Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,207,580 (GRCm39) |
V282E |
probably benign |
Het |
Adam26b |
T |
C |
8: 43,973,296 (GRCm39) |
T569A |
possibly damaging |
Het |
Adam6a |
A |
G |
12: 113,509,609 (GRCm39) |
N661D |
probably damaging |
Het |
Adck1 |
G |
A |
12: 88,407,865 (GRCm39) |
A199T |
probably benign |
Het |
Adhfe1 |
A |
G |
1: 9,628,438 (GRCm39) |
Y270C |
probably damaging |
Het |
Aldh16a1 |
C |
T |
7: 44,796,731 (GRCm39) |
R256H |
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,459,748 (GRCm39) |
M466T |
possibly damaging |
Het |
Aspm |
C |
T |
1: 139,397,131 (GRCm39) |
L908F |
probably damaging |
Het |
Atp8b2 |
T |
A |
3: 89,853,287 (GRCm39) |
T743S |
probably benign |
Het |
Bag2 |
G |
T |
1: 33,786,022 (GRCm39) |
T100K |
probably damaging |
Het |
Camk2a |
A |
G |
18: 61,076,246 (GRCm39) |
|
probably benign |
Het |
Ccdc158 |
A |
G |
5: 92,781,262 (GRCm39) |
Y848H |
probably damaging |
Het |
Ccp110 |
T |
G |
7: 118,324,653 (GRCm39) |
V725G |
possibly damaging |
Het |
Cdh6 |
A |
G |
15: 13,051,418 (GRCm39) |
V405A |
probably benign |
Het |
Ces2g |
T |
C |
8: 105,694,094 (GRCm39) |
|
probably null |
Het |
Cfap157 |
A |
G |
2: 32,667,554 (GRCm39) |
F510L |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,250,722 (GRCm39) |
M669K |
possibly damaging |
Het |
Cnot10 |
C |
T |
9: 114,456,532 (GRCm39) |
A168T |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,868,565 (GRCm39) |
V1371A |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,872,560 (GRCm39) |
L547P |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,325,226 (GRCm39) |
C483R |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,395,762 (GRCm39) |
L3888Q |
probably damaging |
Het |
Dpysl2 |
A |
T |
14: 67,066,888 (GRCm39) |
Y182N |
probably damaging |
Het |
Eif4g1 |
T |
A |
16: 20,500,923 (GRCm39) |
F509L |
probably benign |
Het |
Evc |
T |
C |
5: 37,458,253 (GRCm39) |
T85A |
probably damaging |
Het |
Farsb |
T |
C |
1: 78,444,609 (GRCm39) |
T283A |
probably benign |
Het |
Fem1al |
G |
T |
11: 29,775,178 (GRCm39) |
A93E |
probably damaging |
Het |
Fgf14 |
C |
A |
14: 124,429,845 (GRCm39) |
R30L |
possibly damaging |
Het |
Gbe1 |
T |
C |
16: 70,275,289 (GRCm39) |
L363P |
probably damaging |
Het |
Gcg |
A |
G |
2: 62,307,189 (GRCm39) |
V124A |
probably damaging |
Het |
Glb1l |
A |
G |
1: 75,176,963 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
T |
C |
11: 48,780,409 (GRCm39) |
E449G |
probably damaging |
Het |
Gon4l |
T |
C |
3: 88,802,655 (GRCm39) |
S1089P |
probably benign |
Het |
Hgd |
T |
C |
16: 37,409,111 (GRCm39) |
L25P |
probably damaging |
Het |
Hnf1a |
T |
C |
5: 115,093,311 (GRCm39) |
H318R |
possibly damaging |
Het |
Hsd17b7 |
A |
C |
1: 169,794,826 (GRCm39) |
V71G |
possibly damaging |
Het |
Hydin |
T |
C |
8: 111,233,126 (GRCm39) |
S1742P |
possibly damaging |
Het |
Kank2 |
T |
C |
9: 21,691,078 (GRCm39) |
E552G |
probably benign |
Het |
Kcnq4 |
C |
A |
4: 120,573,810 (GRCm39) |
R217L |
probably damaging |
Het |
Klrg2 |
T |
C |
6: 38,604,540 (GRCm39) |
*201W |
probably null |
Het |
Kndc1 |
T |
C |
7: 139,501,821 (GRCm39) |
S953P |
probably benign |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Lonp1 |
A |
G |
17: 56,933,587 (GRCm39) |
V96A |
probably benign |
Het |
Mgat4e |
T |
