Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004P03Rik |
T |
C |
12: 17,057,185 (GRCm39) |
D104G |
probably damaging |
Het |
2810021J22Rik |
T |
C |
11: 58,771,750 (GRCm39) |
S411P |
probably damaging |
Het |
Adcy2 |
T |
C |
13: 68,876,024 (GRCm39) |
R493G |
probably benign |
Het |
Adcy8 |
A |
G |
15: 64,609,287 (GRCm39) |
I874T |
probably benign |
Het |
Ano2 |
G |
T |
6: 125,957,087 (GRCm39) |
E619* |
probably null |
Het |
Apob |
A |
G |
12: 8,056,456 (GRCm39) |
K1613R |
probably benign |
Het |
Arhgef10 |
T |
A |
8: 15,006,963 (GRCm39) |
F476Y |
probably damaging |
Het |
Bmf |
G |
A |
2: 118,377,283 (GRCm39) |
A74V |
probably damaging |
Het |
Cadps |
T |
C |
14: 12,467,139 (GRCm38) |
E925G |
possibly damaging |
Het |
Ccdc162 |
T |
C |
10: 41,557,682 (GRCm39) |
D181G |
possibly damaging |
Het |
Ccdc85c |
A |
T |
12: 108,173,434 (GRCm39) |
C387S |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,374,410 (GRCm39) |
V974A |
possibly damaging |
Het |
Cplx3 |
T |
A |
9: 57,516,483 (GRCm39) |
I407F |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,250,488 (GRCm39) |
F1703S |
probably damaging |
Het |
Dsg3 |
C |
A |
18: 20,672,793 (GRCm39) |
D821E |
probably benign |
Het |
Ecel1 |
G |
T |
1: 87,080,668 (GRCm39) |
|
probably null |
Het |
Edn1 |
A |
T |
13: 42,458,729 (GRCm39) |
|
probably null |
Het |
Egfr |
G |
A |
11: 16,808,980 (GRCm39) |
C58Y |
probably damaging |
Het |
Fam184a |
T |
C |
10: 53,574,596 (GRCm39) |
N282D |
probably benign |
Het |
Fhit |
T |
A |
14: 9,870,091 (GRCm38) |
Q63L |
probably damaging |
Het |
Gabarapl2 |
T |
C |
8: 112,669,150 (GRCm39) |
V36A |
probably benign |
Het |
Glis1 |
T |
C |
4: 107,424,842 (GRCm39) |
V151A |
probably benign |
Het |
Gm12695 |
A |
G |
4: 96,650,217 (GRCm39) |
S210P |
probably damaging |
Het |
Gpat4 |
TAGAAGA |
TAGA |
8: 23,672,865 (GRCm39) |
|
probably benign |
Het |
H2-M10.4 |
G |
A |
17: 36,772,688 (GRCm39) |
A98V |
probably benign |
Het |
Hhat |
C |
A |
1: 192,277,362 (GRCm39) |
G366C |
probably damaging |
Het |
Hydin |
C |
A |
8: 111,189,154 (GRCm39) |
A1186E |
probably damaging |
Het |
Itgb2 |
T |
A |
10: 77,385,937 (GRCm39) |
|
probably null |
Het |
Kank1 |
C |
T |
19: 25,387,398 (GRCm39) |
A329V |
possibly damaging |
Het |
Kdm4b |
T |
A |
17: 56,708,675 (GRCm39) |
S1070T |
probably benign |
Het |
Kyat1 |
A |
G |
2: 30,078,277 (GRCm39) |
Y101H |
probably damaging |
Het |
Map4k5 |
T |
C |
12: 69,858,140 (GRCm39) |
K679R |
probably benign |
Het |
Mill1 |
A |
T |
7: 17,989,853 (GRCm39) |
D45V |
probably damaging |
Het |
Nox4 |
C |
G |
7: 86,946,716 (GRCm39) |
I137M |
probably benign |
Het |
Odf4 |
A |
G |
11: 68,813,665 (GRCm39) |
|
probably null |
Het |
Ostf1 |
A |
T |
19: 18,558,652 (GRCm39) |
D210E |
probably damaging |
Het |
Paxip1 |
A |
T |
5: 27,966,675 (GRCm39) |
|
probably null |
Het |
Pitrm1 |
A |
G |
13: 6,606,578 (GRCm39) |
T211A |
probably benign |
Het |
Pla2g4f |
A |
G |
2: 120,135,496 (GRCm39) |
S393P |
probably damaging |
Het |
Plppr3 |
T |
C |
10: 79,703,359 (GRCm39) |
T42A |
probably damaging |
Het |
Plxna4 |
C |
A |
6: 32,142,779 (GRCm39) |
G1559W |
probably damaging |
Het |
Ppp1r13l |
T |
C |
7: 19,109,308 (GRCm39) |
|
probably null |
Het |
Prex1 |
C |
T |
2: 166,480,252 (GRCm39) |
V163M |
probably damaging |
Het |
Prl6a1 |
A |
G |
13: 27,500,307 (GRCm39) |
T93A |
probably benign |
Het |
Psg16 |
T |
C |
7: 16,824,459 (GRCm39) |
V81A |
probably benign |
Het |
Rbm33 |
A |
T |
5: 28,613,280 (GRCm39) |
|
probably benign |
Het |
Rest |
C |
T |
5: 77,423,090 (GRCm39) |
P298L |
possibly damaging |
Het |
Rhobtb3 |
G |
A |
13: 76,027,051 (GRCm39) |
R441* |
probably null |
Het |
Rims4 |
T |
A |
2: 163,706,914 (GRCm39) |
K155* |
probably null |
Het |
Rps6kb1 |
C |
T |
11: 86,410,713 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
C |
13: 11,707,532 (GRCm39) |
D2835G |
probably damaging |
Het |
Sc5d |
