Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
G |
10: 28,986,237 |
V19A |
probably benign |
Het |
3632451O06Rik |
T |
C |
14: 49,768,410 |
|
probably null |
Het |
4931409K22Rik |
C |
A |
5: 24,552,688 |
R177L |
probably damaging |
Het |
6820408C15Rik |
T |
C |
2: 152,440,854 |
Y210H |
probably damaging |
Het |
Aars |
T |
A |
8: 111,043,250 |
I327N |
possibly damaging |
Het |
Abca6 |
T |
A |
11: 110,218,281 |
N688Y |
possibly damaging |
Het |
Ablim3 |
T |
C |
18: 61,814,311 |
K457R |
probably benign |
Het |
Acsm2 |
A |
T |
7: 119,563,637 |
N45Y |
probably damaging |
Het |
Agxt2 |
T |
C |
15: 10,373,831 |
S108P |
probably damaging |
Het |
Akr1cl |
A |
T |
1: 65,021,429 |
M174K |
probably benign |
Het |
Bfsp1 |
G |
A |
2: 143,841,763 |
R214W |
probably damaging |
Het |
Cby3 |
A |
G |
11: 50,359,516 |
D183G |
probably damaging |
Het |
Clip2 |
T |
C |
5: 134,503,253 |
D566G |
possibly damaging |
Het |
Colgalt1 |
A |
G |
8: 71,620,757 |
I341V |
probably benign |
Het |
Cyp2c38 |
T |
A |
19: 39,401,709 |
D349V |
probably damaging |
Het |
Degs2 |
C |
T |
12: 108,692,192 |
C176Y |
probably benign |
Het |
Dhx16 |
A |
T |
17: 35,891,065 |
T995S |
probably damaging |
Het |
Dicer1 |
A |
T |
12: 104,713,156 |
C521S |
probably damaging |
Het |
Dopey2 |
T |
C |
16: 93,762,315 |
S532P |
probably benign |
Het |
Dpysl4 |
T |
G |
7: 139,090,338 |
M124R |
probably damaging |
Het |
Eml6 |
A |
G |
11: 29,777,001 |
|
probably null |
Het |
Erbb4 |
A |
T |
1: 68,331,234 |
V395D |
probably damaging |
Het |
Esf1 |
T |
C |
2: 140,158,486 |
D460G |
possibly damaging |
Het |
F830045P16Rik |
G |
A |
2: 129,463,714 |
H247Y |
probably benign |
Het |
Fsbp |
T |
A |
4: 11,583,965 |
S221R |
probably benign |
Het |
Fstl5 |
T |
A |
3: 76,410,622 |
N198K |
possibly damaging |
Het |
Gemin5 |
G |
T |
11: 58,139,080 |
H855Q |
probably damaging |
Het |
Gjd3 |
T |
C |
11: 98,982,709 |
E103G |
probably benign |
Het |
I0C0044D17Rik |
A |
G |
4: 98,820,234 |
|
probably benign |
Het |
Itgb4 |
A |
T |
11: 116,007,357 |
R1646W |
probably damaging |
Het |
Klri2 |
A |
T |
6: 129,738,874 |
C121S |
probably benign |
Het |
Lamc3 |
A |
G |
2: 31,915,996 |
Y703C |
probably damaging |
Het |
Lrrc10 |
A |
G |
10: 117,045,883 |
N154S |
probably damaging |
Het |
Lrriq1 |
A |
G |
10: 103,214,456 |
F812L |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,161,981 |
A516T |
possibly damaging |
Het |
Nav1 |
T |
C |
1: 135,452,272 |
Y1564C |
probably damaging |
Het |
Ndufc1 |
T |
C |
3: 51,408,243 |
T25A |
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,903,659 |
M23V |
probably benign |
Het |
Nnt |
A |
G |
13: 119,404,550 |
|
probably null |
Het |
Nolc1 |
G |
C |
19: 46,079,022 |
|
probably null |
Het |
Nrg1 |
A |
T |
8: 31,824,508 |
M289K |
probably benign |
Het |
Oas3 |
G |
T |
5: 120,777,574 |
H17Q |
possibly damaging |
Het |
Olfr1030 |
A |
G |
2: 85,983,857 |
K6E |
probably benign |
Het |
Olfr239 |
A |
G |
17: 33,199,456 |
Y132C |
probably damaging |
Het |
Olfr30 |
A |
G |
11: 58,455,838 |
I37T |
probably benign |
Het |
Olfr957 |
C |
T |
9: 39,511,354 |
R122H |
possibly damaging |
Het |
Parp9 |
T |
C |
16: 35,967,697 |
Y612H |
probably benign |
Het |
Pcdh1 |
A |
T |
18: 38,199,230 |
M240K |
possibly damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,400,934 |
|
probably benign |
Het |
Plpp2 |
A |
G |
10: 79,530,684 |
V42A |
probably damaging |
Het |
Ppic |
C |
T |
18: 53,407,062 |
V172M |
probably damaging |
Het |
Ppp1r9b |
A |
G |
11: 95,001,324 |
|
silent |
Het |
Prop1 |
A |
G |
11: 50,953,325 |
V27A |
possibly damaging |
Het |
Psmc5 |
A |
G |
11: 106,262,416 |
T295A |
probably benign |
Het |
Rpa1 |
A |
G |
11: 75,312,691 |
|
probably null |
Het |
Rrp12 |
A |
G |
19: 41,871,737 |
F1016L |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,683,697 |
I242F |
probably damaging |
Het |
Slco1a6 |
T |
A |
6: 142,086,434 |
H655L |
probably benign |
Het |
Sp140 |
G |
A |
1: 85,610,824 |
|
probably null |
Het |
Syne1 |
A |
G |
10: 5,348,694 |
I1071T |
possibly damaging |
Het |
Tbc1d9b |
A |
G |
11: 50,149,832 |
D392G |
probably damaging |
Het |
Tcaim |
G |
A |
9: 122,818,773 |
|
probably null |
Het |
Tgm3 |
T |
A |
2: 130,047,782 |
V632E |
probably damaging |
Het |
Triobp |
C |
A |
15: 79,002,148 |
R1830S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,811,243 |
L5176Q |
possibly damaging |
Het |
Vps8 |
A |
G |
16: 21,581,579 |
T1266A |
probably benign |
Het |
Znfx1 |
T |
C |
2: 167,039,010 |
I285V |
possibly damaging |
Het |
|