Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
A |
5: 124,227,909 (GRCm39) |
I111F |
probably benign |
Het |
Abcc12 |
A |
C |
8: 87,255,048 (GRCm39) |
|
probably benign |
Het |
Adgre1 |
G |
T |
17: 57,754,860 (GRCm39) |
V653L |
probably damaging |
Het |
Aebp2 |
T |
A |
6: 140,593,707 (GRCm39) |
D230E |
probably damaging |
Het |
Asap3 |
A |
G |
4: 135,956,768 (GRCm39) |
|
probably benign |
Het |
Bod1l |
T |
C |
5: 41,974,441 (GRCm39) |
E2291G |
probably damaging |
Het |
Casp8 |
A |
T |
1: 58,872,864 (GRCm39) |
S267C |
probably damaging |
Het |
Cchcr1 |
T |
C |
17: 35,836,233 (GRCm39) |
V341A |
probably damaging |
Het |
Cd2ap |
T |
A |
17: 43,126,980 (GRCm39) |
|
probably null |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Clip1 |
T |
A |
5: 123,728,897 (GRCm39) |
E1155D |
probably damaging |
Het |
Cntrl |
G |
A |
2: 35,010,061 (GRCm39) |
R245H |
probably damaging |
Het |
Cyp2b23 |
A |
T |
7: 26,380,842 (GRCm39) |
S128T |
probably benign |
Het |
Dhrs11 |
A |
T |
11: 84,712,579 (GRCm39) |
I196N |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,971,675 (GRCm39) |
|
probably benign |
Het |
Edc3 |
A |
T |
9: 57,655,686 (GRCm39) |
I479F |
possibly damaging |
Het |
Emg1 |
T |
A |
6: 124,682,009 (GRCm39) |
M172L |
probably benign |
Het |
Epha7 |
G |
A |
4: 28,938,680 (GRCm39) |
V512I |
probably benign |
Het |
Exoc7 |
T |
C |
11: 116,197,731 (GRCm39) |
D27G |
probably benign |
Het |
Fasl |
C |
A |
1: 161,615,760 (GRCm39) |
C32F |
probably benign |
Het |
Flg |
A |
T |
3: 93,187,307 (GRCm39) |
H253L |
probably benign |
Het |
Fnip2 |
A |
T |
3: 79,386,812 (GRCm39) |
D971E |
possibly damaging |
Het |
Gab2 |
A |
G |
7: 96,948,280 (GRCm39) |
Y290C |
probably damaging |
Het |
Gm17067 |
T |
A |
7: 42,360,104 (GRCm39) |
I43L |
possibly damaging |
Het |
Gpld1 |
A |
G |
13: 25,146,305 (GRCm39) |
Y183C |
probably damaging |
Het |
Gpr137c |
C |
A |
14: 45,516,392 (GRCm39) |
P327T |
probably benign |
Het |
Hepacam2 |
A |
G |
6: 3,494,477 (GRCm39) |
M1T |
probably null |
Het |
Ighv5-4 |
A |
T |
12: 113,561,060 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
A |
T |
5: 24,750,440 (GRCm39) |
|
probably benign |
Het |
Itgb8 |
T |
A |
12: 119,131,740 (GRCm39) |
E635V |
possibly damaging |
Het |
Kat14 |
T |
C |
2: 144,245,982 (GRCm39) |
V469A |
probably damaging |
Het |
Kcnj15 |
C |
T |
16: 95,097,329 (GRCm39) |
T317I |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Klhl18 |
A |
T |
9: 110,265,151 (GRCm39) |
L285Q |
probably damaging |
Het |
Krt90 |
G |
A |
15: 101,471,218 (GRCm39) |
R15W |
probably damaging |
Het |
Krtap4-8 |
A |
T |
11: 99,670,863 (GRCm39) |
C203S |
unknown |
Het |
Lsp1 |
C |
T |
7: 142,040,098 (GRCm39) |
S75F |
probably damaging |
Het |
Map1b |
A |
G |
13: 99,567,580 (GRCm39) |
S1714P |
unknown |
Het |
Mcm2 |
A |
G |
6: 88,865,234 (GRCm39) |
I481T |
probably damaging |
Het |
Mcpt9 |
T |
C |
14: 56,265,136 (GRCm39) |
T122A |
probably benign |
Het |
Megf10 |
A |
T |
18: 57,422,465 (GRCm39) |
R947W |
probably damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,072 (GRCm39) |
V199D |
probably damaging |
Het |
Or51ai2 |
A |
T |
7: 103,586,616 (GRCm39) |
N10Y |
possibly damaging |
Het |
Pank4 |
A |
G |
4: 155,054,058 (GRCm39) |
Y79C |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,670,171 (GRCm39) |
N386K |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,022,928 (GRCm39) |
M362V |
probably benign |
Het |
Phc2 |
T |
C |
4: 128,637,351 (GRCm39) |
|
probably null |
Het |
Pou4f1 |
C |
T |
14: 104,703,611 (GRCm39) |
A274T |
unknown |
Het |
Proc |
A |
G |
18: 32,256,758 (GRCm39) |
L303P |
probably damaging |
Het |
Ptk2b |
C |
T |
14: 66,394,517 (GRCm39) |
G821D |
possibly damaging |
Het |
Rlim |
T |
C |
X: 103,006,267 (GRCm39) |
T545A |
probably benign |
Het |
Serpinb6c |
T |
C |
13: 34,077,888 (GRCm39) |
N161D |
probably benign |
Het |
Sf3b1 |
G |
A |
1: 55,058,548 (GRCm39) |
Q14* |
probably null |
Het |
Sh3d19 |
G |
A |
3: 86,014,534 (GRCm39) |
V442M |
possibly damaging |
Het |
Slc30a8 |
A |
G |
15: 52,185,097 (GRCm39) |
I140V |
