Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankk1 |
T |
C |
9: 49,328,072 (GRCm39) |
N369S |
probably damaging |
Het |
Atp13a3 |
C |
T |
16: 30,151,182 (GRCm39) |
A1043T |
probably benign |
Het |
AY358078 |
G |
A |
14: 52,057,762 (GRCm39) |
V287I |
unknown |
Het |
Cemip |
T |
C |
7: 83,636,661 (GRCm39) |
E324G |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,431,052 (GRCm39) |
D1487E |
possibly damaging |
Het |
Dscam |
G |
A |
16: 96,517,273 (GRCm39) |
Q879* |
probably null |
Het |
Eci2 |
A |
G |
13: 35,174,759 (GRCm39) |
L50P |
probably damaging |
Het |
Erp44 |
A |
T |
4: 48,236,964 (GRCm39) |
H65Q |
probably benign |
Het |
Fahd1 |
A |
T |
17: 25,068,570 (GRCm39) |
I169N |
probably damaging |
Het |
Galm |
T |
C |
17: 80,488,996 (GRCm39) |
I214T |
probably benign |
Het |
Gipc3 |
T |
A |
10: 81,178,968 (GRCm39) |
N42Y |
probably damaging |
Het |
H2-Eb2 |
A |
T |
17: 34,554,741 (GRCm39) |
|
probably benign |
Het |
Itgb3 |
A |
T |
11: 104,523,174 (GRCm39) |
I113F |
probably damaging |
Het |
Lef1 |
T |
G |
3: 130,994,051 (GRCm39) |
Y342* |
probably null |
Het |
Lilrb4a |
G |
A |
10: 51,368,103 (GRCm39) |
D168N |
possibly damaging |
Het |
Or51b6b |
T |
A |
7: 103,309,860 (GRCm39) |
Y199F |
probably damaging |
Het |
Or5m10 |
T |
A |
2: 85,717,275 (GRCm39) |
F44I |
probably benign |
Het |
Orc1 |
T |
G |
4: 108,445,926 (GRCm39) |
S15A |
possibly damaging |
Het |
Pdk2 |
C |
T |
11: 94,919,324 (GRCm39) |
G317D |
probably benign |
Het |
Rab37 |
T |
C |
11: 115,051,543 (GRCm39) |
S217P |
probably benign |
Het |
Rere |
C |
T |
4: 150,699,289 (GRCm39) |
|
probably benign |
Het |
Sirt1 |
A |
G |
10: 63,160,982 (GRCm39) |
S357P |
probably damaging |
Het |
Smpdl3b |
T |
A |
4: 132,461,024 (GRCm39) |
E351V |
probably benign |
Het |
Sox6 |
C |
A |
7: 115,149,310 (GRCm39) |
G355W |
probably damaging |
Het |
Spopfm2 |
T |
A |
3: 94,083,662 (GRCm39) |
S50C |
probably damaging |
Het |
Srpk2 |
G |
T |
5: 23,723,705 (GRCm39) |
A502E |
probably damaging |
Het |
Trim67 |
G |
A |
8: 125,549,869 (GRCm39) |
V500I |
probably benign |
Het |
Ube2v2 |
A |
G |
16: 15,394,922 (GRCm39) |
V83A |
probably benign |
Het |
Usp43 |
A |
T |
11: 67,747,113 (GRCm39) |
S865T |
probably benign |
Het |
Vdac1 |
G |
A |
11: 52,267,371 (GRCm39) |
|
probably null |
Het |
Vmn2r69 |
T |
A |
7: 85,060,990 (GRCm39) |
H198L |
possibly damaging |
Het |
Vmn2r93 |
T |
C |
17: 18,546,032 (GRCm39) |
C635R |
probably damaging |
Het |
|
Other mutations in Scn11a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Scn11a
|
APN |
9 |
119,599,572 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00272:Scn11a
|
APN |
9 |
119,645,669 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00332:Scn11a
|
APN |
9 |
119,598,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00533:Scn11a
|
APN |
9 |
119,603,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00972:Scn11a
|
APN |
9 |
119,623,004 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01338:Scn11a
|
APN |
9 |
119,613,227 (GRCm39) |
splice site |
probably benign |
|
IGL01534:Scn11a
|
APN |
9 |
119,609,888 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01838:Scn11a
|
APN |
9 |
119,587,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01991:Scn11a
|
APN |
9 |
119,648,970 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02290:Scn11a
|
APN |
9 |
119,603,508 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02454:Scn11a
|
APN |
9 |
119,587,610 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02517:Scn11a
|
APN |
9 |
119,621,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Scn11a
|
APN |
9 |
119,633,555 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Scn11a
|
APN |
9 |
119,634,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Scn11a
|
APN |
9 |
119,619,029 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03171:Scn11a
|
APN |
9 |
119,648,913 (GRCm39) |
missense |
probably benign |
0.00 |
Kleinie
|
