Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,862,763 (GRCm39) |
I240M |
probably benign |
Het |
Abcd3 |
A |
T |
3: 121,558,710 (GRCm39) |
D595E |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,025,614 (GRCm39) |
|
probably null |
Het |
Arpc1b |
A |
G |
5: 145,062,555 (GRCm39) |
D223G |
probably damaging |
Het |
Atp6ap1l |
T |
A |
13: 91,046,866 (GRCm39) |
T104S |
probably benign |
Het |
BC005537 |
T |
C |
13: 24,989,969 (GRCm39) |
|
probably null |
Het |
Ccdc9b |
T |
C |
2: 118,587,903 (GRCm39) |
D477G |
possibly damaging |
Het |
Chrdl2 |
T |
C |
7: 99,666,197 (GRCm39) |
V39A |
possibly damaging |
Het |
Clmp |
C |
G |
9: 40,693,737 (GRCm39) |
S318W |
probably damaging |
Het |
Cmas |
T |
C |
6: 142,717,853 (GRCm39) |
S323P |
probably damaging |
Het |
Cnksr3 |
T |
C |
10: 7,079,132 (GRCm39) |
T80A |
probably benign |
Het |
Ddx25 |
T |
C |
9: 35,453,298 (GRCm39) |
Y484C |
probably damaging |
Het |
Dennd6b |
A |
G |
15: 89,073,075 (GRCm39) |
V154A |
probably damaging |
Het |
Dmxl1 |
G |
A |
18: 49,990,316 (GRCm39) |
V252I |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,341,876 (GRCm39) |
Y3003C |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,370,480 (GRCm39) |
|
probably null |
Het |
Dppa4 |
G |
A |
16: 48,111,596 (GRCm39) |
A194T |
probably damaging |
Het |
Dst |
T |
C |
1: 34,228,527 (GRCm39) |
V2218A |
possibly damaging |
Het |
Dytn |
G |
C |
1: 63,673,032 (GRCm39) |
S457C |
probably damaging |
Het |
Fndc3a |
G |
A |
14: 72,777,768 (GRCm39) |
Q1101* |
probably null |
Het |
Focad |
A |
T |
4: 88,275,679 (GRCm39) |
|
probably null |
Het |
Gas2l2 |
T |
A |
11: 83,312,907 (GRCm39) |
T802S |
probably benign |
Het |
Gm5093 |
A |
G |
17: 46,750,622 (GRCm39) |
F135S |
probably benign |
Het |
Gmeb1 |
A |
T |
4: 131,969,759 (GRCm39) |
D71E |
possibly damaging |
Het |
Heatr5b |
G |
A |
17: 79,124,992 (GRCm39) |
R587C |
probably damaging |
Het |
Jakmip2 |
T |
C |
18: 43,692,279 (GRCm39) |
|
probably null |
Het |
Mier3 |
T |
A |
13: 111,841,778 (GRCm39) |
L111Q |
probably damaging |
Het |
Mrgprg |
G |
A |
7: 143,318,779 (GRCm39) |
S111F |
possibly damaging |
Het |
Mybl1 |
T |
C |
1: 9,741,901 (GRCm39) |
K677R |
probably benign |
Het |
Nhsl1 |
T |
C |
10: 18,407,323 (GRCm39) |
S1486P |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,642,114 (GRCm39) |
I783T |
probably benign |
Het |
Or10d4c |
A |
T |
9: 39,558,459 (GRCm39) |
T146S |
probably benign |
Het |
Or5an1c |
A |
T |
19: 12,218,956 (GRCm39) |
I23K |
probably benign |
Het |
Pigr |
A |
T |
1: 130,769,281 (GRCm39) |
I31L |
probably benign |
Het |
Plaat5 |
A |
G |
19: 7,616,999 (GRCm39) |
|
probably benign |
Het |
Pole2 |
G |
A |
12: 69,254,703 (GRCm39) |
L381F |
probably benign |
Het |
Pramel6 |
T |
A |
2: 87,338,917 (GRCm39) |
M39K |
possibly damaging |
Het |
Rapgef6 |
T |
A |
11: 54,530,553 (GRCm39) |
|
probably null |
Het |
Rinl |
T |
C |
7: 28,496,329 (GRCm39) |
C437R |
probably damaging |
Het |
Shank1 |
T |
C |
7: 43,965,499 (GRCm39) |
S192P |
unknown |
Het |
Slc2a10 |
A |
T |
2: 165,359,570 (GRCm39) |
Y478F |
probably damaging |
Het |
Slc37a3 |
A |
T |
6: 39,343,877 (GRCm39) |
L12H |
probably damaging |
Het |
Slit2 |
T |
A |
5: 48,414,393 (GRCm39) |
C970S |
possibly damaging |
Het |
Stard9 |
T |
C |
2: 120,496,857 (GRCm39) |
S119P |
probably damaging |
Het |
