Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,899,098 (GRCm39) |
N693K |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,841,454 (GRCm39) |
V845D |
probably damaging |
Het |
Anxa8 |
T |
A |
14: 33,819,896 (GRCm39) |
F269Y |
probably benign |
Het |
Anxa8 |
T |
A |
14: 33,819,897 (GRCm39) |
F295L |
possibly damaging |
Het |
Aox4 |
C |
G |
1: 58,268,025 (GRCm39) |
L202V |
probably damaging |
Het |
Ap3s2 |
A |
G |
7: 79,559,617 (GRCm39) |
V104A |
probably benign |
Het |
Aqp3 |
G |
A |
4: 41,094,843 (GRCm39) |
|
probably benign |
Het |
Arhgef26 |
C |
T |
3: 62,355,680 (GRCm39) |
H751Y |
probably benign |
Het |
Asic4 |
A |
T |
1: 75,446,331 (GRCm39) |
Q291L |
possibly damaging |
Het |
Bap1 |
T |
C |
14: 30,978,681 (GRCm39) |
Y31H |
probably damaging |
Het |
Brf1 |
A |
T |
12: 112,924,759 (GRCm39) |
V655D |
probably damaging |
Het |
Cebpz |
A |
G |
17: 79,238,820 (GRCm39) |
S663P |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,744,693 (GRCm39) |
D357G |
probably benign |
Het |
Cfap36 |
T |
C |
11: 29,194,073 (GRCm39) |
T90A |
probably benign |
Het |
Ciita |
A |
T |
16: 10,330,134 (GRCm39) |
D803V |
probably damaging |
Het |
Clnk |
C |
A |
5: 38,931,951 (GRCm39) |
|
probably benign |
Het |
Cyp46a1 |
A |
G |
12: 108,317,470 (GRCm39) |
N158S |
probably damaging |
Het |
Cyp4f13 |
A |
G |
17: 33,160,080 (GRCm39) |
I98T |
possibly damaging |
Het |
Def8 |
G |
A |
8: 124,183,234 (GRCm39) |
A278T |
probably damaging |
Het |
Dll3 |
T |
A |
7: 28,000,746 (GRCm39) |
D103V |
possibly damaging |
Het |
Dnai1 |
T |
A |
4: 41,629,814 (GRCm39) |
M446K |
possibly damaging |
Het |
Dppa4 |
A |
T |
16: 48,111,425 (GRCm39) |
T85S |
probably benign |
Het |
Eif4g1 |
A |
T |
16: 20,494,095 (GRCm39) |
H57L |
probably damaging |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Fn1 |
T |
A |
1: 71,663,269 (GRCm39) |
Q1073L |
possibly damaging |
Het |
Foxp4 |
T |
C |
17: 48,180,104 (GRCm39) |
D599G |
unknown |
Het |
Frrs1 |
T |
C |
3: 116,675,456 (GRCm39) |
V128A |
possibly damaging |
Het |
Gcfc2 |
G |
A |
6: 81,926,935 (GRCm39) |
D608N |
probably damaging |
Het |
Gm1043 |
T |
C |
5: 37,350,317 (GRCm39) |
|
probably benign |
Het |
Gm5148 |
T |
C |
3: 37,768,926 (GRCm39) |
E98G |
probably benign |
Het |
Gpr141 |
T |
C |
13: 19,936,428 (GRCm39) |
I116V |
probably benign |
Het |
Hic1 |
T |
C |
11: 75,058,169 (GRCm39) |
N240S |
probably damaging |
Het |
Hpx |
G |
A |
7: 105,241,445 (GRCm39) |
T322I |
probably damaging |
Het |
Hs3st4 |
A |
T |
7: 123,996,416 (GRCm39) |
M361L |
probably benign |
Het |
Ifrd1 |
A |
G |
12: 40,257,129 (GRCm39) |
|
probably benign |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Klk1b21 |
T |
A |
7: 43,755,319 (GRCm39) |
C173S |
probably damaging |
Het |
Krt25 |
A |
T |
11: 99,213,524 (GRCm39) |
