Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
C |
A |
17: 46,634,996 (GRCm39) |
V336L |
probably benign |
Het |
Acbd4 |
T |
C |
11: 102,996,194 (GRCm39) |
L165P |
possibly damaging |
Het |
Adam10 |
T |
C |
9: 70,673,236 (GRCm39) |
S456P |
possibly damaging |
Het |
Adgre4 |
T |
C |
17: 56,109,096 (GRCm39) |
F368L |
probably damaging |
Het |
Ahcyl1 |
G |
T |
3: 107,572,834 (GRCm39) |
Y528* |
probably null |
Het |
Aldh3b3 |
G |
A |
19: 4,014,516 (GRCm39) |
V84M |
probably damaging |
Het |
Cdca8 |
C |
T |
4: 124,824,896 (GRCm39) |
G78E |
probably damaging |
Het |
Cry2 |
T |
C |
2: 92,254,899 (GRCm39) |
D152G |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,627,032 (GRCm39) |
Y266C |
probably benign |
Het |
Dkk4 |
T |
C |
8: 23,115,336 (GRCm39) |
F62S |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,427,994 (GRCm39) |
V207I |
probably benign |
Het |
Dthd1 |
T |
C |
5: 63,000,255 (GRCm39) |
C526R |
probably damaging |
Het |
Dubr |
A |
T |
16: 50,552,866 (GRCm39) |
|
noncoding transcript |
Het |
F5 |
T |
C |
1: 163,979,542 (GRCm39) |
|
probably benign |
Het |
Flcn |
A |
C |
11: 59,691,870 (GRCm39) |
W260G |
possibly damaging |
Het |
Fmnl1 |
G |
A |
11: 103,084,562 (GRCm39) |
|
probably null |
Het |
Frem2 |
A |
T |
3: 53,455,056 (GRCm39) |
D2173E |
probably benign |
Het |
Fstl4 |
C |
T |
11: 52,959,477 (GRCm39) |
Q173* |
probably null |
Het |
Gfra3 |
G |
A |
18: 34,823,640 (GRCm39) |
P381S |
unknown |
Het |
Gm28308 |
C |
A |
6: 52,190,291 (GRCm39) |
|
probably benign |
Het |
Gm8730 |
T |
A |
8: 103,592,379 (GRCm39) |
|
noncoding transcript |
Het |
Gzmd |
T |
C |
14: 56,368,683 (GRCm39) |
|
probably null |
Het |
Hexb |
A |
G |
13: 97,317,600 (GRCm39) |
Y366H |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,322,046 (GRCm39) |
H4566L |
probably benign |
Het |
Ifi213 |
G |
A |
1: 173,417,986 (GRCm39) |
T142I |
possibly damaging |
Het |
Kif13b |
T |
A |
14: 65,010,513 (GRCm39) |
C1271S |
probably damaging |
Het |
Krtap9-5 |
G |
T |
11: 99,840,286 (GRCm39) |
C329F |
unknown |
Het |
Larp1 |
G |
T |
11: 57,932,439 (GRCm39) |
G207W |
probably damaging |
Het |
Lfng |
A |
G |
5: 140,600,194 (GRCm39) |
D368G |
probably damaging |
Het |
Mbd5 |
G |
A |
2: 49,148,291 (GRCm39) |
V834I |
possibly damaging |
Het |
Mterf1b |
T |
A |
5: 4,247,263 (GRCm39) |
Y301* |
probably null |
Het |
Myh7b |
T |
C |
2: 155,472,434 (GRCm39) |
I1305T |
possibly damaging |
Het |
Naip2 |
A |
T |
13: 100,285,320 (GRCm39) |
I1292N |
probably damaging |
Het |
Nmral1 |
A |
G |
16: 4,532,422 (GRCm39) |
F130L |
probably damaging |
Het |
Nos1 |
A |
G |
5: 118,017,450 (GRCm39) |
N271S |
probably benign |
Het |
Nrap |
A |
G |
19: 56,374,458 (GRCm39) |
S23P |
probably damaging |
Het |
Or12d16-ps1 |
A |
T |
17: 37,705,662 (GRCm39) |
N77I |
probably damaging |
Het |
Or2aj4 |
A |
T |
16: 19,385,263 (GRCm39) |
Y123* |
probably null |
Het |
Or4e2 |
T |
C |
14: 52,688,671 (GRCm39) |
I267T |
probably benign |
Het |
Or6c210 |
T |
C |
10: 129,496,185 (GRCm39) |
V170A |
probably benign |
Het |
Pkdcc |
C |
G |
17: 83,523,290 (GRCm39) |
C132W |
probably damaging |
Het |
Plekhg6 |
G |
A |
6: 125,350,144 (GRCm39) |
L265F |
probably benign |
Het |
Prkaa1 |
A |
G |
15: 5,208,177 (GRCm39) |