C |
T |
9: 42,169,946 (GRCm39) |
V92I |
probably benign |
Het |
Sell |
A |
T |
1: 163,893,829 (GRCm39) |
I175F |
probably damaging |
Het |
Serpinb6d |
A |
G |
13: 33,855,211 (GRCm39) |
D295G |
probably damaging |
Het |
Sphk1 |
A |
G |
11: 116,426,106 (GRCm39) |
D96G |
probably damaging |
Het |
Spns3 |
A |
T |
11: 72,428,096 (GRCm39) |
V228D |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,469,828 (GRCm39) |
S4500G |
probably damaging |
Het |
Syt9 |
T |
A |
7: 107,035,678 (GRCm39) |
C232S |
possibly damaging |
Het |
Terf1 |
A |
G |
1: 15,889,185 (GRCm39) |
I176V |
possibly damaging |
Het |
Tln2 |
C |
T |
9: 67,209,854 (GRCm39) |
A428T |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,499,711 (GRCm39) |
N321S |
probably benign |
Het |
Tomm40 |
A |
G |
7: 19,435,761 (GRCm39) |
I323T |
probably benign |
Het |
Try5 |
T |
A |
6: 41,288,233 (GRCm39) |
Q240L |
possibly damaging |
Het |
Vmn1r213 |
A |
T |
13: 23,195,800 (GRCm39) |
I128L |
probably benign |
Het |
Vmn2r80 |
T |
C |
10: 79,030,162 (GRCm39) |
F663L |
possibly damaging |
Het |
Znfx1 |
T |
A |
2: 166,880,950 (GRCm39) |
Y278F |
probably damaging |
Het |
Zpbp2 |
A |
G |
11: 98,442,117 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Myo3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01014:Myo3a
|
APN |
2 |
22,337,284 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01307:Myo3a
|
APN |
2 |
22,448,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01413:Myo3a
|
APN |
2 |
22,302,411 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01655:Myo3a
|
APN |
2 |
22,428,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01767:Myo3a
|
APN |
2 |
22,428,033 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01803:Myo3a
|
APN |
2 |
22,245,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01969:Myo3a
|
APN |
2 |
22,302,499 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02043:Myo3a
|
APN |
2 |
22,404,776 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02124:Myo3a
|
APN |
2 |
22,467,538 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02174:Myo3a
|
APN |
2 |
22,337,204 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02649:Myo3a
|
APN |
2 |
22,328,418 (GRCm39) |
missense |
probably benign |
|
IGL02976:Myo3a
|
APN |
2 |
22,434,494 (GRCm39) |
nonsense |
probably null |
|
IGL03328:Myo3a
|
APN |
2 |
22,468,210 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03376:Myo3a
|
APN |
2 |
22,490,086 (GRCm39) |
splice site |
probably benign |
|
lose
|
UTSW |
2 |
22,448,332 (GRCm39) |
nonsense |
probably null |
|
snooze
|
UTSW |
2 |
22,287,445 (GRCm39) |
missense |
probably damaging |
0.99 |
A5278:Myo3a
|
UTSW |
2 |
22,328,464 (GRCm39) |
missense |
probably benign |
0.27 |
PIT4445001:Myo3a
|
UTSW |
2 |
22,434,457 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0008:Myo3a
|
UTSW |
2 |
22,469,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0099:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0103:Myo3a
|
UTSW |
2 |
22,436,360 (GRCm39) |
splice site |
probably benign |
|
R0103:Myo3a
|
UTSW |
2 |
22,436,360 (GRCm39) |
splice site |
probably benign |
|
R0212:Myo3a
|
UTSW |
2 |
22,296,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0282:Myo3a
|
UTSW |
2 |
22,250,409 (GRCm39) |
missense |
probably benign |
0.03 |
R0492:Myo3a
|
UTSW |
2 |
22,328,447 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0498:Myo3a
|
UTSW |
2 |
22,467,441 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0594:Myo3a
|
UTSW |
2 |
22,436,370 (GRCm39) |
splice site |
probably benign |
|
R0609:Myo3a
|
UTSW |
2 |
22,401,110 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0609:Myo3a
|
UTSW |
2 |
22,338,324 (GRCm39) |
missense |
probably benign |
0.29 |
R0827:Myo3a
|
UTSW |
2 |
22,448,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R0968:Myo3a
|
UTSW |
2 |
22,448,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Myo3a
