Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts5 |
A |
G |
16: 85,666,881 (GRCm39) |
V537A |
possibly damaging |
Het |
Adcy10 |
A |
T |
1: 165,342,949 (GRCm39) |
I272F |
possibly damaging |
Het |
Adcy6 |
A |
G |
15: 98,502,609 (GRCm39) |
S2P |
probably damaging |
Het |
Agap1 |
A |
G |
1: 89,765,528 (GRCm39) |
|
probably null |
Het |
Aldh3a2 |
A |
G |
11: 61,155,928 (GRCm39) |
V116A |
probably benign |
Het |
Ankdd1b |
A |
T |
13: 96,569,913 (GRCm39) |
|
probably null |
Het |
Antxrl |
G |
A |
14: 33,782,906 (GRCm39) |
V233I |
probably damaging |
Het |
Atp8b5 |
A |
G |
4: 43,302,590 (GRCm39) |
I38V |
probably benign |
Het |
Atxn7l2 |
A |
G |
3: 108,115,748 (GRCm39) |
|
probably benign |
Het |
Bfsp2 |
A |
T |
9: 103,357,424 (GRCm39) |
M1K |
probably null |
Het |
Camsap3 |
T |
A |
8: 3,653,968 (GRCm39) |
I520N |
possibly damaging |
Het |
Cenpc1 |
C |
T |
5: 86,161,369 (GRCm39) |
V854I |
possibly damaging |
Het |
Csnk2a1 |
T |
C |
2: 152,099,347 (GRCm39) |
L88S |
probably damaging |
Het |
Dcaf17 |
A |
G |
2: 70,903,517 (GRCm39) |
N171D |
probably damaging |
Het |
Dctn1 |
G |
C |
6: 83,174,490 (GRCm39) |
A1077P |
possibly damaging |
Het |
Dock1 |
T |
C |
7: 134,453,338 (GRCm39) |
|
probably benign |
Het |
Egfr |
A |
T |
11: 16,839,920 (GRCm39) |
I645L |
probably benign |
Het |
Gdpd1 |
T |
G |
11: 86,950,335 (GRCm39) |
K79N |
possibly damaging |
Het |
Ggt5 |
A |
T |
10: 75,445,742 (GRCm39) |
L432F |
probably benign |
Het |
Gm11060 |
A |
G |
2: 104,924,097 (GRCm39) |
T22A |
unknown |
Het |
Gpr132 |
G |
A |
12: 112,815,860 (GRCm39) |
T322I |
possibly damaging |
Het |
Grin1 |
G |
A |
2: 25,182,442 (GRCm39) |
R940* |
probably null |
Het |
Hip1 |
T |
C |
5: 135,467,486 (GRCm39) |
T316A |
probably benign |
Het |
Hnrnpm |
A |
G |
17: 33,885,462 (GRCm39) |
|
probably benign |
Het |
Hsd3b5 |
G |
A |
3: 98,526,846 (GRCm39) |
T200I |
probably benign |
Het |
Hspa9 |
A |
T |
18: 35,071,659 (GRCm39) |
L647H |
probably damaging |
Het |
Itgad |
T |
C |
7: 127,791,309 (GRCm39) |
I727T |
probably benign |
Het |
Kcnma1 |
T |
C |
14: 23,513,268 (GRCm39) |
D522G |
probably damaging |
Het |
Lipf |
C |
T |
19: 33,948,132 (GRCm39) |
|
probably benign |
Het |
Ly6i |
T |
C |
15: 74,854,904 (GRCm39) |
D2G |
possibly damaging |
Het |
Mast1 |
G |
A |
8: 85,647,264 (GRCm39) |
P631L |
probably damaging |
Het |
Mmp1b |
G |
C |
9: 7,386,693 (GRCm39) |
L144V |
probably damaging |
Het |
Msh6 |
A |
G |
17: 88,292,186 (GRCm39) |
S314G |
probably benign |
Het |
Nefm |
A |
G |
14: 68,358,828 (GRCm39) |
L402P |
probably damaging |
Het |
Nrxn2 |
T |
C |
19: 6,531,476 (GRCm39) |
F697S |
probably damaging |
Het |
Or13c7b |
A |
T |
4: 43,820,639 (GRCm39) |
C241S |
probably damaging |
Het |
Pex13 |
A |
G |
11: 23,599,422 (GRCm39) |
I363T |
probably benign |
Het |
Plcb3 |
T |
C |
19: 6,932,414 (GRCm39) |
R1082G |
possibly damaging |
Het |
Psg28 |
A |
T |
7: 18,161,889 (GRCm39) |
S205T |
possibly damaging |
Het |
Pxt1 |
C |
A |
17: 29,153,756 (GRCm39) |
V26L |
possibly damaging |
Het |
Ripk2 |
G |
A |
4: 16,163,239 (GRCm39) |
T53M |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,741,161 (GRCm39) |
V495A |
probably benign |
Het |
Snrpa |
T |
C |
7: 26,892,362 (GRCm39) |
K66R |
probably benign |
Het |
Srgap1 |
T |
A |
10: 121,732,643 (GRCm39) |
E145V |
probably damaging |
Het |
Suz12 |
A |
G |
11: 79,922,939 (GRCm39) |
T694A |
probably benign |
Het |
Tatdn2 |
T |
A |
6: 113,681,288 (GRCm39) |
D440E |
probably benign |
Het |
Tbc1d21 |
A |
G |
9: 58,270,096 (GRCm39) |
|
probably null |
Het |
Tbc1d31 |
T |
A |
15: 57,815,034 (GRCm39) |
Y570* |
probably null |
Het |
Tbc1d32 |
A |
T |
10: 56,053,575 (GRCm39) |
|
probably benign |
Het |
Tdrd5 |
G |
C |
1: 156,087,406 (GRCm39) |
Q839E |
probably benign |
Het |
Tecpr2 |
A |
G |
12: 110,935,387 (GRCm39) |
N1402S |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,953,153 (GRCm39) |
D921G |
probably damaging |
Het |
Tll1 |
A |
G |
8: 64,491,524 (GRCm39) |
V803A |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Trpm4 |
T |
C |
7: 44,966,480 (GRCm39) |
E461G |
probably damaging |
Het |
Zp3 |
T |
A |
5: 136,013,042 (GRCm39) |
I152N |
probably damaging |
Het |
|
Other mutations in Myo5c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Myo5c
