Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco2 |
G |
A |
15: 81,895,285 (GRCm38) |
A97T |
probably damaging |
Het |
Adat1 |
T |
C |
8: 111,979,362 (GRCm38) |
S371G |
probably benign |
Het |
Aoc3 |
T |
G |
11: 101,332,045 (GRCm38) |
I369R |
possibly damaging |
Het |
Apobr |
A |
T |
7: 126,587,522 (GRCm38) |
|
probably null |
Het |
Arhgap12 |
A |
T |
18: 6,111,774 (GRCm38) |
C69S |
probably damaging |
Het |
Astn2 |
A |
G |
4: 66,119,063 (GRCm38) |
|
probably benign |
Het |
Bcas1 |
T |
C |
2: 170,406,821 (GRCm38) |
D60G |
probably damaging |
Het |
Cacnb4 |
T |
A |
2: 52,477,771 (GRCm38) |
D62V |
probably damaging |
Het |
Cbx8 |
C |
A |
11: 119,040,792 (GRCm38) |
R20L |
probably damaging |
Het |
Ccdc92 |
G |
A |
5: 124,836,273 (GRCm38) |
T64M |
probably benign |
Het |
Cps1 |
G |
T |
1: 67,205,199 (GRCm38) |
S1135I |
probably null |
Het |
Eml2 |
G |
A |
7: 19,179,350 (GRCm38) |
R91H |
probably damaging |
Het |
Fbxl3 |
G |
A |
14: 103,082,877 (GRCm38) |
P426L |
probably damaging |
Het |
Fhod3 |
T |
A |
18: 25,110,239 (GRCm38) |
|
probably null |
Het |
Gabrb2 |
T |
C |
11: 42,597,694 (GRCm38) |
I329T |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,723,571 (GRCm38) |
D745E |
possibly damaging |
Het |
Lacc1 |
T |
A |
14: 77,034,030 (GRCm38) |
N239I |
probably damaging |
Het |
Lamb2 |
T |
A |
9: 108,486,798 (GRCm38) |
C1008S |
probably damaging |
Het |
Man2b1 |
G |
A |
8: 85,090,936 (GRCm38) |
V349I |
probably benign |
Het |
Mib1 |
A |
G |
18: 10,811,985 (GRCm38) |
T961A |
possibly damaging |
Het |
Mmp24 |
A |
G |
2: 155,813,988 (GRCm38) |
I449V |
possibly damaging |
Het |
Olfr156 |
A |
G |
4: 43,821,175 (GRCm38) |
F62S |
probably damaging |
Het |
Olfr497 |
T |
A |
7: 108,422,915 (GRCm38) |
C115S |
probably benign |
Het |
Pgr |
A |
G |
9: 8,958,419 (GRCm38) |
E809G |
probably damaging |
Het |
Ppp1r3g |
T |
A |
13: 35,969,620 (GRCm38) |
V341E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,700,653 (GRCm38) |
S1091T |
probably benign |
Het |
Rab44 |
G |
A |
17: 29,139,897 (GRCm38) |
R353K |
probably benign |
Het |
Reck |
G |
A |
4: 43,891,001 (GRCm38) |
M46I |
probably benign |
Het |
Rorb |
G |
T |
19: 18,977,628 (GRCm38) |
S208Y |
possibly damaging |
Het |
Serinc2 |
G |
T |
4: 130,254,054 (GRCm38) |
T410N |
possibly damaging |
Het |
Slc23a2 |
G |
A |
2: 132,056,782 (GRCm38) |
R612* |
probably null |
Het |
Slx4 |
T |
C |
16: 3,994,909 (GRCm38) |
E145G |
probably damaging |
Het |
Spag16 |
A |
G |
1: 70,493,830 (GRCm38) |
D556G |
probably damaging |
Het |
Spopl |
C |
T |
2: 23,517,945 (GRCm38) |
V241M |
probably damaging |
Het |
Ssfa2 |
T |
A |
2: 79,657,820 (GRCm38) |
V749E |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,172,332 (GRCm38) |
