Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430038I01Rik |
C |
T |
7: 136,989,321 (GRCm39) |
R60Q |
probably benign |
Het |
Angpt4 |
C |
T |
2: 151,771,311 (GRCm39) |
T209I |
probably benign |
Het |
Ap3b1 |
T |
C |
13: 94,616,393 (GRCm39) |
|
probably benign |
Het |
Aplp1 |
A |
C |
7: 30,143,867 (GRCm39) |
V56G |
probably damaging |
Het |
Asns |
G |
A |
6: 7,676,299 (GRCm39) |
P419L |
probably damaging |
Het |
Atxn7 |
A |
T |
14: 14,100,846 (GRCm38) |
H844L |
probably damaging |
Het |
Cd14 |
A |
G |
18: 36,859,288 (GRCm39) |
Y56H |
probably benign |
Het |
Cd300lb |
C |
T |
11: 114,819,225 (GRCm39) |
V135I |
probably damaging |
Het |
Cep152 |
C |
T |
2: 125,425,813 (GRCm39) |
A851T |
probably benign |
Het |
Cfap74 |
C |
T |
4: 155,545,344 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
A |
6: 8,175,708 (GRCm39) |
I47L |
probably benign |
Het |
Dnaaf9 |
T |
C |
2: 130,578,492 (GRCm39) |
H664R |
probably damaging |
Het |
Eef1d |
T |
C |
15: 75,774,808 (GRCm39) |
T200A |
probably benign |
Het |
Exoc1l |
A |
G |
5: 76,664,377 (GRCm39) |
I155M |
probably damaging |
Het |
Faap100 |
A |
T |
11: 120,262,973 (GRCm39) |
M795K |
probably benign |
Het |
Gabpb1 |
C |
T |
2: 126,500,454 (GRCm39) |
R15Q |
possibly damaging |
Het |
Gata4 |
C |
A |
14: 63,438,933 (GRCm39) |
M381I |
probably benign |
Het |
Gm5114 |
A |
G |
7: 39,058,282 (GRCm39) |
S446P |
possibly damaging |
Het |
Gnb1 |
T |
A |
4: 155,636,146 (GRCm39) |
N155K |
probably benign |
Het |
Haspin |
G |
A |
11: 73,029,044 (GRCm39) |
T15M |
probably damaging |
Het |
Heatr5a |
A |
G |
12: 51,971,955 (GRCm39) |
L745P |
probably damaging |
Het |
Kcng3 |
T |
A |
17: 83,895,812 (GRCm39) |
|
probably benign |
Het |
Kif15 |
A |
T |
9: 122,828,350 (GRCm39) |
N887I |
possibly damaging |
Het |
Kif26a |
T |
C |
12: 112,135,397 (GRCm39) |
|
probably benign |
Het |
Kif9 |
G |
A |
9: 110,348,679 (GRCm39) |
C738Y |
probably benign |
Het |
Kifc2 |
G |
T |
15: 76,551,300 (GRCm39) |
C613F |
probably benign |
Het |
Klf12 |
A |
G |
14: 100,224,865 (GRCm39) |
|
probably null |
Het |
Lrp1 |
A |
T |
10: 127,381,520 (GRCm39) |
I3826N |
probably benign |
Het |
Map2k4 |
A |
G |
11: 65,610,437 (GRCm39) |
|
probably benign |
Het |
Or51m1 |
T |
C |
7: 103,578,708 (GRCm39) |
V226A |
probably benign |
Het |
Pax4 |
T |
C |
6: 28,442,448 (GRCm39) |
T285A |
probably benign |
Het |
Pcdhb5 |
A |
G |
18: 37,455,137 (GRCm39) |
N506D |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,367,405 (GRCm39) |
G768S |
probably benign |
Het |
Plb1 |
G |
T |
5: 32,430,457 (GRCm39) |
G138V |
probably benign |
Het |
Poln |
A |
C |
5: 34,272,762 (GRCm39) |
V398G |
possibly damaging |
Het |
Poteg |
A |
G |
8: 27,952,105 (GRCm39) |
|
probably benign |
Het |
Rapgef1 |
C |
A |
2: 29,614,780 (GRCm39) |
|
probably benign |
Het |
Rbm43 |
A |
T |
2: 51,815,722 (GRCm39) |
D166E |
probably benign |
Het |
Rhobtb2 |
T |
C |
14: 70,026,137 (GRCm39) |
T602A |
probably benign |
Het |
Samd3 |
G |
A |
10: 26,147,398 (GRCm39) |
|
probably benign |
Het |
Sbno2 |
A |
C |
10: 79,894,174 (GRCm39) |
|
probably benign |
Het |
Sec1 |
A |
G |
7: 45,328,759 (GRCm39) |
V96A |
probably benign |
Het |
Senp7 |
A |
C |
16: 55,973,933 (GRCm39) |
S385R |
possibly damaging |
Het |
Sgk3 |
T |
C |
1: 9,955,902 (GRCm39) |
V301A |
probably damaging |
Het |
Sgpl1 |
A |
T |
10: 60,938,392 (GRCm39) |
M467K |
probably damaging |
Het |
Slc22a26 |
A |
G |
19: 7,779,618 (GRCm39) |
I66T |
probably benign |
Het |
Stra6 |
G |
A |
9: 58,058,752 (GRCm39) |
|
probably null |
Het |
Tfrc |
T |
A |
16: 32,434,214 (GRCm39) |
|
probably null |
Het |