|
APN |
9 |
75,150,162 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo5c
|
APN |
9 |
75,196,463 (GRCm39) |
missense |
probably benign |
|
IGL01503:Myo5c
|
APN |
9 |
75,170,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Myo5c
|
APN |
9 |
75,208,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Myo5c
|
APN |
9 |
75,176,864 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01956:Myo5c
|
APN |
9 |
75,150,158 (GRCm39) |
splice site |
probably null |
|
IGL02127:Myo5c
|
APN |
9 |
75,208,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Myo5c
|
APN |
9 |
75,153,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Myo5c
|
APN |
9 |
75,173,442 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03052:Myo5c
|
APN |
9 |
75,159,798 (GRCm39) |
splice site |
probably benign |
|
IGL03179:Myo5c
|
APN |
9 |
75,163,148 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03224:Myo5c
|
APN |
9 |
75,185,525 (GRCm39) |
missense |
probably benign |
0.01 |
Marked
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
pixie
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
PIT4142001:Myo5c
|
UTSW |
9 |
75,191,230 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4431001:Myo5c
|
UTSW |
9 |
75,159,853 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0126:Myo5c
|
UTSW |
9 |
75,176,807 (GRCm39) |
missense |
probably benign |
0.05 |
R0266:Myo5c
|
UTSW |
9 |
75,191,498 (GRCm39) |
splice site |
probably benign |
|
R0345:Myo5c
|
UTSW |
9 |
75,204,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Myo5c
|
UTSW |
9 |
75,192,303 (GRCm39) |
splice site |
probably benign |
|
R0602:Myo5c
|
UTSW |
9 |
75,173,478 (GRCm39) |
splice site |
probably null |
|
R0675:Myo5c
|
UTSW |
9 |
75,185,571 (GRCm39) |
missense |
probably benign |
|
R0798:Myo5c
|
UTSW |
9 |
75,165,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Myo5c
|
UTSW |
9 |
75,178,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Myo5c
|
UTSW |
9 |
75,198,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1072:Myo5c
|
UTSW |
9 |
75,199,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Myo5c
|
UTSW |
9 |
75,193,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Myo5c
|
UTSW |
9 |
75,183,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Myo5c
|
UTSW |
9 |
75,208,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Myo5c
|
UTSW |
9 |
75,174,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R1616:Myo5c
|
UTSW |
9 |
75,203,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Myo5c
|
UTSW |
9 |
75,184,357 (GRCm39) |
missense |
probably benign |
0.09 |
R1800:Myo5c
|
UTSW |
9 |
75,153,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Myo5c
|
UTSW |
9 |
75,180,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Myo5c
|
UTSW |
9 |
75,157,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Myo5c
|
UTSW |
9 |
75,157,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R1897:Myo5c
|
UTSW |
9 |
75,199,523 (GRCm39) |
missense |
probably benign |
0.20 |
R1898:Myo5c
|
UTSW |
9 |
75,204,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Myo5c
|
UTSW |
9 |
75,196,337 (GRCm39) |
unclassified |
probably benign |
|
R2063:Myo5c
|
UTSW |
9 |
75,189,150 (GRCm39) |
missense |
probably benign |
0.19 |
R2230:Myo5c
|
UTSW |
9 |
75,180,888 (GRCm39) |
missense |
probably benign |
|
R2519:Myo5c
|
UTSW |
9 |
75,157,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2520:Myo5c
|
UTSW |
9 |
75,204,931 (GRCm39) |
nonsense |
probably null |
|
R3034:Myo5c
|
UTSW |
9 |
75,193,859 (GRCm39) |
missense |
probably benign |
0.44 |
R3117:Myo5c
|
UTSW |
9 |
75,173,476 (GRCm39) |
critical splice donor site |
probably null |
|
R3432:Myo5c
|
UTSW |
9 |
75,170,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R3751:Myo5c
|
UTSW |
9 |
75,183,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4132:Myo5c
|
UTSW |
9 |
75,159,850 (GRCm39) |
missense |
probably benign |
0.00 |
R4173:Myo5c
|
UTSW |
9 |
75,153,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Myo5c
|
UTSW |
9 |
75,191,224 (GRCm39) |
missense |
probably benign |
0.01 |
R4429:Myo5c
|
UTSW |
9 |
75,201,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4574:Myo5c
|
UTSW |
9 |
75,176,893 (GRCm39) |
missense |
