Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,622,212 (GRCm39) |
V372F |
probably benign |
Het |
Adcy10 |
G |
A |
1: 165,347,464 (GRCm39) |
C393Y |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,669 (GRCm39) |
I681S |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,540,485 (GRCm39) |
|
probably benign |
Het |
Akr1a1 |
A |
T |
4: 116,497,092 (GRCm39) |
V156E |
probably damaging |
Het |
Alk |
T |
G |
17: 72,202,734 (GRCm39) |
D1167A |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,620,453 (GRCm39) |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,385,221 (GRCm39) |
N288K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,398,133 (GRCm39) |
|
probably null |
Het |
Asxl2 |
G |
A |
12: 3,524,618 (GRCm39) |
|
probably null |
Het |
Atp6v0a1 |
A |
G |
11: 100,946,413 (GRCm39) |
H802R |
probably damaging |
Het |
B4galnt1 |
A |
G |
10: 127,007,691 (GRCm39) |
T531A |
possibly damaging |
Het |
Cecr2 |
A |
G |
6: 120,733,530 (GRCm39) |
N506D |
possibly damaging |
Het |
Crebrf |
T |
C |
17: 26,978,839 (GRCm39) |
V509A |
probably damaging |
Het |
Cyp4f40 |
A |
T |
17: 32,894,590 (GRCm39) |
I413F |
probably null |
Het |
Defb12 |
C |
A |
8: 19,164,342 (GRCm39) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,312,674 (GRCm39) |
E4297G |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,775,038 (GRCm39) |
T207N |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,565,783 (GRCm39) |
Q416* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,536,222 (GRCm39) |
L284P |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,287,739 (GRCm39) |
I595F |
probably benign |
Het |
Gm9920 |
A |
G |
15: 54,972,371 (GRCm39) |
|
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,981,084 (GRCm39) |
K783E |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,055,277 (GRCm39) |
S1052P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 58,002,252 (GRCm39) |
I192V |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,586,803 (GRCm39) |
D722G |
probably damaging |
Het |
Lepr |
T |
C |
4: 101,672,216 (GRCm39) |
V1080A |
possibly damaging |
Het |
Lpin1 |
C |
T |
12: 16,613,656 (GRCm39) |
G504S |
probably damaging |
Het |
Lrit2 |
A |
C |
14: 36,791,140 (GRCm39) |
Q273P |
possibly damaging |
Het |
Mlkl |
T |
A |
8: 112,054,569 (GRCm39) |
E189D |
probably benign |
Het |
Mttp |
C |
T |
3: 137,810,790 (GRCm39) |
R608H |
probably benign |
Het |
Nav2 |
T |
C |
7: 49,238,908 (GRCm39) |
V2011A |
probably benign |
Het |
Nos2 |
A |
T |
11: 78,848,317 (GRCm39) |
I1075F |
probably benign |
Het |
Npat |
A |
G |
9: 53,461,336 (GRCm39) |
|
probably null |
Het |
Nucks1 |
T |
C |
1: 131,846,771 (GRCm39) |
F16L |
probably damaging |
Het |
Nus1 |
T |
C |
10: 52,305,309 (GRCm39) |
S150P |
possibly damaging |
Het |
Odad1 |
C |
T |
7: 45,591,506 (GRCm39) |
R257* |
probably null |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or4c123 |
G |
T |
2: 89,127,506 (GRCm39) |
T36K |
probably damaging |
Het |
Or8b35 |
A |
T |
9: 37,903,908 (GRCm39) |
Y40F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,731,367 (GRCm39) |
T3290A |
unknown |
Het |
Pign |
A |
T |
1: 105,585,537 (GRCm39) |
F4Y |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,696,406 (GRCm39) |
N233D |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,397,652 (GRCm39) |
M1325L |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scaf11 |
T |
A |
15: 96,315,001 (GRCm39) |
H1227L |
possibly damaging |
Het |
Sec31b |
G |
T |
19: 44,507,076 (GRCm39) |
P840T |
probably damaging |
Het |
Slc16a9 |
T |
A |
10: 70,118,958 (GRCm39) |
L426I |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc34a1 |