Stim2 |
C |
A |
5: 54,273,451 (GRCm39) |
D568E |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Traf3 |
A |
G |
12: 111,221,757 (GRCm39) |
E306G |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Ttll6 |
T |
C |
11: 96,049,714 (GRCm39) |
S811P |
possibly damaging |
Het |
Ubr7 |
A |
G |
12: 102,735,437 (GRCm39) |
K299E |
probably benign |
Het |
Urb1 |
C |
A |
16: 90,593,380 (GRCm39) |
V251L |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,422,590 (GRCm39) |
E183D |
probably damaging |
Het |
Zfp35 |
T |
G |
18: 24,136,557 (GRCm39) |
Y300* |
probably null |
Het |
Zfp414 |
C |
T |
17: 33,849,012 (GRCm39) |
T33I |
probably damaging |
Het |
|
Other mutations in Zfp938 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Zfp938
|
APN |
10 |
82,063,355 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00743:Zfp938
|
APN |
10 |
82,062,317 (GRCm39) |
missense |
probably benign |
|
IGL01764:Zfp938
|
APN |
10 |
82,063,624 (GRCm39) |
splice site |
probably benign |
|
IGL01814:Zfp938
|
APN |
10 |
82,062,052 (GRCm39) |
missense |
probably benign |
|
IGL02244:Zfp938
|
APN |
10 |
82,061,906 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02865:Zfp938
|
APN |
10 |
82,062,026 (GRCm39) |
missense |
probably benign |
0.33 |
R0372:Zfp938
|
UTSW |
10 |
82,063,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Zfp938
|
UTSW |
10 |
82,061,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Zfp938
|
UTSW |
10 |
82,061,253 (GRCm39) |
missense |
probably benign |
0.00 |
R1672:Zfp938
|
UTSW |
10 |
82,060,982 (GRCm39) |
missense |
probably benign |
|
R1929:Zfp938
|
UTSW |
10 |
82,061,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Zfp938
|
UTSW |
10 |
82,061,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Zfp938
|
UTSW |
10 |
82,061,876 (GRCm39) |
missense |
probably benign |
|
R2271:Zfp938
|
UTSW |
10 |
82,061,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Zfp938
|
UTSW |
10 |
82,061,340 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4502:Zfp938
|
UTSW |
10 |
82,062,105 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4503:Zfp938
|
UTSW |
10 |
82,062,105 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4886:Zfp938
|
UTSW |
10 |
82,061,957 (GRCm39) |
missense |
probably benign |
0.33 |
R4934:Zfp938
|
UTSW |
10 |
82,062,012 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5174:Zfp938
|
UTSW |
10 |
82,061,838 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5410:Zfp938
|
UTSW |
10 |
82,061,092 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6284:Zfp938
|
UTSW |
10 |
82,063,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6491:Zfp938
|
UTSW |
10 |
82,063,363 (GRCm39) |
makesense |
probably null |
|
R6575:Zfp938
|
UTSW |
10 |
82,061,160 (GRCm39) |
nonsense |
probably null |
|
R6649:Zfp938
|
UTSW |
10 |
82,061,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R7992:Zfp938
|
UTSW |
10 |
82,061,777 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8211:Zfp938
|
UTSW |
10 |
82,062,419 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8313:Zfp938
|
UTSW |
10 |
82,061,422 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8963:Zfp938
|
UTSW |
10 |
82,061,287 (GRCm39) |
missense |
possibly damaging |
0.61 |
X0066:Zfp938
|
UTSW |
10 |
82,061,931 (GRCm39) |
missense |
probably benign |
0.33 |
|