Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
G |
T |
6: 128,557,582 |
N837K |
possibly damaging |
Het |
Adam29 |
A |
T |
8: 55,872,161 |
C419* |
probably null |
Het |
Adamts7 |
C |
A |
9: 90,185,795 |
S446* |
probably null |
Het |
Ager |
A |
G |
17: 34,600,620 |
R371G |
probably damaging |
Het |
Apobr |
T |
A |
7: 126,586,457 |
V380E |
possibly damaging |
Het |
Arhgap26 |
T |
C |
18: 39,246,845 |
S105P |
|
Het |
Atrip |
A |
G |
9: 109,073,838 |
F56S |
probably damaging |
Het |
Bag2 |
T |
C |
1: 33,746,824 |
Y139C |
|
Het |
Bccip |
C |
T |
7: 133,717,617 |
Q146* |
probably null |
Het |
Btbd10 |
G |
A |
7: 113,351,824 |
R20W |
possibly damaging |
Het |
Catsperd |
T |
A |
17: 56,655,156 |
N443K |
probably damaging |
Het |
Cdh26 |
G |
A |
2: 178,462,616 |
E265K |
probably benign |
Het |
Cep76 |
T |
C |
18: 67,634,815 |
R216G |
probably damaging |
Het |
Cnot1 |
T |
A |
8: 95,749,032 |
M1000L |
probably benign |
Het |
Cyp1a1 |
A |
G |
9: 57,702,787 |
T495A |
possibly damaging |
Het |
Cyp2w1 |
T |
A |
5: 139,356,715 |
M421K |
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,149,478 |
T1453A |
probably benign |
Het |
Dnah5 |
G |
T |
15: 28,409,266 |
W3610L |
probably damaging |
Het |
Dnajc10 |
G |
A |
2: 80,349,293 |
G724R |
probably damaging |
Het |
Dst |
T |
A |
1: 34,188,504 |
I1726N |
possibly damaging |
Het |
Dync2h1 |
A |
T |
9: 7,139,462 |
L1391* |
probably null |
Het |
Dzank1 |
T |
C |
2: 144,476,092 |
S718G |
probably benign |
Het |
E230025N22Rik |
T |
C |
18: 36,686,837 |
D300G |
probably damaging |
Het |
Ebf3 |
T |
C |
7: 137,312,369 |
I131V |
possibly damaging |
Het |
Eif3g |
T |
C |
9: 20,896,130 |
I131V |
probably benign |
Het |
Eppk1 |
T |
A |
15: 76,106,303 |
Q2126L |
possibly damaging |
Het |
Fam83h |
T |
C |
15: 76,002,333 |
R1052G |
probably benign |
Het |
Fry |
A |
T |
5: 150,295,808 |
|
probably benign |
Het |
Ggt6 |
C |
T |
11: 72,437,297 |
H208Y |
possibly damaging |
Het |
Gm15821 |
T |
A |
17: 34,214,261 |
E28V |
unknown |
Het |
Gprin2 |
T |
C |
14: 34,195,000 |
Q271R |
probably damaging |
Het |
Gsdmd |
T |
C |
15: 75,867,204 |
F477L |
probably benign |
Het |
Hes7 |
T |
C |
11: 69,122,956 |
S214P |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,457,955 |
H4871R |
possibly damaging |
Het |
Il15ra |
G |
A |
2: 11,718,422 |
V86I |
possibly damaging |
Het |
Il17rb |
C |
A |
14: 30,002,900 |
|
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,118,677 |
|
probably benign |
Het |
Kcnab2 |
T |
C |
4: 152,407,178 |
Y63C |
probably damaging |
Het |
Kctd17 |
A |
T |
15: 78,430,082 |
Y84F |
probably damaging |
Het |
Lama1 |
T |
A |
17: 67,812,496 |
V2656E |
|
Het |
Lama2 |
T |
C |
10: 26,984,371 |
N3040S |
probably benign |
Het |
Ldha |
C |
T |
7: 46,851,009 |
R173C |
