Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,906,048 (GRCm39) |
T806A |
possibly damaging |
Het |
Adgre1 |
T |
G |
17: 57,726,338 (GRCm39) |
L403R |
probably damaging |
Het |
Alox12 |
A |
T |
11: 70,133,398 (GRCm39) |
|
probably null |
Het |
Ankib1 |
A |
T |
5: 3,763,210 (GRCm39) |
D506E |
possibly damaging |
Het |
Ascc3 |
T |
G |
10: 50,597,935 (GRCm39) |
Y1268D |
probably damaging |
Het |
Bik |
A |
G |
15: 83,425,624 (GRCm39) |
M42V |
probably benign |
Het |
Bola1 |
A |
T |
3: 96,104,517 (GRCm39) |
S26T |
probably benign |
Het |
Bub1 |
T |
C |
2: 127,643,201 (GRCm39) |
I1048V |
probably benign |
Het |
Cad |
A |
G |
5: 31,219,564 (GRCm39) |
N621S |
probably damaging |
Het |
Camkv |
C |
A |
9: 107,822,799 (GRCm39) |
N69K |
possibly damaging |
Het |
Ccdc110 |
T |
C |
8: 46,395,876 (GRCm39) |
M589T |
probably benign |
Het |
Ccdc154 |
T |
A |
17: 25,389,864 (GRCm39) |
V498E |
probably damaging |
Het |
Ccr1l1 |
A |
G |
9: 123,777,691 (GRCm39) |
L252P |
probably damaging |
Het |
Cdh1 |
T |
C |
8: 107,390,953 (GRCm39) |
C690R |
probably damaging |
Het |
Cfap157 |
T |
G |
2: 32,668,175 (GRCm39) |
|
probably null |
Het |
Cux2 |
A |
G |
5: 122,025,540 (GRCm39) |
S43P |
possibly damaging |
Het |
Cyb5rl |
C |
T |
4: 106,925,880 (GRCm39) |
P21S |
probably damaging |
Het |
Cyp51 |
T |
G |
5: 4,136,594 (GRCm39) |
Q400P |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,137,152 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,642,688 (GRCm39) |
V1104I |
possibly damaging |
Het |
Ephb4 |
A |
G |
5: 137,352,688 (GRCm39) |
I90M |
probably benign |
Het |
Fam13c |
A |
G |
10: 70,378,523 (GRCm39) |
N269S |
probably damaging |
Het |
Fam83c |
T |
A |
2: 155,673,444 (GRCm39) |
Y248F |
possibly damaging |
Het |
Fat2 |
A |
G |
11: 55,194,542 (GRCm39) |
F1166L |
probably benign |
Het |
Fem1a |
A |
G |
17: 56,564,686 (GRCm39) |
N260D |
probably benign |
Het |
Fnbp4 |
T |
A |
2: 90,597,743 (GRCm39) |
|
probably null |
Het |
Fut9 |
T |
A |
4: 25,619,733 (GRCm39) |
*360Y |
probably null |
Het |
Fut9 |
T |
A |
4: 25,619,734 (GRCm39) |
*360L |
probably null |
Het |
Gm3727 |
T |
A |
14: 7,264,625 (GRCm38) |
Q10L |
probably damaging |
Het |
Gpat2 |
G |
A |
2: 127,270,211 (GRCm39) |
V75M |
probably damaging |
Het |
Haspin |
A |
C |
11: 73,027,456 (GRCm39) |
N544K |
probably damaging |
Het |
Havcr1 |
A |
G |
11: 46,669,379 (GRCm39) |
N286S |
probably benign |
Het |
Lrp6 |
A |
C |
6: 134,436,246 (GRCm39) |
C1307G |
probably damaging |
Het |
Lrrc2 |
A |
C |
9: 110,808,645 (GRCm39) |
H294P |
possibly damaging |
Het |
Mettl25b |
A |
T |
3: 87,834,360 (GRCm39) |
|
probably null |
Het |
Mon2 |
A |
C |
10: 122,878,269 (GRCm39) |
|
probably null |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mrgprb1 |
T |
C |
7: 48,097,070 (GRCm39) |
I281V |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,569,294 (GRCm39) |
E118G |
probably damaging |
Het |
Nefh |
T |
C |
11: 4,893,872 (GRCm39) |
D394G |
probably damaging |
Het |
Neurl4 |
A |
G |
11: 69,794,047 (GRCm39) |
T168A |
probably benign |
Het |
Or10s1 |
A |
G |
9: 39,986,211 (GRCm39) |
N207D |
possibly damaging |
Het |
Or1j18 |
T |
A |
2: 36,624,713 (GRCm39) |
C127S |
probably damaging |
Het |
Or51a10 |
T |
C |
7: 103,698,845 (GRCm39) |
T239A |
probably benign |
Het |
Or5ak4 |
A |
T |
2: 85,161,446 (GRCm39) |
N265K |
probably benign |
Het |
Oxsr1 |
A |
C |
9: 119,123,498 (GRCm39) |
M92R |
probably damaging |
Het |
Pde8a |
T |
C |
7: 80,945,516 (GRCm39) |
|
probably null |
Het |
Pex5l |
T |
A |
3: 33,007,281 (GRCm39) |
|
probably null |
Het |
Pik3r4 |
T |
A |
9: 105,549,984 (GRCm39) |
M1025K |
probably benign |
Het |
Plch1 |
C |
T |
3: 63,605,903 (GRCm39) |
E1325K |
probably benign |
Het |
Plin2 |
A |
T |
4: 86,586,669 (GRCm39) |
V54E |
