Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,660,352 |
S1219P |
possibly damaging |
Het |
A2ml1 |
A |
G |
6: 128,561,526 |
Y644H |
probably damaging |
Het |
Abca9 |
T |
G |
11: 110,117,076 |
R1232S |
possibly damaging |
Het |
Acsf2 |
C |
T |
11: 94,573,149 |
V70M |
probably benign |
Het |
Ampd1 |
A |
G |
3: 103,079,130 |
I42V |
probably benign |
Het |
Arhgap10 |
A |
G |
8: 77,344,638 |
|
probably null |
Het |
Atp1a4 |
A |
T |
1: 172,244,408 |
L432Q |
probably damaging |
Het |
Bbs12 |
T |
A |
3: 37,320,449 |
C349S |
possibly damaging |
Het |
Bnc2 |
A |
G |
4: 84,292,770 |
V479A |
possibly damaging |
Het |
C130060K24Rik |
A |
G |
6: 65,441,385 |
|
probably benign |
Het |
Cald1 |
A |
T |
6: 34,771,108 |
K761* |
probably null |
Het |
Cd177 |
C |
T |
7: 24,752,263 |
G443R |
probably null |
Het |
Cdc42bpb |
T |
C |
12: 111,325,976 |
D375G |
probably damaging |
Het |
Chsy3 |
T |
C |
18: 59,176,196 |
Y174H |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,531,926 |
S782N |
unknown |
Het |
Crtac1 |
C |
T |
19: 42,309,190 |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,582,527 |
D3683V |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,845,043 |
L62P |
probably damaging |
Het |
Cyp3a57 |
A |
T |
5: 145,371,057 |
K208* |
probably null |
Het |
Dnaaf2 |
A |
T |
12: 69,197,348 |
L313Q |
probably damaging |
Het |
Dtl |
A |
G |
1: 191,546,568 |
L394P |
probably benign |
Het |
Ehhadh |
T |
C |
16: 21,766,555 |
E192G |
probably benign |
Het |
Fads2 |
T |
C |
19: 10,082,633 |
I226V |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,270,382 |
E3174G |
probably damaging |
Het |
Galnt14 |
C |
T |
17: 73,574,831 |
R91Q |
probably damaging |
Het |
Hdhd5 |
G |
T |
6: 120,510,291 |
D368E |
probably benign |
Het |
Hk3 |
T |
A |
13: 55,010,804 |
I528F |
probably damaging |
Het |
Hrasls |
T |
A |
16: 29,220,437 |
Y90N |
probably benign |
Het |
Il10ra |
A |
C |
9: 45,255,653 |
S533R |
possibly damaging |
Het |
Itpr3 |
G |
T |
17: 27,086,976 |
K169N |
probably benign |
Het |
Lrrc17 |
A |
G |
5: 21,575,266 |
T413A |
probably benign |
Het |
Mcm2 |
C |
T |
6: 88,884,071 |
D882N |
probably benign |
Het |
Met |
T |
C |
6: 17,562,198 |
V1186A |
probably damaging |
Het |
Msh5 |
C |
T |
17: 35,029,652 |
|
probably null |
Het |
Nav3 |
T |
C |
10: 109,764,787 |
I1326M |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,850,896 |
I314V |
probably benign |
Het |
Olfr1510 |
A |
C |
14: 52,410,768 |
F35V |
probably damaging |
Het |
Olfr920 |
T |
A |
9: 38,756,116 |
Y143N |
probably benign |
Het |
Pim1 |
A |
G |
17: 29,493,746 |
E211G |
probably damaging |
Het |
Ppp1r12b |
A |
T |
1: 134,776,406 |
D903E |
probably benign |
Het |
Ptpn14 |
T |
C |
1: 189,851,032 |
L692P |
probably benign |
Het |
Ptprt |
A |
G |
2: 162,135,218 |
C387R |
probably damaging |
Het |
Scarb1 |
A |
G |
5: 125,304,277 |
Y68H |
possibly damaging |
Het |
Shisa6 |
T |
A |
11: 66,217,974 |
D359V |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,188,073 |
S1297P |
probably damaging |
Het |
Sik1 |
T |
C |
17: 31,850,151 |
D250G |
probably damaging |
Het |
Slamf7 |
A |
G |
1: 171,639,067 |
L190S |
probably damaging |
Het |
Slc22a3 |
G |
A |
17: 12,433,468 |
P423L |
probably damaging |
Het |
Slc35e2 |
A |
T |
4: 155,612,680 |
E217V |
probably damaging |
Het |
Spocd1 |
A |
T |
4: 129,956,461 |
N760I |
probably damaging |
Het |
Tas2r136 |
G |
T |
6: 132,777,331 |
P278T |
possibly damaging |
Het |
Tchhl1 |
A |
T |
3: 93,470,529 |
Q180L |
probably benign |
Het |
Tmem151b |
T |
A |
17: 45,547,084 |
T79S |
probably benign |
Het |
Tomm70a |
T |
A |
16: 57,144,742 |
C430S |
probably benign |
Het |
Trbv16 |
T |
A |
6: 41,152,002 |
L40Q |
probably damaging |
Het |
Trmt1l |
T |
G |
1: 151,440,843 |
I32S |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,425,330 |
T2011A |
probably damaging |
Het |
Urb1 |
C |
T |
16: 90,772,764 |
W1358* |
probably null |
Het |
Usp31 |
T |
G |
7: 121,649,475 |
H915P |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,003,511 |
M79K |
possibly damaging |
Het |
Vmn2r14 |
A |
G |
5: 109,221,356 |
I117T |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,869,351 |
H2667R |
possibly damaging |
Het |
Vwa5b1 |
G |
A |
4: 138,578,651 |
T912M |
possibly damaging |
Het |
Zfp709 |
G |
A |
8: 71,889,519 |
C264Y |
probably benign |
Het |
Zkscan5 |
A |
G |
5: 145,220,088 |
I467V |
probably benign |
Het |
Zxdc |
A |
T |
6: 90,370,299 |
D214V |
probably damaging |
Het |
|