|
UTSW |
2 |
22,434,456 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1301:Myo3a
|
UTSW |
2 |
22,271,906 (GRCm39) |
splice site |
probably benign |
|
R1352:Myo3a
|
UTSW |
2 |
22,328,486 (GRCm39) |
critical splice donor site |
probably null |
|
R1443:Myo3a
|
UTSW |
2 |
22,287,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Myo3a
|
UTSW |
2 |
22,467,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Myo3a
|
UTSW |
2 |
22,467,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1517:Myo3a
|
UTSW |
2 |
22,287,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R1565:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Myo3a
|
UTSW |
2 |
22,455,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Myo3a
|
UTSW |
2 |
22,404,638 (GRCm39) |
missense |
probably benign |
0.03 |
R1822:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Myo3a
|
UTSW |
2 |
22,345,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Myo3a
|
UTSW |
2 |
22,401,054 (GRCm39) |
missense |
probably benign |
|
R1837:Myo3a
|
UTSW |
2 |
22,467,604 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1867:Myo3a
|
UTSW |
2 |
22,404,657 (GRCm39) |
missense |
probably benign |
0.00 |
R1917:Myo3a
|
UTSW |
2 |
22,296,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Myo3a
|
UTSW |
2 |
22,455,008 (GRCm39) |
missense |
probably benign |
0.02 |
R1937:Myo3a
|
UTSW |
2 |
22,401,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Myo3a
|
UTSW |
2 |
22,246,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Myo3a
|
UTSW |
2 |
22,468,140 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2091:Myo3a
|
UTSW |
2 |
22,338,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R2115:Myo3a
|
UTSW |
2 |
22,250,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Myo3a
|
UTSW |
2 |
22,468,186 (GRCm39) |
missense |
probably benign |
0.42 |
R2126:Myo3a
|
UTSW |
2 |
22,468,186 (GRCm39) |
missense |
probably benign |
0.42 |
R2216:Myo3a
|
UTSW |
2 |
22,467,783 (GRCm39) |
missense |
probably benign |
0.00 |
R2413:Myo3a
|
UTSW |
2 |
22,467,924 (GRCm39) |
missense |
probably benign |
0.00 |
R2964:Myo3a
|
UTSW |
2 |
22,345,067 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3196:Myo3a
|
UTSW |
2 |
22,404,679 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3837:Myo3a
|
UTSW |
2 |
22,455,121 (GRCm39) |
splice site |
probably benign |
|
R3905:Myo3a
|
UTSW |
2 |
22,448,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Myo3a
|
UTSW |
2 |
22,455,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R4014:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4015:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4017:Myo3a
|
UTSW |
2 |
22,468,182 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4043:Myo3a
|
UTSW |
2 |
22,338,350 (GRCm39) |
splice site |
probably benign |
|
R4044:Myo3a
|
UTSW |
2 |
22,467,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R4057:Myo3a
|
UTSW |
2 |
22,270,971 (GRCm39) |
missense |
probably benign |
0.01 |
R4192:Myo3a
|
UTSW |
2 |
22,412,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Myo3a
|
UTSW |
2 |
22,345,089 (GRCm39) |
missense |
probably benign |
0.14 |
R4321:Myo3a
|
UTSW |
2 |
22,271,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Myo3a
|
UTSW |
2 |
22,467,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R4398:Myo3a
|
UTSW |
2 |
22,467,854 (GRCm39) |
missense |
probably benign |
|
R4446:Myo3a
|
UTSW |
2 |
22,490,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Myo3a
|
UTSW |
2 |
22,287,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5096:Myo3a
|
UTSW |
2 |
22,464,254 (GRCm39) |
missense |
probably benign |
0.16 |
R5183:Myo3a
|
UTSW |
2 |
22,468,170 (GRCm39) |
missense |
probably benign |
0.05 |
R5458:Myo3a
|
UTSW |
2 |
22,250,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Myo3a
|
UTSW |
2 |
22,448,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5522:Myo3a