probably damaging |
Het |
Prss47 |
A |
T |
13: 65,192,887 (GRCm39) |
I298N |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,097,546 (GRCm39) |
R1017G |
probably benign |
Het |
Psg19 |
T |
A |
7: 18,530,911 (GRCm39) |
Y81F |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Serpinb1a |
T |
C |
13: 33,034,397 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2a |
A |
T |
19: 47,266,794 (GRCm39) |
V265E |
probably damaging |
Het |
Slc22a17 |
A |
T |
14: 55,146,282 (GRCm39) |
Y337* |
probably null |
Het |
Slc25a27 |
A |
G |
17: 43,968,663 (GRCm39) |
V138A |
probably benign |
Het |
Slc4a2 |
A |
G |
5: 24,636,314 (GRCm39) |
Y220C |
probably damaging |
Het |
Slc66a3 |
G |
A |
12: 17,039,840 (GRCm39) |
L192F |
probably damaging |
Het |
Stab1 |
A |
T |
14: 30,890,392 (GRCm39) |
S20T |
probably benign |
Het |
Tcstv2a |
A |
T |
13: 120,725,633 (GRCm39) |
Q99L |
probably damaging |
Het |
Thsd1 |
G |
T |
8: 22,728,538 (GRCm39) |
|
probably benign |
Het |
Tmem204 |
G |
A |
17: 25,299,566 (GRCm39) |
|
probably benign |
Het |
Toporsl |
T |
A |
4: 52,612,072 (GRCm39) |
F655Y |
possibly damaging |
Het |
Vmn2r98 |
A |
G |
17: 19,301,553 (GRCm39) |
K852E |
unknown |
Het |
Wdpcp |
T |
G |
11: 21,641,884 (GRCm39) |
L174R |
probably damaging |
Het |
Zbbx |
G |
A |
3: 75,019,414 (GRCm39) |
P99S |
probably damaging |
Het |
Zfhx4 |
C |
T |
3: 5,468,418 (GRCm39) |
P2859S |
probably benign |
Het |
Zfp600 |
A |
T |
4: 146,133,488 (GRCm39) |
R719* |
probably null |
Het |
Zfp697 |
C |
A |
3: 98,335,330 (GRCm39) |
A365E |
unknown |
Het |
Zfp957 |
A |
C |
14: 79,451,053 (GRCm39) |
S249A |
probably benign |
Het |
|
Other mutations in Tom1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Tom1l1
|
APN |
11 |
90,565,566 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01995:Tom1l1
|
APN |
11 |
90,540,687 (GRCm39) |
missense |
probably damaging |
0.96 |
R0057:Tom1l1
|
UTSW |
11 |
90,575,975 (GRCm39) |
splice site |
probably benign |
|
R1557:Tom1l1
|
UTSW |
11 |
90,547,210 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1614:Tom1l1
|
UTSW |
11 |
90,574,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Tom1l1
|
UTSW |
11 |
90,547,177 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2517:Tom1l1
|
UTSW |
11 |
90,561,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3745:Tom1l1
|
UTSW |
11 |
90,548,567 (GRCm39) |
missense |
probably benign |
0.01 |
R4614:Tom1l1
|
UTSW |
11 |
90,561,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Tom1l1
|
UTSW |
11 |
90,537,675 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4755:Tom1l1
|
UTSW |
11 |
90,575,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5397:Tom1l1
|
UTSW |
11 |
90,552,600 (GRCm39) |
missense |
probably benign |
0.02 |
R6294:Tom1l1
|
UTSW |
11 |
90,552,587 (GRCm39) |
nonsense |
probably null |
|
R6733:Tom1l1
|
UTSW |
11 |
90,575,886 (GRCm39) |
critical splice donor site |
probably null |
|
R6911:Tom1l1
|
UTSW |
11 |
90,534,987 (GRCm39) |
splice site |
probably null |
|
R7103:Tom1l1
|
UTSW |
11 |
90,561,907 (GRCm39) |
splice site |
probably null |
|
R7489:Tom1l1
|
UTSW |
11 |
90,547,185 (GRCm39) |
missense |
probably benign |
0.00 |
R7696:Tom1l1
|
UTSW |
11 |
90,563,741 (GRCm39) |
missense |
probably benign |
0.02 |
R8244:Tom1l1
|
UTSW |
11 |
90,548,647 (GRCm39) |
missense |
probably benign |
0.13 |
R8787:Tom1l1
|
UTSW |
11 |
90,561,931 (GRCm39) |
missense |
probably benign |
0.00 |
R9205:Tom1l1
|
UTSW |
11 |
90,548,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Tom1l1
|
UTSW |
11 |
90,540,648 (GRCm39) |
small deletion |
probably benign |
|
R9308:Tom1l1
|
UTSW |
11 |
90,540,648 (GRCm39) |
small deletion |
probably benign |
|
R9309:Tom1l1
|
UTSW |
11 |
90,540,648 (GRCm39) |
small deletion |
probably benign |
|
|