C |
1: 134,469,478 (GRCm39) |
K189E |
possibly damaging |
Het |
Msantd5f8 |
A |
G |
4: 73,805,457 (GRCm39) |
S351P |
probably damaging |
Het |
Msh2 |
G |
A |
17: 88,026,187 (GRCm39) |
V722I |
possibly damaging |
Het |
Mtcl3 |
A |
C |
10: 29,026,390 (GRCm39) |
M491L |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,982,641 (GRCm39) |
Y1632H |
probably damaging |
Het |
Nlrc4 |
T |
G |
17: 74,743,032 (GRCm39) |
K862T |
probably damaging |
Het |
Notch4 |
A |
T |
17: 34,806,154 (GRCm39) |
Q1750L |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,972,849 (GRCm39) |
V2066I |
possibly damaging |
Het |
Or2v2 |
T |
C |
11: 49,003,993 (GRCm39) |
K187E |
probably damaging |
Het |
Or4c15 |
T |
A |
2: 88,760,627 (GRCm39) |
I11L |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,156 (GRCm39) |
I215N |
probably damaging |
Het |
Or52d13 |
A |
T |
7: 103,110,243 (GRCm39) |
Y57* |
probably null |
Het |
Or5m8 |
T |
C |
2: 85,823,075 (GRCm39) |
S305P |
probably damaging |
Het |
Pde7a |
T |
A |
3: 19,295,655 (GRCm39) |
|
probably benign |
Het |
Pign |
A |
T |
1: 105,575,892 (GRCm39) |
Y249* |
probably null |
Het |
Ppp1r17 |
A |
T |
6: 56,003,449 (GRCm39) |
E87D |
probably damaging |
Het |
Prss3 |
T |
A |
6: 41,350,857 (GRCm39) |
Q211L |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,526,989 (GRCm39) |
E413G |
probably benign |
Het |
Rnf150 |
A |
G |
8: 83,590,712 (GRCm39) |
H25R |
probably damaging |
Het |
Scamp2 |
T |
C |
9: 57,488,934 (GRCm39) |
|
probably null |
Het |
Scap |
T |
A |
9: 110,203,410 (GRCm39) |
|
probably benign |
Het |
Sdc2 |
A |
C |
15: 33,032,602 (GRCm39) |
K175N |
probably damaging |
Het |
Serpinb6d |
T |
A |
13: 33,851,547 (GRCm39) |
|
probably null |
Het |
Sh3tc2 |
A |
G |
18: 62,146,164 (GRCm39) |
N1181S |
probably benign |
Het |
Slc44a2 |
T |
C |
9: 21,259,441 (GRCm39) |
I46T |
probably damaging |
Het |
Slfn8 |
A |
G |
11: 82,908,540 (GRCm39) |
M1T |
probably null |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Spata1 |
C |
G |
3: 146,175,529 (GRCm39) |
D326H |
probably damaging |
Het |
Tbck |
T |
G |
3: 132,507,288 (GRCm39) |
S753R |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,876,070 (GRCm39) |
I340M |
probably benign |
Het |
Tmprss6 |
T |
A |
15: 78,330,877 (GRCm39) |
Y50F |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,194,078 (GRCm39) |
S701T |
probably benign |
Het |
Trbv17 |
A |
T |
6: 41,140,223 (GRCm39) |
N26I |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,771,531 (GRCm39) |
S248T |
probably damaging |
Het |
Vmn2r53 |
T |
G |
7: 12,335,330 (GRCm39) |
Q110P |
probably damaging |
Het |
Vmn2r75 |
A |
G |
7: 85,797,611 (GRCm39) |
V734A |
probably benign |
Het |
Wfdc11 |
A |
T |
2: 164,507,415 (GRCm39) |
M14K |
probably null |
Het |
Xcr1 |
T |
A |
9: 123,685,712 (GRCm39) |
M17L |
probably benign |
Het |
Zbtb40 |
A |
G |
4: 136,716,070 (GRCm39) |
I965T |
probably damaging |
Het |
Zfp760 |
A |
T |
17: 21,942,511 (GRCm39) |
H562L |
probably damaging |
Het |
Zfp760 |
A |
T |
17: 21,942,516 (GRCm39) |
R564* |
probably null |
Het |
Znf41-ps |
T |
A |
4: 145,555,283 (GRCm39) |
|
noncoding transcript |
Het |
Zyg11a |
A |
T |
4: 108,067,387 (GRCm39) |
I41N |
probably damaging |
Het |
|
Other mutations in Insyn2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Insyn2b