F485I |
probably benign |
Het |
Trmo |
C |
T |
4: 46,382,140 (GRCm38) |
V326M |
probably damaging |
Het |
Tssk5 |
T |
C |
15: 76,372,211 (GRCm38) |
D336G |
probably damaging |
Het |
Ttyh2 |
A |
T |
11: 114,710,963 (GRCm38) |
Q471L |
possibly damaging |
Het |
Wdr33 |
A |
C |
18: 31,893,079 (GRCm38) |
Q944H |
unknown |
Het |
Wdr55 |
G |
A |
18: 36,760,395 (GRCm38) |
V37M |
possibly damaging |
Het |
Zbtb18 |
A |
T |
1: 177,447,121 (GRCm38) |
S7C |
probably damaging |
Het |
Zfhx4 |
G |
A |
3: 5,399,620 (GRCm38) |
V1638M |
possibly damaging |
Het |
Zfp81 |
A |
T |
17: 33,334,703 (GRCm38) |
I379N |
possibly damaging |
Het |
|
Other mutations in Myo7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Myo7b
|
APN |
18 |
32,021,556 (GRCm38) |
utr 5 prime |
probably benign |
|
IGL01799:Myo7b
|
APN |
18 |
31,962,770 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01881:Myo7b
|
APN |
18 |
32,000,267 (GRCm38) |
splice site |
probably benign |
|
IGL01883:Myo7b
|
APN |
18 |
31,998,151 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01934:Myo7b
|
APN |
18 |
32,001,341 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01980:Myo7b
|
APN |
18 |
31,961,900 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL02506:Myo7b
|
APN |
18 |
31,967,154 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02704:Myo7b
|
APN |
18 |
31,966,961 (GRCm38) |
missense |
probably benign |
0.13 |
IGL02929:Myo7b
|
APN |
18 |
31,994,925 (GRCm38) |
missense |
probably benign |
0.19 |
IGL03149:Myo7b
|
APN |
18 |
32,014,302 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03335:Myo7b
|
APN |
18 |
31,985,020 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL03372:Myo7b
|
APN |
18 |
31,998,601 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03385:Myo7b
|
APN |
18 |
31,989,577 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4131001:Myo7b
|
UTSW |
18 |
31,961,206 (GRCm38) |
missense |
probably benign |
0.17 |
PIT4445001:Myo7b
|
UTSW |
18 |
31,962,352 (GRCm38) |
missense |
probably damaging |
0.96 |
PIT4445001:Myo7b
|
UTSW |
18 |
31,959,466 (GRCm38) |
missense |
possibly damaging |
0.80 |
R0034:Myo7b
|
UTSW |
18 |
31,960,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R0138:Myo7b
|
UTSW |
18 |
32,010,151 (GRCm38) |
missense |
probably damaging |
1.00 |
R0149:Myo7b
|
UTSW |
18 |
32,014,209 (GRCm38) |
missense |
probably damaging |
1.00 |
R0226:Myo7b
|
UTSW |
18 |
31,972,896 (GRCm38) |
missense |
probably benign |
0.00 |
R0312:Myo7b
|
UTSW |
18 |
32,014,337 (GRCm38) |
missense |
possibly damaging |
0.68 |
R0361:Myo7b
|
UTSW |
18 |
32,014,209 (GRCm38) |
missense |
probably damaging |
1.00 |
R0506:Myo7b
|
UTSW |
18 |
31,964,386 (GRCm38) |
