Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833439L19Rik |
A |
T |
13: 54,700,519 (GRCm39) |
M273K |
probably benign |
Het |
Aar2 |
A |
G |
2: 156,393,361 (GRCm39) |
D250G |
probably benign |
Het |
Acly |
T |
A |
11: 100,407,711 (GRCm39) |
Y213F |
probably benign |
Het |
Adgrg5 |
G |
A |
8: 95,668,133 (GRCm39) |
M399I |
|
Het |
Adhfe1 |
T |
C |
1: 9,623,634 (GRCm39) |
L95P |
probably damaging |
Het |
Ano7 |
G |
A |
1: 93,322,180 (GRCm39) |
C396Y |
probably damaging |
Het |
Apob |
T |
A |
12: 8,066,125 (GRCm39) |
Y4365N |
probably damaging |
Het |
Arfgap3 |
C |
T |
15: 83,192,366 (GRCm39) |
R411H |
probably damaging |
Het |
Bbs7 |
T |
C |
3: 36,661,818 (GRCm39) |
Y127C |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,382,982 (GRCm39) |
T793A |
probably benign |
Het |
Casp8ap2 |
T |
A |
4: 32,643,807 (GRCm39) |
V960E |
possibly damaging |
Het |
Cd200l1 |
G |
T |
16: 45,264,237 (GRCm39) |
T107N |
possibly damaging |
Het |
Cdkl3 |
A |
G |
11: 51,895,770 (GRCm39) |
T6A |
probably benign |
Het |
Cdkn2aip |
T |
C |
8: 48,166,654 (GRCm39) |
D51G |
probably benign |
Het |
Cdpf1 |
G |
T |
15: 85,692,527 (GRCm39) |
S52* |
probably null |
Het |
Celf5 |
T |
A |
10: 81,303,925 (GRCm39) |
D177V |
probably damaging |
Het |
Cep164 |
A |
G |
9: 45,682,897 (GRCm39) |
V931A |
probably damaging |
Het |
Cog6 |
T |
C |
3: 52,900,907 (GRCm39) |
D457G |
probably damaging |
Het |
Col4a2 |
G |
T |
8: 11,496,157 (GRCm39) |
V1593L |
probably benign |
Het |
Dlg5 |
C |
G |
14: 24,204,681 (GRCm39) |
M1287I |
probably benign |
Het |
Dmrt1 |
T |
C |
19: 25,523,362 (GRCm39) |
S238P |
probably benign |
Het |
Dpysl2 |
A |
G |
14: 67,099,927 (GRCm39) |
M103T |
probably benign |
Het |
Emsy |
C |
A |
7: 98,262,256 (GRCm39) |
A608S |
probably benign |
Het |
Entr1 |
A |
G |
2: 26,278,645 (GRCm39) |
F21S |
unknown |
Het |
Entrep2 |
C |
T |
7: 64,806,056 (GRCm39) |
G6S |
probably benign |
Het |
Exoc5 |
A |
T |
14: 49,253,086 (GRCm39) |
C576S |
probably damaging |
Het |
Fignl1 |
A |
G |
11: 11,752,219 (GRCm39) |
S279P |
probably benign |
Het |
Gimap1 |
A |
G |
6: 48,719,386 (GRCm39) |
R71G |
unknown |
Het |
Gm26727 |
A |
T |
2: 67,263,263 (GRCm39) |
M88K |
probably damaging |
Het |
Gm45861 |
T |
A |
8: 28,045,436 (GRCm39) |
W1066R |
unknown |
Het |
Gpr15 |
A |
G |
16: 58,538,249 (GRCm39) |
L280S |
possibly damaging |
Het |
Grin1 |
C |
T |
2: 25,187,422 (GRCm39) |
W629* |
probably null |
Het |
Grk5 |
C |
T |
19: 61,078,467 (GRCm39) |
P508L |
possibly damaging |
Het |
Hgf |
A |
T |
5: 16,766,029 (GRCm39) |
D55V |
probably damaging |
Het |
Hipk1 |
T |
A |
3: 103,668,890 (GRCm39) |
D502V |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,489,758 (GRCm39) |
K4394E |
probably damaging |
Het |
Llgl2 |
A |
G |
11: 115,740,467 (GRCm39) |
T388A |
probably damaging |
Het |
Lsm14a |
G |
T |
7: 34,088,898 (GRCm39) |
S2R |
probably damaging |
Het |
Madd |
A |
T |
