Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
A |
G |
7: 45,754,943 (GRCm39) |
I1525T |
probably benign |
Het |
Agtpbp1 |
A |
G |
13: 59,648,392 (GRCm39) |
V476A |
probably benign |
Het |
Aipl1 |
A |
G |
11: 71,922,256 (GRCm39) |
I151T |
probably benign |
Het |
Apc |
C |
T |
18: 34,445,971 (GRCm39) |
R938* |
probably null |
Het |
Atp2a2 |
A |
G |
5: 122,596,554 (GRCm39) |
F855S |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,223,075 (GRCm39) |
T261A |
possibly damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,365,900 (GRCm39) |
D370G |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,736,025 (GRCm39) |
I2964V |
probably damaging |
Het |
Clec16a |
T |
C |
16: 10,386,375 (GRCm39) |
V158A |
probably damaging |
Het |
Col6a5 |
G |
A |
9: 105,741,806 (GRCm39) |
T2371I |
probably damaging |
Het |
Cpne8 |
T |
C |
15: 90,503,929 (GRCm39) |
T79A |
probably damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,780,413 (GRCm39) |
R145G |
probably damaging |
Het |
Disc1 |
G |
A |
8: 125,851,289 (GRCm39) |
W391* |
probably null |
Het |
Dnah8 |
G |
A |
17: 30,941,988 (GRCm39) |
V1745I |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,376,886 (GRCm39) |
V1557A |
probably benign |
Het |
Egfem1 |
T |
A |
3: 29,637,145 (GRCm39) |
Y194N |
probably damaging |
Het |
Eif4a3 |
A |
G |
11: 119,179,705 (GRCm39) |
Y361H |
probably damaging |
Het |
Esd |
T |
A |
14: 74,982,153 (GRCm39) |
S189R |
possibly damaging |
Het |
Fancf |
A |
T |
7: 51,511,196 (GRCm39) |
Y269* |
probably null |
Het |
Fbln2 |
A |
T |
6: 91,248,569 (GRCm39) |
H1078L |
possibly damaging |
Het |
Fbxw13 |
A |
G |
9: 109,010,592 (GRCm39) |
|
probably null |
Het |
Fcgr2b |
A |
T |
1: 170,790,941 (GRCm39) |
V284D |
probably benign |
Het |
Fuz |
G |
A |
7: 44,549,718 (GRCm39) |
G363R |
probably damaging |
Het |
Gas7 |
A |
G |
11: 67,574,234 (GRCm39) |
E403G |
probably damaging |
Het |
Gnl1 |
A |
G |
17: 36,291,581 (GRCm39) |
D49G |
possibly damaging |
Het |
Gucy2g |
A |
G |
19: 55,214,445 (GRCm39) |
V561A |
probably benign |
Het |
H1f7 |
A |
T |
15: 98,154,216 (GRCm39) |
V311E |
unknown |
Het |
Hebp2 |
T |
C |
10: 18,420,122 (GRCm39) |
T104A |
probably benign |
Het |
Ighv1-19 |
T |
A |
12: 114,672,377 (GRCm39) |
Q80L |
probably benign |
Het |
Kctd19 |
T |
A |
8: 106,122,959 (GRCm39) |
|
probably null |
Het |
Kdm3b |
T |
C |
18: 34,955,428 (GRCm39) |
L905P |
probably damaging |
Het |
Klkb1 |
T |
C |
8: 45,735,814 (GRCm39) |
D183G |
probably benign |
Het |
Krt6b |
T |
C |
15: 101,588,460 (GRCm39) |
R67G |
possibly damaging |
Het |
Krt75 |
T |
C |
15: 101,482,248 (GRCm39) |
I7V |
probably benign |
Het |
Lpo |
A |
T |
11: 87,697,751 (GRCm39) |
N685K |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,538,070 (GRCm39) |
I1202N |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,572 (GRCm38) |
M1482K |
probably benign |
Het |
Mylk |
T |
A |
16: 34,791,810 (GRCm39) |
V1494E |
probably damaging |
Het |
Neurl4 |
A |
G |
11: 69,801,913 (GRCm39) |
D17G |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,647,725 (GRCm39) |
Y228C |
probably damaging |
Het |
Nprl2 |
G |
A |
9: 107,420,273 (GRCm39) |
|
