Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
G |
17: 24,484,949 (GRCm39) |
I1521T |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,740,693 (GRCm39) |
I145N |
probably damaging |
Het |
Ago3 |
C |
A |
4: 126,248,798 (GRCm39) |
|
probably null |
Het |
Agrn |
A |
T |
4: 156,257,297 (GRCm39) |
W1178R |
probably benign |
Het |
Akap3 |
A |
T |
6: 126,843,267 (GRCm39) |
I629L |
probably benign |
Het |
Aknad1 |
T |
G |
3: 108,682,560 (GRCm39) |
Y545* |
probably null |
Het |
Anapc1 |
C |
A |
2: 128,454,930 (GRCm39) |
V1925F |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,799,943 (GRCm39) |
|
probably null |
Het |
Cfap157 |
T |
C |
2: 32,669,413 (GRCm39) |
E294G |
probably damaging |
Het |
Cfd |
G |
A |
10: 79,728,331 (GRCm39) |
G231S |
probably damaging |
Het |
Csf2ra |
A |
G |
19: 61,215,300 (GRCm39) |
V105A |
probably damaging |
Het |
Dhtkd1 |
A |
T |
2: 5,922,591 (GRCm39) |
W523R |
probably damaging |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dnajc22 |
A |
C |
15: 98,999,085 (GRCm39) |
Y90S |
possibly damaging |
Het |
Ebna1bp2 |
A |
G |
4: 118,482,772 (GRCm39) |
K254E |
probably damaging |
Het |
Gfpt1 |
A |
T |
6: 87,033,168 (GRCm39) |
D131V |
probably damaging |
Het |
Gm5460 |
A |
G |
14: 33,763,982 (GRCm39) |
I21V |
unknown |
Het |
H2-T9 |
A |
G |
17: 36,438,686 (GRCm39) |
I235T |
possibly damaging |
Het |
Htr1d |
C |
T |
4: 136,169,664 (GRCm39) |
|
probably benign |
Het |
Kndc1 |
G |
A |
7: 139,516,749 (GRCm39) |
E1570K |
probably damaging |
Het |
Kntc1 |
T |
C |
5: 123,919,789 (GRCm39) |
Y887H |
probably damaging |
Het |
Kti12 |
T |
C |
4: 108,705,679 (GRCm39) |
S198P |
probably benign |
Het |
Mcmdc2 |
A |
T |
1: 10,010,643 (GRCm39) |
I604F |
unknown |
Het |
Mmp8 |
A |
T |
9: 7,563,196 (GRCm39) |
D253V |
probably damaging |
Het |
Muc4 |
T |
C |
16: 32,569,509 (GRCm39) |
S252P |
possibly damaging |
Het |
Ncoa7 |
T |
C |
10: 30,530,435 (GRCm39) |
I749V |
probably benign |
Het |
Nfrkb |
A |
G |
9: 31,325,311 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,904,477 (GRCm39) |
T7166A |
probably benign |
Het |
Obsl1 |
A |
G |
1: 75,466,313 (GRCm39) |
S1472P |
probably damaging |
Het |
Or14j7 |
T |
A |
17: 38,234,567 (GRCm39) |
L37M |
probably benign |
Het |
Or1e20-ps1 |
T |
A |
11: 73,324,536 (GRCm39) |
D172V |
unknown |
Het |
Orc1 |
A |
C |
4: 108,445,884 (GRCm39) |
M1L |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,813,742 (GRCm39) |
S4069T |
possibly damaging |
Het |
Pus1 |
T |
C |
5: 110,921,798 (GRCm39) |
*442W |
probably null |
Het |
Rgma |
A |
C |
7: 73,059,139 (GRCm39) |
D97A |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,746,279 (GRCm39) |
K3834E |
probably benign |
Het |
Sars2 |
T |
C |
7: 28,452,866 (GRCm39) |
V475A |
probably benign |
Het |
Scamp2 |
A |
T |
9: 57,494,385 (GRCm39) |
T253S |
probably benign |
Het |
Skint9 |
C |
T |
4: 112,248,174 (GRCm39) |
W190* |
probably null |
Het |
Spata31d1e |
G |
A |
13: 59,891,254 (GRCm39) |
Q189* |
probably null |
Het |
Sv2b |
C |
T |
7: 74,767,450 (GRCm39) |
V649I |
possibly damaging |
Het |
Synpo2 |
A |
G |
3: 122,906,835 (GRCm39) |
V827A |
probably benign |
Het |
Tiparp |
A |
T |
3: 65,460,948 (GRCm39) |
I646F |
probably damaging |
Het |
Topaz1 |
G |
A |
9: 122,577,480 (GRCm39) |
G130D |
probably damaging |
Het |
Trio |
TACCTTGTTACTGAGCCCTTCTCACCTTCACAGACACCTTGTTACTGAGCCCTTCTCACCTTCACAGATACCTTGTTACTGAGCCCTTCTC |
TACCTTGTTACTGAGCCCTTCTCACCTTCACAGATACCTTGTTACTGAGCCCTTCTC |
15: 27,742,399 (GRCm39) |
|
probably benign |
Het |
Ttll7 |
C |
T |
3: 146,619,051 (GRCm39) |
P319S |
possibly damaging |
Het |
Umodl1 |
T |
A |
17: 31,201,318 (GRCm39) |
F416I |
possibly damaging |
Het |
Vmn2r104 |
T |
C |
17: 20,261,088 (GRCm39) |
D445G |
probably benign |
Het |
Wnk2 |
A |
G |
13: 49,235,462 (GRCm39) |
V651A |
possibly damaging |
Het |
Zbtb21 |
C |
T |
16: 97,751,112 (GRCm39) |
S1057N |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,815,950 (GRCm39) |
C667S |
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 |
R1454:Myo5c
|
UTSW |
9 |
75,170,348 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
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 |
|