Tmem30b |
T |
C |
12: 73,592,779 (GRCm39) |
Y112C |
probably damaging |
Het |
Trap1 |
A |
T |
16: 3,886,894 (GRCm39) |
|
probably benign |
Het |
Trpc1 |
A |
G |
9: 95,631,814 (GRCm39) |
S43P |
probably damaging |
Het |
Tsku |
T |
C |
7: 98,001,870 (GRCm39) |
T154A |
possibly damaging |
Het |
Uroc1 |
T |
C |
6: 90,322,292 (GRCm39) |
V272A |
probably damaging |
Het |
Vmn1r69 |
T |
A |
7: 10,314,738 (GRCm39) |
|
probably benign |
Het |
Vmn2r1 |
T |
A |
3: 63,997,435 (GRCm39) |
W364R |
probably damaging |
Het |
Wnk2 |
G |
T |
13: 49,221,556 (GRCm39) |
T377K |
possibly damaging |
Het |
Zfta |
C |
A |
19: 7,397,724 (GRCm39) |
H90Q |
probably damaging |
Het |
Zscan20 |
T |
C |
4: 128,479,455 (GRCm39) |
N1012S |
probably damaging |
Het |
|
Other mutations in Myo7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Myo7b
|
APN |
18 |
32,154,609 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01799:Myo7b
|
APN |
18 |
32,095,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01881:Myo7b
|
APN |
18 |
32,133,320 (GRCm39) |
splice site |
probably benign |
|
IGL01883:Myo7b
|
APN |
18 |
32,131,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Myo7b
|
APN |
18 |
32,134,394 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01980:Myo7b
|
APN |
18 |
32,094,953 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02506:Myo7b
|
APN |
18 |
32,100,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Myo7b
|
APN |
18 |
32,100,014 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02929:Myo7b
|
APN |
18 |
32,127,978 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03149:Myo7b
|
APN |
18 |
32,147,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03335:Myo7b
|
APN |
18 |
32,118,073 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03372:Myo7b
|
APN |
18 |
32,131,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03385:Myo7b
|
APN |
18 |
32,122,630 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Myo7b
|
UTSW |
18 |
32,094,259 (GRCm39) |
missense |
probably benign |
0.17 |
PIT4445001:Myo7b
|
UTSW |
18 |
32,095,405 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4445001:Myo7b
|
UTSW |
18 |
32,092,519 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0138:Myo7b
|
UTSW |
18 |
32,143,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Myo7b
|
UTSW |
18 |
32,147,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Myo7b
|
UTSW |
18 |
32,105,949 (GRCm39) |
missense |
probably benign |
0.00 |
R0312:Myo7b
|
UTSW |
18 |
32,147,390 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0361:Myo7b
|
UTSW |
18 |
32,147,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Myo7b
|
UTSW |
18 |
32,097,439 (GRCm39) |
critical splice donor site |
probably null |
|
R0524:Myo7b
|
UTSW |
18 |
32,146,477 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0645:Myo7b
|
UTSW |
18 |
32,127,962 (GRCm39) |
missense |
probably benign |
0.10 |
R0724:Myo7b
|
UTSW |
18 |
32,138,602 (GRCm39) |
splice site |
probably benign |
|
R0731:Myo7b
|
UTSW |
18 |
32,094,878 (GRCm39) |
splice site |
probably null |
|
R0762:Myo7b
|
UTSW |
18 |
32,116,997 (GRCm39) |
missense |
probably benign |
0.01 |
R0843:Myo7b
|
UTSW |
18 |
32,107,137 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0894:Myo7b
|
UTSW |
18 |
32,133,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0966:Myo7b
|
UTSW |
18 |
32,131,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Myo7b
|
UTSW |
18 |
32,127,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Myo7b
|
UTSW |
18 |
32,116,805 (GRCm39) |
splice site |
probably benign |
|
R1523:Myo7b
|
UTSW |
18 |
