Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610010F05Rik |
A |
G |
11: 23,625,100 |
L58P |
probably damaging |
Het |
4933427D14Rik |
T |
C |
11: 72,189,586 |
E418G |
probably damaging |
Het |
9930012K11Rik |
C |
A |
14: 70,157,622 |
V28L |
possibly damaging |
Het |
Abtb2 |
C |
T |
2: 103,709,425 |
R712* |
probably null |
Het |
Acvr1c |
C |
T |
2: 58,287,705 |
G171S |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,753,288 |
A1783E |
probably benign |
Het |
Anapc4 |
A |
T |
5: 52,848,828 |
Q149L |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,628,527 |
V824A |
possibly damaging |
Het |
Ankrd31 |
G |
C |
13: 96,831,586 |
C577S |
probably benign |
Het |
Apol7c |
T |
C |
15: 77,526,074 |
N224S |
probably benign |
Het |
Arl14 |
A |
T |
3: 69,222,696 |
T59S |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,612,472 |
I870K |
probably damaging |
Het |
B4galt1 |
A |
T |
4: 40,807,796 |
V335E |
probably benign |
Het |
C2cd3 |
C |
T |
7: 100,390,241 |
P216S |
probably benign |
Het |
Cchcr1 |
C |
A |
17: 35,529,118 |
N711K |
possibly damaging |
Het |
Chd2 |
A |
G |
7: 73,497,810 |
F467L |
possibly damaging |
Het |
Cntn6 |
A |
T |
6: 104,861,946 |
E987V |
possibly damaging |
Het |
Col11a2 |
T |
A |
17: 34,053,598 |
L286H |
probably damaging |
Het |
Cwc22 |
C |
T |
2: 77,929,448 |
R85Q |
possibly damaging |
Het |
Cyp7a1 |
A |
C |
4: 6,272,587 |
F209V |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,614,882 |
T189A |
possibly damaging |
Het |
Dusp16 |
A |
T |
6: 134,725,879 |
C216* |
probably null |
Het |
Fan1 |
T |
A |
7: 64,372,486 |
N340Y |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,328,158 |
N1993S |
probably damaging |
Het |
Fbxw22 |
A |
G |
9: 109,383,962 |
S306P |
probably benign |
Het |
Ferd3l |
T |
C |
12: 33,928,652 |
S55P |
probably benign |
Het |
Fpr-rs3 |
A |
G |
17: 20,624,298 |
S194P |
possibly damaging |
Het |
Gm19965 |
G |
A |
1: 116,820,879 |
D97N |
probably benign |
Het |
Gtpbp2 |
A |
G |
17: 46,167,988 |
|
probably benign |
Het |
Hcn3 |
A |
C |
3: 89,159,845 |
I72S |
possibly damaging |
Het |
Hist1h3f |
G |
T |
13: 23,544,590 |
V36L |
probably benign |
Het |
Hk3 |
T |
A |
13: 55,014,465 |
N109Y |
probably damaging |
Het |
Iqub |
T |
C |
6: 24,505,738 |
E57G |
possibly damaging |
Het |
Kcnk3 |
T |
A |
5: 30,622,053 |
M149K |
possibly damaging |
Het |
Kcp |
C |
T |
6: 29,505,720 |
G51D |
probably benign |
Het |
Kif26a |
C |
A |
12: 112,146,829 |
A53D |
probably damaging |
Het |
Lifr |
T |
A |
15: 7,172,937 |
I353K |
probably benign |
Het |
Llph |
A |
T |
10: 120,231,284 |
N102I |
probably damaging |
Het |
Lmo3 |
C |
A |
6: 138,416,568 |
R18L |
possibly damaging |
Het |
Lrrc46 |
T |
C |
11: 97,035,545 |
E175G |
probably benign |
Het |
Ltk |
A |
T |
2: 119,754,594 |
C128* |
probably null |
Het |
Map1b |
T |
C |
13: 99,434,767 |
E482G |
probably damaging |
Het |
Mapk8ip2 |
T |
C |
15: 89,460,452 |
V740A |
probably damaging |
Het |
Miga2 |
T |
C |
2: 30,371,163 |
W157R |
probably benign |
