Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox2 |
C |
T |
14: 8,256,789 (GRCm38) |
E25K |
probably damaging |
Het |
Acss2 |
A |
G |
2: 155,392,032 (GRCm39) |
Y218C |
probably benign |
Het |
Armc8 |
C |
T |
9: 99,378,203 (GRCm39) |
|
probably null |
Het |
Aspg |
G |
A |
12: 112,089,824 (GRCm39) |
G454D |
probably damaging |
Het |
Atp9b |
T |
C |
18: 80,809,051 (GRCm39) |
T623A |
|
Het |
Cacna1e |
A |
G |
1: 154,357,411 (GRCm39) |
L655P |
probably damaging |
Het |
Cant1 |
T |
A |
11: 118,302,281 (GRCm39) |
N12I |
probably damaging |
Het |
Cep63 |
T |
C |
9: 102,475,382 (GRCm39) |
T445A |
probably benign |
Het |
Clstn1 |
A |
T |
4: 149,698,564 (GRCm39) |
D50V |
possibly damaging |
Het |
Col4a4 |
T |
C |
1: 82,431,076 (GRCm39) |
M1609V |
unknown |
Het |
Dand5 |
A |
T |
8: 85,542,938 (GRCm39) |
C179* |
probably null |
Het |
Dbndd1 |
A |
G |
8: 124,233,547 (GRCm39) |
L153P |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,306,454 (GRCm39) |
I437V |
probably benign |
Het |
Dnhd1 |
T |
A |
7: 105,344,223 (GRCm39) |
S1856T |
probably benign |
Het |
Dpp8 |
T |
A |
9: 64,973,700 (GRCm39) |
Y641* |
probably null |
Het |
Dthd1 |
G |
A |
5: 63,039,626 (GRCm39) |
R676H |
probably benign |
Het |
Efl1 |
C |
T |
7: 82,426,733 (GRCm39) |
T1077M |
probably damaging |
Het |
Eif3e |
G |
T |
15: 43,138,709 (GRCm39) |
Q83K |
probably benign |
Het |
Firrm |
A |
T |
1: 163,795,907 (GRCm39) |
M428K |
probably benign |
Het |
Gfm2 |
G |
A |
13: 97,286,910 (GRCm39) |
A170T |
probably damaging |
Het |
Gm14496 |
T |
A |
2: 181,642,256 (GRCm39) |
H642Q |
probably benign |
Het |
Gmip |
G |
A |
8: 70,269,693 (GRCm39) |
R596Q |
possibly damaging |
Het |
Hook1 |
A |
T |
4: 95,910,510 (GRCm39) |
Q708L |
probably damaging |
Het |
Krtap9-3 |
G |
A |
11: 99,488,526 (GRCm39) |
R119C |
unknown |
Het |
Lnpk |
A |
C |
2: 74,381,403 (GRCm39) |
|
probably null |
Het |
Lrp1 |
G |
T |
10: 127,429,334 (GRCm39) |
Y484* |
probably null |
Het |
Lrrc8e |
C |
T |
8: 4,285,185 (GRCm39) |
P470L |
probably damaging |
Het |
Mapre1 |
A |
G |
2: 153,606,960 (GRCm39) |
N231D |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,405,503 (GRCm39) |
N937K |
unknown |
Het |
Ndufaf7 |
T |
C |
17: 79,253,900 (GRCm39) |
|
probably null |
Het |
Nlrp5 |
A |
T |
7: 23,118,225 (GRCm39) |
I650F |
probably benign |
Het |
Notch1 |
T |
C |
2: 26,359,845 (GRCm39) |
D1290G |
probably benign |
Het |
Or7g27 |
C |
T |
9: 19,250,320 (GRCm39) |
A188V |
possibly damaging |
Het |
Or8b46 |
T |
C |
9: 38,450,665 (GRCm39) |
I158T |
probably damaging |
Het |
Orc4 |
C |
T |
2: 48,826,783 (GRCm39) |
|
probably null |
Het |
Plekhm2 |
A |
G |
4: 141,357,949 (GRCm39) |
V664A |
probably benign |
Het |
Pom121l2 |
T |
G |
13: 22,168,402 (GRCm39) |
I891S |
probably benign |
Het |
Prkcsh |
T |
C |
9: 21,923,982 (GRCm39) |
Y425H |
probably damaging |
Het |
Prps1l1 |
A |
C |
12: 35,035,559 (GRCm39) |
T225P |
probably damaging |
Het |
Prr18 |
T |
G |
17: 8,560,324 (GRCm39) |
V160G |
probably damaging |
Het |
Psd2 |
T |
A |
18: 36,143,798 (GRCm39) |
F701L |
probably damaging |
Het |
Sclt1 |
T |
C |
3: 41,601,931 (GRCm39) |
E593G |
probably damaging |
Het |
Sdk1 |
T |
C |
5: 141,948,548 (GRCm39) |
I631T |
probably benign |
Het |
Sirt1 |
A |
T |
10: 63,171,487 (GRCm39) |
D231E |
probably benign |
Het |
Slc22a30 |
C |
T |
19: 8,378,259 (GRCm39) |
C139Y |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,624,974 (GRCm39) |
N274I |
probably damaging |
Het |
Spocd1 |
A |
G |
4: 129,847,398 (GRCm39) |
Q529R |
|
Het |
Trarg1 |
T |
A |
11: 76,571,098 (GRCm39) |
L38Q |
probably damaging |
Het |
Trbv3 |
T |
A |
6: 41,025,530 (GRCm39) |
L40H |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,761,264 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,578,519 (GRCm39) |
Y24125H |
probably damaging |
Het |
Ush1g |
C |
A |
11: 115,209,056 (GRCm39) |
L379F |
probably damaging |
Het |
Vipr1 |
G |
A |
9: 121,471,993 (GRCm39) |
|
probably null |
Het |
Vmn2r73 |
A |
T |
7: 85,506,795 (GRCm39) |
M839K |
|
Het |
Wee1 |
T |
C |
7: 109,721,917 (GRCm39) |
S121P |
probably damaging |
Het |
Zfp608 |
T |
C |
18: 55,030,274 (GRCm39) |
K1222R |
probably 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 |
|
R3911:Cnnm2
|
UTSW |
19 |
46,866,375 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
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 |
|