32,099,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Myo7b
|
UTSW |
18 |
32,127,962 (GRCm39) |
missense |
probably benign |
0.10 |
R1623:Myo7b
|
UTSW |
18 |
32,133,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Myo7b
|
UTSW |
18 |
32,094,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Myo7b
|
UTSW |
18 |
32,127,950 (GRCm39) |
missense |
probably benign |
|
R1786:Myo7b
|
UTSW |
18 |
32,127,950 (GRCm39) |
missense |
probably benign |
|
R1796:Myo7b
|
UTSW |
18 |
32,119,728 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1907:Myo7b
|
UTSW |
18 |
32,110,052 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2027:Myo7b
|
UTSW |
18 |
32,118,013 (GRCm39) |
missense |
probably benign |
|
R2102:Myo7b
|
UTSW |
18 |
32,133,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Myo7b
|
UTSW |
18 |
32,116,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Myo7b
|
UTSW |
18 |
32,110,096 (GRCm39) |
missense |
probably benign |
0.41 |
R2323:Myo7b
|
UTSW |
18 |
32,104,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R2365:Myo7b
|
UTSW |
18 |
32,147,384 (GRCm39) |
missense |
probably damaging |
0.98 |
R3078:Myo7b
|
UTSW |
18 |
32,100,237 (GRCm39) |
missense |
probably benign |
0.04 |
R3522:Myo7b
|
UTSW |
18 |
32,143,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Myo7b
|
UTSW |
18 |
32,107,165 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3880:Myo7b
|
UTSW |
18 |
32,102,567 (GRCm39) |
missense |
probably damaging |
0.96 |
R4334:Myo7b
|
UTSW |
18 |
32,110,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4343:Myo7b
|
UTSW |
18 |
32,116,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R4497:Myo7b
|
UTSW |
18 |
32,147,282 (GRCm39) |
missense |
probably benign |
0.06 |
R4498:Myo7b
|
UTSW |
18 |
32,147,282 (GRCm39) |
missense |
probably benign |
0.06 |
R4551:Myo7b
|
UTSW |
18 |
32,118,161 (GRCm39) |
missense |
probably benign |
0.01 |
R4593:Myo7b
|
UTSW |
18 |
32,146,428 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4616:Myo7b
|
UTSW |
18 |
32,136,540 (GRCm39) |
splice site |
probably null |
|
R4646:Myo7b
|
UTSW |
18 |
32,127,422 (GRCm39) |
missense |
probably benign |
0.25 |
R4648:Myo7b
|
UTSW |
18 |
32,100,178 (GRCm39) |
splice site |
probably null |
|
R4737:Myo7b
|
UTSW |
18 |
32,131,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Myo7b
|
UTSW |
18 |
32,094,953 (GRCm39) |
missense |
probably benign |
0.00 |
R4790:Myo7b
|
UTSW |
18 |
32,133,158 (GRCm39) |
splice site |
probably null |
|
R4909:Myo7b
|
UTSW |
18 |
32,097,489 (GRCm39) |
missense |
probably benign |
0.01 |
R5027:Myo7b
|
UTSW |
18 |
32,108,265 (GRCm39) |
missense |
probably benign |
0.22 |
R5034:Myo7b
|
UTSW |
18 |
32,104,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Myo7b
|
UTSW |
18 |
32,116,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R5266:Myo7b
|
UTSW |
18 |
32,131,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Myo7b
|
UTSW |
18 |
32,131,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Myo7b
|
UTSW |
18 |
32,116,972 (GRCm39) |
missense |
probably damaging |
0.96 |
R5457:Myo7b
|
UTSW |
18 |
32,104,503 (GRCm39) |
splice site |
probably null |
|
R5540:Myo7b
|
UTSW |
18 |
32,140,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5628:Myo7b
|
UTSW |
18 |
32,107,240 (GRCm39) |
missense |
probably benign |
|
R5815:Myo7b
|
UTSW |
18 |
32,099,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Myo7b
|
UTSW |
18 |
32,101,043 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6137:Myo7b
|
UTSW |
18 |
32,133,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo7b
|
UTSW |
18 |