critical splice donor site |
probably null |
|
R0524:Myo7b
|
UTSW |
18 |
32,013,424 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0645:Myo7b
|
UTSW |
18 |
31,994,909 (GRCm38) |
missense |
probably benign |
0.10 |
R0724:Myo7b
|
UTSW |
18 |
32,005,549 (GRCm38) |
splice site |
probably benign |
|
R0731:Myo7b
|
UTSW |
18 |
31,961,825 (GRCm38) |
splice site |
probably null |
|
R0762:Myo7b
|
UTSW |
18 |
31,983,944 (GRCm38) |
missense |
probably benign |
0.01 |
R0843:Myo7b
|
UTSW |
18 |
31,974,084 (GRCm38) |
missense |
possibly damaging |
0.83 |
R0894:Myo7b
|
UTSW |
18 |
32,000,070 (GRCm38) |
missense |
probably damaging |
1.00 |
R0966:Myo7b
|
UTSW |
18 |
31,998,763 (GRCm38) |
missense |
probably damaging |
1.00 |
R1205:Myo7b
|
UTSW |
18 |
31,994,342 (GRCm38) |
missense |
probably damaging |
1.00 |
R1387:Myo7b
|
UTSW |
18 |
31,983,752 (GRCm38) |
splice site |
probably benign |
|
R1523:Myo7b
|
UTSW |
18 |
31,966,876 (GRCm38) |
missense |
probably damaging |
1.00 |
R1544:Myo7b
|
UTSW |
18 |
31,994,909 (GRCm38) |
missense |
probably benign |
0.10 |
R1623:Myo7b
|
UTSW |
18 |
32,000,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R1780:Myo7b
|
UTSW |
18 |
31,961,185 (GRCm38) |
missense |
probably damaging |
1.00 |
R1785:Myo7b
|
UTSW |
18 |
31,994,897 (GRCm38) |
missense |
probably benign |
|
R1786:Myo7b
|
UTSW |
18 |
31,994,897 (GRCm38) |
missense |
probably benign |
|
R1796:Myo7b
|
UTSW |
18 |
31,986,675 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1907:Myo7b
|
UTSW |
18 |
31,976,999 (GRCm38) |
missense |
possibly damaging |
0.89 |
R2027:Myo7b
|
UTSW |
18 |
31,984,960 (GRCm38) |
missense |
probably benign |
|
R2102:Myo7b
|
UTSW |
18 |
31,999,978 (GRCm38) |
missense |
probably damaging |
1.00 |
R2174:Myo7b
|
UTSW |
18 |
31,983,557 (GRCm38) |
missense |
probably damaging |
1.00 |
R2272:Myo7b
|
UTSW |
18 |
31,977,043 (GRCm38) |
missense |
probably benign |
0.41 |
R2323:Myo7b
|
UTSW |
18 |
31,971,345 (GRCm38) |
missense |
probably damaging |
1.00 |
R2365:Myo7b
|
UTSW |
18 |
32,014,331 (GRCm38) |
missense |
probably damaging |
0.98 |
R3078:Myo7b
|
UTSW |
18 |
31,967,184 (GRCm38) |
missense |
probably benign |
0.04 |
R3522:Myo7b
|
UTSW |
18 |
32,010,079 (GRCm38) |
missense |
probably damaging |
1.00 |
R3788:Myo7b
|
UTSW |
18 |
31,974,112 (GRCm38) |
missense |
possibly damaging |
0.95 |
R3880:Myo7b
|
UTSW |
18 |
31,969,514 (GRCm38) |
missense |
probably damaging |
0.96 |
R4334:Myo7b
|
UTSW |
18 |
31,976,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R4343:Myo7b
|
UTSW |
18 |
31,983,627 (GRCm38) |
missense |
probably damaging |
1.00 |
R4498:Myo7b
|
UTSW |
18 |
32,014,229 (GRCm38) |
missense |
probably benign |
0.06 |
R4551:Myo7b
|
UTSW |
18 |
