Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
Actl9 |
A |
G |
17: 33,653,062 (GRCm39) |
N374S |
probably benign |
Het |
Adam34l |
T |
C |
8: 44,079,508 (GRCm39) |
N239D |
probably damaging |
Het |
Ahcyl2 |
T |
A |
6: 29,768,555 (GRCm39) |
|
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,720,464 (GRCm39) |
M1501T |
probably benign |
Het |
Asb17 |
A |
T |
3: 153,550,175 (GRCm39) |
D69V |
probably damaging |
Het |
Atp13a5 |
T |
C |
16: 29,082,202 (GRCm39) |
Y877C |
probably damaging |
Het |
Atrip |
T |
C |
9: 108,894,271 (GRCm39) |
Q64R |
probably benign |
Het |
Auts2 |
A |
G |
5: 131,505,730 (GRCm39) |
|
probably benign |
Het |
Cacna2d1 |
G |
T |
5: 16,564,068 (GRCm39) |
R893L |
probably damaging |
Het |
Ccdc138 |
C |
T |
10: 58,409,458 (GRCm39) |
R596C |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,288,628 (GRCm39) |
Y353C |
probably damaging |
Het |
Cdon |
T |
C |
9: 35,400,330 (GRCm39) |
Y1015H |
probably damaging |
Het |
Chsy3 |
T |
C |
18: 59,312,543 (GRCm39) |
Y339H |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,136,744 (GRCm39) |
W190R |
probably benign |
Het |
Ddx1 |
A |
T |
12: 13,273,993 (GRCm39) |
I570N |
probably damaging |
Het |
Duox1 |
G |
A |
2: 122,167,798 (GRCm39) |
R1027H |
probably benign |
Het |
Dync1h1 |
C |
T |
12: 110,593,326 (GRCm39) |
Q1198* |
probably null |
Het |
Ecel1 |
G |
A |
1: 87,081,975 (GRCm39) |
S246L |
probably damaging |
Het |
Fam228b |
T |
G |
12: 4,813,042 (GRCm39) |
R109S |
probably damaging |
Het |
Fut9 |
T |
A |
4: 25,799,245 (GRCm39) |
|
probably benign |
Het |
Gm5592 |
A |
G |
7: 40,939,159 (GRCm39) |
R814G |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,897,746 (GRCm39) |
K233E |
probably benign |
Het |
Gramd1c |
A |
G |
16: 43,811,026 (GRCm39) |
Y438H |
probably damaging |
Het |
Gsdmc |
A |
T |
15: 63,673,882 (GRCm39) |
D134E |
possibly damaging |
Het |
Gxylt2 |
A |
G |
6: 100,760,142 (GRCm39) |
I226V |
probably benign |
Het |
Hc |
T |
C |
2: 34,903,544 (GRCm39) |
I1037V |
probably benign |
Het |
Hspa4 |
T |
G |
11: 53,179,950 (GRCm39) |
R69S |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,829,354 (GRCm39) |
S508P |
probably damaging |
Het |
Krt7 |
G |
A |
15: 101,310,428 (GRCm39) |
R25H |
probably benign |
Het |
Lhfpl6 |
T |
A |
3: 52,950,854 (GRCm39) |
S43T |
possibly damaging |
Het |
Lrrc7 |
T |
A |
3: 157,887,217 (GRCm39) |
K394N |
possibly damaging |
Het |
Lypd4 |
A |
T |
7: 24,566,240 (GRCm39) |
L28Q |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,161,481 (GRCm39) |
E798G |
probably benign |
Het |
Mta1 |
T |
A |
12: 113,097,145 (GRCm39) |
|
probably null |
Het |
Mtg2 |
A |
T |
2: 179,725,183 (GRCm39) |
Q132L |
possibly damaging |
Het |
Myh1 |
G |
T |
11: 67,096,874 (GRCm39) |
E382* |
probably null |
Het |
Nckap5 |
A |
T |
1: 125,904,786 (GRCm39) |
F144L |
possibly damaging |
Het |
Nfrkb |
T |
A |
9: 31,300,351 (GRCm39) |
|
probably null |
Het |
Nmt2 |
C |
T |
2: 3,285,429 (GRCm39) |
P5L |
probably benign |
Het |
Nsmf |
T |
C |
2: 24,945,073 (GRCm39) |
|
probably null |
Het |
Oprl1 |
C |
T |
2: 181,360,795 (GRCm39) |
R257C |
probably damaging |
Het |
Or51q1 |
A |
T |
7: 103,628,581 (GRCm39) |
M61L |
probably damaging |
Het |
Or5a1 |
T |
A |
19: 12,097,420 (GRCm39) |
I219F |
probably benign |
Het |
Pcdhgc3 |
T |
A |
18: 37,940,638 (GRCm39) |
N346K |
probably damaging |
Het |
Pcnt |
G |
A |
10: 76,190,911 (GRCm39) |
P2791S |
probably benign |
Het |
Pdia3 |
A |
G |
2: 121,244,620 (GRCm39) |
N11S |
probably benign |
Het |
Pik3c2g |
A |
T |
6: 139,841,928 (GRCm39) |
T778S |
probably benign |
Het |
Pik3ip1 |
T |
A |
11: 3,283,520 (GRCm39) |
I75N |
probably damaging |
Het |
Pla2g4d |
A |
T |
2: 120,112,176 (GRCm39) |
Y118* |
probably null |
Het |
Ppargc1b |
A |
G |
18: 61,440,336 (GRCm39) |
S845P |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 142,905,937 (GRCm39) |
L50* |
probably null |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pxdn |
G |
A |
12: 30,053,140 (GRCm39) |
V926I |
probably benign |
Het |
Rab11fip2 |
A |
T |
19: 59,925,799 (GRCm39) |
N139K |
probably damaging |
Het |
Rcn2 |
T |
A |
9: 55,960,300 (GRCm39) |
M189K |
probably damaging |
Het |
Rev1 |
A |
T |
1: 38,113,570 (GRCm39) |
|
probably benign |
Het |
Rhbg |
C |
A |
3: 88,152,441 (GRCm39) |
G368C |
probably damaging |
Het |
Rnf214 |
A |
G |
9: 45,811,042 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
T |
C |
4: 124,618,959 (GRCm39) |
S307P |
probably benign |
Het |
Slc6a18 |
T |
A |
13: 73,814,442 (GRCm39) |
Y494F |
probably damaging |
Het |
Son |
T |
C |
16: 91,454,552 (GRCm39) |
S1100P |
probably damaging |
Het |
Spag16 |
T |
G |
1: 69,892,511 (GRCm39) |
N97K |
probably benign |
Het |
Tmem192 |
T |
C |
8: 65,412,163 (GRCm39) |
V114A |
possibly damaging |
Het |
Urb1 |
G |
T |
16: 90,553,059 (GRCm39) |
P1901T |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,419,459 (GRCm39) |
T601A |
probably damaging |
Het |
Wdtc1 |
G |
T |
4: 133,036,162 (GRCm39) |
T126K |
possibly damaging |
Het |
Xirp2 |
T |
C |
2: 67,356,014 (GRCm39) |
Y3592H |
possibly damaging |
Het |
Xylt2 |
A |
T |
11: 94,560,842 (GRCm39) |
V232E |
probably damaging |
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 |
R4685:Myo3a
|
UTSW |
2 |
22,412,233 (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 |
|