|
APN |
11 |
34,353,011 (GRCm39) |
missense |
probably benign |
|
IGL01867:Insyn2b
|
APN |
11 |
34,353,065 (GRCm39) |
missense |
probably benign |
0.39 |
PIT4677001:Insyn2b
|
UTSW |
11 |
34,353,122 (GRCm39) |
missense |
probably benign |
|
R0317:Insyn2b
|
UTSW |
11 |
34,352,826 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1165:Insyn2b
|
UTSW |
11 |
34,352,740 (GRCm39) |
missense |
probably benign |
|
R1710:Insyn2b
|
UTSW |
11 |
34,354,263 (GRCm39) |
splice site |
probably null |
|
R2083:Insyn2b
|
UTSW |
11 |
34,352,141 (GRCm39) |
missense |
probably benign |
0.01 |
R2096:Insyn2b
|
UTSW |
11 |
34,352,936 (GRCm39) |
missense |
probably benign |
0.03 |
R3820:Insyn2b
|
UTSW |
11 |
34,353,007 (GRCm39) |
missense |
probably benign |
0.01 |
R3821:Insyn2b
|
UTSW |
11 |
34,353,007 (GRCm39) |
missense |
probably benign |
0.01 |
R3822:Insyn2b
|
UTSW |
11 |
34,353,007 (GRCm39) |
missense |
probably benign |
0.01 |
R3969:Insyn2b
|
UTSW |
11 |
34,369,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R3970:Insyn2b
|
UTSW |
11 |
34,369,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R3980:Insyn2b
|
UTSW |
11 |
34,352,678 (GRCm39) |
missense |
probably benign |
0.00 |
R4092:Insyn2b
|
UTSW |
11 |
34,351,935 (GRCm39) |
start gained |
probably benign |
|
R4231:Insyn2b
|
UTSW |
11 |
34,353,143 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Insyn2b
|
UTSW |
11 |
34,353,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R4938:Insyn2b
|
UTSW |
11 |
34,352,231 (GRCm39) |
missense |
probably damaging |
0.98 |
R5269:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5287:Insyn2b
|
UTSW |
11 |
34,353,058 (GRCm39) |
missense |
probably benign |
0.12 |
R5358:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5359:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Insyn2b
|
UTSW |
11 |
34,352,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Insyn2b
|
UTSW |
11 |
34,353,058 (GRCm39) |
missense |
probably benign |
0.12 |
R5705:Insyn2b
|
UTSW |
11 |
34,354,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R6282:Insyn2b
|
UTSW |
11 |
34,352,819 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7030:Insyn2b
|
UTSW |
11 |
34,352,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R7069:Insyn2b
|
UTSW |
11 |
34,352,677 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7178:Insyn2b
|
UTSW |
11 |
34,352,359 (GRCm39) |
missense |
probably damaging |
0.96 |
R7180:Insyn2b
|
UTSW |
11 |
34,369,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Insyn2b
|
UTSW |
11 |
34,352,539 (GRCm39) |
missense |
probably benign |
0.00 |
R7789:Insyn2b
|
UTSW |
11 |
34,352,537 (GRCm39) |
missense |
probably benign |
|
R7832:Insyn2b
|
UTSW |
11 |
34,353,034 (GRCm39) |
missense |
probably benign |
|
R8377:Insyn2b
|
UTSW |
11 |
34,351,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R8930:Insyn2b
|
UTSW |
11 |
34,352,707 (GRCm39) |
missense |
probably benign |
0.00 |
R8932:Insyn2b
|
UTSW |
11 |
34,352,707 (GRCm39) |
missense |
probably benign |
0.00 |
R9407:Insyn2b
|
UTSW |
11 |
34,352,072 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Insyn2b
|
UTSW |
11 |
34,353,188 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Insyn2b
|
UTSW |
11 |
34,352,725 (GRCm39) |
missense |
probably benign |
0.01 |
|