unknown |
Het |
Lig1 |
A |
G |
7: 13,303,820 |
I665M |
probably damaging |
Het |
Lipe |
G |
A |
7: 25,384,498 |
A412V |
probably damaging |
Het |
Lrrc63 |
T |
C |
14: 75,084,844 |
T607A |
probably benign |
Het |
Majin |
G |
A |
19: 6,213,397 |
|
probably null |
Het |
Map3k19 |
A |
G |
1: 127,830,438 |
L335P |
probably benign |
Het |
Map3k9 |
A |
G |
12: 81,772,733 |
L249P |
probably damaging |
Het |
Mb21d1 |
C |
A |
9: 78,442,505 |
V192L |
probably benign |
Het |
Muc5b |
G |
T |
7: 141,872,472 |
D4769Y |
probably damaging |
Het |
Myh9 |
T |
C |
15: 77,768,992 |
T1382A |
probably benign |
Het |
Nedd4l |
T |
A |
18: 65,178,924 |
D407E |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,422,383 |
I160V |
possibly damaging |
Het |
Nmrk1 |
A |
G |
19: 18,639,792 |
|
probably benign |
Het |
Nnmt |
C |
A |
9: 48,592,161 |
K188N |
probably damaging |
Het |
Nup153 |
T |
A |
13: 46,684,233 |
Q1171L |
probably benign |
Het |
Olfr1012 |
T |
G |
2: 85,759,535 |
L280F |
possibly damaging |
Het |
Oplah |
T |
A |
15: 76,303,217 |
E556V |
probably benign |
Het |
Otog |
A |
G |
7: 46,288,096 |
D1743G |
probably benign |
Het |
Otogl |
T |
C |
10: 107,777,571 |
Y2011C |
probably damaging |
Het |
Pbx4 |
C |
T |
8: 69,864,447 |
P118L |
probably benign |
Het |
Plekha6 |
T |
A |
1: 133,285,261 |
S757T |
probably benign |
Het |
Plk5 |
C |
G |
10: 80,357,996 |
R40G |
probably damaging |
Het |
Polr3a |
C |
T |
14: 24,469,411 |
S643N |
probably damaging |
Het |
Pwp1 |
T |
A |
10: 85,882,881 |
L304Q |
probably damaging |
Het |
Qrich2 |
GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG |
GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG |
11: 116,457,541 |
|
probably benign |
Het |
Rab11fip1 |
A |
G |
8: 27,154,708 |
F350L |
probably benign |
Het |
Safb2 |
T |
C |
17: 56,566,614 |
E683G |
probably damaging |
Het |
Scarb1 |
A |
T |
5: 125,304,350 |
N43K |
probably damaging |
Het |
Serpina3k |
A |
G |
12: 104,340,971 |
E154G |
probably damaging |
Het |
Sgsm3 |
T |
A |
15: 81,007,981 |
V250D |
probably damaging |
Het |
Slit1 |
T |
A |
19: 41,624,529 |
I851F |
probably benign |
Het |
Spag4 |
G |
A |
2: 156,068,504 |
G350E |
probably damaging |
Het |
Sult2a7 |
A |
T |
7: 14,491,830 |
L77Q |
probably damaging |
Het |
Tbc1d2 |
T |
A |
4: 46,607,062 |
T783S |
probably damaging |
Het |
Thoc6 |
T |
C |
17: 23,669,888 |
E182G |
|
Het |
Tmem132a |
A |
T |
19: 10,860,161 |
I595N |
probably damaging |
Het |
Trim69 |
A |
G |
2: 122,173,290 |
N240S |
probably benign |
Het |
Ush1c |
A |
T |
7: 46,197,190 |
|
probably benign |
Het |
Wnk4 |
T |
G |
11: 101,262,815 |
Y234* |
probably null |
Het |
Zfp943 |
A |
G |
17: 21,992,340 |
N136D |
possibly damaging |
Het |
Znhit2 |
G |
A |
19: 6,061,639 |
R138H |
possibly damaging |
Het |
|