Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
C |
T |
2: 69,108,153 (GRCm39) |
A715T |
probably benign |
Het |
Ampd2 |
A |
G |
3: 107,983,005 (GRCm39) |
Y641H |
probably damaging |
Het |
Aqp4 |
A |
T |
18: 15,531,248 (GRCm39) |
V171E |
probably damaging |
Het |
Arid4a |
T |
A |
12: 71,121,729 (GRCm39) |
S381R |
probably damaging |
Het |
Armc8 |
T |
G |
9: 99,419,784 (GRCm39) |
N51H |
probably damaging |
Het |
Asic5 |
T |
A |
3: 81,928,308 (GRCm39) |
Y424N |
probably damaging |
Het |
Bcl11a |
A |
T |
11: 24,114,069 (GRCm39) |
K471* |
probably null |
Het |
Birc6 |
A |
G |
17: 74,996,307 (GRCm39) |
T4494A |
probably damaging |
Het |
Btbd9 |
A |
G |
17: 30,746,409 (GRCm39) |
I139T |
probably benign |
Het |
Ccdc60 |
C |
A |
5: 116,310,527 (GRCm39) |
R178S |
possibly damaging |
Het |
Cd163 |
C |
T |
6: 124,286,128 (GRCm39) |
A226V |
probably benign |
Het |
Cibar2 |
C |
A |
8: 120,896,443 (GRCm39) |
|
probably null |
Het |
Cog1 |
T |
G |
11: 113,542,863 (GRCm39) |
S170A |
probably benign |
Het |
Cwc15 |
T |
C |
9: 14,419,211 (GRCm39) |
L169P |
probably damaging |
Het |
Cyp3a25 |
A |
T |
5: 145,923,643 (GRCm39) |
D333E |
probably benign |
Het |
Ddc |
C |
T |
11: 11,779,132 (GRCm39) |
V331I |
probably benign |
Het |
Dlc1 |
T |
A |
8: 37,325,205 (GRCm39) |
T367S |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,943,514 (GRCm39) |
D3183G |
possibly damaging |
Het |
Eif2a |
T |
A |
3: 58,452,486 (GRCm39) |
Y165* |
probably null |
Het |
Eml6 |
T |
C |
11: 29,727,267 (GRCm39) |
D1285G |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,713,008 (GRCm39) |
|
probably null |
Het |
Fbn1 |
T |
C |
2: 125,187,883 (GRCm39) |
T1549A |
probably benign |
Het |
Fezf2 |
T |
C |
14: 12,342,713 (GRCm38) |
Y384C |
probably damaging |
Het |
Flvcr1 |
A |
T |
1: 190,740,370 (GRCm39) |
V550E |
probably benign |
Het |
Gcm2 |
A |
G |
13: 41,259,347 (GRCm39) |
W41R |
probably damaging |
Het |
Gli2 |
A |
T |
1: 118,782,247 (GRCm39) |
M160K |
possibly damaging |
Het |
Gpr61 |
C |
T |
3: 108,057,623 (GRCm39) |
R346H |
probably damaging |
Het |
Hoxa5 |
A |
T |
6: 52,181,135 (GRCm39) |
S66T |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,541,883 (GRCm39) |
V781D |
possibly damaging |
Het |
Kdm3b |
G |
A |
18: 34,929,915 (GRCm39) |
V220M |
probably damaging |
Het |
Klhl25 |
T |
A |
7: 75,516,268 (GRCm39) |
Y391* |
probably null |
Het |
Mc2r |
A |
T |
18: 68,540,880 (GRCm39) |
Y138N |
probably damaging |
Het |
Mtap |
C |
A |
4: 89,074,821 (GRCm39) |
D106E |
probably benign |
Het |
Nup43 |
G |
T |
10: 7,543,435 (GRCm39) |
W37L |
probably damaging |
Het |
Nxpe2 |
T |
A |
9: 48,237,663 (GRCm39) |
E197D |
probably damaging |
Het |
Odad1 |
T |
C |
7: 45,591,179 (GRCm39) |
I218T |
probably damaging |
Het |
Or10d1c |
C |
A |
9: 38,893,779 (GRCm39) |
C187F |
probably damaging |
Het |
Or55b4 |
T |
A |
7: 102,133,321 (GRCm39) |
*335C |
probably null |
Het |
Or5p60 |
T |
C |
7: 107,723,663 (GRCm39) |
Y269C |
probably damaging |
Het |
Or8h8 |
A |
T |
2: 86,753,126 (GRCm39) |
V250D |
possibly damaging |
Het |
Pitrm1 |
A |
G |
13: 6,605,611 (GRCm39) |
H186R |
probably damaging |
Het |
Pklr |
C |
T |
3: 89,052,188 (GRCm39) |
R467C |
probably damaging |
Het |
Plxna2 |
A |
G |
1: 194,326,401 (GRCm39) |
N112D |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Ppp3cb |
A |
C |
14: 20,558,682 (GRCm39) |
|
probably null |
Het |
R3hcc1l |
C |
T |
19: 42,571,865 (GRCm39) |
R135* |
probably null |
Het |
Ralyl |
A |
C |
3: 14,180,761 (GRCm39) |
D68A |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
S100a1 |
T |
C |
3: 90,418,619 (GRCm39) |
N65S |
probably damaging |
Het |
Slc5a5 |
T |
A |
8: 71,342,865 (GRCm39) |
M232L |
probably benign |
Het |
Tet3 |
A |
T |
6: 83,350,305 (GRCm39) |
N1054K |
probably damaging |
Het |
Tg |
A |
G |
15: 66,570,408 (GRCm39) |
N1427D |
probably benign |
Het |
Tns1 |
A |
C |
1: 73,956,831 (GRCm39) |
V530G |
probably damaging |
Het |
Trcg1 |
C |
A |
9: 57,153,156 (GRCm39) |
Q600K |
possibly damaging |
Het |
Tshz3 |
A |
G |
7: 36,468,131 (GRCm39) |
E40G |
probably damaging |
Het |
Usp34 |
T |
C |
11: 23,334,420 (GRCm39) |
F1138S |
possibly damaging |
Het |
Vmn2r26 |
C |
T |
6: 124,038,603 (GRCm39) |
T726I |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,148,440 (GRCm39) |
R112* |
probably null |
Het |
Vwa2 |
G |
T |
19: 56,897,426 (GRCm39) |
R577L |
probably benign |
Het |
Vwa3b |
A |
C |
1: 37,196,511 (GRCm39) |
Q46P |
probably damaging |
Het |
Wdr25 |
T |
A |
12: 108,958,725 (GRCm39) |
|
probably null |
Het |
Wrap53 |
A |
G |
11: 69,453,226 (GRCm39) |
L405P |
probably damaging |
Het |
Zfp629 |
C |
A |
7: 127,211,161 (GRCm39) |
W216L |
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 |
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 |
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 |
|