Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
T |
7: 40,993,521 |
I296F |
possibly damaging |
Het |
Adamts19 |
C |
T |
18: 58,837,512 |
T56M |
possibly damaging |
Het |
Armc4 |
T |
C |
18: 7,217,965 |
N583S |
probably benign |
Het |
Axdnd1 |
T |
G |
1: 156,341,889 |
E802D |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,631,053 |
V2630A |
probably benign |
Het |
Capn5 |
A |
T |
7: 98,131,195 |
F323I |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,191,759 |
E206G |
probably damaging |
Het |
Cmah |
T |
G |
13: 24,456,915 |
N382K |
probably benign |
Het |
Col11a1 |
A |
T |
3: 114,131,593 |
D25V |
probably damaging |
Het |
Cyp2d41-ps |
G |
T |
15: 82,779,220 |
|
noncoding transcript |
Het |
Cyp3a59 |
A |
G |
5: 146,099,851 |
K288E |
possibly damaging |
Het |
Cyr61 |
T |
C |
3: 145,648,658 |
D166G |
probably benign |
Het |
Dclre1a |
A |
C |
19: 56,529,590 |
I1019S |
probably damaging |
Het |
Fat2 |
G |
T |
11: 55,262,325 |
A3687D |
possibly damaging |
Het |
Flg2 |
T |
A |
3: 93,203,497 |
V944E |
unknown |
Het |
Galntl5 |
T |
C |
5: 25,198,463 |
V177A |
possibly damaging |
Het |
Gm14295 |
A |
T |
2: 176,811,014 |
N766Y |
probably benign |
Het |
Gm15433 |
T |
A |
1: 84,964,112 |
|
noncoding transcript |
Het |
Gm2431 |
C |
T |
7: 142,258,332 |
G8E |
unknown |
Het |
Gm5435 |
T |
A |
12: 82,495,426 |
|
noncoding transcript |
Het |
Gprc5c |
G |
T |
11: 114,864,267 |
V257L |
possibly damaging |
Het |
Grip1 |
T |
C |
10: 119,985,480 |
I350T |
probably benign |
Het |
Guf1 |
T |
A |
5: 69,560,486 |
F196I |
probably damaging |
Het |
Kcng4 |
G |
T |
8: 119,626,279 |
D297E |
probably damaging |
Het |
Khdrbs2 |
G |
A |
1: 32,472,692 |
R246Q |
probably damaging |
Het |
Layn |
T |
C |
9: 51,068,161 |
E148G |
probably damaging |
Het |
Lrig3 |
T |
A |
10: 126,009,919 |
V739E |
probably damaging |
Het |
Lyg1 |
A |
G |
1: 37,947,267 |
W129R |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,199,857 |
T1567I |
probably damaging |
Het |
Nus1 |
T |
A |
10: 52,429,256 |
L12* |
probably null |
Het |
Olfr2 |
A |
T |
7: 107,001,443 |
V139D |
possibly damaging |
Het |
Olfr354 |
A |
G |
2: 36,907,101 |
I52V |
probably benign |
Het |
Otop1 |
A |
G |
5: 38,297,916 |
N218S |
probably benign |
Het |
Pcif1 |
T |
A |
2: 164,885,379 |
N90K |
probably damaging |
Het |
Phf2 |
T |
C |
13: 48,820,042 |
|
probably null |
Het |
Piezo2 |
T |
A |
18: 63,146,856 |
I215F |
probably damaging |
Het |
Pitpnm2 |
G |
T |
5: 124,130,321 |
C553* |
probably null |
Het |
Prdm1 |
A |
G |
10: 44,450,228 |
V115A |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,816,752 |
D3587G |
probably damaging |
Het |
Sez6l |
A |
T |
5: 112,422,024 |
Y883* |
probably null |
Het |
Sh3rf2 |
A |
C |
18: 42,111,138 |
H223P |
probably damaging |
Het |
Slco1a5 |
C |
T |
6: 142,242,113 |
C500Y |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,066,737 |
H610L |
probably benign |
Het |
Syn3 |
T |
C |
10: 86,294,628 |
*244W |
probably null |
Het |
Sytl2 |
A |
T |
7: 90,375,689 |
D295V |
probably damaging |
Het |
Tnfrsf1a |
T |
A |
6: 125,358,077 |
C44S |
probably damaging |
Het |
Ttc6 |
T |
G |
12: 57,673,204 |
L854V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,766,258 |
I18358V |
probably benign |
Het |
Vmn2r108 |
A |
G |
17: 20,463,136 |
V602A |
probably damaging |
Het |
Zap70 |
A |
G |
1: 36,779,009 |
|
probably benign |
Het |
Zfhx2 |
T |
C |
14: 55,066,846 |
E1227G |
possibly damaging |
Het |
Znhit3 |
G |
A |
11: 84,916,084 |
|
probably null |
Het |
Zpbp2 |
A |
G |
11: 98,551,410 |
|
probably benign |
Het |
|