T473A |
probably benign |
Het |
Prpf3 |
G |
A |
3: 95,743,801 (GRCm39) |
Q451* |
probably null |
Het |
Psma5-ps |
T |
A |
10: 85,150,065 (GRCm39) |
|
noncoding transcript |
Het |
Ptprh |
T |
A |
7: 4,600,996 (GRCm39) |
D127V |
possibly damaging |
Het |
Rab36 |
T |
C |
10: 74,877,765 (GRCm39) |
|
probably null |
Het |
Rasa1 |
A |
T |
13: 85,386,282 (GRCm39) |
Y427* |
probably null |
Het |
Rgs11 |
T |
C |
17: 26,423,521 (GRCm39) |
|
probably null |
Het |
Serpinb13 |
C |
T |
1: 106,910,574 (GRCm39) |
S66L |
probably damaging |
Het |
Shank2 |
G |
A |
7: 143,974,342 (GRCm39) |
V1087I |
probably benign |
Het |
Slc39a10 |
A |
C |
1: 46,875,173 (GRCm39) |
M43R |
probably benign |
Het |
Slc40a1 |
T |
A |
1: 45,951,473 (GRCm39) |
Q228L |
probably benign |
Het |
Slc45a1 |
A |
T |
4: 150,722,996 (GRCm39) |
L296Q |
probably benign |
Het |
Stambpl1 |
A |
G |
19: 34,213,691 (GRCm39) |
T307A |
probably benign |
Het |
Stt3a |
T |
C |
9: 36,644,225 (GRCm39) |
T705A |
possibly damaging |
Het |
Tec |
G |
A |
5: 72,980,980 (GRCm39) |
|
probably benign |
Het |
Trp63 |
A |
T |
16: 25,684,012 (GRCm39) |
T300S |
possibly damaging |
Het |
Vmn1r235 |
A |
G |
17: 21,482,623 (GRCm39) |
H316R |
probably benign |
Het |
Vmn2r1 |
A |
G |
3: 64,012,074 (GRCm39) |
H645R |
possibly damaging |
Het |
Wdfy4 |
A |
G |
14: 32,831,505 (GRCm39) |
I907T |
possibly damaging |
Het |
Zcchc10 |
A |
G |
11: 53,218,151 (GRCm39) |
T33A |
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,710,560 (GRCm39) |
V761D |
probably damaging |
Het |
Zfp358 |
T |
C |
8: 3,546,146 (GRCm39) |
|
probably null |
Het |
Zfp661 |
G |
A |
2: 127,419,468 (GRCm39) |
P224L |
probably damaging |
Het |
Zfp937 |
T |
C |
2: 150,078,706 (GRCm39) |
M33T |
probably damaging |
Het |
Zfp955a |
T |
C |
17: 33,461,040 (GRCm39) |
H364R |
probably damaging |
Het |
|
Other mutations in Myo16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Myo16
|
APN |
8 |
10,488,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00567:Myo16
|
APN |
8 |
10,512,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00671:Myo16
|
APN |
8 |
10,411,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00897:Myo16
|
APN |
8 |
10,365,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01458:Myo16
|
APN |
8 |
10,485,853 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Myo16
|
APN |
8 |
10,420,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Myo16
|
APN |
8 |
10,450,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01680:Myo16
|
APN |
8 |
10,322,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01747:Myo16
|
APN |
8 |
10,654,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Myo16
|
APN |
8 |
10,411,088 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02203:Myo16
|
APN |
8 |
10,620,132 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02506:Myo16
|
APN |
8 |
10,440,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02819:Myo16
|
APN |
8 |
10,372,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Myo16
|
APN |
8 |
10,582,990 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02943:Myo16
|
APN |
8 |
10,450,595 (GRCm39) |
splice site |
probably benign |
|
IGL03347:Myo16
|
APN |
8 |
10,426,120 (GRCm39) |