32,121,602 (GRCm39) |
missense |
probably benign |
0.00 |
R6218:Myo7b
|
UTSW |
18 |
32,092,507 (GRCm39) |
missense |
probably benign |
0.10 |
R6256:Myo7b
|
UTSW |
18 |
32,116,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Myo7b
|
UTSW |
18 |
32,146,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Myo7b
|
UTSW |
18 |
32,131,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Myo7b
|
UTSW |
18 |
32,127,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R6438:Myo7b
|
UTSW |
18 |
32,099,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Myo7b
|
UTSW |
18 |
32,123,322 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7030:Myo7b
|
UTSW |
18 |
32,104,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Myo7b
|
UTSW |
18 |
32,131,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R7210:Myo7b
|
UTSW |
18 |
32,140,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7218:Myo7b
|
UTSW |
18 |
32,114,054 (GRCm39) |
missense |
probably benign |
0.05 |
R7378:Myo7b
|
UTSW |
18 |
32,099,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R7458:Myo7b
|
UTSW |
18 |
32,121,604 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7517:Myo7b
|
UTSW |
18 |
32,146,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R7559:Myo7b
|
UTSW |
18 |
32,116,413 (GRCm39) |
missense |
probably benign |
0.01 |
R7667:Myo7b
|
UTSW |
18 |
32,094,958 (GRCm39) |
missense |
probably benign |
|
R7737:Myo7b
|
UTSW |
18 |
32,147,257 (GRCm39) |
nonsense |
probably null |
|
R7942:Myo7b
|
UTSW |
18 |
32,146,422 (GRCm39) |
missense |
probably damaging |
0.98 |
R8030:Myo7b
|
UTSW |
18 |
32,131,135 (GRCm39) |
missense |
probably damaging |
0.96 |
R8114:Myo7b
|
UTSW |
18 |
32,098,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Myo7b
|
UTSW |
18 |
32,104,408 (GRCm39) |
missense |
probably damaging |
0.96 |
R8341:Myo7b
|
UTSW |
18 |
32,116,979 (GRCm39) |
missense |
probably benign |
0.39 |
R8406:Myo7b
|
UTSW |
18 |
32,092,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Myo7b
|
UTSW |
18 |
32,095,757 (GRCm39) |
missense |
probably benign |
0.00 |
R8517:Myo7b
|
UTSW |
18 |
32,100,244 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8537:Myo7b
|
UTSW |
18 |
32,110,142 (GRCm39) |
missense |
probably benign |
0.08 |
R8546:Myo7b
|
UTSW |
18 |
32,123,201 (GRCm39) |
missense |
probably benign |
0.19 |
R8721:Myo7b
|
UTSW |
18 |
32,140,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Myo7b
|
UTSW |
18 |
32,114,124 (GRCm39) |
missense |
probably benign |
0.03 |
R8841:Myo7b
|
UTSW |
18 |
32,097,490 (GRCm39) |
missense |
probably benign |
0.06 |
R8853:Myo7b
|
UTSW |
18 |
32,119,744 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8960:Myo7b
|
UTSW |
18 |
32,127,299 (GRCm39) |
splice site |
probably benign |
|
R8984:Myo7b
|
UTSW |
18 |
32,099,402 (GRCm39) |
missense |
probably null |
0.68 |
R9356:Myo7b
|
UTSW |
18 |
32,110,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Myo7b
|
UTSW |
18 |
32,093,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9364:Myo7b
|
UTSW |
18 |
32,133,413 (GRCm39) |
missense |
probably benign |
0.12 |
R9405:Myo7b
|
UTSW |
18 |
32,109,356 (GRCm39) |
missense |
probably benign |
0.00 |
R9533:Myo7b
|
UTSW |
18 |
32,108,297 (GRCm39) |
missense |
probably benign |
0.27 |
R9776:Myo7b
|
UTSW |
18 |
32,133,068 (GRCm39) |
missense |
probably benign |
0.45 |
X0027:Myo7b
|
UTSW |
18 |
32,098,689 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo7b
|
UTSW |
18 |
32,114,051 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1177:Myo7b
|
UTSW |
18 |
32,118,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|