Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acin1 |
A |
T |
14: 54,901,995 (GRCm39) |
V559E |
probably benign |
Het |
Adamts20 |
A |
G |
15: 94,236,340 (GRCm39) |
F844L |
probably benign |
Het |
Adcy5 |
C |
A |
16: 35,118,794 (GRCm39) |
D1048E |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,259,630 (GRCm39) |
C768* |
probably null |
Het |
Aldh18a1 |
G |
T |
19: 40,553,282 (GRCm39) |
Q487K |
probably damaging |
Het |
Aldh3b1 |
G |
A |
19: 3,971,271 (GRCm39) |
|
probably benign |
Het |
Asb18 |
T |
G |
1: 89,896,302 (GRCm39) |
D246A |
probably benign |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
Bcl2l15 |
A |
G |
3: 103,745,914 (GRCm39) |
|
probably null |
Het |
Brd10 |
A |
T |
19: 29,720,998 (GRCm39) |
S743T |
probably damaging |
Het |
Cage1 |
T |
A |
13: 38,207,309 (GRCm39) |
K285* |
probably null |
Het |
Ccn2 |
A |
C |
10: 24,472,695 (GRCm39) |
T202P |
probably damaging |
Het |
Cldn17 |
A |
G |
16: 88,303,444 (GRCm39) |
L95P |
probably damaging |
Het |
Cldn20 |
A |
T |
17: 3,583,157 (GRCm39) |
D110V |
probably damaging |
Het |
Cnot10 |
T |
C |
9: 114,444,067 (GRCm39) |
T443A |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Col23a1 |
T |
C |
11: 51,418,716 (GRCm39) |
Y135H |
unknown |
Het |
Cse1l |
T |
C |
2: 166,768,331 (GRCm39) |
S210P |
probably damaging |
Het |
Cspg4 |
T |
G |
9: 56,796,027 (GRCm39) |
V1254G |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,709,404 (GRCm39) |
T1415A |
probably damaging |
Het |
Epc2 |
A |
G |
2: 49,422,117 (GRCm39) |
Y337C |
probably damaging |
Het |
Epha2 |
A |
G |
4: 141,049,963 (GRCm39) |
S799G |
probably damaging |
Het |
Fndc10 |
A |
G |
4: 155,779,355 (GRCm39) |
Y133C |
probably damaging |
Het |
Gli3 |
G |
T |
13: 15,900,882 (GRCm39) |
S1423I |
probably benign |
Het |
Gm6034 |
A |
T |
17: 36,354,045 (GRCm39) |
|
probably benign |
Het |
Grik2 |
C |
A |
10: 49,399,842 (GRCm39) |
W296L |
possibly damaging |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Il6 |
T |
A |
5: 30,218,490 (GRCm39) |
Y46N |
possibly damaging |
Het |
Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
Itga9 |
A |
G |
9: 118,527,374 (GRCm39) |
|
probably benign |
Het |
Kcna7 |
T |
C |
7: 45,056,345 (GRCm39) |
V187A |
possibly damaging |
Het |
Kdm5b |
G |
T |
1: 134,540,919 (GRCm39) |
|
probably benign |
Het |
Knl1 |
T |
G |
2: 118,906,815 (GRCm39) |
S1635A |
probably damaging |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lox |
T |
G |
18: 52,653,983 (GRCm39) |
|
probably null |
Het |
Mdc1 |
A |
G |
17: 36,158,718 (GRCm39) |
D366G |
possibly damaging |
Het |
Meiob |
T |
C |
17: 25,053,021 (GRCm39) |
C344R |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,867,002 (GRCm39) |
M551K |
probably damaging |
Het |
Mrps15 |
A |
G |
4: 125,945,187 (GRCm39) |
T125A |
probably benign |
Het |
Mtmr14 |
A |
G |
6: 113,230,693 (GRCm39) |
H99R |
probably damaging |
Het |
Mup4 |
A |
G |
4: 59,960,598 (GRCm39) |
M1T |
probably null |
Het |
Mup5 |
G |
A |
4: 61,750,607 (GRCm39) |
R179* |
probably null |
Het |
Ncoa3 |
T |
G |
2: 165,911,221 (GRCm39) |
V1326G |
possibly damaging |
Het |
Noa1 |
A |
T |
5: 77,455,428 (GRCm39) |
N429K |
probably benign |
Het |
Nrxn1 |
C |
T |
17: 90,469,832 (GRCm39) |
A241T |
probably damaging |
Het |
Or1p1 |
A |
T |
11: 74,180,126 (GRCm39) |
Y218F |
probably damaging |
Het |
Or2t49 |
C |
T |
11: 58,392,765 (GRCm39) |
V206M |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,471 (GRCm39) |
S233L |
probably damaging |
Het |
Peg3 |
C |
A |
7: 6,712,900 (GRCm39) |
S774I |
possibly damaging |
Het |
