4: 61,753,317 (GRCm39) |
Y15N |
possibly damaging |
Het |
Mx1 |
T |
A |
16: 97,256,329 (GRCm39) |
M197L |
probably damaging |
Het |
N4bp2 |
C |
T |
5: 65,964,483 (GRCm39) |
T844I |
probably benign |
Het |
Nlrc3 |
T |
A |
16: 3,781,859 (GRCm39) |
R517W |
probably damaging |
Het |
Nos3 |
A |
T |
5: 24,573,995 (GRCm39) |
I227F |
probably damaging |
Het |
Or52a5 |
A |
G |
7: 103,427,267 (GRCm39) |
F95S |
probably benign |
Het |
Pabpc2 |
A |
G |
18: 39,906,953 (GRCm39) |
N73D |
probably damaging |
Het |
Pcdhb18 |
A |
G |
18: 37,624,820 (GRCm39) |
R717G |
probably benign |
Het |
Pcsk5 |
T |
A |
19: 17,413,964 (GRCm39) |
M1702L |
probably benign |
Het |
Plxna2 |
A |
C |
1: 194,431,614 (GRCm39) |
|
probably benign |
Het |
Polr2a |
A |
G |
11: 69,630,755 (GRCm39) |
M1221T |
possibly damaging |
Het |
Polr2b |
A |
G |
5: 77,473,948 (GRCm39) |
D384G |
probably damaging |
Het |
Ppl |
T |
A |
16: 4,925,438 (GRCm39) |
H67L |
probably benign |
Het |
Psmd5 |
A |
G |
2: 34,757,035 (GRCm39) |
L63S |
probably damaging |
Het |
Psme1 |
A |
G |
14: 55,818,222 (GRCm39) |
T150A |
probably damaging |
Het |
Rapgef5 |
C |
T |
12: 117,621,940 (GRCm39) |
R33C |
probably damaging |
Het |
Rela |
G |
A |
19: 5,695,359 (GRCm39) |
R295H |
probably damaging |
Het |
Rpe65 |
T |
A |
3: 159,320,421 (GRCm39) |
V326E |
probably damaging |
Het |
Scn5a |
C |
A |
9: 119,391,563 (GRCm39) |
R43L |
probably damaging |
Het |
Skida1 |
T |
C |
2: 18,051,143 (GRCm39) |
|
probably benign |
Het |
Slc4a4 |
G |
A |
5: 89,283,587 (GRCm39) |
A469T |
probably benign |
Het |
Spaca7 |
G |
T |
8: 12,630,991 (GRCm39) |
E48* |
probably null |
Het |
Syn3 |
G |
T |
10: 85,970,908 (GRCm39) |
T238K |
probably benign |
Het |
Taok1 |
A |
G |
11: 77,470,626 (GRCm39) |
S60P |
probably benign |
Het |
Tecpr1 |
A |
G |
5: 144,151,128 (GRCm39) |
I256T |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,552,196 (GRCm39) |
|
probably null |
Het |
Tex15 |
A |
G |
8: 34,061,511 (GRCm39) |
T588A |
probably damaging |
Het |
Tgfbi |
T |
A |
13: 56,780,004 (GRCm39) |
|
probably benign |
Het |
Tmem62 |
G |
A |
2: 120,814,843 (GRCm39) |
A169T |
probably benign |
Het |
Tnc |
A |
G |
4: 63,924,621 (GRCm39) |
S1026P |
probably benign |
Het |
Tnik |
T |
C |
3: 28,658,418 (GRCm39) |
S568P |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,804,888 (GRCm39) |
I947F |
probably damaging |
Het |
Ttc27 |
T |
A |
17: 75,170,402 (GRCm39) |
L832Q |
possibly damaging |
Het |
U2surp |
C |
T |
9: 95,363,793 (GRCm39) |
|
probably benign |
Het |
Ube4a |
A |
T |
9: 44,841,064 (GRCm39) |
D1009E |
possibly damaging |
Het |
Unc13d |
T |
C |
11: 115,965,262 (GRCm39) |
E192G |
probably benign |
Het |
Vmn2r71 |
T |
C |
7: 85,273,352 (GRCm39) |
V722A |
possibly damaging |
Het |
Zfp386 |
T |
C |
12: 116,023,709 (GRCm39) |
S476P |
probably damaging |
Het |
Zfp644 |
A |
T |
5: 106,786,199 (GRCm39) |
V116D |
probably damaging |
Het |
Zfyve16 |
T |
A |
13: 92,644,755 (GRCm39) |
N1149I |
probably benign |
Het |
|
Other mutations in Acta2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Acta2
|
APN |
19 |
34,229,191 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01802:Acta2
|
APN |
19 |
34,220,836 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01945:Acta2
|
APN |
19 |
34,229,254 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02136:Acta2
|
APN |
19 |
34,229,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Acta2
|
APN |
19 |
34,222,310 (GRCm39) |
critical splice donor site |
probably null |
|
R0648:Acta2
|
UTSW |
19 |
34,225,934 (GRCm39) |
missense |
probably benign |
|
R1393:Acta2
|
UTSW |
19 |
34,219,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Acta2
|
UTSW |
19 |
34,220,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2338:Acta2
|
UTSW |
19 |
34,225,941 (GRCm39) |
splice site |
probably benign |
|
R3113:Acta2
|
UTSW |
19 |
34,220,752 (GRCm39) |
missense |
probably benign |
|
R3940:Acta2
|
UTSW |
19 |
34,220,880 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3955:Acta2
|
UTSW |
19 |
34,229,126 (GRCm39) |
splice site |
probably benign |
|
R4765:Acta2
|
UTSW |
19 |
34,223,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4826:Acta2
|
UTSW |
19 |
34,229,223 (GRCm39) |
nonsense |
probably null |
|
R6453:Acta2
|
UTSW |
19 |
34,224,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6754:Acta2
|
UTSW |
19 |
34,222,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Acta2
|
UTSW |
19 |
34,229,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7311:Acta2
|
UTSW |
19 |
34,219,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7463:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7536:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7537:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7605:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7609:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7610:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7613:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7626:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7627:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7803:Acta2
|
UTSW |
19 |
34,220,818 (GRCm39) |
missense |
probably benign |
|
R7872:Acta2
|
UTSW |
19 |
34,220,839 (GRCm39) |
missense |
probably damaging |
0.99 |
R8801:Acta2
|
UTSW |
19 |
34,229,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R9059:Acta2
|
UTSW |
19 |
34,219,155 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9191:Acta2
|
UTSW |
19 |
34,222,480 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9487:Acta2
|
UTSW |
19 |
34,225,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R9675:Acta2
|
UTSW |
19 |
34,223,612 (GRCm39) |
missense |
|
|
R9776:Acta2
|
UTSW |
19 |
34,223,481 (GRCm39) |
missense |
probably benign |
0.01 |
|