V65E |
probably benign |
Het |
Lrrc15 |
A |
T |
16: 30,092,267 (GRCm39) |
D357E |
possibly damaging |
Het |
Lrrd1 |
T |
A |
5: 3,901,345 (GRCm39) |
V550E |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,334,540 (GRCm39) |
Y1490H |
probably damaging |
Het |
Macrod1 |
A |
G |
19: 7,174,281 (GRCm39) |
|
probably benign |
Het |
Mcm5 |
T |
A |
8: 75,847,508 (GRCm39) |
V435D |
probably damaging |
Het |
Mctp1 |
C |
T |
13: 76,975,831 (GRCm39) |
R478C |
probably damaging |
Het |
Med10 |
T |
C |
13: 69,959,817 (GRCm39) |
|
probably benign |
Het |
Mrpl4 |
T |
C |
9: 20,919,888 (GRCm39) |
Y280H |
probably benign |
Het |
Msrb3 |
T |
C |
10: 120,687,892 (GRCm39) |
E61G |
probably damaging |
Het |
Myo1c |
T |
C |
11: 75,551,827 (GRCm39) |
Y337H |
possibly damaging |
Het |
Myrfl |
T |
A |
10: 116,685,138 (GRCm39) |
R81W |
probably damaging |
Het |
Neil1 |
T |
C |
9: 57,051,030 (GRCm39) |
|
probably benign |
Het |
Neto2 |
A |
G |
8: 86,367,673 (GRCm39) |
I357T |
possibly damaging |
Het |
Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
Nkx6-3 |
T |
C |
8: 23,643,607 (GRCm39) |
S3P |
probably benign |
Het |
Or52h7 |
A |
T |
7: 104,214,210 (GRCm39) |
I261L |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,512,863 (GRCm39) |
I54T |
possibly damaging |
Het |
Prex2 |
A |
T |
1: 11,355,267 (GRCm39) |
|
probably benign |
Het |
Psapl1 |
T |
A |
5: 36,361,975 (GRCm39) |
V189E |
probably damaging |
Het |
Ptdss2 |
T |
G |
7: 140,735,232 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,307,322 (GRCm39) |
C661R |
probably benign |
Het |
Rpap1 |
T |
C |
2: 119,595,380 (GRCm39) |
|
probably null |
Het |
Rrp1b |
A |
G |
17: 32,279,426 (GRCm39) |
T696A |
probably benign |
Het |
Sacm1l |
T |
A |
9: 123,377,982 (GRCm39) |
H87Q |
probably benign |
Het |
Serpinb11 |
T |
A |
1: 107,305,260 (GRCm39) |
M212K |
probably damaging |
Het |
Tbc1d22a |
C |
A |
15: 86,183,885 (GRCm39) |
T248K |
probably damaging |
Het |
Tcerg1 |
C |
T |
18: 42,701,679 (GRCm39) |
|
probably benign |
Het |
Tpst1 |
T |
A |
5: 130,130,627 (GRCm39) |
H32Q |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,818,600 (GRCm39) |
V1412E |
possibly damaging |
Het |
Usp19 |
C |
A |
9: 108,378,514 (GRCm39) |
P1326Q |
possibly damaging |
Het |
Vmn1r235 |
T |
A |
17: 21,482,596 (GRCm39) |
M307K |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,487,048 (GRCm39) |
T616S |
probably damaging |
Het |
Vps13a |
G |
A |
19: 16,637,863 (GRCm39) |
T2406I |
possibly damaging |
Het |
Zbtb26 |
T |
A |
2: 37,326,053 (GRCm39) |
M328L |
probably benign |
Het |
Zp2 |
A |
G |
7: 119,736,423 (GRCm39) |
F340S |
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 |
R0034:Myo7b
|
UTSW |
18 |
32,093,913 (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 |
|