probably null |
Het |
Nxf1 |
A |
G |
19: 8,739,669 (GRCm39) |
|
probably null |
Het |
Or4a39 |
A |
G |
2: 89,236,770 (GRCm39) |
F218L |
probably benign |
Het |
Or52u1 |
A |
T |
7: 104,237,730 (GRCm39) |
N240Y |
probably damaging |
Het |
Pde3b |
A |
G |
7: 114,118,847 (GRCm39) |
E662G |
possibly damaging |
Het |
Plekhm3 |
G |
A |
1: 64,977,078 (GRCm39) |
R131C |
probably damaging |
Het |
Plpp7 |
T |
C |
2: 31,985,950 (GRCm39) |
S43P |
probably benign |
Het |
Pramel5 |
A |
G |
4: 143,998,187 (GRCm39) |
L352P |
probably damaging |
Het |
Prepl |
T |
C |
17: 85,395,902 (GRCm39) |
S27G |
probably benign |
Het |
Ptprd |
A |
G |
4: 76,051,542 (GRCm39) |
I227T |
probably damaging |
Het |
Pttg1ip |
C |
T |
10: 77,419,854 (GRCm39) |
Q6* |
probably null |
Het |
Rgl1 |
C |
T |
1: 152,424,813 (GRCm39) |
|
probably null |
Het |
Riiad1 |
C |
A |
3: 94,380,173 (GRCm39) |
G41* |
probably null |
Het |
Rnf214 |
C |
T |
9: 45,807,486 (GRCm39) |
R239H |
probably damaging |
Het |
Rpap3 |
C |
T |
15: 97,584,407 (GRCm39) |
V346I |
probably benign |
Het |
Scaf4 |
G |
A |
16: 90,048,831 (GRCm39) |
Q328* |
probably null |
Het |
Slc5a8 |
T |
A |
10: 88,740,774 (GRCm39) |
|
probably null |
Het |
Slc9a8 |
A |
G |
2: 167,288,449 (GRCm39) |
T183A |
probably benign |
Het |
Sod3 |
A |
T |
5: 52,525,736 (GRCm39) |
H145L |
probably damaging |
Het |
Sp4 |
A |
G |
12: 118,263,341 (GRCm39) |
V235A |
probably damaging |
Het |
Spp1 |
A |
C |
5: 104,588,153 (GRCm39) |
E185A |
possibly damaging |
Het |
Susd1 |
A |
T |
4: 59,351,679 (GRCm39) |
W461R |
probably benign |
Het |
Svil |
A |
C |
18: 5,095,516 (GRCm39) |
K1124Q |
probably damaging |
Het |
Tdrd12 |
A |
T |
7: 35,186,720 (GRCm39) |
|
probably null |
Het |
Terb1 |
A |
T |
8: 105,221,795 (GRCm39) |
N168K |
probably benign |
Het |
Tnnt1 |
A |
G |
7: 4,510,573 (GRCm39) |
L216P |
probably damaging |
Het |
Ttc28 |
A |
G |
5: 111,424,121 (GRCm39) |
K1463E |
probably damaging |
Het |
Twf2 |
T |
G |
9: 106,089,098 (GRCm39) |
|
probably null |
Het |
Urb1 |
C |
T |
16: 90,602,299 (GRCm39) |
R90Q |
probably damaging |
Het |
Wdr45b |
A |
T |
11: 121,219,650 (GRCm39) |
C299* |
probably null |
Het |
Wrap73 |
A |
G |
4: 154,237,138 (GRCm39) |
S54G |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,888,931 (GRCm39) |
K323R |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,378,582 (GRCm39) |
I302T |
possibly damaging |
Het |
|
Other mutations in Sec23a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00815:Sec23a
|
APN |
12 |
59,039,068 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01836:Sec23a
|
APN |
12 |
59,018,073 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01906:Sec23a
|
APN |
12 |
59,053,830 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Sec23a
|
APN |
12 |
59,048,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02507:Sec23a
|
APN |
12 |
59,053,884 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02816:Sec23a
|
APN |
12 |
59,025,331 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03060:Sec23a
|
APN |
12 |
59,032,891 (GRCm39) |
missense |
probably benign |
|
R0308:Sec23a
|
UTSW |
12 |
59,053,985 (GRCm39) |
nonsense |
probably null |
