Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533K18Rik |
A |
G |
10: 70,872,202 |
|
noncoding transcript |
Het |
Abca3 |
G |
T |
17: 24,376,473 |
C328F |
possibly damaging |
Het |
Aldh5a1 |
T |
C |
13: 24,918,512 |
N323D |
possibly damaging |
Het |
Atp5c1 |
T |
C |
2: 10,068,666 |
Y32C |
probably damaging |
Het |
Capn3 |
T |
G |
2: 120,502,186 |
|
probably null |
Het |
Ccdc113 |
C |
A |
8: 95,551,238 |
D275E |
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,242,719 |
F562I |
possibly damaging |
Het |
Cd96 |
T |
C |
16: 46,109,127 |
T152A |
possibly damaging |
Het |
Cdh7 |
T |
A |
1: 110,061,140 |
D257E |
probably damaging |
Het |
Cilp2 |
T |
C |
8: 69,881,204 |
D1048G |
probably benign |
Het |
Clrn2 |
T |
G |
5: 45,460,066 |
L93R |
probably damaging |
Het |
Crat |
C |
A |
2: 30,409,966 |
G134V |
probably damaging |
Het |
Dis3 |
A |
T |
14: 99,097,745 |
N140K |
probably benign |
Het |
Dmxl2 |
T |
A |
9: 54,445,376 |
|
probably benign |
Het |
Dus1l |
T |
A |
11: 120,793,079 |
Q181L |
probably damaging |
Het |
Ece1 |
A |
G |
4: 137,948,544 |
T410A |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,421,048 |
H90L |
probably damaging |
Het |
Gm16602 |
G |
A |
13: 19,336,570 |
|
probably benign |
Het |
Gm1966 |
T |
C |
7: 106,602,537 |
D500G |
probably damaging |
Het |
Gpr152 |
T |
A |
19: 4,142,952 |
V164E |
probably damaging |
Het |
Grik3 |
A |
C |
4: 125,694,036 |
I650L |
possibly damaging |
Het |
Gzmm |
A |
T |
10: 79,695,062 |
T233S |
probably benign |
Het |
H2-Q4 |
T |
A |
17: 35,383,312 |
V341D |
probably benign |
Het |
Igsf21 |
A |
G |
4: 140,027,718 |
|
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,860,657 |
|
probably benign |
Het |
Kntc1 |
T |
G |
5: 123,781,658 |
V864G |
probably damaging |
Het |
Lnx1 |
T |
C |
5: 74,620,155 |
E235G |
possibly damaging |
Het |
Man2b1 |
G |
T |
8: 85,097,430 |
K985N |
probably benign |
Het |
Map4k1 |
C |
A |
7: 29,001,619 |
P670Q |
probably damaging |
Het |
Mapk8ip1 |
C |
A |
2: 92,388,974 |
|
probably null |
Het |
Mettl16 |
T |
A |
11: 74,792,267 |
Y178* |
probably null |
Het |
Mrpl11 |
T |
A |
19: 4,963,421 |
|
probably null |
Het |
Nup85 |
T |
C |
11: 115,569,714 |
S140P |
possibly damaging |
Het |
Olfr1140 |
T |
C |
2: 87,746,598 |
V134A |
probably benign |
Het |
Olfr1301 |
T |
A |
2: 111,755,005 |
V252E |
probably damaging |
Het |
Olfr301 |
T |
C |
7: 86,412,959 |
L199P |
possibly damaging |
Het |
Olfr352 |
T |
C |
2: 36,870,520 |
|
probably benign |
Het |
Pcdhb2 |
T |
A |
18: 37,295,322 |
L116* |
probably null |
Het |
Pdcd7 |
C |
A |
9: 65,346,703 |
R188S |
probably damaging |
Het |
Pdk2 |
T |
C |
11: 95,027,285 |
Y374C |
probably damaging |
Het |
Ppp1r12a |
G |
T |
10: 108,234,021 |
D224Y |
probably damaging |
Het |
Ppp2r2d |
T |
A |
7: 138,876,635 |
Y169N |
probably damaging |
Het |
Prcp |
A |
C |
7: 92,910,213 |
T162P |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,342,142 |
S873P |
probably benign |
Het |
Ptpn2 |
T |
C |
18: 67,681,553 |
T129A |
probably benign |
Het |
Rtkn |
G |
A |
6: 83,146,061 |
R68H |
probably damaging |
Het |
Sall4 |
C |
T |
2: 168,755,856 |
D355N |
probably damaging |
Het |
Scn7a |
A |
G |
2: 66,703,852 |
V493A |
probably benign |
Het |
Sema4b |
G |
A |
7: 80,215,696 |
A140T |
probably damaging |
Het |
Shisa6 |
C |
A |
11: 66,217,828 |
G408C |
possibly damaging |
Het |
Slc7a9 |
G |
T |
7: 35,454,164 |
V197F |
probably damaging |
Het |
Spata2 |
A |
T |
2: 167,484,151 |
D249E |
probably damaging |
Het |
Stk36 |
T |
A |
1: 74,633,638 |
V1013E |
probably benign |
Het |
Tcp10a |
T |
C |
17: 7,343,500 |
V336A |
probably damaging |
Het |
Tfb2m |
A |
T |
1: 179,537,844 |
V185D |
possibly damaging |
Het |
Tgm7 |
T |
A |
2: 121,106,915 |
Y76F |
probably benign |
Het |
Tph1 |
T |
C |
7: 46,653,753 |
Y267C |
probably damaging |
Het |
Ube2d1 |
A |
G |
10: 71,255,826 |
|
probably benign |
Het |
Vps4a |
A |
G |
8: 107,036,924 |
D72G |
probably benign |
Het |
Wipf2 |
T |
A |
11: 98,890,803 |
V56D |
possibly damaging |
Het |
Wisp3 |
A |
G |
10: 39,158,310 |
Y99H |
probably damaging |
Het |
Zfp750 |
C |
A |
11: 121,512,165 |
V586L |
probably benign |
Het |
Zfp831 |
A |
G |
2: 174,644,606 |
E358G |
possibly damaging |
Het |
|