Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot2 |
A |
G |
12: 83,992,917 |
Y400C |
probably benign |
Het |
Agbl1 |
A |
G |
7: 76,409,332 |
M237V |
|
Het |
Arntl2 |
A |
G |
6: 146,806,442 |
T21A |
probably benign |
Het |
Atrnl1 |
C |
A |
19: 57,611,379 |
S9* |
probably null |
Het |
BC031181 |
A |
T |
18: 75,009,335 |
K71* |
probably null |
Het |
Brpf1 |
A |
T |
6: 113,314,874 |
M294L |
probably benign |
Het |
Camk2g |
T |
G |
14: 20,739,342 |
D382A |
possibly damaging |
Het |
Ccdc33 |
T |
A |
9: 58,118,465 |
R94W |
probably damaging |
Het |
Cd244 |
T |
A |
1: 171,577,255 |
L225Q |
probably damaging |
Het |
Chsy1 |
G |
T |
7: 66,171,030 |
V338F |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,362,450 |
I170V |
unknown |
Het |
Col6a2 |
G |
T |
10: 76,607,756 |
Q492K |
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,859,316 |
V3168L |
probably benign |
Het |
Fam206a |
A |
G |
4: 56,804,218 |
I78V |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,977,542 |
K1402E |
possibly damaging |
Het |
Ghdc |
C |
T |
11: 100,769,667 |
A127T |
probably benign |
Het |
Glp1r |
T |
C |
17: 30,930,598 |
|
probably null |
Het |
Gm15922 |
T |
C |
7: 3,739,282 |
E82G |
probably damaging |
Het |
Gm19410 |
A |
T |
8: 35,809,099 |
M1637L |
probably benign |
Het |
Gm906 |
T |
G |
13: 50,247,086 |
K401N |
probably benign |
Het |
Grm5 |
T |
G |
7: 88,130,251 |
D998E |
probably benign |
Het |
Krtcap3 |
A |
G |
5: 31,252,560 |
T157A |
probably damaging |
Het |
Luc7l2 |
A |
G |
6: 38,603,464 |
R333G |
unknown |
Het |
Mdc1 |
T |
G |
17: 35,850,881 |
S895R |
probably benign |
Het |
Mef2a |
G |
A |
7: 67,295,394 |
T80M |
probably damaging |
Het |
Mitd1 |
T |
A |
1: 37,885,275 |
I65F |
probably benign |
Het |
Mms19 |
A |
G |
19: 41,944,572 |
L1026P |
probably damaging |
Het |
Mtbp |
G |
T |
15: 55,609,526 |
V629L |
unknown |
Het |
Ncapd3 |
T |
A |
9: 27,055,505 |
I545N |
possibly damaging |
Het |
Nin |
G |
A |
12: 70,042,768 |
T1291M |
|
Het |
Olfr1487 |
A |
T |
19: 13,619,833 |
I181F |
probably damaging |
Het |
Olfr419 |
T |
A |
1: 174,250,218 |
K236N |
probably damaging |
Het |
Orc3 |
G |
T |
4: 34,587,032 |
C352* |
probably null |
Het |
Oxct2b |
G |
A |
4: 123,117,757 |
G490D |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,479,405 |
T473S |
probably benign |
Het |
Phkg2 |
G |
A |
7: 127,582,902 |
G365D |
probably damaging |
Het |
Ppp2r3a |
A |
T |
9: 101,211,712 |
F471I |
probably benign |
Het |
Prl3d1 |
T |
C |
13: 27,100,035 |
C196R |
possibly damaging |
Het |
Prmt1 |
A |
T |
7: 44,984,128 |
F14L |
probably benign |
Het |
Prox1 |
A |
G |
1: 190,162,221 |
L9P |
probably damaging |
Het |
Ptpn13 |
T |
A |
5: 103,540,983 |
F881I |
probably benign |
Het |
Rab3ip |
A |
G |
10: 116,914,139 |
I363T |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,761,209 |
E134G |
probably damaging |
Het |
Rapgef6 |
C |
T |
11: 54,694,453 |
P1559L |
probably benign |
Het |
Rnf180 |
T |
C |
13: 105,167,588 |
K507E |
probably damaging |
Het |
Rpl3l |
T |
C |
17: 24,730,986 |
I53T |
probably benign |
Het |
Rtl1 |
T |
C |
12: 109,591,008 |
I1466V |
unknown |
Het |
Saxo2 |
A |
G |
7: 82,635,351 |
Y100H |
probably damaging |
Het |
Selenoh |
G |
T |
2: 84,670,380 |
R39S |
probably damaging |
Het |
Sgsm2 |
A |
G |
11: 74,865,497 |
V342A |
probably damaging |
Het |
Slc26a9 |
T |
A |
1: 131,763,244 |
F587I |
possibly damaging |
Het |
Smoc1 |
A |
T |
12: 81,105,908 |
Q91L |
possibly damaging |
Het |
Spag9 |
A |
C |
11: 93,996,563 |
H98P |
possibly damaging |
Het |
T2 |
T |
A |
17: 8,418,215 |
C337* |
probably null |
Het |
Tbc1d19 |
A |
G |
5: 53,897,035 |
Y455C |
probably damaging |
Het |
Thbd |
A |
G |
2: 148,407,420 |
L176P |
probably damaging |
Het |
Tmem116 |
A |
G |
5: 121,452,189 |
|
probably null |
Het |
Tmem25 |
C |
T |
9: 44,798,343 |
V54I |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 45,321,809 |
V378I |
probably benign |
Het |
Trrap |
G |
T |
5: 144,842,612 |
W3129C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,728,316 |
D29740E |
probably damaging |
Het |
Vcan |
C |
T |
13: 89,685,114 |
C3073Y |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,910,982 |
D388E |
probably benign |
Het |
|