critical splice acceptor site |
probably null |
|
3-1:Myo16
|
UTSW |
8 |
10,488,869 (GRCm39) |
missense |
probably damaging |
0.99 |
P0016:Myo16
|
UTSW |
8 |
10,450,596 (GRCm39) |
splice site |
probably benign |
|
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Myo16
|
UTSW |
8 |
10,619,790 (GRCm39) |
missense |
probably benign |
0.01 |
R0195:Myo16
|
UTSW |
8 |
10,365,538 (GRCm39) |
splice site |
probably benign |
|
R0418:Myo16
|
UTSW |
8 |
10,619,918 (GRCm39) |
missense |
probably benign |
0.01 |
R0576:Myo16
|
UTSW |
8 |
10,612,318 (GRCm39) |
critical splice donor site |
probably null |
|
R0627:Myo16
|
UTSW |
8 |
10,489,689 (GRCm39) |
missense |
probably benign |
0.15 |
R0826:Myo16
|
UTSW |
8 |
10,426,285 (GRCm39) |
splice site |
probably benign |
|
R0835:Myo16
|
UTSW |
8 |
10,322,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Myo16
|
UTSW |
8 |
10,440,183 (GRCm39) |
missense |
probably benign |
0.17 |
R1052:Myo16
|
UTSW |
8 |
10,620,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1180:Myo16
|
UTSW |
8 |
10,446,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Myo16
|
UTSW |
8 |
10,610,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1503:Myo16
|
UTSW |
8 |
10,552,817 (GRCm39) |
missense |
probably benign |
0.44 |
R1733:Myo16
|
UTSW |
8 |
10,492,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R1873:Myo16
|
UTSW |
8 |
10,322,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Myo16
|
UTSW |
8 |
10,372,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2013:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Myo16
|
UTSW |
8 |
10,426,260 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Myo16
|
UTSW |
8 |
10,322,633 (GRCm39) |
missense |
probably benign |
0.08 |
R2214:Myo16
|
UTSW |
8 |
10,488,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2351:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2352:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2357:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2566:Myo16
|
UTSW |
8 |
10,644,820 (GRCm39) |
missense |
probably benign |
0.43 |
R3402:Myo16
|
UTSW |
8 |
10,434,719 (GRCm39) |
missense |
probably benign |
|
R3870:Myo16
|
UTSW |
8 |
10,492,239 (GRCm39) |
missense |
probably benign |
0.25 |
R4080:Myo16
|
UTSW |
8 |
10,612,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Myo16
|
UTSW |
8 |
10,485,869 (GRCm39) |
missense |
probably benign |
0.01 |
R4631:Myo16
|
UTSW |
8 |
10,556,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Myo16
|
UTSW |
8 |
10,485,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Myo16
|
UTSW |
8 |
10,619,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R4852:Myo16
|
UTSW |
8 |
10,423,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Myo16
|
UTSW |
8 |
10,488,892 (GRCm39) |
missense |
probably damaging |
0.98 |
R4993:Myo16
|
UTSW |
8 |
10,526,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R5077:Myo16
|
UTSW |
8 |
10,372,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Myo16
|
UTSW |
8 |
10,526,114 (GRCm39) |
missense |
probably benign |
|
R5170:Myo16
|
UTSW |
8 |
10,619,745 (GRCm39) |
missense |
probably benign |
0.30 |
R5203:Myo16
|
UTSW |
8 |
10,410,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5246:Myo16
