Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610030E20Rik |
C |
T |
6: 72,324,635 (GRCm39) |
T56M |
probably damaging |
Het |
Adamtsl5 |
C |
T |
10: 80,181,372 (GRCm39) |
S36N |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,750,704 (GRCm39) |
|
probably benign |
Het |
Ago1 |
A |
G |
4: 126,354,210 (GRCm39) |
F200S |
probably damaging |
Het |
Akr1cl |
T |
C |
1: 65,063,865 (GRCm39) |
D108G |
possibly damaging |
Het |
Aopep |
A |
G |
13: 63,208,954 (GRCm39) |
D357G |
probably benign |
Het |
Arhgef3 |
A |
T |
14: 27,123,743 (GRCm39) |
D468V |
probably benign |
Het |
Aspn |
T |
C |
13: 49,705,353 (GRCm39) |
C72R |
possibly damaging |
Het |
Baz2b |
T |
C |
2: 59,792,485 (GRCm39) |
T548A |
possibly damaging |
Het |
Birc6 |
G |
A |
17: 74,906,368 (GRCm39) |
|
probably null |
Het |
Btnl2 |
A |
T |
17: 34,577,249 (GRCm39) |
T135S |
possibly damaging |
Het |
Ccnl1 |
T |
A |
3: 65,865,282 (GRCm39) |
I90F |
possibly damaging |
Het |
Ccnt1 |
T |
C |
15: 98,463,024 (GRCm39) |
|
probably null |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Cfap45 |
A |
G |
1: 172,357,501 (GRCm39) |
D85G |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,737,941 (GRCm39) |
D2319V |
unknown |
Het |
Cma1 |
T |
C |
14: 56,181,989 (GRCm39) |
M14V |
possibly damaging |
Het |
Cmtm1 |
T |
C |
8: 105,036,774 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
A |
G |
4: 63,249,559 (GRCm39) |
H1738R |
unknown |
Het |
Colq |
T |
A |
14: 31,275,794 (GRCm39) |
D41V |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,337,166 (GRCm39) |
T2437A |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,611,139 (GRCm39) |
D3755G |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,150,545 (GRCm39) |
Y1349C |
probably damaging |
Het |
Eps8 |
C |
T |
6: 137,505,569 (GRCm39) |
R53Q |
possibly damaging |
Het |
Fbf1 |
T |
C |
11: 116,043,594 (GRCm39) |
D405G |
probably benign |
Het |
Fen1 |
C |
T |
19: 10,177,674 (GRCm39) |
E257K |
possibly damaging |
Het |
Gstm7 |
A |
T |
3: 107,834,271 (GRCm39) |
M198K |
possibly damaging |
Het |
Hook3 |
A |
T |
8: 26,563,675 (GRCm39) |
S190T |
probably benign |
Het |
Htra4 |
A |
C |
8: 25,520,526 (GRCm39) |
|
probably null |
Het |
Ighv1-15 |
T |
C |
12: 114,621,116 (GRCm39) |
I70V |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,470,324 (GRCm39) |
N452Y |
probably damaging |
Het |
Insyn2a |
T |
G |
7: 134,519,427 (GRCm39) |
K368Q |
probably damaging |
Het |
Iqcf5 |
T |
A |
9: 106,393,020 (GRCm39) |
N92K |
possibly damaging |
Het |
Itk |
A |
G |
11: 46,246,661 (GRCm39) |
Y186H |
probably damaging |
Het |
Klhdc10 |
T |
C |
6: 30,446,690 (GRCm39) |
S282P |
probably benign |
Het |
Klhl18 |
T |
A |
9: 110,305,577 (GRCm39) |
E29V |
possibly damaging |
Het |
Ky |
T |
C |
9: 102,402,614 (GRCm39) |
S140P |
probably damaging |
Het |
Lmntd2 |
T |
C |
7: 140,793,550 (GRCm39) |
E112G |
unknown |
Het |
Lrrc36 |
C |
A |
8: 106,178,718 (GRCm39) |
D304E |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,400,273 (GRCm39) |
F674Y |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,361,013 (GRCm39) |
D1111N |
probably benign |
Het |
Osbpl8 |
T |
G |
10: 111,107,941 (GRCm39) |
N312K |
possibly damaging |
Het |
Otogl |
C |
T |
10: 107,731,637 (GRCm39) |
C168Y |
probably damaging |
Het |
Phldb2 |
T |
G |
16: 45,645,934 (GRCm39) |
T171P |
probably benign |
Het |
Ppef2 |
A |
T |
5: 92,386,841 (GRCm39) |
F365L |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Ryr1 |
G |
A |
7: 28,795,596 (GRCm39) |
T1105I |
probably benign |
Het |
Sclt1 |
T |
A |
3: 41,617,889 (GRCm39) |
*29L |
probably null |
Het |
Serpinb9c |
T |
A |
13: 33,334,262 (GRCm39) |
Y288F |
probably benign |
Het |
Setd1a |
T |
A |
7: 127,385,366 (GRCm39) |
M691K |
probably benign |
Het |
Sftpc |
T |
C |
14: 70,760,059 (GRCm39) |
E66G |
probably damaging |
Het |
Spata31h1 |
T |
C |
10: 82,131,934 (GRCm39) |
I359V |
probably benign |
Het |
Thnsl2 |
T |
C |
6: 71,118,303 (GRCm39) |
T42A |
probably benign |
Het |
Tram1 |
T |
C |
1: 13,640,199 (GRCm39) |
D285G |
probably benign |
Het |
Ttn |
G |
A |
2: 76,675,374 (GRCm39) |
P11137L |
unknown |
Het |
Ttn |
C |
A |
2: 76,727,103 (GRCm39) |
V5821F |
unknown |
Het |
Ttn |
A |
T |
2: 76,566,584 (GRCm39) |
I28103K |
probably damaging |
Het |
Usp38 |
T |
A |
8: 81,740,945 (GRCm39) |
M41L |
probably benign |
Het |
Zcwpw1 |
T |
G |
5: 137,815,753 (GRCm39) |
Y419D |
possibly damaging |
Het |
Zfp407 |
G |
A |
18: 84,577,525 (GRCm39) |
A1196V |
possibly damaging |
Het |
Zfp446 |
T |
A |
7: 12,712,970 (GRCm39) |
S103T |
possibly 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 |
IGL02057:Scn11a
|
APN |
9 |
119,594,536 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|