31,985,108 (GRCm38) |
missense |
probably benign |
0.01 |
R4593:Myo7b
|
UTSW |
18 |
32,013,375 (GRCm38) |
missense |
possibly damaging |
0.77 |
R4616:Myo7b
|
UTSW |
18 |
32,003,487 (GRCm38) |
splice site |
probably null |
|
R4646:Myo7b
|
UTSW |
18 |
31,994,369 (GRCm38) |
missense |
probably benign |
0.25 |
R4648:Myo7b
|
UTSW |
18 |
31,967,125 (GRCm38) |
splice site |
probably null |
|
R4737:Myo7b
|
UTSW |
18 |
31,998,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R4765:Myo7b
|
UTSW |
18 |
31,961,900 (GRCm38) |
missense |
probably benign |
0.00 |
R4790:Myo7b
|
UTSW |
18 |
32,000,105 (GRCm38) |
splice site |
probably null |
|
R4909:Myo7b
|
UTSW |
18 |
31,964,436 (GRCm38) |
missense |
probably benign |
0.01 |
R5027:Myo7b
|
UTSW |
18 |
31,975,212 (GRCm38) |
missense |
probably benign |
0.22 |
R5034:Myo7b
|
UTSW |
18 |
31,971,387 (GRCm38) |
missense |
probably damaging |
1.00 |
R5112:Myo7b
|
UTSW |
18 |
31,983,587 (GRCm38) |
missense |
probably damaging |
1.00 |
R5266:Myo7b
|
UTSW |
18 |
31,998,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R5267:Myo7b
|
UTSW |
18 |
31,998,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R5348:Myo7b
|
UTSW |
18 |
31,983,919 (GRCm38) |
missense |
probably damaging |
0.96 |
R5457:Myo7b
|
UTSW |
18 |
31,971,450 (GRCm38) |
splice site |
probably null |
|
R5540:Myo7b
|
UTSW |
18 |
32,007,090 (GRCm38) |
missense |
probably damaging |
1.00 |
R5628:Myo7b
|
UTSW |
18 |
31,974,187 (GRCm38) |
missense |
probably benign |
|
R5815:Myo7b
|
UTSW |
18 |
31,966,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R6062:Myo7b
|
UTSW |
18 |
31,967,990 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6137:Myo7b
|
UTSW |
18 |
31,999,974 (GRCm38) |
missense |
probably damaging |
1.00 |
R6158:Myo7b
|
UTSW |
18 |
31,988,549 (GRCm38) |
missense |
probably benign |
0.00 |
R6218:Myo7b
|
UTSW |
18 |
31,959,454 (GRCm38) |
missense |
probably benign |
0.10 |
R6256:Myo7b
|
UTSW |
18 |
31,983,695 (GRCm38) |
missense |
probably damaging |
1.00 |
R6257:Myo7b
|
UTSW |
18 |
32,013,415 (GRCm38) |
missense |
probably damaging |
1.00 |
R6265:Myo7b
|
UTSW |
18 |
31,998,150 (GRCm38) |
missense |
probably damaging |
1.00 |
R6302:Myo7b
|
UTSW |
18 |
31,994,386 (GRCm38) |
missense |
probably damaging |
0.98 |
R6438:Myo7b
|
UTSW |
18 |
31,966,329 (GRCm38) |
missense |
probably damaging |
1.00 |
R6654:Myo7b
|
UTSW |
18 |
31,990,269 (GRCm38) |
missense |
possibly damaging |
0.46 |
R7030:Myo7b
|
UTSW |
18 |
31,971,573 (GRCm38) |
missense |
probably damaging |
1.00 |
R7090:Myo7b
|
UTSW |
18 |
31,998,712 (GRCm38) |
missense |
probably damaging |
1.00 |
R7210:Myo7b
|
UTSW |
18 |
32,007,102 (GRCm38) |
missense |
probably damaging |
1.00 |
R7218:Myo7b
|
