Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
C |
T |
12: 113,453,894 (GRCm39) |
S237L |
probably damaging |
Het |
Ank3 |
T |
G |
10: 69,644,709 (GRCm39) |
L58V |
probably damaging |
Het |
Arsb |
A |
T |
13: 93,926,574 (GRCm39) |
I115F |
possibly damaging |
Het |
Atad2b |
T |
C |
12: 5,023,970 (GRCm39) |
Y32H |
probably damaging |
Het |
Brd1 |
A |
C |
15: 88,598,201 (GRCm39) |
M515R |
probably benign |
Het |
Cbx7 |
A |
G |
15: 79,803,023 (GRCm39) |
S30P |
possibly damaging |
Het |
Cdk12 |
A |
G |
11: 98,136,114 (GRCm39) |
T1123A |
unknown |
Het |
Cep170b |
A |
G |
12: 112,707,379 (GRCm39) |
D375G |
probably damaging |
Het |
Clcn3 |
T |
C |
8: 61,390,369 (GRCm39) |
K164E |
probably benign |
Het |
Clip4 |
A |
C |
17: 72,163,459 (GRCm39) |
K677T |
probably damaging |
Het |
Clrn2 |
T |
C |
5: 45,617,540 (GRCm39) |
I137T |
possibly damaging |
Het |
Cntln |
T |
C |
4: 84,802,816 (GRCm39) |
S39P |
probably damaging |
Het |
Crocc2 |
T |
A |
1: 93,143,353 (GRCm39) |
N1318K |
probably benign |
Het |
Emc1 |
C |
T |
4: 139,098,976 (GRCm39) |
Q820* |
probably null |
Het |
Fbxl2 |
G |
A |
9: 113,818,451 (GRCm39) |
T170I |
probably damaging |
Het |
Fyb2 |
A |
G |
4: 104,852,975 (GRCm39) |
T552A |
probably damaging |
Het |
Garin5b |
A |
G |
7: 4,762,358 (GRCm39) |
V257A |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Helz2 |
C |
T |
2: 180,875,260 (GRCm39) |
E1745K |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,269,006 (GRCm39) |
Y2213H |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,184,986 (GRCm39) |
Y24H |
possibly damaging |
Het |
Inpp5d |
T |
A |
1: 87,627,397 (GRCm39) |
L566Q |
probably damaging |
Het |
Itgb2 |
C |
A |
10: 77,384,431 (GRCm39) |
P184H |
probably damaging |
Het |
Kcnb2 |
T |
A |
1: 15,781,436 (GRCm39) |
D769E |
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,741,666 (GRCm39) |
M3087T |
possibly damaging |
Het |
Ltbp3 |
A |
G |
19: 5,795,800 (GRCm39) |
|
probably null |
Het |
Ms4a6b |
A |
G |
19: 11,497,728 (GRCm39) |
E9G |
probably damaging |
Het |
Nat3 |
G |
A |
8: 67,976,831 (GRCm39) |
|
probably null |
Het |
Ndufaf1 |
A |
T |
2: 119,490,534 (GRCm39) |
D175E |
probably damaging |
Het |
Nop58 |
T |
G |
1: 59,750,471 (GRCm39) |
|
probably benign |
Het |
Or10al6 |
A |
G |
17: 38,083,326 (GRCm39) |
T261A |
probably benign |
Het |
Or8s16 |
A |
G |
15: 98,211,219 (GRCm39) |
Y71H |
possibly damaging |
Het |
P3h4 |
C |
T |
11: 100,302,575 (GRCm39) |
E354K |
probably benign |
Het |
Plekhm2 |
T |
G |
4: 141,356,843 (GRCm39) |
T787P |
possibly damaging |
Het |
Ppia |
C |
T |
11: 6,368,230 (GRCm39) |
T37I |
probably benign |
Het |
Reln |
T |
A |
5: 22,200,511 (GRCm39) |
M1330L |
probably benign |
Het |
Ric1 |
A |
G |
19: 29,539,426 (GRCm39) |
E53G |
probably benign |
Het |
Sgip1 |
T |
A |
4: 102,823,482 (GRCm39) |
V721E |
probably damaging |
Het |
Slc33a1 |
A |
T |
3: 63,850,709 (GRCm39) |
D538E |
probably benign |
Het |
Son |
T |
C |
16: 91,471,629 (GRCm39) |
|
|
Het |
Srebf1 |
A |
T |
11: 60,094,341 (GRCm39) |
S591R |
probably damaging |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Taok2 |
G |
A |
7: 126,469,319 (GRCm39) |
R1170W |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,845,688 (GRCm39) |
V210E |
probably benign |
Het |
Ttc6 |
T |
A |
12: 57,775,249 (GRCm39) |
N1648K |
possibly damaging |
Het |
Vgll3 |
C |
T |
16: 65,636,131 (GRCm39) |
P94L |
probably damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,349,362 (GRCm39) |
V740E |
probably damaging |
Het |
Yeats2 |
A |
G |
16: 20,040,460 (GRCm39) |
E1127G |
possibly damaging |
Het |
Zfp709 |
T |
A |
8: 72,643,329 (GRCm39) |
Y252N |
probably damaging |
Het |
|
Other mutations in Gm2381 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02309:Gm2381
|
APN |
7 |
42,472,033 (GRCm39) |
splice site |
probably benign |
|
R0266:Gm2381
|
UTSW |
7 |
42,469,372 (GRCm39) |
nonsense |
probably null |
|
R0617:Gm2381
|
UTSW |
7 |
42,469,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Gm2381
|
UTSW |
7 |
42,469,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R0849:Gm2381
|
UTSW |
7 |
42,469,372 (GRCm39) |
nonsense |
probably null |
|
R1340:Gm2381
|
UTSW |
7 |
42,469,828 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1549:Gm2381
|
UTSW |
7 |
42,471,825 (GRCm39) |
missense |
probably benign |
0.09 |
R1702:Gm2381
|
UTSW |
7 |
42,469,655 (GRCm39) |
missense |
probably benign |
0.08 |
R1708:Gm2381
|
UTSW |
7 |
42,469,649 (GRCm39) |
missense |
probably benign |
0.05 |
R1909:Gm2381
|
UTSW |
7 |
42,469,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Gm2381
|
UTSW |
7 |
42,469,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R2849:Gm2381
|
UTSW |
7 |
42,469,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R4437:Gm2381
|
UTSW |
7 |
42,469,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Gm2381
|
UTSW |
7 |
42,469,425 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:Gm2381
|
UTSW |
7 |
42,471,820 (GRCm39) |
missense |
probably benign |
0.12 |
R6370:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6372:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R6688:Gm2381
|
UTSW |
7 |
42,470,010 (GRCm39) |
missense |
probably benign |
0.00 |
R7150:Gm2381
|
UTSW |
7 |
42,469,888 (GRCm39) |
missense |
probably benign |
0.04 |
R7336:Gm2381
|
UTSW |
7 |
42,471,804 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8692:Gm2381
|
UTSW |
7 |
42,472,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Gm2381
|
UTSW |
7 |
42,469,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|