2: 91,000,544 (GRCm39) |
M507K |
possibly damaging |
Het |
Map2k3 |
G |
T |
11: 60,837,472 (GRCm39) |
V191L |
|
Het |
Mapk8ip1 |
A |
G |
2: 92,217,060 (GRCm39) |
S421P |
probably damaging |
Het |
Marchf7 |
C |
T |
2: 60,064,785 (GRCm39) |
R354* |
probably null |
Het |
Myc |
T |
G |
15: 61,859,935 (GRCm39) |
C204G |
probably damaging |
Het |
Nampt |
A |
G |
12: 32,900,528 (GRCm39) |
H491R |
possibly damaging |
Het |
Noct |
C |
T |
3: 51,157,267 (GRCm39) |
Q202* |
probably null |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or10b1 |
T |
A |
10: 78,355,949 (GRCm39) |
F169Y |
probably damaging |
Het |
Osbpl10 |
G |
A |
9: 115,052,804 (GRCm39) |
V451M |
probably damaging |
Het |
Osr2 |
T |
A |
15: 35,303,061 (GRCm39) |
F312Y |
probably benign |
Het |
Parp16 |
A |
T |
9: 65,137,097 (GRCm39) |
I108F |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,885,888 (GRCm39) |
T1656A |
unknown |
Het |
Pnpla8 |
A |
G |
12: 44,330,657 (GRCm39) |
I374V |
probably benign |
Het |
Prss23 |
T |
C |
7: 89,159,931 (GRCm39) |
N46S |
probably benign |
Het |
Ptger2 |
T |
C |
14: 45,226,476 (GRCm39) |
W19R |
possibly damaging |
Het |
Rbl2 |
T |
C |
8: 91,805,527 (GRCm39) |
S195P |
probably damaging |
Het |
Rnf169 |
C |
T |
7: 99,575,477 (GRCm39) |
V373I |
probably damaging |
Het |
Sclt1 |
C |
A |
3: 41,629,837 (GRCm39) |
E325* |
probably null |
Het |
Sergef |
C |
T |
7: 46,284,913 (GRCm39) |
S43N |
probably benign |
Het |
Slc35f3 |
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CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
8: 127,115,777 (GRCm39) |
|
probably benign |
Het |
Slc3a2 |
T |
C |
19: 8,685,370 (GRCm39) |
D472G |
probably damaging |
Het |
Slc43a3 |
T |
C |
2: 84,780,800 (GRCm39) |
F342L |
probably benign |
Het |
Slc44a4 |
A |
T |
17: 35,140,670 (GRCm39) |
I288F |
probably benign |
Het |
Snupn |
T |
A |
9: 56,877,915 (GRCm39) |
N151K |
possibly damaging |
Het |
Srbd1 |
A |
T |
17: 86,437,550 (GRCm39) |
D264E |
probably benign |
Het |
Srpra |
A |
T |
9: 35,125,569 (GRCm39) |
T378S |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,141,762 (GRCm39) |
D613G |
possibly damaging |
Het |
Sycp2l |
C |
T |
13: 41,326,132 (GRCm39) |
P246L |
|
Het |
Tcf20 |
T |
C |
15: 82,736,037 (GRCm39) |
R1805G |
probably benign |
Het |
Tob1 |
T |
A |
11: 94,104,880 (GRCm39) |
F139I |
probably damaging |
Het |
Traj9 |
A |
G |
14: 54,446,871 (GRCm39) |
T8A |
unknown |
Het |
Trank1 |
G |
T |
9: 111,220,537 (GRCm39) |
D2425Y |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,738,071 (GRCm39) |
S4202L |
unknown |
Het |
Ttn |
A |
T |
2: 76,577,267 (GRCm39) |
M24542K |
probably damaging |
Het |
Vcam1 |
T |
C |
3: 115,911,105 (GRCm39) |
Y431C |
probably damaging |
Het |
Vcpkmt |
G |
A |
12: 69,627,936 (GRCm39) |
R175C |
probably damaging |
Het |
Vmn2r51 |
A |
T |
7: 9,839,479 (GRCm39) |
D36E |
probably benign |
Het |
Vmn2r61 |
A |
G |