probably benign |
Het |
Spata1 |
T |
A |
3: 146,181,079 (GRCm39) |
N293I |
probably damaging |
Het |
Strap |
T |
G |
6: 137,712,380 (GRCm39) |
C10G |
probably damaging |
Het |
Tcf7 |
C |
A |
11: 52,173,793 (GRCm39) |
|
probably benign |
Het |
Tmem114 |
A |
T |
16: 8,230,054 (GRCm39) |
M116K |
probably damaging |
Het |
Tmem63b |
A |
G |
17: 45,988,884 (GRCm39) |
S113P |
probably damaging |
Het |
Tmtc3 |
A |
C |
10: 100,284,888 (GRCm39) |
N582K |
probably damaging |
Het |
Tnfrsf11b |
G |
A |
15: 54,119,578 (GRCm39) |
|
probably benign |
Het |
Tns2 |
T |
C |
15: 102,022,272 (GRCm39) |
|
probably null |
Het |
Trim30a |
A |
G |
7: 104,060,348 (GRCm39) |
V476A |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,132,151 (GRCm39) |
V791D |
probably benign |
Het |
Vmn2r99 |
T |
C |
17: 19,614,635 (GRCm39) |
F785S |
possibly damaging |
Het |
Vps35l |
A |
G |
7: 118,345,613 (GRCm39) |
T49A |
possibly damaging |
Het |
Wdr35 |
A |
T |
12: 9,036,077 (GRCm39) |
I283F |
probably benign |
Het |
Wnt10b |
G |
T |
15: 98,672,219 (GRCm39) |
A166E |
possibly damaging |
Het |
|
Other mutations in Cnnm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Cnnm2
|
APN |
19 |
46,751,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01971:Cnnm2
|
APN |
19 |
46,860,115 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02003:Cnnm2
|
APN |
19 |
46,856,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Cnnm2
|
APN |
19 |
46,865,827 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02185:Cnnm2
|
APN |
19 |
46,751,434 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02652:Cnnm2
|
APN |
19 |
46,751,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02682:Cnnm2
|
APN |
19 |
46,750,515 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03009:Cnnm2
|
APN |
19 |
46,865,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03378:Cnnm2
|
APN |
19 |
46,866,473 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1581:Cnnm2
|
UTSW |
19 |
46,751,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R3700:Cnnm2
|
UTSW |
19 |
46,750,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Cnnm2
|
UTSW |
19 |
46,750,232 (GRCm39) |
nonsense |
probably null |
|
R4508:Cnnm2
|
UTSW |
19 |
46,865,709 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Cnnm2
|
UTSW |
19 |
46,751,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4878:Cnnm2
|
UTSW |
19 |
46,847,522 (GRCm39) |
missense |
probably benign |
0.45 |
R5154:Cnnm2
|
UTSW |
19 |
46,751,571 (GRCm39) |
missense |
probably benign |
0.02 |
R5445:Cnnm2
|
UTSW |
19 |
46,865,727 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5771:Cnnm2
|
UTSW |
19 |
46,845,434 (GRCm39) |
splice site |
probably null |
|
R5914:Cnnm2
|
UTSW |
19 |
46,751,616 (GRCm39) |
missense |
probably benign |
0.07 |
R6263:Cnnm2
|
UTSW |
19 |
46,845,344 (GRCm39) |
missense |
probably benign |
0.30 |
R6715:Cnnm2
|
UTSW |
19 |
46,842,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6881:Cnnm2
|
UTSW |
19 |
46,865,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Cnnm2
|
UTSW |
19 |
46,847,379 (GRCm39) |
splice site |
probably null |
|
R7022:Cnnm2
|
UTSW |
19 |
46,750,989 (GRCm39) |
missense |
probably damaging |
0.98 |
R7486:Cnnm2
|
UTSW |
19 |
46,750,513 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7600:Cnnm2
|
UTSW |
19 |
46,750,506 (GRCm39) |
missense |
probably benign |
0.02 |
R7648:Cnnm2
|
UTSW |
19 |
46,866,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R7800:Cnnm2
|
UTSW |
19 |
46,866,420 (GRCm39) |
missense |
probably benign |
0.28 |
R8867:Cnnm2
|
UTSW |
19 |
46,750,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R8971:Cnnm2
|
UTSW |
19 |
46,845,362 (GRCm39) |
missense |
probably benign |
0.28 |
R9433:Cnnm2
|
UTSW |
19 |
46,750,807 (GRCm39) |
missense |
probably benign |
0.23 |
R9463:Cnnm2
|
UTSW |
19 |
46,750,990 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Cnnm2
|
UTSW |
19 |
46,750,902 (GRCm39) |
missense |
probably benign |
0.05 |
X0018:Cnnm2
|
UTSW |
19 |
46,751,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|