Het |
Mlip |
A |
G |
9: 77,102,393 |
*837Q |
probably null |
Het |
Mroh2a |
G |
T |
1: 88,254,935 |
R1195L |
possibly damaging |
Het |
Myl1 |
T |
C |
1: 66,945,058 |
|
probably benign |
Het |
Olfr365 |
T |
C |
2: 37,202,177 |
L312P |
possibly damaging |
Het |
Olfr448 |
T |
C |
6: 42,896,816 |
Y122H |
probably benign |
Het |
Olfr613 |
A |
G |
7: 103,551,868 |
I28V |
probably benign |
Het |
P3h3 |
A |
T |
6: 124,857,368 |
V107D |
probably benign |
Het |
Papolb |
A |
T |
5: 142,528,896 |
S331T |
possibly damaging |
Het |
Pars2 |
T |
G |
4: 106,654,503 |
V494G |
probably benign |
Het |
Pcdhb3 |
C |
A |
18: 37,301,710 |
T243K |
probably benign |
Het |
Pde9a |
T |
A |
17: 31,470,724 |
M415K |
probably damaging |
Het |
Ppp1r9b |
G |
A |
11: 94,992,148 |
A201T |
probably benign |
Het |
Prl |
A |
G |
13: 27,064,959 |
N197S |
possibly damaging |
Het |
Prl2c1 |
T |
A |
13: 27,851,741 |
M32K |
probably benign |
Het |
Prrt4 |
T |
C |
6: 29,170,738 |
S572G |
possibly damaging |
Het |
Psd |
T |
A |
19: 46,322,419 |
D397V |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,945,480 |
Y213* |
probably null |
Het |
Ptcd3 |
T |
A |
6: 71,897,110 |
|
probably null |
Het |
Ptprk |
T |
G |
10: 28,334,484 |
F167L |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,616,944 |
V472A |
probably damaging |
Het |
Scnn1g |
T |
C |
7: 121,740,353 |
L125S |
probably damaging |
Het |
Sec16a |
T |
C |
2: 26,430,112 |
Y1438C |
probably damaging |
Het |
Serinc3 |
C |
T |
2: 163,634,446 |
S155N |
probably benign |
Het |
Slc3a2 |
A |
T |
19: 8,713,632 |
V78E |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 34,921,068 |
L23Q |
probably damaging |
Het |
Slco5a1 |
C |
T |
1: 12,881,196 |
|
probably benign |
Het |
Slit1 |
A |
G |
19: 41,616,715 |
M899T |
probably benign |
Het |
Sorl1 |
A |
G |
9: 42,022,392 |
I1094T |
probably benign |
Het |
Spag9 |
T |
A |
11: 94,081,370 |
L258Q |
probably benign |
Het |
Strip1 |
T |
C |
3: 107,618,936 |
E488G |
possibly damaging |
Het |
Stx18 |
G |
A |
5: 38,104,891 |
D30N |
possibly damaging |
Het |
Sync |
T |
C |
4: 129,287,790 |
|
probably null |
Het |
Syncrip |
A |
G |
9: 88,476,796 |
V220A |
probably damaging |
Het |
Tagln2 |
T |
C |
1: 172,505,909 |
I110T |
probably benign |
Het |
Taok1 |
T |
C |
11: 77,541,801 |
T729A |
probably benign |
Het |
Tgfbrap1 |
C |
T |
1: 43,067,599 |
V75I |
possibly damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,017,066 |
T24A |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,713,157 |
D2221E |
probably damaging |
Het |
Triml1 |
A |
G |
8: 43,130,566 |
S333P |
probably damaging |
Het |
Trp53bp1 |
C |
A |
2: 121,199,113 |
R1862L |
probably damaging |
Het |
Tsc22d1 |
T |
G |
14: 76,418,292 |
I737S |
possibly damaging |
Het |
U2af2 |
A |
T |
7: 5,079,274 |
K462N |
possibly damaging |
Het |
Ubap2 |
A |
C |
4: 41,233,631 |
N86K |
probably damaging |
Het |
Uso1 |
A |
G |
5: 92,195,348 |
K764E |
probably benign |
Het |
Vmn1r192 |
T |
A |
13: 22,187,952 |
M33L |
probably benign |
Het |
|