|
UTSW |
2 |
22,464,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Myo3a
|
UTSW |
2 |
22,448,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Myo3a
|
UTSW |
2 |
22,467,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:Myo3a
|
UTSW |
2 |
22,412,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Myo3a
|
UTSW |
2 |
22,404,737 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6602:Myo3a
|
UTSW |
2 |
22,467,799 (GRCm39) |
missense |
probably damaging |
0.96 |
R6671:Myo3a
|
UTSW |
2 |
22,299,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R6743:Myo3a
|
UTSW |
2 |
22,366,475 (GRCm39) |
missense |
probably benign |
0.24 |
R6865:Myo3a
|
UTSW |
2 |
22,464,313 (GRCm39) |
missense |
probably benign |
0.00 |
R6961:Myo3a
|
UTSW |
2 |
22,250,369 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Myo3a
|
UTSW |
2 |
22,337,188 (GRCm39) |
missense |
probably benign |
0.04 |
R7215:Myo3a
|
UTSW |
2 |
22,250,378 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7301:Myo3a
|
UTSW |
2 |
22,436,504 (GRCm39) |
critical splice donor site |
probably null |
|
R7318:Myo3a
|
UTSW |
2 |
22,448,332 (GRCm39) |
nonsense |
probably null |
|
R7447:Myo3a
|
UTSW |
2 |
22,436,464 (GRCm39) |
missense |
probably benign |
0.27 |
R7456:Myo3a
|
UTSW |
2 |
22,412,255 (GRCm39) |
missense |
probably benign |
0.08 |
R7528:Myo3a
|
UTSW |
2 |
22,270,925 (GRCm39) |
nonsense |
probably null |
|
R7731:Myo3a
|
UTSW |
2 |
22,287,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Myo3a
|
UTSW |
2 |
22,245,954 (GRCm39) |
missense |
probably damaging |
0.99 |
R8054:Myo3a
|
UTSW |
2 |
22,464,329 (GRCm39) |
missense |
probably benign |
0.00 |
R8140:Myo3a
|
UTSW |
2 |
22,412,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Myo3a
|
UTSW |
2 |
22,287,476 (GRCm39) |
critical splice donor site |
probably null |
|
R8346:Myo3a
|
UTSW |
2 |
22,448,434 (GRCm39) |
critical splice donor site |
probably null |
|
R8421:Myo3a
|
UTSW |
2 |
22,366,935 (GRCm39) |
missense |
probably benign |
0.07 |
R8495:Myo3a
|
UTSW |
2 |
22,401,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R8551:Myo3a
|
UTSW |
2 |
22,337,277 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Myo3a
|
UTSW |
2 |
22,296,607 (GRCm39) |
splice site |
probably benign |
|
R8757:Myo3a
|
UTSW |
2 |
22,448,319 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8759:Myo3a
|
UTSW |
2 |
22,448,319 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8779:Myo3a
|
UTSW |
2 |
22,250,404 (GRCm39) |
nonsense |
probably null |
|
R8828:Myo3a
|
UTSW |
2 |
22,245,864 (GRCm39) |
missense |
probably benign |
0.01 |
R8910:Myo3a
|
UTSW |
2 |
22,464,280 (GRCm39) |
missense |
probably benign |
0.01 |
R8916:Myo3a
|
UTSW |
2 |
22,457,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Myo3a
|
UTSW |
2 |
22,401,074 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9028:Myo3a
|
UTSW |
2 |
22,490,099 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9046:Myo3a
|
UTSW |
2 |
22,448,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R9120:Myo3a
|
UTSW |
2 |
22,436,464 (GRCm39) |
missense |
probably benign |
0.27 |
R9153:Myo3a
|
UTSW |
2 |
22,404,744 (GRCm39) |
missense |
probably benign |
0.02 |
R9191:Myo3a
|
UTSW |
2 |
22,469,841 (GRCm39) |
missense |
probably benign |
0.24 |
R9258:Myo3a
|
UTSW |
2 |
22,467,545 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9436:Myo3a
|
UTSW |
2 |
22,412,235 (GRCm39) |
nonsense |
probably null |
|
R9464:Myo3a
|
UTSW |
2 |
22,232,383 (GRCm39) |
start gained |
probably benign |
|
R9487:Myo3a
|
UTSW |
2 |
22,245,862 (GRCm39) |
missense |
probably benign |
|
R9719:Myo3a
|
UTSW |
2 |
22,436,493 (GRCm39) |
missense |
probably benign |
0.02 |
R9799:Myo3a
|
UTSW |
2 |
22,490,181 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo3a
|
UTSW |
2 |
22,508,152 (GRCm39) |
missense |
possibly damaging |
0.58 |
|