probably benign |
0.00 |
R4791:Myo5c
|
UTSW |
9 |
75,198,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Myo5c
|
UTSW |
9 |
75,152,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Myo5c
|
UTSW |
9 |
75,199,484 (GRCm39) |
missense |
probably damaging |
0.97 |
R4881:Myo5c
|
UTSW |
9 |
75,191,434 (GRCm39) |
missense |
probably benign |
0.00 |
R4900:Myo5c
|
UTSW |
9 |
75,180,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Myo5c
|
UTSW |
9 |
75,204,791 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4966:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
R5057:Myo5c
|
UTSW |
9 |
75,208,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5347:Myo5c
|
UTSW |
9 |
75,202,487 (GRCm39) |
missense |
probably null |
1.00 |
R5399:Myo5c
|
UTSW |
9 |
75,195,356 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5440:Myo5c
|
UTSW |
9 |
75,165,407 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5569:Myo5c
|
UTSW |
9 |
75,180,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5600:Myo5c
|
UTSW |
9 |
75,196,436 (GRCm39) |
missense |
probably benign |
0.00 |
R5606:Myo5c
|
UTSW |
9 |
75,182,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Myo5c
|
UTSW |
9 |
75,180,185 (GRCm39) |
missense |
probably benign |
0.00 |
R5798:Myo5c
|
UTSW |
9 |
75,191,480 (GRCm39) |
missense |
probably benign |
0.04 |
R5865:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.97 |
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
R6143:Myo5c
|
UTSW |
9 |
75,157,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Myo5c
|
UTSW |
9 |
75,180,893 (GRCm39) |
missense |
probably benign |
|
R6253:Myo5c
|
UTSW |
9 |
75,152,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Myo5c
|
UTSW |
9 |
75,182,836 (GRCm39) |
missense |
probably benign |
|
R6307:Myo5c
|
UTSW |
9 |
75,180,198 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6358:Myo5c
|
UTSW |
9 |
75,203,294 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6450:Myo5c
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
R6598:Myo5c
|
UTSW |
9 |
75,153,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6618:Myo5c
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
R6774:Myo5c
|
UTSW |
9 |
75,196,468 (GRCm39) |
missense |
probably benign |
0.05 |
R6865:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
R6996:Myo5c
|
UTSW |
9 |
75,157,746 (GRCm39) |
missense |
probably benign |
0.01 |
R7023:Myo5c
|
UTSW |
9 |
75,208,738 (GRCm39) |
missense |
probably damaging |
0.98 |
R7123:Myo5c
|
UTSW |
9 |
75,196,505 (GRCm39) |
missense |
probably benign |
|
R7250:Myo5c
|
UTSW |
9 |
75,169,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Myo5c
|
UTSW |
9 |
75,176,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7340:Myo5c
|
UTSW |
9 |
75,196,423 (GRCm39) |
missense |
probably benign |
|
R7382:Myo5c
|
UTSW |
9 |
75,211,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Myo5c
|
UTSW |
9 |
75,158,809 (GRCm39) |
splice site |
probably null |
|
R7788:Myo5c
|
UTSW |
9 |
75,186,627 (GRCm39) |
missense |
probably damaging |
0.98 |
R7956:Myo5c
|
UTSW |
9 |
75,159,845 (GRCm39) |
missense |
probably benign |
|
R8082:Myo5c
|
UTSW |
9 |
75,182,793 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8290:Myo5c
|
UTSW |
9 |
75,196,178 (GRCm39) |
missense |
probably benign |
0.01 |
R8406:Myo5c
|
UTSW |
9 |
75,182,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R8481:Myo5c
|
UTSW |
9 |
75,208,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8489:Myo5c
|
UTSW |
9 |
75,180,128 (GRCm39) |
missense |
probably damaging |
0.98 |
R8505:Myo5c
|
UTSW |
9 |
75,153,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8685:Myo5c
|
UTSW |
9 |
75,192,229 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8806:Myo5c
|
UTSW |
9 |
75,150,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Myo5c
|
UTSW |
9 |
75,185,585 (GRCm39) |
missense |
probably benign |
0.10 |
R9323:Myo5c
|
UTSW |
9 |
75,153,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R9639:Myo5c
|
UTSW |
9 |
75,165,477 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Myo5c
|
UTSW |
9 |
75,152,341 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo5c
|
UTSW |
9 |
75,153,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|