Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438A13Rik |
T |
C |
3: 37,038,517 |
|
probably benign |
Het |
Abcb10 |
C |
T |
8: 123,954,315 |
R714Q |
possibly damaging |
Het |
Abcb5 |
T |
A |
12: 118,936,087 |
I282L |
probably benign |
Het |
Aox1 |
A |
T |
1: 58,078,465 |
E835D |
probably benign |
Het |
Arhgap17 |
C |
T |
7: 123,321,874 |
|
probably null |
Het |
Calcr |
C |
T |
6: 3,693,718 |
V359I |
probably benign |
Het |
Chd9 |
T |
A |
8: 91,015,267 |
|
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,017,029 |
|
probably benign |
Het |
Dnajc11 |
A |
G |
4: 151,970,861 |
E171G |
possibly damaging |
Het |
Efhd1 |
T |
C |
1: 87,264,684 |
F79L |
possibly damaging |
Het |
Fam83a |
A |
T |
15: 57,993,077 |
|
probably null |
Het |
Fam98a |
A |
G |
17: 75,540,105 |
|
probably benign |
Het |
Ficd |
A |
G |
5: 113,738,253 |
Y163C |
probably damaging |
Het |
Filip1l |
T |
C |
16: 57,506,804 |
S66P |
probably damaging |
Het |
Fmo5 |
A |
G |
3: 97,635,593 |
Y73C |
probably damaging |
Het |
Galnt12 |
C |
A |
4: 47,122,566 |
R574S |
possibly damaging |
Het |
Klc3 |
C |
A |
7: 19,395,062 |
G461W |
probably damaging |
Het |
Lmo7 |
A |
T |
14: 101,912,079 |
T973S |
possibly damaging |
Het |
Loxl1 |
C |
A |
9: 58,311,910 |
G326V |
possibly damaging |
Het |
Lrrc24 |
A |
G |
15: 76,718,304 |
V127A |
probably benign |
Het |
Lyrm1 |
T |
C |
7: 119,916,131 |
|
probably benign |
Het |
Med28 |
G |
A |
5: 45,522,469 |
V65I |
probably damaging |
Het |
Mgat4c |
T |
C |
10: 102,388,461 |
Y179H |
probably damaging |
Het |
Micall1 |
A |
C |
15: 79,114,681 |
N58T |
probably damaging |
Het |
Ncoa4 |
T |
A |
14: 32,173,420 |
M72K |
possibly damaging |
Het |
Nutm1 |
T |
C |
2: 112,248,933 |
Q879R |
probably benign |
Het |
Olfr1428 |
C |
T |
19: 12,109,148 |
V133I |
probably benign |
Het |
Olfr870 |
T |
A |
9: 20,171,167 |
I135F |
probably damaging |
Het |
Olfr965 |
T |
A |
9: 39,720,035 |
D269E |
probably benign |
Het |
Phf11b |
T |
C |
14: 59,324,924 |
I177M |
probably damaging |
Het |
Pin1rt1 |
T |
G |
2: 104,714,707 |
I27L |
probably benign |
Het |
Plxna2 |
T |
C |
1: 194,762,550 |
V750A |
possibly damaging |
Het |
Pou5f1 |
A |
T |
17: 35,510,039 |
N126I |
possibly damaging |
Het |
Ptprn |
A |
T |
1: 75,247,873 |
H946Q |
possibly damaging |
Het |
Rnf43 |
G |
T |
11: 87,732,304 |
G744* |
probably null |
Het |
Rsbn1 |
C |
A |
3: 103,953,629 |
|
probably benign |
Het |
Sars2 |
T |
A |
7: 28,746,781 |
I145N |
possibly damaging |
Het |
Sh3tc2 |
A |
T |
18: 62,011,880 |
E1135V |
probably damaging |
Het |
Shroom1 |
A |
G |
11: 53,463,379 |
D42G |
probably benign |
Het |
Sidt2 |
A |
G |
9: 45,942,683 |
|
probably null |
Het |
Slc39a8 |
T |
C |
3: 135,886,797 |
|
probably benign |
Het |
Slc9c1 |
T |
C |
16: 45,599,758 |
S1059P |
probably benign |
Het |
Socs6 |
A |
T |
18: 88,869,846 |
M315K |
probably benign |
Het |
Soga3 |
T |
A |
10: 29,198,949 |
F911Y |
probably damaging |
Het |
Speer2 |
T |
C |
16: 69,857,977 |
E200G |
probably damaging |
Het |
Sult2a5 |
T |
A |
7: 13,624,182 |
|
probably null |
Het |
Tmbim1 |
A |
T |
1: 74,291,699 |
I168N |
possibly damaging |
Het |
Trim38 |
T |
C |
13: 23,782,963 |
V131A |
probably damaging |
Het |
Ube2o |
A |
G |
11: 116,541,642 |
S833P |
probably damaging |
Het |
Uggt2 |
T |
C |
14: 119,075,346 |
I350M |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,509,489 |
D640G |
probably damaging |
Het |
Vmn2r54 |
C |
T |
7: 12,632,428 |
C193Y |
probably damaging |
Het |
|