T |
C |
13: 23,996,575 (GRCm39) |
S27P |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,299 (GRCm39) |
S310P |
possibly damaging |
Het |
Tmem245 |
G |
A |
4: 56,947,084 (GRCm39) |
R110C |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,735,152 (GRCm39) |
Y953C |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,684,775 (GRCm39) |
|
probably null |
Het |
Ush2a |
G |
A |
1: 188,644,320 (GRCm39) |
V4561I |
probably benign |
Het |
Vmn1r192 |
C |
T |
13: 22,371,801 (GRCm39) |
V140I |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,656,026 (GRCm39) |
I330N |
probably damaging |
Het |
Vmn2r99 |
T |
C |
17: 19,599,531 (GRCm39) |
V405A |
probably damaging |
Het |
Wdhd1 |
A |
C |
14: 47,509,678 (GRCm39) |
V172G |
probably benign |
Het |
Zfhx3 |
C |
T |
8: 109,677,817 (GRCm39) |
R2956C |
possibly damaging |
Het |
Zfp446 |
T |
C |
7: 12,716,178 (GRCm39) |
L283P |
possibly damaging |
Het |
Zfp82 |
T |
C |
7: 29,756,591 (GRCm39) |
K164E |
probably damaging |
Het |
|
Other mutations in Dpysl5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02177:Dpysl5
|
APN |
5 |
30,902,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Dpysl5
|
APN |
5 |
30,946,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Dpysl5
|
UTSW |
5 |
30,935,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R0788:Dpysl5
|
UTSW |
5 |
30,946,185 (GRCm39) |
critical splice donor site |
probably null |
|
R1716:Dpysl5
|
UTSW |
5 |
30,935,338 (GRCm39) |
missense |
probably benign |
0.00 |
R2016:Dpysl5
|
UTSW |
5 |
30,948,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Dpysl5
|
UTSW |
5 |
30,948,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Dpysl5
|
UTSW |
5 |
30,948,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R2965:Dpysl5
|
UTSW |
5 |
30,948,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4440:Dpysl5
|
UTSW |
5 |
30,949,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R4863:Dpysl5
|
UTSW |
5 |
30,941,687 (GRCm39) |
missense |
probably benign |
0.08 |
R4918:Dpysl5
|
UTSW |
5 |
30,949,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R6379:Dpysl5
|
UTSW |
5 |
30,935,317 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6621:Dpysl5
|
UTSW |
5 |
30,941,813 (GRCm39) |
critical splice donor site |
probably null |
|
R7199:Dpysl5
|
UTSW |
5 |
30,940,539 (GRCm39) |
missense |
probably benign |
0.21 |
R7232:Dpysl5
|
UTSW |
5 |
30,949,642 (GRCm39) |
missense |
probably benign |
0.03 |
R7388:Dpysl5
|
UTSW |
5 |
30,902,805 (GRCm39) |
missense |
probably benign |
|
R7446:Dpysl5
|
UTSW |
5 |
30,936,231 (GRCm39) |
missense |
probably benign |
0.00 |
R7868:Dpysl5
|
UTSW |
5 |
30,902,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Dpysl5
|
UTSW |
5 |
30,953,658 (GRCm39) |
missense |
probably benign |
0.28 |
R8428:Dpysl5
|
UTSW |
5 |
30,902,811 (GRCm39) |
missense |
probably damaging |
0.99 |
R8835:Dpysl5
|
UTSW |
5 |
30,936,282 (GRCm39) |
critical splice donor site |
probably null |
|
R8888:Dpysl5
|
UTSW |
5 |
30,902,687 (GRCm39) |
missense |
probably benign |
0.01 |
R8943:Dpysl5
|
UTSW |
5 |
30,935,375 (GRCm39) |
missense |
probably benign |
0.33 |
R9033:Dpysl5
|
UTSW |
5 |
30,948,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Dpysl5
|
UTSW |
5 |
30,935,397 (GRCm39) |
missense |
probably benign |
0.45 |
R9305:Dpysl5
|
UTSW |
5 |
30,948,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Dpysl5
|
UTSW |
5 |
30,935,399 (GRCm39) |
nonsense |
probably null |
|
R9700:Dpysl5
|
UTSW |
5 |
30,904,417 (GRCm39) |
nonsense |
probably null |
|
Z1176:Dpysl5
|
UTSW |
5 |
30,935,464 (GRCm39) |
missense |
probably benign |
0.01 |
|