Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5830411N06Rik |
G |
A |
7: 140,296,826 |
C710Y |
probably damaging |
Het |
A1bg |
A |
T |
15: 60,921,234 |
L8Q |
probably damaging |
Het |
Abca4 |
T |
C |
3: 122,148,901 |
V1681A |
probably damaging |
Het |
Abce1 |
G |
T |
8: 79,690,293 |
A363E |
probably benign |
Het |
Adgrl2 |
T |
C |
3: 148,859,164 |
Y256C |
probably damaging |
Het |
Afm |
T |
C |
5: 90,547,881 |
C416R |
probably damaging |
Het |
Ahnak |
T |
A |
19: 9,006,917 |
V1855D |
probably damaging |
Het |
Alb |
A |
T |
5: 90,468,593 |
H319L |
probably benign |
Het |
Ankrd35 |
G |
T |
3: 96,684,903 |
R835L |
probably damaging |
Het |
Atg2b |
T |
C |
12: 105,649,155 |
D1014G |
possibly damaging |
Het |
Cdk6 |
T |
A |
5: 3,344,436 |
Y24N |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,752,473 |
N323K |
probably damaging |
Het |
Cops9 |
A |
T |
1: 92,639,767 |
|
probably benign |
Het |
Crybg1 |
T |
C |
10: 44,003,510 |
T561A |
probably benign |
Het |
Dcdc5 |
T |
C |
2: 106,365,433 |
|
noncoding transcript |
Het |
Fam149b |
A |
G |
14: 20,363,300 |
T196A |
possibly damaging |
Het |
Fam217a |
C |
A |
13: 34,910,297 |
C402F |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,253,889 |
V4053E |
probably benign |
Het |
Fcgbp |
T |
C |
7: 28,091,579 |
V755A |
probably damaging |
Het |
Fxr1 |
C |
A |
3: 34,068,976 |
S641R |
probably benign |
Het |
Gata5 |
A |
T |
2: 180,334,254 |
M39K |
probably benign |
Het |
Gon4l |
T |
A |
3: 88,899,971 |
D1658E |
probably damaging |
Het |
Gpr180 |
C |
T |
14: 118,162,698 |
T426M |
probably damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,584,297 |
T121I |
probably benign |
Het |
Helq |
T |
C |
5: 100,762,593 |
E1039G |
probably damaging |
Het |
Hibch |
T |
A |
1: 52,901,247 |
Y192N |
probably damaging |
Het |
Hp1bp3 |
A |
G |
4: 138,222,115 |
I41M |
probably damaging |
Het |
Itpripl2 |
G |
T |
7: 118,489,878 |
P486Q |
probably benign |
Het |
Kcnj6 |
T |
C |
16: 94,833,201 |
D17G |
probably benign |
Het |
Kprp |
T |
A |
3: 92,824,336 |
Y469F |
unknown |
Het |
Kremen2 |
T |
C |
17: 23,742,255 |
T373A |
probably benign |
Het |
Lgi4 |
A |
G |
7: 31,061,137 |
Y39C |
possibly damaging |
Het |
Lgr5 |
T |
C |
10: 115,478,504 |
D176G |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,588,463 |
S785G |
probably benign |
Het |
Ltbp1 |
A |
T |
17: 75,291,330 |
Q920L |
probably benign |
Het |
Map2 |
A |
G |
1: 66,416,037 |
E1362G |
probably damaging |
Het |
Nkx2-6 |
T |
C |
14: 69,171,823 |
S8P |
probably damaging |
Het |
Olfr93 |
T |
C |
17: 37,151,594 |
Q126R |
probably benign |
Het |
Pde4dip |
C |
T |
3: 97,747,576 |
R888Q |
possibly damaging |
Het |
Per1 |
A |
G |
11: 69,103,445 |
H494R |
probably damaging |
Het |
Pira2 |
A |
G |
7: 3,842,546 |
F280L |
probably benign |
Het |
Plekhm3 |
C |
T |
1: 64,937,986 |
W108* |
probably null |
Het |
Ptcd3 |
A |
G |
6: 71,902,936 |
S113P |
probably damaging |
Het |
Scarf1 |
T |
C |
11: 75,514,016 |
L42P |
possibly damaging |
Het |
Skint1 |
A |
C |
4: 112,019,056 |
Q58P |
probably damaging |
Het |
Spata7 |
A |
T |
12: 98,669,331 |
N438I |
probably damaging |
Het |
Spdya |
C |
A |
17: 71,569,131 |
D164E |
probably damaging |
Het |
Speer3 |
G |
A |
5: 13,794,768 |
|
probably null |
Het |
Ssc4d |
A |
T |
5: 135,970,196 |
L51H |
probably damaging |
Het |
Steap1 |
A |
G |
5: 5,740,579 |
I123T |
possibly damaging |
Het |
Styx |
T |
A |
14: 45,371,026 |
F147I |
possibly damaging |
Het |
Suv39h2 |
T |
A |
2: 3,474,853 |
|
probably benign |
Het |
Tfb2m |
A |
G |
1: 179,545,881 |
V84A |
probably benign |
Het |
Tlcd1 |
T |
G |
11: 78,178,936 |
V25G |
probably benign |
Het |
Tmem79 |
T |
C |
3: 88,332,563 |
Y280C |
probably damaging |
Het |
Trim5 |
T |
A |
7: 104,276,835 |
N173I |
probably damaging |
Het |
Ttc17 |
A |
T |
2: 94,377,682 |
D194E |
probably damaging |
Het |
Zfp2 |
T |
C |
11: 50,900,157 |
E353G |
possibly damaging |
Het |
|