|
UTSW |
8 |
10,612,212 (GRCm39) |
nonsense |
probably null |
|
R5517:Myo16
|
UTSW |
8 |
10,610,226 (GRCm39) |
missense |
probably benign |
0.22 |
R5567:Myo16
|
UTSW |
8 |
10,372,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Myo16
|
UTSW |
8 |
10,619,606 (GRCm39) |
missense |
probably benign |
0.01 |
R5749:Myo16
|
UTSW |
8 |
10,463,245 (GRCm39) |
missense |
probably benign |
0.01 |
R6131:Myo16
|
UTSW |
8 |
10,619,877 (GRCm39) |
missense |
probably benign |
|
R6213:Myo16
|
UTSW |
8 |
10,420,963 (GRCm39) |
critical splice donor site |
probably null |
|
R6216:Myo16
|
UTSW |
8 |
10,365,494 (GRCm39) |
missense |
probably benign |
0.01 |
R6240:Myo16
|
UTSW |
8 |
10,420,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6628:Myo16
|
UTSW |
8 |
10,620,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R6935:Myo16
|
UTSW |
8 |
10,619,820 (GRCm39) |
missense |
probably benign |
0.37 |
R6996:Myo16
|
UTSW |
8 |
10,619,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Myo16
|
UTSW |
8 |
10,619,673 (GRCm39) |
missense |
unknown |
|
R7164:Myo16
|
UTSW |
8 |
10,619,585 (GRCm39) |
missense |
unknown |
|
R7255:Myo16
|
UTSW |
8 |
10,549,169 (GRCm39) |
missense |
unknown |
|
R7266:Myo16
|
UTSW |
8 |
10,322,687 (GRCm39) |
missense |
unknown |
|
R7319:Myo16
|
UTSW |
8 |
10,526,185 (GRCm39) |
splice site |
probably null |
|
R7398:Myo16
|
UTSW |
8 |
10,612,183 (GRCm39) |
missense |
unknown |
|
R7442:Myo16
|
UTSW |
8 |
10,322,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Myo16
|
UTSW |
8 |
10,450,589 (GRCm39) |
missense |
unknown |
|
R7539:Myo16
|
UTSW |
8 |
10,411,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7622:Myo16
|
UTSW |
8 |
10,426,238 (GRCm39) |
missense |
unknown |
|
R7794:Myo16
|
UTSW |
8 |
10,619,913 (GRCm39) |
missense |
unknown |
|
R7903:Myo16
|
UTSW |
8 |
10,426,265 (GRCm39) |
missense |
probably null |
|
R8055:Myo16
|
UTSW |
8 |
10,612,186 (GRCm39) |
missense |
unknown |
|
R8078:Myo16
|
UTSW |
8 |
10,612,078 (GRCm39) |
missense |
unknown |
|
R8081:Myo16
|
UTSW |
8 |
10,372,743 (GRCm39) |
missense |
unknown |
|
R8679:Myo16
|
UTSW |
8 |
10,411,042 (GRCm39) |
missense |
unknown |
|
R8700:Myo16
|
UTSW |
8 |
10,463,172 (GRCm39) |
missense |
unknown |
|
R8939:Myo16
|
UTSW |
8 |
10,524,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R8955:Myo16
|
UTSW |
8 |
10,426,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Myo16
|
UTSW |
8 |
10,619,700 (GRCm39) |
missense |
unknown |
|
R9187:Myo16
|
UTSW |
8 |
10,492,233 (GRCm39) |
missense |
unknown |
|
R9219:Myo16
|
UTSW |
8 |
10,492,236 (GRCm39) |
missense |
unknown |
|
R9287:Myo16
|
UTSW |
8 |
10,526,114 (GRCm39) |
missense |
unknown |
|
R9327:Myo16
|
UTSW |
8 |
10,489,705 (GRCm39) |
critical splice donor site |
probably null |
|
R9763:Myo16
|
UTSW |
8 |
10,450,528 (GRCm39) |
missense |
unknown |
|
R9765:Myo16
|
UTSW |
8 |
10,620,401 (GRCm39) |
missense |
probably damaging |
0.97 |
R9790:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
R9791:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
X0066:Myo16
|
UTSW |
8 |
10,426,185 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo16
|
UTSW |
8 |
10,524,691 (GRCm39) |
missense |
unknown |
|
|