UTSW |
18 |
31,981,001 (GRCm38) |
missense |
probably benign |
0.05 |
R7378:Myo7b
|
UTSW |
18 |
31,966,239 (GRCm38) |
missense |
probably damaging |
1.00 |
R7458:Myo7b
|
UTSW |
18 |
31,988,551 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7517:Myo7b
|
UTSW |
18 |
32,013,267 (GRCm38) |
missense |
probably damaging |
0.99 |
R7559:Myo7b
|
UTSW |
18 |
31,983,360 (GRCm38) |
missense |
probably benign |
0.01 |
R7667:Myo7b
|
UTSW |
18 |
31,961,905 (GRCm38) |
missense |
probably benign |
|
R7737:Myo7b
|
UTSW |
18 |
32,014,204 (GRCm38) |
nonsense |
probably null |
|
R7942:Myo7b
|
UTSW |
18 |
32,013,369 (GRCm38) |
missense |
probably damaging |
0.98 |
R8030:Myo7b
|
UTSW |
18 |
31,998,082 (GRCm38) |
missense |
probably damaging |
0.96 |
R8114:Myo7b
|
UTSW |
18 |
31,965,624 (GRCm38) |
missense |
probably damaging |
1.00 |
R8338:Myo7b
|
UTSW |
18 |
31,971,355 (GRCm38) |
missense |
probably damaging |
0.96 |
R8341:Myo7b
|
UTSW |
18 |
31,983,926 (GRCm38) |
missense |
probably benign |
0.39 |
R8406:Myo7b
|
UTSW |
18 |
31,959,813 (GRCm38) |
missense |
probably damaging |
1.00 |
R8464:Myo7b
|
UTSW |
18 |
31,962,704 (GRCm38) |
missense |
probably benign |
0.00 |
R8517:Myo7b
|
UTSW |
18 |
31,967,191 (GRCm38) |
missense |
possibly damaging |
0.87 |
R8537:Myo7b
|
UTSW |
18 |
31,977,089 (GRCm38) |
missense |
probably benign |
0.08 |
R8546:Myo7b
|
UTSW |
18 |
31,990,148 (GRCm38) |
missense |
probably benign |
0.19 |
R8721:Myo7b
|
UTSW |
18 |
32,007,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R8770:Myo7b
|
UTSW |
18 |
31,981,071 (GRCm38) |
missense |
probably benign |
0.03 |
R8841:Myo7b
|
UTSW |
18 |
31,964,437 (GRCm38) |
missense |
probably benign |
0.06 |
R8853:Myo7b
|
UTSW |
18 |
31,986,691 (GRCm38) |
missense |
possibly damaging |
0.67 |
R8960:Myo7b
|
UTSW |
18 |
31,994,246 (GRCm38) |
splice site |
probably benign |
|
R8984:Myo7b
|
UTSW |
18 |
31,966,349 (GRCm38) |
missense |
probably null |
0.68 |
R9356:Myo7b
|
UTSW |
18 |
31,977,043 (GRCm38) |
missense |
probably damaging |
1.00 |
R9357:Myo7b
|
UTSW |
18 |
31,960,076 (GRCm38) |
missense |
probably damaging |
1.00 |
R9364:Myo7b
|
UTSW |
18 |
32,000,360 (GRCm38) |
missense |
probably benign |
0.12 |
R9405:Myo7b
|
UTSW |
18 |
31,976,303 (GRCm38) |
missense |
probably benign |
0.00 |
R9533:Myo7b
|
UTSW |
18 |
31,975,244 (GRCm38) |
missense |
probably benign |
0.27 |
R9776:Myo7b
|
UTSW |
18 |
32,000,015 (GRCm38) |
missense |
probably benign |
0.45 |
X0027:Myo7b
|
UTSW |
18 |
31,965,636 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Myo7b
|
UTSW |
18 |
31,980,998 (GRCm38) |
missense |
possibly damaging |
0.82 |
Z1177:Myo7b
|
UTSW |
18 |
31,985,056 (GRCm38) |
missense |
probably damaging |
1.00 |
|