|
R0361:Sec23a
|
UTSW |
12 |
59,037,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Sec23a
|
UTSW |
12 |
59,031,953 (GRCm39) |
missense |
probably benign |
0.07 |
R0720:Sec23a
|
UTSW |
12 |
59,018,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1084:Sec23a
|
UTSW |
12 |
59,031,921 (GRCm39) |
missense |
probably damaging |
0.97 |
R1156:Sec23a
|
UTSW |
12 |
59,048,622 (GRCm39) |
missense |
probably benign |
|
R1438:Sec23a
|
UTSW |
12 |
59,048,796 (GRCm39) |
missense |
probably damaging |
0.98 |
R1446:Sec23a
|
UTSW |
12 |
59,025,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Sec23a
|
UTSW |
12 |
59,032,972 (GRCm39) |
splice site |
probably null |
|
R1705:Sec23a
|
UTSW |
12 |
59,048,652 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1997:Sec23a
|
UTSW |
12 |
59,048,793 (GRCm39) |
missense |
probably benign |
|
R2051:Sec23a
|
UTSW |
12 |
59,037,754 (GRCm39) |
splice site |
probably null |
|
R2081:Sec23a
|
UTSW |
12 |
59,045,067 (GRCm39) |
nonsense |
probably null |
|
R4201:Sec23a
|
UTSW |
12 |
59,048,791 (GRCm39) |
missense |
probably benign |
0.00 |
R4706:Sec23a
|
UTSW |
12 |
59,029,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R4724:Sec23a
|
UTSW |
12 |
59,025,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R5375:Sec23a
|
UTSW |
12 |
59,053,791 (GRCm39) |
missense |
probably benign |
0.15 |
R5858:Sec23a
|
UTSW |
12 |
59,019,821 (GRCm39) |
missense |
probably damaging |
0.98 |
R6539:Sec23a
|
UTSW |
12 |
59,031,998 (GRCm39) |
missense |
probably benign |
0.00 |
R6558:Sec23a
|
UTSW |
12 |
59,051,338 (GRCm39) |
missense |
probably benign |
0.03 |
R6616:Sec23a
|
UTSW |
12 |
59,043,941 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6716:Sec23a
|
UTSW |
12 |
59,015,609 (GRCm39) |
missense |
probably benign |
0.09 |
R7078:Sec23a
|
UTSW |
12 |
59,039,069 (GRCm39) |
missense |
probably benign |
0.07 |
R7155:Sec23a
|
UTSW |
12 |
59,036,229 (GRCm39) |
missense |
probably benign |
0.03 |
R7367:Sec23a
|
UTSW |
12 |
59,013,785 (GRCm39) |
missense |
probably benign |
|
R7923:Sec23a
|
UTSW |
12 |
59,039,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R8178:Sec23a
|
UTSW |
12 |
59,053,980 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8557:Sec23a
|
UTSW |
12 |
59,052,056 (GRCm39) |
missense |
probably damaging |
0.96 |
R8839:Sec23a
|
UTSW |
12 |
59,037,781 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9141:Sec23a
|
UTSW |
12 |
59,053,890 (GRCm39) |
missense |
probably benign |
0.42 |
R9213:Sec23a
|
UTSW |
12 |
59,048,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Sec23a
|
UTSW |
12 |
59,053,890 (GRCm39) |
missense |
probably benign |
0.42 |
R9508:Sec23a
|
UTSW |
12 |
59,036,185 (GRCm39) |
missense |
probably benign |
0.00 |
R9520:Sec23a
|
UTSW |
12 |
59,031,974 (GRCm39) |
missense |
probably benign |
|
R9562:Sec23a
|
UTSW |
12 |
59,048,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9608:Sec23a
|
UTSW |
12 |
59,019,804 (GRCm39) |
missense |
probably benign |
|
R9797:Sec23a
|
UTSW |
12 |
59,052,060 (GRCm39) |
nonsense |
probably null |
|
Z1088:Sec23a
|
UTSW |
12 |
59,051,362 (GRCm39) |
missense |
probably benign |
0.01 |
|