Phyh |
A |
G |
2: 4,942,620 (GRCm39) |
K321R |
probably null |
Het |
Plcg1 |
T |
A |
2: 160,573,840 (GRCm39) |
M35K |
probably damaging |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Ppargc1b |
T |
A |
18: 61,440,275 (GRCm39) |
|
probably null |
Het |
Prcd |
A |
C |
11: 116,548,371 (GRCm39) |
S27R |
probably benign |
Het |
Prx |
T |
A |
7: 27,216,948 (GRCm39) |
M622K |
probably benign |
Het |
Psmd1 |
T |
A |
1: 85,999,567 (GRCm39) |
D51E |
probably damaging |
Het |
Psmd13 |
C |
T |
7: 140,463,430 (GRCm39) |
T38I |
probably damaging |
Het |
Ptprf |
A |
C |
4: 118,082,096 (GRCm39) |
D1047E |
possibly damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Riiad1 |
G |
A |
3: 94,380,176 (GRCm39) |
P40S |
possibly damaging |
Het |
Rnft1 |
T |
A |
11: 86,377,096 (GRCm39) |
N53K |
probably benign |
Het |
Scn4a |
C |
T |
11: 106,211,646 (GRCm39) |
R1457H |
probably benign |
Het |
Sema6c |
A |
T |
3: 95,078,099 (GRCm39) |
I492F |
probably damaging |
Het |
Shbg |
T |
C |
11: 69,505,798 (GRCm39) |
H403R |
probably damaging |
Het |
Slc15a5 |
A |
T |
6: 138,049,845 (GRCm39) |
|
probably benign |
Het |
Slc38a1 |
G |
A |
15: 96,485,016 (GRCm39) |
T221M |
probably damaging |
Het |
Slc6a16 |
T |
A |
7: 44,910,600 (GRCm39) |
V375E |
possibly damaging |
Het |
Slc6a17 |
T |
A |
3: 107,379,492 (GRCm39) |
M559L |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,181,373 (GRCm39) |
|
probably benign |
Het |
Sorcs2 |
G |
A |
5: 36,184,092 (GRCm39) |
R965W |
probably damaging |
Het |
St8sia4 |
C |
A |
1: 95,581,394 (GRCm39) |
R116L |
probably damaging |
Het |
Tcaf1 |
A |
C |
6: 42,652,272 (GRCm39) |
S737A |
possibly damaging |
Het |
Thbs2 |
T |
A |
17: 14,899,072 (GRCm39) |
Y676F |
probably benign |
Het |
Tmod2 |
A |
G |
9: 75,493,324 (GRCm39) |
|
probably benign |
Het |
Trim75 |
T |
C |
8: 65,435,391 (GRCm39) |
|
probably null |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp54 |
A |
T |
14: 20,633,508 (GRCm39) |
Y37* |
probably null |
Het |
Vill |
T |
C |
9: 118,895,082 (GRCm39) |
F100S |
probably damaging |
Het |
Vstm5 |
A |
G |
9: 15,168,663 (GRCm39) |
R76G |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,032,321 (GRCm39) |
T540A |
probably benign |
Het |
Zfp947 |
A |
C |
17: 22,365,184 (GRCm39) |
N163K |
probably benign |
Het |
Zfyve26 |
T |
C |
12: 79,308,573 (GRCm39) |
H228R |
possibly damaging |
Het |
|
Other mutations in Gmip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00790:Gmip
|
APN |
8 |
70,269,661 (GRCm39) |
nonsense |
probably null |
|
IGL02529:Gmip
|
APN |
8 |
70,269,439 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03185:Gmip
|
APN |
8 |
70,262,433 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03328:Gmip
|
APN |
8 |
70,264,261 (GRCm39) |
missense |
possibly damaging |
0.79 |
microdot
|
UTSW |
8 |
70,266,785 (GRCm39) |
missense |
probably damaging |
1.00 |
minnox
|
UTSW |
8 |
70,270,452 (GRCm39) |
missense |
probably benign |
0.02 |
puncta
|
UTSW |
8 |
70,268,736 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0110:Gmip
|
UTSW |
8 |
70,268,259 (GRCm39) |
unclassified |
probably benign |
|
R0329:Gmip
|
UTSW |
8 |
70,263,468 (GRCm39) |
missense |
probably benign |
0.06 |
R0330:Gmip
|
UTSW |
8 |
70,263,468 (GRCm39) |
missense |
probably benign |
0.06 |
R0510:Gmip
|
UTSW |
8 |
70,268,259 (GRCm39) |
unclassified |
probably benign |
|
R0638:Gmip
|
UTSW |
8 |
70,264,095 (GRCm39) |
splice site |
probably benign |
|
R1692:Gmip
|
UTSW |
8 |
70,266,553 (GRCm39) |
missense |
probably benign |
|
R1755:Gmip
|
UTSW |
8 |