UTSW |
9 |
119,632,569 (GRCm39) |
missense |
probably benign |
0.16 |
H8441:Scn11a
|
UTSW |
9 |
119,636,976 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4449001:Scn11a
|
UTSW |
9 |
119,599,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Scn11a
|
UTSW |
9 |
119,648,928 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Scn11a
|
UTSW |
9 |
119,619,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Scn11a
|
UTSW |
9 |
119,640,226 (GRCm39) |
missense |
probably benign |
0.41 |
R0828:Scn11a
|
UTSW |
9 |
119,584,073 (GRCm39) |
missense |
probably benign |
0.00 |
R0893:Scn11a
|
UTSW |
9 |
119,632,396 (GRCm39) |
splice site |
probably null |
|
R0932:Scn11a
|
UTSW |
9 |
119,636,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Scn11a
|
UTSW |
9 |
119,624,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R1161:Scn11a
|
UTSW |
9 |
119,584,123 (GRCm39) |
nonsense |
probably null |
|
R1162:Scn11a
|
UTSW |
9 |
119,634,710 (GRCm39) |
splice site |
probably benign |
|
R1310:Scn11a
|
UTSW |
9 |
119,584,123 (GRCm39) |
nonsense |
probably null |
|
R1589:Scn11a
|
UTSW |
9 |
119,598,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Scn11a
|
UTSW |
9 |
119,633,478 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1781:Scn11a
|
UTSW |
9 |
119,584,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R1812:Scn11a
|
UTSW |
9 |
119,609,931 (GRCm39) |
nonsense |
probably null |
|
R1901:Scn11a
|
UTSW |
9 |
119,608,102 (GRCm39) |
nonsense |
probably null |
|
R1978:Scn11a
|
UTSW |
9 |
119,609,861 (GRCm39) |
nonsense |
probably null |
|
R1985:Scn11a
|
UTSW |
9 |
119,583,744 (GRCm39) |
missense |
probably benign |
0.19 |
R2022:Scn11a
|
UTSW |
9 |
119,640,274 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2072:Scn11a
|
UTSW |
9 |
119,640,274 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2098:Scn11a
|
UTSW |
9 |
119,621,560 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2163:Scn11a
|
UTSW |
9 |
119,584,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R2250:Scn11a
|
UTSW |
9 |
119,587,668 (GRCm39) |
missense |
probably benign |
0.01 |
R2373:Scn11a
|
UTSW |
9 |
119,642,252 (GRCm39) |
missense |
probably benign |
0.43 |
R2508:Scn11a
|
UTSW |
9 |
119,594,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R3757:Scn11a
|
UTSW |
9 |
119,632,569 (GRCm39) |
missense |
probably benign |
0.16 |
R3767:Scn11a
|
UTSW |
9 |
119,613,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3770:Scn11a
|
UTSW |
9 |
119,613,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R4089:Scn11a
|
UTSW |
9 |
119,624,719 (GRCm39) |
splice site |
probably null |
|
R4092:Scn11a
|
UTSW |
9 |
119,619,036 (GRCm39) |
missense |
probably benign |
0.03 |
R4247:Scn11a
|
UTSW |
9 |
119,636,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R4279:Scn11a
|
UTSW |
9 |
119,583,428 (GRCm39) |
missense |
probably benign |
0.25 |
R4299:Scn11a
|
UTSW |
9 |
119,594,572 (GRCm39) |
missense |
probably damaging |
0.97 |
R4403:Scn11a
|
UTSW |
9 |
119,624,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R4468:Scn11a
|
UTSW |
9 |
119,584,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Scn11a
|
UTSW |
9 |
119,584,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Scn11a
|
UTSW |
9 |
119,644,269 (GRCm39) |
splice site |
probably null |
|
R4739:Scn11a
|
UTSW |
9 |
119,583,627 (GRCm39) |
missense |
probably benign |
0.39 |
R4809:Scn11a
|
UTSW |
9 |
119,648,936 (GRCm39) |
missense |
probably benign |
0.00 |
R4954:Scn11a
|
UTSW |
9 |
119,587,725 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5012:Scn11a
|
UTSW |
9 |
119,609,944 (GRCm39) |
missense |
probably benign |
0.31 |
R5044:Scn11a
|
UTSW |
9 |
119,648,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R5222:Scn11a
|
UTSW |
9 |
119,644,268 (GRCm39) |
splice site |
probably null |
|
R5224:Scn11a
|
UTSW |
9 |
119,583,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Scn11a
|
UTSW |
9 |
