Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
C |
8: 24,651,786 |
K256E |
probably damaging |
Het |
Adam20 |
T |
A |
8: 40,796,558 |
H568Q |
probably benign |
Het |
Ambp |
A |
G |
4: 63,151,468 |
L107P |
probably damaging |
Het |
Art1 |
T |
C |
7: 102,107,334 |
F244S |
probably damaging |
Het |
Asxl2 |
C |
A |
12: 3,501,458 |
L1067I |
probably damaging |
Het |
Atm |
T |
C |
9: 53,459,823 |
T2242A |
probably benign |
Het |
Atp2c1 |
C |
T |
9: 105,421,573 |
|
probably null |
Het |
Bptf |
A |
G |
11: 107,043,791 |
Y2819H |
probably damaging |
Het |
Caskin1 |
G |
A |
17: 24,505,694 |
R1152H |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,866,432 |
L868Q |
probably damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,760,915 |
E178G |
unknown |
Het |
Dclk1 |
G |
T |
3: 55,487,307 |
R103S |
probably damaging |
Het |
Des |
A |
G |
1: 75,360,730 |
T105A |
probably damaging |
Het |
Ebf3 |
T |
C |
7: 137,225,884 |
T262A |
probably benign |
Het |
Epha4 |
A |
G |
1: 77,382,939 |
V759A |
probably damaging |
Het |
Fam192a |
C |
A |
8: 94,575,779 |
C208F |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,089,196 |
F1078I |
probably damaging |
Het |
Il20 |
T |
C |
1: 130,910,781 |
I60V |
probably benign |
Het |
Kif3c |
A |
T |
12: 3,365,981 |
M1L |
probably benign |
Het |
Lhfpl5 |
A |
T |
17: 28,576,037 |
I13F |
probably damaging |
Het |
Lin28b |
C |
T |
10: 45,381,228 |
G218E |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,482,353 |
N2530K |
possibly damaging |
Het |
Matn2 |
T |
A |
15: 34,316,605 |
F31Y |
possibly damaging |
Het |
Mcm6 |
T |
C |
1: 128,348,933 |
N307D |
probably benign |
Het |
Mmp16 |
A |
T |
4: 18,054,491 |
R332S |
probably benign |
Het |
Mpdz |
T |
A |
4: 81,369,592 |
T477S |
probably benign |
Het |
Mrpl47 |
T |
C |
3: 32,730,186 |
D145G |
probably damaging |
Het |
Myo6 |
T |
C |
9: 80,242,221 |
S150P |
probably damaging |
Het |
Naca |
C |
A |
10: 128,040,179 |
S360* |
probably null |
Het |
Olfr319 |
C |
T |
11: 58,702,087 |
P129S |
possibly damaging |
Het |
Phip |
C |
A |
9: 82,875,395 |
A1575S |
probably benign |
Het |
Plxna2 |
T |
C |
1: 194,644,556 |
M266T |
probably benign |
Het |
Ppp1r16a |
C |
T |
15: 76,693,669 |
Q328* |
probably null |
Het |
Prag1 |
T |
C |
8: 36,103,267 |
F335L |
probably benign |
Het |
Prmt2 |
A |
G |
10: 76,222,565 |
Y137H |
probably damaging |
Het |
Ptgds |
T |
C |
2: 25,467,345 |
D184G |
possibly damaging |
Het |
Ptpn5 |
T |
C |
7: 47,088,611 |
Y241C |
probably benign |
Het |
Pxdn |
G |
A |
12: 30,003,402 |
V1193M |
probably benign |
Het |
Raet1e |
T |
A |
10: 22,182,087 |
|
probably benign |
Het |
Rttn |
A |
G |
18: 88,983,810 |
D282G |
probably benign |
Het |
Sis |
G |
A |
3: 72,911,949 |
R1425* |
probably null |
Het |
Slco2a1 |
G |
T |
9: 103,082,383 |
M559I |
probably damaging |
Het |
Spata4 |
C |
T |
8: 54,600,844 |
A15V |
probably damaging |
Het |
Spop |
T |
C |
11: 95,470,627 |
S14P |
probably benign |
Het |
Tcof1 |
A |
T |
18: 60,835,850 |
D230E |
possibly damaging |
Het |
Thap8 |
T |
A |
7: 30,280,669 |
Y46* |
probably null |
Het |
Tmem55b |
T |
C |
14: 50,930,306 |
E54G |
probably damaging |
Het |
Tubgcp5 |
T |
A |
7: 55,806,055 |
L277* |
probably null |
Het |
Ubxn10 |
A |
T |
4: 138,720,570 |
V265E |
probably damaging |
Het |
Ugt2b36 |
T |
A |
5: 87,091,989 |
Y179F |
probably benign |
Het |
Wdr37 |
A |
C |
13: 8,835,252 |
|
probably null |
Het |
Zfp593 |
A |
G |
4: 134,244,913 |
V94A |
probably benign |
Het |
|