7: 41,949,917 (GRCm39) |
E779G |
probably damaging |
Het |
Zfp831 |
T |
C |
2: 174,487,938 (GRCm39) |
L871P |
possibly damaging |
Het |
|
Other mutations in F830016B08Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:F830016B08Rik
|
APN |
18 |
60,433,340 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:F830016B08Rik
|
APN |
18 |
60,433,058 (GRCm39) |
missense |
probably benign |
0.00 |
FR4342:F830016B08Rik
|
UTSW |
18 |
60,433,013 (GRCm39) |
small insertion |
probably benign |
|
R0172:F830016B08Rik
|
UTSW |
18 |
60,433,036 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0375:F830016B08Rik
|
UTSW |
18 |
60,433,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1517:F830016B08Rik
|
UTSW |
18 |
60,433,970 (GRCm39) |
nonsense |
probably null |
|
R1791:F830016B08Rik
|
UTSW |
18 |
60,433,589 (GRCm39) |
missense |
probably benign |
0.01 |
R2413:F830016B08Rik
|
UTSW |
18 |
60,433,365 (GRCm39) |
nonsense |
probably null |
|
R2696:F830016B08Rik
|
UTSW |
18 |
60,433,808 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3607:F830016B08Rik
|
UTSW |
18 |
60,433,780 (GRCm39) |
nonsense |
probably null |
|
R4612:F830016B08Rik
|
UTSW |
18 |
60,434,087 (GRCm39) |
missense |
probably benign |
0.42 |
R4621:F830016B08Rik
|
UTSW |
18 |
60,433,939 (GRCm39) |
missense |
probably benign |
0.01 |
R4752:F830016B08Rik
|
UTSW |
18 |
60,434,153 (GRCm39) |
missense |
probably benign |
0.00 |
R5755:F830016B08Rik
|
UTSW |
18 |
60,433,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:F830016B08Rik
|
UTSW |
18 |
60,433,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6183:F830016B08Rik
|
UTSW |
18 |
60,432,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6272:F830016B08Rik
|
UTSW |
18 |
60,433,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:F830016B08Rik
|
UTSW |
18 |
60,433,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:F830016B08Rik
|
UTSW |
18 |
60,433,052 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:F830016B08Rik
|
UTSW |
18 |
60,433,150 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8289:F830016B08Rik
|
UTSW |
18 |
60,433,360 (GRCm39) |
missense |
probably benign |
0.45 |
R9034:F830016B08Rik
|
UTSW |
18 |
60,433,141 (GRCm39) |
missense |
probably damaging |
0.96 |
R9600:F830016B08Rik
|
UTSW |
18 |
60,433,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R9614:F830016B08Rik
|
UTSW |
18 |
60,433,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9633:F830016B08Rik
|
UTSW |
18 |
60,432,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R9638:F830016B08Rik
|
UTSW |
18 |
60,432,956 (GRCm39) |
missense |
probably benign |
0.00 |
R9684:F830016B08Rik
|
UTSW |
18 |
60,433,043 (GRCm39) |
missense |
probably damaging |
0.97 |
RF044:F830016B08Rik
|
UTSW |
18 |
60,433,010 (GRCm39) |
small insertion |
probably benign |
|
RF054:F830016B08Rik
|
UTSW |
18 |
60,433,010 (GRCm39) |
small insertion |
probably benign |
|
|