119,598,974 (GRCm39) |
missense |
probably damaging |
0.97 |
R5555:Scn11a
|
UTSW |
9 |
119,584,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R5711:Scn11a
|
UTSW |
9 |
119,618,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Scn11a
|
UTSW |
9 |
119,640,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Scn11a
|
UTSW |
9 |
119,613,082 (GRCm39) |
missense |
probably benign |
|
R6057:Scn11a
|
UTSW |
9 |
119,594,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Scn11a
|
UTSW |
9 |
119,624,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Scn11a
|
UTSW |
9 |
119,583,933 (GRCm39) |
missense |
probably benign |
0.00 |
R6892:Scn11a
|
UTSW |
9 |
119,636,035 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6908:Scn11a
|
UTSW |
9 |
119,621,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Scn11a
|
UTSW |
9 |
119,594,580 (GRCm39) |
missense |
probably benign |
0.04 |
R7112:Scn11a
|
UTSW |
9 |
119,583,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Scn11a
|
UTSW |
9 |
119,588,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Scn11a
|
UTSW |
9 |
119,648,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R7265:Scn11a
|
UTSW |
9 |
119,644,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7302:Scn11a
|
UTSW |
9 |
119,636,017 (GRCm39) |
missense |
probably benign |
0.03 |
R7391:Scn11a
|
UTSW |
9 |
119,624,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Scn11a
|
UTSW |
9 |
119,587,692 (GRCm39) |
missense |
probably benign |
0.01 |
R7479:Scn11a
|
UTSW |
9 |
119,588,941 (GRCm39) |
missense |
probably benign |
0.38 |
R7608:Scn11a
|
UTSW |
9 |
119,644,379 (GRCm39) |
splice site |
probably null |
|
R7768:Scn11a
|
UTSW |
9 |
119,644,338 (GRCm39) |
missense |
probably benign |
0.13 |
R7785:Scn11a
|
UTSW |
9 |
119,645,622 (GRCm39) |
missense |
probably benign |
0.00 |
R7794:Scn11a
|
UTSW |
9 |
119,594,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R7818:Scn11a
|
UTSW |
9 |
119,613,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R7884:Scn11a
|
UTSW |
9 |
119,633,617 (GRCm39) |
missense |
probably benign |
0.01 |
R7988:Scn11a
|
UTSW |
9 |
119,594,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R8049:Scn11a
|
UTSW |
9 |
119,584,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8127:Scn11a
|
UTSW |
9 |
119,633,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Scn11a
|
UTSW |
9 |
119,632,548 (GRCm39) |
missense |
probably benign |
|
R8344:Scn11a
|
UTSW |
9 |
119,611,036 (GRCm39) |
missense |
probably benign |
0.00 |
R8346:Scn11a
|
UTSW |
9 |
119,608,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Scn11a
|
UTSW |
9 |
119,618,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R8819:Scn11a
|
UTSW |
9 |
119,645,586 (GRCm39) |
missense |
probably benign |
0.19 |
R8820:Scn11a
|
UTSW |
9 |
119,645,586 (GRCm39) |
missense |
probably benign |
0.19 |
R8837:Scn11a
|
UTSW |
9 |
119,621,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Scn11a
|
UTSW |
9 |
119,623,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Scn11a
|
UTSW |
9 |
119,603,363 (GRCm39) |
nonsense |
probably null |
|
R8975:Scn11a
|
UTSW |
9 |
119,587,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:Scn11a
|
UTSW |
9 |
119,588,989 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9222:Scn11a
|
UTSW |
9 |
119,611,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R9355:Scn11a
|
UTSW |
9 |
119,584,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Scn11a
|
UTSW |
9 |
119,624,774 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9712:Scn11a
|
UTSW |
9 |
119,619,076 (GRCm39) |
nonsense |
probably null |
|
R9766:Scn11a
|
UTSW |
9 |
119,584,181 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Scn11a
|
UTSW |
9 |
119,584,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn11a
|
UTSW |
9 |
119,648,886 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn11a
|
UTSW |
9 |
119,584,064 (GRCm39) |
missense |
possibly damaging |
0.94 |
|