70,266,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Gmip
|
UTSW |
8 |
70,267,127 (GRCm39) |
missense |
probably benign |
|
R1894:Gmip
|
UTSW |
8 |
70,273,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1926:Gmip
|
UTSW |
8 |
70,268,170 (GRCm39) |
missense |
probably benign |
0.41 |
R2005:Gmip
|
UTSW |
8 |
70,266,693 (GRCm39) |
missense |
probably benign |
|
R4280:Gmip
|
UTSW |
8 |
70,266,251 (GRCm39) |
unclassified |
probably benign |
|
R4281:Gmip
|
UTSW |
8 |
70,266,251 (GRCm39) |
unclassified |
probably benign |
|
R4282:Gmip
|
UTSW |
8 |
70,266,251 (GRCm39) |
unclassified |
probably benign |
|
R4283:Gmip
|
UTSW |
8 |
70,266,251 (GRCm39) |
unclassified |
probably benign |
|
R5221:Gmip
|
UTSW |
8 |
70,266,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R5512:Gmip
|
UTSW |
8 |
70,270,540 (GRCm39) |
missense |
probably benign |
0.00 |
R5521:Gmip
|
UTSW |
8 |
70,270,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Gmip
|
UTSW |
8 |
70,270,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Gmip
|
UTSW |
8 |
70,269,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Gmip
|
UTSW |
8 |
70,270,022 (GRCm39) |
missense |
probably benign |
0.28 |
R6228:Gmip
|
UTSW |
8 |
70,268,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R6775:Gmip
|
UTSW |
8 |
70,268,285 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6787:Gmip
|
UTSW |
8 |
70,266,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Gmip
|
UTSW |
8 |
70,263,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Gmip
|
UTSW |
8 |
70,263,824 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6852:Gmip
|
UTSW |
8 |
70,270,641 (GRCm39) |
nonsense |
probably null |
|
R6934:Gmip
|
UTSW |
8 |
70,273,576 (GRCm39) |
missense |
probably benign |
|
R7010:Gmip
|
UTSW |
8 |
70,264,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R7122:Gmip
|
UTSW |
8 |
70,270,452 (GRCm39) |
missense |
probably benign |
0.02 |
R7254:Gmip
|
UTSW |
8 |
70,269,118 (GRCm39) |
splice site |
probably null |
|
R7351:Gmip
|
UTSW |
8 |
70,270,034 (GRCm39) |
missense |
probably benign |
0.01 |
R7360:Gmip
|
UTSW |
8 |
70,263,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Gmip
|
UTSW |
8 |
70,273,149 (GRCm39) |
missense |
probably benign |
|
R7577:Gmip
|
UTSW |
8 |
70,267,085 (GRCm39) |
missense |
probably benign |
0.17 |
R7718:Gmip
|
UTSW |
8 |
70,270,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R8018:Gmip
|
UTSW |
8 |
70,268,143 (GRCm39) |
missense |
probably benign |
0.41 |
R8080:Gmip
|
UTSW |
8 |
70,268,736 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8694:Gmip
|
UTSW |
8 |
70,270,485 (GRCm39) |
missense |
probably benign |
|
R8750:Gmip
|
UTSW |
8 |
70,273,134 (GRCm39) |
missense |
probably benign |
0.01 |
R8826:Gmip
|
UTSW |
8 |
70,268,748 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8917:Gmip
|
UTSW |
8 |
70,270,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Gmip
|
UTSW |
8 |
70,269,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Gmip
|
UTSW |
8 |
70,273,298 (GRCm39) |
missense |
probably damaging |
0.96 |
R9350:Gmip
|
UTSW |
8 |
70,263,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R9463:Gmip
|
UTSW |
8 |
70,269,693 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9547:Gmip
|
UTSW |
8 |
70,273,381 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9771:Gmip
|
UTSW |
8 |
70,266,718 (GRCm39) |
missense |
probably benign |
0.44 |
X0063:Gmip
|
UTSW |
8 |
70,262,466 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gmip
|
UTSW |
8 |
70,268,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|